p38 Mitogen-Activated Protein Kinases
A mitogen-activated protein kinase subfamily that regulates a variety of cellular processes including CELL GROWTH PROCESSES; CELL DIFFERENTIATION; APOPTOSIS; and cellular responses to INFLAMMATION. The P38 MAP kinases are regulated by CYTOKINE RECEPTORS and can be activated in response to bacterial pathogens.
MAP Kinase Signaling System
An intracellular signaling system involving the MAP kinase cascades (three-membered protein kinase cascades). Various upstream activators, which act in response to extracellular stimuli, trigger the cascades by activating the first member of a cascade, MAP KINASE KINASE KINASES; (MAPKKKs). Activated MAPKKKs phosphorylate MITOGEN-ACTIVATED PROTEIN KINASE KINASES which in turn phosphorylate the MITOGEN-ACTIVATED PROTEIN KINASES; (MAPKs). The MAPKs then act on various downstream targets to affect gene expression. In mammals, there are several distinct MAP kinase pathways including the ERK (extracellular signal-regulated kinase) pathway, the SAPK/JNK (stress-activated protein kinase/c-jun kinase) pathway, and the p38 kinase pathway. There is some sharing of components among the pathways depending on which stimulus originates activation of the cascade.
Mitogen-Activated Protein Kinases
A superfamily of PROTEIN-SERINE-THREONINE KINASES that are activated by diverse stimuli via protein kinase cascades. They are the final components of the cascades, activated by phosphorylation by MITOGEN-ACTIVATED PROTEIN KINASE KINASES, which in turn are activated by mitogen-activated protein kinase kinase kinases (MAP KINASE KINASE KINASES).
Oxidoreductases Acting on Sulfur Group Donors
A malignant neoplasm that may be classified either as a glioma or as a primitive neuroectodermal tumor of childhood (see NEUROECTODERMAL TUMOR, PRIMITIVE). The tumor occurs most frequently in the first decade of life with the most typical location being the cerebellar vermis. Histologic features include a high degree of cellularity, frequent mitotic figures, and a tendency for the cells to organize into sheets or form rosettes. Medulloblastoma have a high propensity to spread throughout the craniospinal intradural axis. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2060-1)
Bence Jones Protein
Fukushima Nuclear Accident
Encyclopedias as Topic
7-Hydroxycoumarins. Substances present in many plants, especially umbelliferae. Umbelliferones are used in sunscreen preparations and may be mutagenic. Their derivatives are used in liver therapy, as reagents, plant growth factors, sunscreens, insecticides, parasiticides, choleretics, spasmolytics, etc.
Molecular Sequence Annotation
Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein.
Phosphatidylinositol 3-kinase and protein kinase C are required for the inhibition of caspase activity by epidermal growth factor. (1/2254)The mechanism by which growth factors exert an anti-apoptotic function on many cell types is not well understood. This issue is addressed in relation to epidermal growth factor (EGF) which inhibits apoptosis induced by staurosporine or wortmannin in an epithelial tumour cell line (CNE-2). The presence of EGF substantially reduced the in vitro Ac-DEVD-AMC hydrolytic activity and almost completely suppressed the intracellular cleavage of poly(ADP-ribose) polymerase in staurosporine- or wortmannin-treated cells. Staurosporine but not wortmannin caused the intracellular proteolytic processing of pro-caspase-3 and this event was transiently inhibited by EGF. Staurosporine-induced apoptosis was not inhibited by EGF in the presence of wortmannin or LY294002. Similarly, EGF failed to inhibit wortmannin-induced apoptosis in the presence of staurosporine, chelerythrine chloride or Go6850. These results suggest that phosphatidylinositol 3-kinase and protein kinase C play a role in the survival function of EGF but the reduction of cellular caspase activity cannot be satisfactorily explained by a lack of pro-caspase-3 activation. (+info)
CPCCOEt, a noncompetitive metabotropic glutamate receptor 1 antagonist, inhibits receptor signaling without affecting glutamate binding. (2/2254)Metabotropic glutamate receptors (mGluRs) are a family of G protein-coupled receptors characterized by a large, extracellular N-terminal domain comprising the glutamate-binding site. In the current study, we examined the pharmacological profile and site of action of the non-amino-acid antagonist 7-hydroxyiminocyclopropan[b]chromen-1a-carboxylic acid ethyl ester (CPCCOEt). CPCCOEt selectively inhibited glutamate-induced increases in intracellular calcium at human mGluR1b (hmGluR1b) with an apparent IC50 of 6.5 microM while having no agonist or antagonist activity at hmGluR2, -4a, -5a, -7b, and -8a up to 100 microM. Schild analysis indicated that CPCCOEt acts in a noncompetitive manner by decreasing the efficacy of glutamate-stimulated phosphoinositide hydrolysis without affecting the EC50 value or Hill coefficient of glutamate. Similarly, CPCCOEt did not displace [3H]glutamate binding to membranes prepared from mGluR1a-expressing cells. To elucidate the site of action, we systematically exchanged segments and single amino acids between hmGluR1b and the related subtype, hmGluR5a. Substitution of Thr815 and Ala818, located at the extracellular surface of transmembrane segment VII, with the homologous amino acids of hmGluR5a eliminated CPCCOEt inhibition of hmGluR1b. In contrast, introduction of Thr815 and Ala818 at the homologous positions of hmGluR5a conferred complete inhibition by CPCCOEt (IC50 = 6.6 microM), i.e., a gain of function. These data suggest that CPCCOEt represents a novel class of G protein-coupled receptor antagonists inhibiting receptor signaling without affecting ligand binding. We propose that the interaction of CPCCOEt with Thr815 and Ala818 of mGluR1 disrupts receptor activation by inhibiting an intramolecular interaction between the agonist-bound extracellular domain and the transmembrane domain. (+info)
Myogenic signaling of phosphatidylinositol 3-kinase requires the serine-threonine kinase Akt/protein kinase B. (3/2254)The oncogene p3k, coding for a constitutively active form of phosphatidylinositol 3-kinase (PI 3-kinase), strongly activates myogenic differentiation. Inhibition of endogenous PI 3-kinase activity with the specific inhibitor LY294002, or with dominant-negative mutants of PI 3-kinase, interferes with myotube formation and with the expression of muscle-specific proteins. Here we demonstrate that a downstream target of PI 3-kinase, serine-threonine kinase Akt, plays an important role in myogenic differentiation. Expression of constitutively active forms of Akt dramatically enhances myotube formation and expression of the muscle-specific proteins MyoD, creatine kinase, myosin heavy chain, and desmin. Transdominant negative forms of Akt inhibit myotube formation and the expression of muscle-specific proteins. The inhibition of myotube formation and the reduced expression of muscle-specific proteins caused by the PI 3-kinase inhibitor LY294002 are completely reversed by constitutively active forms of Akt. Wild-type cellular Akt effects a partial reversal of LY294002-induced inhibition of myogenic differentiation. This result suggests that Akt can substitute for PI 3-kinase in the stimulation of myogenesis; Akt may be an essential downstream component of PI 3-kinase-induced muscle differentiation. (+info)
Autophosphorylation of p110delta phosphoinositide 3-kinase: a new paradigm for the regulation of lipid kinases in vitro and in vivo. (4/2254)Phosphoinositide 3-kinases (PI3Ks) are lipid kinases which also possess an in vitro protein kinase activity towards themselves or their adaptor proteins. The physiological relevance of these phosphorylations is unclear at present. Here, the protein kinase activity of the tyrosine kinase-linked PI3K, p110delta, is characterized and its functional impact assessed. In vitro autophosphorylation of p110delta completely down-regulates its lipid kinase activity. The single site of autophosphorylation was mapped to Ser1039 at the C-terminus of p110delta. Antisera specific for phospho-Ser1039 revealed a very low level of phosphorylation of this residue in cell lines. However, p110delta that is recruited to activated receptors (such as CD28 in T cells) shows a time-dependent increase in Ser1039 phosphorylation and a concomitant decrease in associated lipid kinase activity. Treatment of cells with okadaic acid, an inhibitor of Ser/Thr phosphatases, also dramatically increases the level of Ser1039-phosphorylated p110delta. LY294002 and wortmannin blocked these in vivo increases in Ser1039 phosphorylation, consistent with the notion that PI3Ks, and possibly p110delta itself, are involved in the in vivo phosphorylation of p110delta. In summary, we show that PI3Ks are subject to regulatory phosphorylations in vivo similar to those identified under in vitro conditions, identifying a new level of control of these signalling molecules. (+info)
Inhibition of phosphatidylinositol 3-kinase induces nitric-oxide synthase in lipopolysaccharide- or cytokine-stimulated C6 glial cells. (5/2254)Nitric oxide (NO) produced by inducible nitric-oxide synthase (iNOS) in different cells including brain cells in response to proinflammatory cytokines plays an important role in the pathophysiology of demyelinating and neurodegenerative diseases. The present study underlines the importance of phosphatidylinositol 3-kinase (PI 3-kinase) in the expression of iNOS in C6 glial cells and rat primary astrocytes. Bacterial lipopolysaccharide (LPS) or interleukin-1beta (IL-1beta) was unable to induce the expression of iNOS and the production of NO in rat C6 glial cells. Similarly, wortmannin and LY294002, compounds that inhibit PI 3-kinase, were also unable to induce the expression of iNOS and the production of NO. However, a combination of wortmannin or LY294002 with LPS or IL-1beta induced the expression of iNOS and the production of NO in C6 glial cells. Consistent with the induction of iNOS, wortmannin also induced iNOS promoter-derived chloramphenicol acetyltransferase activity in LPS- or IL-1beta-treated C6 glial cells. The expression of iNOS by LPS in C6 glial cells expressing a dominant-negative mutant of p85alpha, the regulatory subunit of PI 3-kinase, further supports the conclusion that inhibition of PI 3-kinase provides a necessary signal for the induction of iNOS. Next we examined the effect of wortmannin on the activation of mitogen-activated protein (MAP) kinase and nuclear factor NF-kappaB in LPS- or IL-1beta-stimulated C6 glial cells. In contrast to the inability of LPS and IL-1beta alone to induce the expression of iNOS, both LPS and IL-1beta individually stimulated MAP kinase activity and induced DNA binding and transcriptional activity of NF-kappaB. Wortmannin alone was unable to activate MAP kinase and NF-kappaB. Moreover, wortmannin had no effect on LPS- or IL-1beta-mediated activation of MAP kinase and NF-kappaB, suggesting that wortmannin induced the expression of iNOS in LPS- or IL-1beta-stimulated C6 glial cells without modulating the activation of MAP kinase and NF-kappaB. Similar to C6 glial cells, wortmannin also stimulated LPS-mediated expression of iNOS and production of NO in astrocytes without affecting the LPS-mediated activation of NF-kappaB. Taken together, the results from specific chemical inhibitors and dominant-negative mutant expression studies demonstrate that apart from the activation of NF-kappaB, inhibition of PI 3-kinase is also necessary for the expression of iNOS and production of NO. (+info)
Anti-apoptotic signaling of the IGF-I receptor in fibroblasts following loss of matrix adhesion. (6/2254)The type 1 insulin-like growth factor receptor (IGF-IR) is known to protect cells from a variety of apoptotic injuries. In several instances, the anti-apoptotic effect of the wild type IGF-IR is more evident under conditions of anchorage-independence than in cells in monolayer cultures. We have investigated IGF-IR signaling in cells in anoikis, a form of apoptosis that occurs when cells are denied attachment to the extra-cellular matrix. IGF-I protects mouse embryo fibroblasts (MEF) from anoikis caused by withdrawal of growth factors. Survival is dependent on the concentration of IGF-I and a sufficient number of functional IGF-I receptors. In this model, IGF-I protection correlates best with ras activation and cell-to-cell aggregation, while PI3-kinase, Akt and MAP kinases seem to play a lesser, alternative role. (+info)
Insulin-like growth factor-1-mediated neuroprotection against oxidative stress is associated with activation of nuclear factor kappaB. (7/2254)The role of insulin-like growth factor 1 (IGF-1) for the treatment of neurodegenerative disorders, such as Alzheimer's disease, has recently gained attention. The present study demonstrates that IGF-1 promotes the survival of rat primary cerebellar neurons and of immortalized hypothalamic rat GT1-7 cells after challenge with oxidative stress induced by hydrogen peroxide (H2O2). Neuroprotective concentrations of IGF-1 specifically induce the transcriptional activity and the DNA binding activity of nuclear factor kappaB (NF-kappaB), a transcription factor that has been suggested to play a neuroprotective role. This induction is associated with increased nuclear translocation of the p65 subunit of NF-kappaB and with degradation of the NF-kappaB inhibitory protein IkappaBalpha. IGF-1-mediated protection of GT1-7 cells against oxidative challenges was mimicked by overexpression of the NF-kappaB subunit c-Rel. Partial inhibition of NF-kappaB baseline activity by overexpression of a dominant-negative IkappaBalpha mutant enhanced the toxicity of H2O2 in GT1-7 cells. The pathway by which IGF-1 promotes neuronal survival and activation of NF-kappaB involves the phosphoinositol (PI) 3-kinase, because both effects of IGF-1 are blocked by LY294002 and wortmannin, two specific PI 3-kinase inhibitors. Taken together, our results provide evidence for a novel molecular link between IGF-1-mediated neuroprotection and induction of NF-kappaB that is dependent on the PI 3-kinase pathway. (+info)
Requirement of phosphatidylinositol 3-kinase activity for bradykinin stimulation of NF-kappaB activation in cultured human epithelial cells. (8/2254)The signaling mechanisms utilized by bradykinin (BK) to activate the transcription factor nuclear factor kappaB (NF-kappaB) are poorly defined. We previously demonstrated that BK-stimulated NF-kappaB activation requires the small GTPase RhoA. We present evidence that BK-induced NF-kappaB activation both activates and requires phosphatidylinositol 3-kinase (PI 3-kinase) in A549 human epithelial cells. Pre-treatment with the PI 3-kinase-specific inhibitors, wortmannin, and LY294002 effectively blocked BK-induced PI 3-kinase activity. Wortmannin and LY294002 also abolished BK-induced NF-kappaB activation, as did transient transfection with a dominant negative mutant of the p85 subunit. BK-stimulated PI 3-kinase activity and NF-kappaB activation were sensitive to pertussis but not cholera toxin, suggesting that the B2 BK receptors transducing the response were coupled to Galphai or Galphao heterotrimeric G proteins. Tumor necrosis factor alpha (TNFalpha) also stimulated increased PI 3-kinase activity, however TNFalpha-stimulated NF-kappaB activation was not affected by the PI 3-kinase inhibitors or the p85 dominant negative mutant. These findings provide evidence that BK-induced NF-kappaB activation utilizes a signaling pathway that requires activity of both RhoA and PI 3-kinase and is distinct from the signaling pathway utilized by TNFalpha. Furthermore, we show that the p85 regulatory subunit is required for activation of PI 3-kinase activity by this G protein-coupled receptor. (+info)
Domino reactions of 2-methyl chromones containing an electron withdrawing group with chromone-fused dienes - PDF Free Download
Domino reactions of 2-methyl chromones containing an electron withdrawing group with chromone-fused dienes Jian Gong, Fuchun Xie, Wenming Ren, Hong Chen and Youhong Hu* State Key Laboratory of Drug Research,
pranlukast hydrate nanopowder dispersion
Page contains details about pranlukast hydrate nanopowder dispersion . It has composition images, properties, Characterization methods, synthesis, applications and reference articles : nano.nature.com
Effect of PI 3-K inhibitors on apoptosis in HEC 1-A, RL | Open-i
Effect of PI 3-K inhibitors on apoptosis in HEC 1-A, RL 95-2 and Ishikawa cells. Control (■), LY294002 (○) and Wortmannin (▲). 2 × 106 cells were plated
銀河系 - 維基百科，自由的百科全書
銀河系包含的恆星數量在2,000億至4,000億顆之間，還有至少1,000億顆的行星。確切的數值取決於質量非常低的恆星，這些恆星很難檢測得到，特別是距離太陽超過300 ly（90 ...
1H-2-Benzopyran-1-one - Alfa Chemistry
Alfa Chemistry is the worlds leading provider for special chemicals. We offer qualified products for 491-31-6(1H-2-Benzopyran-1-one),please inquire us for 491-31-6(1H-2-Benzopyran-1-one).
LY 2584702 tosylate | S6K1 inhibitor | LY 2779964 | LY2584702 | CAS [1082949-68-5] - [1082949-67-4] | Axon 2464 | Axon Ligand™...
LY 2584702 tosylate | S6K1 inhibitor | LY 2779964 | LY2584702 | LY2779964 | CAS [1082949-68-5] - [1082949-67-4] | Axon 2464 | Axon Ligand™ with >98% purity available from supplier Axon Medchem, prime source of life science reagents for your research
The multi-faceted roles of the PI3K-AKT pathway in melanoma - pdf descargar
The multi-faceted roles of the PI3K-AKT pathway in melanoma. . Biblioteca virtual para leer y descargar libros, documentos, trabajos y tesis universitarias en PDF. Material universiario, documentación y tareas realizadas por universitarios en nuestra biblioteca. Para descargar gratis y para leer online.
LY 294002 | PI3K inhibitor | LY294002 | CAS [154447-36-6] | Axon 1366 | Axon Ligand™ with |99% purity available from stock from...
LY 294002 | PI3K inhibitor | LY294002 | CAS [154447-36-6] | Axon 1366 | Axon Ligand™ with >99% purity available from supplier Axon Medchem, prime source of life science reagents for your research
PTMScan Direct PI3K / Akt Proteomic Service | CST
Information and case study data for the PTMScan Direct PI3K / Akt Service offered by CST, which allows for targeted screening of 105 proteins within the Akt pathway.
LY2140023 | LY404039 Prodrug | MCE
LY2140023 是一种口服有效的 LY404039 的前药。LY404039 是一种选择性的代谢型谷氨酸 2/3 受体激动剂。LY2140023 有用于精神分裂症的潜力。- 高纯度，全球文献引用。
Impact of the phosphatidylinositide 3-kinase signaling pathway on the cardioprotection induced by intermittent hypoxia |...
BACKGROUND: Exposure to intermittent hypoxia (IH) may enhance cardiac function and protects heart against ischemia-reperfusion (I/R) injury. To elucidate the underlying mechanisms, we developed a cardioprotective IH model that was characterized at hemodynamic, biochemical and molecular levels. METHODS: Mice were exposed to 4 daily IH cycles (each composed of 2-min at 6-8% O2 followed by 3-min reoxygenation for 5 times) for 14 days, with normoxic mice as controls. Mice were then anesthetized and subdivided in various subgroups for analysis of contractility (pressure-volume loop), morphology, biochemistry or resistance to I/R (30-min occlusion of the left anterior descending coronary artery (LAD) followed by reperfusion and measurement of the area at risk and infarct size). In some mice, the phosphatidylinositide 3-kinase (PI3K) inhibitor wortmannin was administered (24 µg/kg ip) 15 min before LAD. RESULTS: We found that IH did not induce myocardial hypertrophy; rather both contractility and ...
Chromones | REACH
Suryo Rahmanto A, Savov V, Brunner A, Bolin S, Weishaupt H, Malyukova A, Rosén G, Cancer M, Hutter S, Sundström A, Kawauchi D, Jones DT, Spruck C, Taylor MD, Cho YJ, Pfister SM, Kool M, Korshunov A, Swartling FJ, Sangfelt O. FBW7 suppression leads to SOX9 stabilization and increased malignancy in medulloblastoma. EMBO J. 2016 10 17; 35(20):2192-2212 ...
5-Methyl-7-oxo-3-phenyl-7H-furo[3,2-g]chromen-6-yl)-acetic acid | 664366-11-4
(5-Methyl-7-oxo-3-phenyl-7H-furo[3,2-g]chromen-6-yl)-acetic acid에 대한 모든 정보는 Chemicalbook 에서 조회 할 수 있습니다.포함:구조식 이미지,카스 번호(CAS),분자식,녹는점,끓는 점,밀도,가격,공급자,MSDS(SDS),GHS,사용,독성,HS세관 코드.온라인 구매 지원.
ChemIDplus - 81816-68-4 - CCULRDJFKNULHF-UHFFFAOYSA-N - Piperazine, 1-(3,4-dihydro-2H-1-benzopyran-4-yl)-4-(2-methoxyphenyl)- -...
81816-68-4 - CCULRDJFKNULHF-UHFFFAOYSA-N - Piperazine, 1-(3,4-dihydro-2H-1-benzopyran-4-yl)-4-(2-methoxyphenyl)- - Similar structures search, synonyms, formulas, resource links, and other chemical information.
TRC | Details of CAS = 105300-40-1, ChemicalName = rac-6-Fluoro-3,4-dihydro-4-oxo-2H-1-benzopyran-2-carboxylic Acid, synonym =...
Buy high quality rac-6-Fluoro-3,4-dihydro-4-oxo-2H-1-benzopyran-2-carboxylic Acid 105300-40-1 from toronto research chemicals Inc.
PI3K inhibitors block L. pneumophila entry into host ce | Open-i
PI3K inhibitors block L. pneumophila entry into host cells.Murine J774A.1 (A, B) that were treated or not treated with different concentrations of LY294002 or (
PKS BLAST table : Aureo 00030
In vitro reconstitution and crystal structure of p-aminobenzoate N-oxygenase (AurF) involved in aureothin biosynthesis.(Proc. Natl. Acad. Sci. U.S.A.)  ...
DGIdb - PRANLUKAST Drug Record
DGIdb, The Drug Gene Interaction Database, is a research resource that can be used to search candidate genes or drugs against the known and potentially druggable genome.
7-(2-Fluorobenzyl)-1,3-dimethyl-8-(4-morpholinyl)-3,7-dihydro-1H-purine-2,6-dione | C18H20FN5O3 | ChemSpider
Structure, properties, spectra, suppliers and links for: 7-(2-Fluorobenzyl)-1,3-dimethyl-8-(4-morpholinyl)-3,7-dihydro-1H-purine-2,6-dione.
Accela Chembio Inc N-METHYL-4-(4-MORPHOLINYL 1G N-METHYL-4-(4-MORPHOLINYL | Fisher Scientific
Shop a large selection of products and learn more about Accela Chembio Inc N-METHYL-4-(4-MORPHOLINYL 1G N-METHYL-4-(4-MORPHOLINYL .
CAS # 480-37-5, Pinostrobin, (S)-2,3-Dihydro-5-hydroxy-7-methoxy-2-phenyl-4H-1-benzopyran-4-one, 5-Hydroxy-7-methoxyflavanone,...
chemBlink provides information about CAS # 480-37-5, Pinostrobin, (S)-2,3-Dihydro-5-hydroxy-7-methoxy-2-phenyl-4H-1-benzopyran-4-one, 5-Hydroxy-7-methoxyflavanone, 5-Hydroxy-7-methoxy-2-phenyl-chroman-4-one, molecular formula: C16H14O4.
2H-1-Benzopyran-2-one,4,6-dihydroxy-3-(3-oxo-1-phenylbutyl)- - Alfa Chemistry
2H-1-Benzopyran-2-one,4,6-dihydroxy-3-(3-oxo-1-phenylbutyl)-/ACM17834025 can be provided in Alfa Chemistry. We are dedicated to provide our customers the best products and services.
Pişika mirovî - Wîkîpediya
Cotek pişikên mirov heye, di nav singekelênê de. Pişik bi şeweya qoçekî ne. Aliyê jorê pişikê zirav û glover e, binê pişikê fireh û çal e û li ser qoqiza navpençikê de cih bû ye. Dilê mirov di navbera herdu pişikan, nezikê pişika çepê de cih digire. Loma pişika çepê ji ya rastê piçûktir e. Pişka rastê sê pil, pişka çepê du pil e. Her pilên(bi îngilîzî:lobe) pişkê jî di nav pişikê de dabeş dibin boy pilên hê hûriktir ên bi navê pilok( bi îngilîzî: lobule). Dora pişikan bi perasûyan û navpençikê dagirtî ye. Pişik pêkhateyek nerm e, dişibe îsfencê û hertim bi hewayê tijî ye. Pişik rasterast bi singekelênê ve giridayî nin in, derveyê pişikan bi perdeya pilûr ve dapoşî ye. Perdeya pilûr ji du çînan pêk tê. Çînek pilûrê bi pişikan ve, çîna din jî bi diwarê singekelên û navpençikê ve girêdayî ye. Valahiya navbera çînên pilûrê, wekî kelêna pilûr bi nav dibe. Xaneyên pilûrê, ...
Antibiotic SL 2052
3H-Furo[4,3,2-de]indeno[4,5-h]-2-benzopyran-3,6,9-trione, 11-(acetyloxy)-1,6b,7,8,9a,10,11,11b-octahydro-1-(methoxymethyl)-9a,11b-dimethyl-, (1S,6bR,9aS,11R,11bR ...
اثر فاز اول درمان پریودنتال بر سطح سرمی آنتی بادی ضد کاردیولیپین در بیماران مبتلا به پریودنتیت مزمن
مقدمه: با توجه به ارتباط بین دهان و دندان و بیماریهای سیستمیک و نقش قطعی عفونتهای دهان و دندان در فرآیندهای پاتولوژیک در نقاط دیگر بدن، هدف از مطالعه حاضر بررسی اثر درمان غیر جراحی پریودنتال بر سطح سرمی آنتی بادی ضد کاردیولیپین (aCLA) است که به طور بالقوه در پاتوژنز بیماری های قلبی عروقی در بیماران پریودنتال نقش دارد.مواد و روش: بیست داوطلب (11 زن و 9 مرد) با میانگین سنی 55/40 سال در این مطالعه شرکت کردند. پریودنتیت مزمن با معاینه کامل پریودنتال تشخیص داده شد. این معاینات شامل اندازه گیری عمق پاکت (PD) و از دست رفتن چسبندگی (AL)، همچنین شاخص پلاک (PI) و شاخص لثه ای (GI) بود
Influence of phosphorohydrazone derivatives of benzopyrones on polymerization and viscosity of fibrin - Acta Biochimica...
The synthesis and antitumour and antibacterial activity of coumarin and chromone phosphorohydrazones have been reported. This study describes influence of phosphorohydrazones derivatives of coumarin and chromone on the polymerization and viscosity of fibrin. The fibrin polymerization assay was performed by the Shen and Lorand method and the clot viscosity was measured on the basis of Shen and Lorand and Marchi and coworkers methods. Among the eight compounds tested, one coumarin derivative and two chromone derivatives showed significant activity ...
The Toxoplasma Blog: Intracellular Networks of the PI3K/AKT and MAPK Pathways for Regulating Toxoplasma gondii-Induced IL-23...
Interleukin (IL)-23 and IL-12 are closely related in structure, and these cytokines regulate both innate and adaptive immunity. However, the precise signaling networks that regulate the production of each in Toxoplasma gondii-infected THP-1 monocytic cells, particularly the PI3K/AKT and MAPK signaling pathways, remain unknown. In the present study, T. gondii infection upregulated the expression of IL-23 and IL-12 in THP-1 cells, and both cytokines increased with parasite dose. IL-23 secretion was strongly inhibited by TLR2 monoclonal antibody (mAb) treatment in a dose-dependent manner and by TLR2 siRNA transfection, whereas IL-12 secretion was strongly inhibited by TLR4 mAb treatment dose-dependently and by TLR4 siRNA transfection. IL-23 production was dose-dependently inhibited by the PI3K inhibitors LY294002 and wortmannin, whereas IL-12 production increased dose-dependently. THP-1 cells exposed to live T. gondii tachyzoites underwent rapid p38 MAPK, ERK1/2 and JNK activation. IL-23 production ...
4-Hydroxy-3-(3-oxo-1-phenylbutyl)-2H-1-benzopyran-2-one, CAS Number: 81-81-2
4-Hydroxy-3-(3-oxo-1-phenylbutyl)-2H-1-benzopyran-2-one - chemical information, properties, structures, articles, patents and more chemical data.
NU7441 | KU-57788 | CAS#503468-95-9 | PI3K inhibitor | MedKoo Biosciences
NU7441, also known as KU-57788, is a highly potent and selective DNA-PK inhibitor (IC50=14 nM), exhibiting ATP-competitive inhibition kinetics. NU7441 increased the cytotoxicity of ionizing radiation and etoposide in SW620, LoVo, and V3-YAC cells but not in V3 cells, confirming that potentiation was due to DNA-PK inhibition. NU7441 substantially retarded the repair of ionizing radiation-induced and etoposide-induced DSB.
Focusing on PTEN Research in Cancer | OncologyPRO
Understanding of mechanisms of resistance to PI3K inhibitors is of paramount importance. PTEN is a major negative regulator of PI3K pathway.
蛋白激酶B - 维基百科，自由的百科全书
Akt1通过抑制凋亡过程从而参与细胞存活途径。Akt1亦能诱导蛋白合成通路，故其在导致骨骼肌肥大及的一般组织生长的细胞通路中是一种重要信号蛋白。因其可以阻断凋亡并继而促进细胞存活，现已表明Akt1在多种肿瘤中起到主要作用。Akt（先亦被称为Akt1）首先是在转化逆转录病毒AKT8中被鉴定为癌基因的。 Akt2在胰岛素信号通路中是一重要的信号分子。需要其来诱导葡萄糖转运。在敲除Akt1但具正常Akt2的小鼠中，血糖稳态不受干扰，但动物体型会较小，这与Akt1在生长中起得作用是一致的。相反，Akt2缺失但具有正常Akt1的的小鼠生长略缺陷且表现出糖尿病表型（胰岛素抵抗），这从另一方面印证了Akt2对胰岛素受体信号通路更具特异性的这一设想。 Akt3似乎主要在脑中表达，但其作用仍未明晰。有报道显示Akt3缺失的小鼠脑部较小。 ...
白小姐救世香港赛马会中特玄机图 【2107年马报资料】 | 0pi3s.cvaps.cn contacts
描述. Reviews, coupons, analysis, whois, global ranking and traffic for 0pi3s.cvaps.cn. Learn more about 0pi3s OR 0pi3s.cvaps.cn. Is 0pi3s.cvaps.cn a scam or a fraud? Coupon for 0pi3s.cvaps.cn
Akt | 陶素生化
Anti- phosphatidylinositol-3-phosphate/phosphatidylinositol 5-kinase, III PAb | Technique alternative | 02012560599 -...
Order Anti-human phosphatidylinositol-3-phosphate phosphatidylinositol 5-kinase type III PAb 02012560599 at Gentaur phosphatidylinositol-3-phosphate/phosphatidylinositol 5-kinase, III PAb
Isopropyl [(2-hexyl-6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy]acetate | C24H32O5 | ChemSpider
Structure, properties, spectra, suppliers and links for: Isopropyl [(2-hexyl-6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy]acetate.
ChemIDplus - 60595-60-0 - KJRCVOWXLZJQKW-UHFFFAOYSA-N - 4H-1-Benzopyran-4-one, 2,5,8-trimethyl- - Similar structures search,...
60595-60-0 - KJRCVOWXLZJQKW-UHFFFAOYSA-N - 4H-1-Benzopyran-4-one, 2,5,8-trimethyl- - Similar structures search, synonyms, formulas, resource links, and other chemical information.
Haplotype: (AKT1_1251C,T) - ( AKT1_IVS14+32G,A) - ( AKT1_IVS14+66C,G) - ( AKT1_IVS14+93C,T) - ( AKT1_IVS+95-98delCTCA)(C-G-C-C-del), (AKT1_1251C,T) - ( AKT1_IVS14+32G,A) - ( AKT1_IVS14+66C,G) - ( AKT1_IVS14+93C,T) - ( AKT1_IVS14+98A,G)(C-G-C-C-A), (AKT1_1251C,T) - ( AKT1_IVS14+32G,A) - ( AKT1_IVS14+66C,G) - ( AKT1_IVS14+93C,T) - ( AKT1_IVS14+98A,G)(C-G-G-C-A), (AKT1_1251C,T) - ( AKT1_IVS14+32G,A) - ( AKT1_IVS14+66C,G) - ( AKT1_IVS14+93C,T) - ( AKT1_IVS14+98A,G) - ( AKT1_IVS14+105_106ins_CTCAC or CTCAG)(C-G-C-C-G-insCTCAG ...
Sca1/Ly6A/E抗体(PE/Cy7 ®)[D7]|Abcam中国|Anti-Sca1/Ly6A/E抗体(PE/Cy7 ®)[D7]
PE/Cy7 ®偶联Sca1 / Ly6A/E抗体[D7](ab93537)可与小鼠样本反应并经Flow Cyt实验严格验证，实验条件参看说明书。Abcam对所有产品均提供质保服务，中国75%以上现货。
LGD1069 | Selective Inhibitors of Protein Methyltransferases
A series of 7-hydroxy, 8-hydroxy and 7,8-dihydroxy synthetic chromone derivatives was evaluated for his or her DPPH free radical scavenging activities. Thirty-six synthetic chromone derivatives (indicated as compounds 1C36) were assessed for his or her antioxidant activities by DPPH radical scavenging assay. As demonstrated in Furniture 1 and ?and2,2, various chromones exhibited different degrees of activity, which range from EC50 = 2.58 to 182.77 M that are stronger than the popular organic antioxidants, e.g., luteolin and quercetin which possessed IC50 = 10.89 and 11.04 M,  respectively. Structure-radical scavenging activity romantic relationship demonstrated how the 7,8-dihydroxy-2-phenyl-3-benzoyl substituted compounds (compounds 29, 30 and 36) exhibited a strong antioxidant activity with low log EC50. This indicated that dihydroxy substitution (cathecol group) on ring A was LGD1069 essential for radical scavenging activity. The presence of benzoyl group at position 3 confers a high ...
Activation of the serine/threonine kinase Akt contributes to the formation, maintenance, and therapeutic resistance of cancer, which is driving development of compounds that inhibit Akt. Phosphatidylinositol ether lipid analogues (PIAs) are analogues of the products of PI3K that inhibit Akt activation, translocation, and the proliferation of a broad spectrum of cancer cell types. To gain insight into the mechanism of PIAs, time-dependent transcriptional profiling of 5 active PIAs and the PI3K inhibitor LY294002 (LY) was performed in NSCLC cells using high-density oligonucleotide arrays. Gene ontology analysis revealed genes involved in apoptosis, wounding response, and angiogenesis were upregulated by PIAs, while genes involved in DNA replication, repair and mitosis were suppressed. Genes that exhibited early differential expression were partitioned into 3 groups; those induced by PIAs only (DUSP1, KLF6, CENTD2, BHLHB2, PREX1), those commonly induced by PIAs and LY (TRIB1, KLF2, RHOB and ...
ZSTK474 | CAS#475110-96-4 | phosphoinositide 3-kinase-specific inhibitor | PI3K inhibitor | MedKoo Biosciences
ZSTK474 is a novel orally applicable phosphoinositide 3-kinase-specific inhibitor that strongly inhibits cancer cell proliferation. Combination treatment using X-rays then ZSTK474 given orally for 8 days, starting 24h post-irradiation, significantly enhanced cell growth inhibition. The combined effect was also observed for clonogenic survival with continuous ZSTK474 treatment. Western blot analysis showed enhanced phosphorylation of Akt and GSK-3β by X-irradiation, whereas phosphorylation was inhibited by ZSTK474 treatment alone. Treatment with ZSTK474 after X-irradiation also inhibited phosphorylation, and remarkably inhibited xenograft tumor growth.
KAKEN - Research Projects | Effect of a phosphatidylinositol 3-kinase inhibitor wortmannin on radiation and bleomycin...
Principal Investigator：HOSOI Yoshio, Project Period (FY)：1997 - 1998, Research Category：Grant-in-Aid for Scientific Research (C), Section：一般, Research Field：Radiation science
Structural Determinants of Isoform Selectivity in PI3K Inhibitors<...
TY - JOUR. T1 - Structural Determinants of Isoform Selectivity in PI3K Inhibitors. AU - Miller, Michelle S.. AU - Thompson, Philip E.. AU - Gabelli, Sandra B. PY - 2019/2/26. Y1 - 2019/2/26. N2 - Phosphatidylinositol 3-kinases (PI3Ks) are important therapeutic targets for the treatment of cancer, thrombosis, and inflammatory and immune diseases. The four highly homologous Class I isoforms, PI3K, PI3K, PI3K and PI3K have unique, non-redundant physiological roles and as such, isoform selectivity has been a key consideration driving inhibitor design and development. In this review, we discuss the structural biology of PI3Ks and how our growing knowledge of structure has influenced the medicinal chemistry of PI3K inhibitors. We present an analysis of the available structure-selectivity-activity relationship data to highlight key insights into how the various regions of the PI3K binding site influence isoform selectivity. The picture that emerges is one that is far from simple and emphasizes the ...
This study found that compounds exhibiting antioxidant properties, i.e., NAC, PBN, and lipoic acid, prevent ANG II from activating the transcription factor NFAT3 in cardiomyocytes. Consistent with the hypothesis that oxidants mediate NFAT3 activation, we found that H2O2 induces activation of NFAT3 transcription factor in a narrow dose range (50-150 μM) within 1-8 h. A chemical inhibitor of ERKs, PD98059, inhibited H2O2 from activating NFAT3. In contrast, the PI3K inhibitor LY249002 and the p38 MAPK inhibitor SB202190 failed to show an inhibitory effect on H2O2-induced NFAT3 activation. A dominant negative form of c-Jun, TAM67, abolished NFAT3 activation. Because PD98059 inhibits the activation of AP-1 transcription factors by H2O2 (46), our data suggest a role of AP-1 downstream of ERKs in the H2O2-induced NFAT3 activation in cardiomyocytes.. Cooperation of NFATs with other families of transcription factors is an important character of NFATs in regulating gene expression. There is evidence that ...
4-[2-(4-Morpholinyl)ethyl]-3-thiosemicarbazide 77644-45-2 Chemical Properties Physical Properties
4-[2-(4-Morpholinyl)ethyl]-3-thiosemicarbazide chemical properties, What are the chemical properties of 4-[2-(4-Morpholinyl)ethyl]-3-thiosemicarbazide 77644-45-2, What are the physical properties of 4-[2-(4-Morpholinyl)ethyl]-3-thiosemicarbazide ect.
AKT/PKB signaling: navigating downstream
The serine/threonine kinase Akt, also known as protein kinase B (PKB), is a central node in cell signaling downstream of growth factors, cytokines, and other cellular stimuli. Aberrant loss or gain of Akt activation underlies the pathophysiological properties of a variety of complex diseases, includ …
Ito, K., Caramori, G. and Adcock, I.M. (2007) Therapeu tic potential of phosphatidylinositol 3-kinase inhibitors in...
Ito, K., Caramori, G. and Adcock, I.M. (2007) Therapeu tic potential of phosphatidylinositol 3-kinase inhibitors in inflammatory respiratory disease. The Journal of Phar macology and Experimental Therapeutics, 321, 1-8. Epub 4 October 2006. doi10.1124/jpet.106.111674
Phospho-AKT1 (Ser473), PE, clone: SDRNR, eBioscience™ 100 Tests; PE Phospho-AKT1 (Ser473), PE, clone: SDRNR, eBioscience™
Phospho-AKT1 (Ser473), PE, clone: SDRNR, eBioscience™ 100 Tests; PE Phospho-AKT1 (Ser473), PE, clone: SDRNR, eBioscience™ Primary Antibodies Ad to Ak
PKB - Bing 词典
必应词典为您提供PKB的释义，网络释义： 民族觉醒党(PARTAI KEBANGKITAN BANGSA)；PACAMOR KUBAR BEARINGS；复兴党；
... is a chromone derivative, a type of phenolic compound found in cloves. It has also been isolated from the fungal ... I. Chromone and naphthoquinone metabolites from a Cylindrocarponspecies". Australian Journal of Chemistry. 25 (4): 875. doi: ... Schönberg, Alexander; Badran, Nasry; Starkowsky, Nicolas A. (1953). "Furo-chromones and -Coumarins. VII. Degradation of ...
Schönberg, Alexander; Badran, Nasry; Starkowsky, Nicolas A. (1955). "Furo-chromones and -Coumarins. XII. Synthesis of Fraxinol ...
Starting from phloroghrcin aldehyde, and building on the 2-methyl-y-pyrone, 2-methyl-5,7-dihydroxy-dfo-yl-chromone was obtained ... Badawi, M.M.; Fayez, M.B.E. (1965). "Natural chromones-I". Tetrahedron. 21 (10): 2925. doi:10.1016/S0040-4020(01)98378-4. ... a compound derivative of chromone (1,4-benzopyrone) and furan. Ammi visnaga, the main source for visnagin, has been used in ...
ISBN 0-398-06179-3. A. A. Ali; M. A. Makboul; A. A. Attia; D. T. Ali (1990). "Chromones and flavans from Pancratium maritimum ...
Mahal, H. S.; Venkataraman, K. (1934). "Synthetical experiments in the chromone. group. XIV. Action of sodamide on 1-acyloxy-2- ... The Baker-Venkataraman rearrangement is often used in the synthesis of chromones and flavones. After the base-catalyzed ... To complete the construction of the chromone or flavone core, cyclodehydration is required. This was commonly afforded by ... rearrangement, treatment with acid generally affords the chromone or flavone core, though other milder methods have been ...
... is a chromone derivative. To date, it has been isolated from plant families such as Polygonaceae, Lamiaceae, ... "2,5-Dimethyl-7-hydroxy chromone". ChemSpider. Royal Society of Chemistry. Retrieved April 18, 2011. CS1 maint: discouraged ...
Cromoglicate is classified as a chromone. Cromolyn is also being tested as a drug to treat insulin-induced lipoatrophy. ... "Inhibition of volume-activated chloride currents in endothelial cells by chromones". Br J Pharmacol. 115 (8): 1393-8. doi: ...
2 (4). Chen, G.; Jin, H. Z.; Li, X. F.; Zhang, Q.; Shen, Y. H.; Yan, S. K.; Zhang, W. D. (2008). "A new chromone glycoside from ...
In a variation the reaction of phenols and beta-ketoesters and phosphorus pentoxide yields a chromone. This reaction is called ... Simonis chromone cyclization. The ketone in the ketoester is activated by P2O5 for reaction with the phenol hydroxyl group ...
The Kostanecki acylation is a method used in organic synthesis to form chromones or coumarins by acylation of O-hydroxyaryl ... If benzoic anhydride (or benzoyl chloride) is used, a particular type of chromone called a flavone is obtained. The mechanism ... Missing or empty ,title= (help) Ellis, G. P. (1977) Chromenes, Chromanones, and Chromones from The Chemistry of Heterocyclic ... "Chromone: A Valid Scaffold in Medicinal Chemistry". Chemical Reviews. 114 (9): 4960-92. doi:10.1021/cr400265z. PMID 24555663. ...
Khadem S, Marles RJ (2011). "Chromone and flavonoid alkaloids: occurrence and bioactivity". Molecules. 17 (1): 191-206. ... contain a nitrogen heterocycle such as a pyridine or piperidine which is covalently bonded to the A-ring of a chromone. One ...
This process, a variant of Allan-Robinson reaction, is in use for the synthesis of flavones and chromones. Through his ... Synthetical experiments in the chromone group. Part XIV. The action of sodamide on 1-acyloxy-2-acetonaphthones". Journal of the ...
... has a strongly acidic chromone skeleton. The 5-hydroxy group increases the activity and, along with the 10-alkyl ... Dahl, R. (1980). "Clinical study of a new orally active chromone in asthma-proxicromil (FPL 57787)". Clin Allergy. 10 (6): 715- ...
"Synthesis of Heterocyclic-Substituted Chromones and Related Compounds as Potential Anticancer Agents1". Journal of Medicinal ...
Monoamine oxidase B
compound #9, #12, Gaspar A, Reis J, Fonseca A, Milhazes N, Viña D, Uriarte E, Borges F (January 2011). "Chromone 3- ... Chromone-3-phenylcarboxamides Isatins Phthalimides 8-Benzyloxycaffeines and CSC analogs (E,E)-8-(4-phenylbutadien-1-yl) ...
Eucryphin, a chromone rhamnoside, can be isolated from the bark of E. cordifolia. The Plant List: A Working List of All Plant ... Eucryphin, a new chromone rhamnoside from the bark of Eucryphia cordifolia. R. Tschesche, S. Delhvi, S. Sepulveda and E. ...
... is a chromone derivative, a phenolic compound found in cloves. It is also one of the compounds responsible for ...
A chromone and three flavonoid glycosides have been reported from the roots. World Conservation Monitoring Centre 1998. In: ...
Gui, Y; Tsao, R; Li, L; Liu, C. M; Wang, J; Zong, X (2011). "Preparative separation of chromones in plant extract of ...
At least 70 of these are terpenoids which come in the form of sesquiterpenes and chromones; no monoterpenes have been detected ...
Chemical compounds isolated from the genus include isoflavones, flavanols, glycosides, pterocarpans, chromone, and ursolic acid ...
Isoflavones like barbigerone, genistin and a chromone 6,7-dimethoxy-2,3-dihydrochromone were identified. The isoflavone ...
"A new chromone and flavone synthesis and its utilization for the synthesis of potentially antitumorigenic polycyclic chromones ...
"Synthesis and evaluation of substituted chroman-4-one and chromone derivatives as sirtuin 2-selective inhibitors". Journal of ...
... is a chemical compound which is a derivative of chromone (1,4-benzopyrone) and furan. Some chemical derivatives ...
It is a derivative of 7-methanesulfonylamino-6-phenoxychromones and is a chromone with two amide groups; it was first published ...
The aloin cells produce anthraquinone and chromone derivatives, which may be responsible for the medicinal attributes of Aloe. ...
4-Pyrone (or γ-pyrone) is found in some natural chemical compounds such as chromone, maltol and kojic acid. Furanone, which has ...
... which can also be used to produce chromones. Coumarin is found naturally in many plants, notably in high concentration in the ...
The n-butanol extract of the root bark of the Cameroonian species has also been shown to contain new chromone glycosides and ... Analyses of Schumanniophyton magnificum have yielded a variety of chromone alkaloids, including schummaniophytine, ...
Chromone - Wikipedia
Derivatives of chromone are collectively known as chromones. Most, though not all, chromones are also phenylpropanoids. 6,7- ... Abstract CID 10286 from PubChem - "4-chromone" Chromones at the US National Library of Medicine Medical Subject Headings (MeSH ... Chromone (or 1,4-benzopyrone) is a derivative of benzopyran with a substituted keto group on the pyran ring. It is an isomer of ... Eucryphin, a chromone rhamnoside, can be isolated from the bark of Eucryphia cordifolia. Cromolyn (disodium cromoglicate) was ...
Frontiers | Repositioning Chromones for Early Anti-inflammatory Treatment of COVID-19 | Pharmacology
This commentary elaborates on the pharmacological rationale of repositioning the mast cell stabilizer chromones as an ... Repositioning Chromones for Early Anti-inflammatory Treatment of COVID-19. Piero Sestili* and Vilberto Stocchi ... Citation: Sestili P and Stocchi V (2020) Repositioning Chromones for Early Anti-inflammatory Treatment of COVID-19. Front. ... This commentary elaborates on the pharmacological rationale of repositioning the mast cell stabilizer chromones as an ...
Marine Drugs | Free Full-Text | Rare Chromones from a Fungal Mutant of the Marine-Derived Penicillium purpurogenum G59
Three new and rare chromones, named epiremisporine B (2), epiremisporine B1 (3) and isoconiochaetone C (4), along with three ... Xia M-W, Cui C-B, Li C-W, Wu C-J, Peng J-X, Li D-H. Rare Chromones from a Fungal Mutant of the Marine-Derived Penicillium ... Xia, M.-W.; Cui, C.-B.; Li, C.-W.; Wu, C.-J.; Peng, J.-X.; Li, D.-H. Rare Chromones from a Fungal Mutant of the Marine-Derived ... Rare Chromones from a Fungal Mutant of the Marine-Derived Penicillium purpurogenum G59. Ming-Wen Xia 1,2. ...
Synthesis, preliminary cytotoxicity evaluation of new 3-formylchromone hydrazones and phosphorohydrazone derivatives of...
Reactions of chromone derivatives 1- 4 with N-substituted hydrazines were described. Hydrazones ( 6, 7a, 8a- c, 9b- e, 10e, 11e ... Reactions of chromone derivatives 1-4 with N-substituted hydrazines were described. Hydrazones (6, 7a, 8a-c, 9b-e, 10e, 11e, 12 ... Huang W, Liu MZ, Li Y, Tan Y, Yang GF (2007) Design, syntheses, and antitumor activity of novel chromone and aurone derivatives ... Lin WH, Fu HZ, Li J, Proksch P (2001) Novel chromone derivatives from marine fungus Aspergillus versicolor isolated from the ...
Tin-free radical reactions under minimal solvent conditions for the synthesis of substituted chromones and coumarins - Green...
This free radical addition process allows for the preparation of a variety of substrates, including substituted chromones and ... chromones. and coumarins J. R. Zimmerman, M. Manpadi and R. Spatney, Green Chem., 2011, 13, 3103 DOI: 10.1039/C1GC15775B ... chromones. and coumarins. . This method is high yielding, conducted at ambient temperature and, in nearly all instances, ...
Marine Drugs | Free Full-Text | Phomopsichin A-D; Four New Chromone Derivatives from Mangrove Endophytic Fungus Phomopsis sp....
... in which a dihydropyran ring is fused with the chromone ring. Compounds 1-5 showed weak inhibitory activities on ... Four new chromone derivatives, phomopsichins A-D (1-4), along with a known compound, phomoxanthone A (5), were isolated from ... Four new chromone derivatives, phomopsichins A-D (1-4), along with a known compound, phomoxanthone A (5), were isolated from ... Huang M, Li J, Liu L, Yin S, Wang J, Lin Y. Phomopsichin A-D; Four New Chromone Derivatives from Mangrove Endophytic Fungus ...
CHROMONE | 491-38-3 | INDOFINE Chemical Company
Comparison of radical scavenging behavior of chromones dihydrogenistein and demethyltexasin-a DFT approach | Springer for...
The present work deals with the validation of radical scavenging behavior of two identical chromones: 4′,5,7 trihydroxy ... DFT Chromones Frontier molecular orbital analysis and molecular docking This is a preview of subscription content, log in to ... Tawfik HA, Ewies EF, El-Hamouly WS (2014) Synthesis of chromones and their applications during the last ten years during the ... The present work deals with the validation of radical scavenging behavior of two identical chromones: 4′,5,7 trihydroxy ...
chromone: Definition, Word Game Analysis
... chromone Best Plays of chromone in Scrabble® and Words With Friends, Length tables of words in chromone, Word growth of ... chromone. 2 letter words in chromone (10 words). ehemenhemenoohonorre ... chromone. in Words With Friends™. The word chromone is playable in Words With Friends™, no blanks required. Because it is ... chromone. in Scrabble®. The word chromone is playable in Scrabble®, no blanks required. Because it is longer than 7 letters, ...
Design, Synthesis and Biological Evaluation of Chromone-based p38 MAP Kinase Inhibitors
DIGITAL.CSIC: Synthesis and Biological Evaluation of Novel Chromone+Donepezil Hybrids for Alzheimer's Disease Therapy
A novel chromone derivative with anti-inflammatory property via inhibition of ROS-dependent activation of TRAF6-ASK1-p38...
4940-39-0 - Chromone-2-carboxylic acid, 97% - Chromocarb - 4-Oxo-4H-1-benzopyran-2-carboxylic acid - A13552 - Alfa Aesar
DISSERTATIONS.SE: Design and Synthesis of Chalcone and Chromone Derivatives as Novel Anticancer Agents
Dissertation: Design and Synthesis of Chalcone and Chromone Derivatives as Novel Anticancer Agents . ... Synthetic chromone precursors, i.e. chalcones, and related dienones were evaluated as antiproliferative agents that interfere ... Keywords: NATURVETENSKAP; NATURAL SCIENCES; Chalcones; Chromones; Fluorescence; Fluorophore; Cellular imaging; Anticancer; ... The study resulted in a series of highly selective ATP-competitive chromone-based p38␣ inhibitors with IC50 values in the ...
Synthesis and Biological Evaluation of Novel Chromone+Donepezil Hybrids for Alzheimer's Disease Therapy | Bentham Science
Synthesis and Biological Evaluation of Novel Chromone+Donepezil Hybrids for Alzheimers Disease Therapy. Author(s): Rim Malek, ... Keywords:Alzheimer disease, antioxidants, cholinesterase, chromone, donepezil, ORAC, passerini reaction.. Abstract:Background: ... Title:Synthesis and Biological Evaluation of Novel Chromone+Donepezil Hybrids for Alzheimers Disease Therapy ... "Synthesis and Biological Evaluation of Novel Chromone+Donepezil Hybrids for Alzheimers Disease Therapy", Current Alzheimer ...
NOPR: Synthesis, Biological Evaluation and Molecular Modeling Studies of Novel Chromone/Aza-Chromone Fused α-Aminophosphonates...
A series of novel chromone/aza-chromone fused α-aminophosphonate derivatives were synthesized in good yields using silica ... Synthesis, Biological Evaluation and Molecular Modeling Studies of Novel Chromone/Aza-Chromone Fused α-Aminophosphonates as Src ... Aza-chromone compound showed Src kinase inhibition with an IC50 value of 15.8 µM. The compounds were subjected to molecular ...
7-fluoro-4-chromone-3-sulfur compounds] - Publikationsserver der Universität Regensburg
Lowe, W., Elz, Sigurd, Reiser, H. und Schott, S. (1994) [7-fluoro-4-chromone-3-sulfur compounds]. Archiv der Pharmazie 327 (4 ... The novel 7-fluoro-4-chromone-3-sulfur compounds 5-12 were synthesized from the sulfinic acid 4, which can be obtained from the ... Animals Aorta, Thoracic/drug effects Chromones/*chemical synthesis/pharmacology Male Muscle, Smooth, Vascular/drug effects Rats ...
Carbamoyl Translocations by an Anionic ortho-Fries and Cumulenolate -Acylation Pathway Regioselective Synthesis of...
KGaA, Weinheim 2127 Zuschriften Table 1: Synthesis of chromone 3-carboxamides 5 a,c-k and 8-carboxamides 6 a,c-f,h-j. Entry ... The biaryl O-carbamate 4 k (entry 20) furnishes the 8-aryl chromone 5 k, which is structurally related to several naturally ... 2008, 120, 2127 -2131 Scheme 2. Synthesis of chromone 3-carboxamide 5 i and 8-carboxamide 6 i. gave us impetus to extend these ... However, their corresponding transformations into chromones 6 a, 6 c, 6 d, and 6 j (entries 2, 6, 8, and 19) require a ...
US 8852657 B2 - Chromones As Therapeutic Agents - The Lens - Free & Open Patent and Scholarly Search
... total chromones. The chromones are isolated as described in detail below. In some embodiments, the one or more chromone is ... The standardized chromone composition from these two species of Aloe contained no less than 1.4% chromones-i.e. aloesin (UP394 ... The standardized chromone composition from two species of Aloe contained no less than 2% chromones-i.e. aloesin (UP394) with ... This standardized chromone composition (UP780) from these two species of Aloe contained no less than 2% chromones-i.e. aloesin ...
Salinity stress induces the production of 2-(2-phenylethyl)chromones and regulates novel classes of responsive genes involved...
... chromones. Salinity stress could induce the production of 41 2-(2-phenylethyl)chromones in A. sinensis calli. We conducted the ... chromones biosynthesis. Forty one 2-(2-phenylethyl)chromones were identified from NaCl-treated A. sinensis calli. 93 041 ... 2-(2-phenylethyl)chromones are principal components responsible for the quality of agarwood. However, the molecular basis of 2 ... Our research indicated that salt stress induced production of several of 2-(2-phenylethyl)chromones in A. sinensis calli. ...
Chromones | REACH
"Chromones" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... This graph shows the total number of publications written about "Chromones" by people in this website by year, and whether " ... Below are the most recent publications written about "Chromones" by people in Profiles. ...
Eugenitin - Wikipedia
Eugenitin is a chromone derivative, a type of phenolic compound found in cloves. It has also been isolated from the fungal ... I. Chromone and naphthoquinone metabolites from a Cylindrocarponspecies". Australian Journal of Chemistry. 25 (4): 875. doi: ... Schönberg, Alexander; Badran, Nasry; Starkowsky, Nicolas A. (1953). "Furo-chromones and -Coumarins. VII. Degradation of ...
Bergapten - Wikipedia
RCSB PDB - QUE Ligand Summary Page
RCSB PDB - STL Ligand Summary Page
Recent advances in the diversification of chromones and flavones by direct C-H bond activation or functionalization
Chromone and flavone are both central backbones of natural products and clinical medicines. Synthesis of diversely ... Recent advances in the diversification of chromones and flavones by direct C-H bond activation or functionalization[J]. Chinese ... Considering the importance of the functionalized chromone and flavone compounds as well as the notable advances in the ... Recent advances in the diversification of chromones and flavones by direct C-H bond activation or functionalization. ...
Antioxidant lignans and chromone glycosides from Eurya japonica<...
Antioxidant lignans and chromone glycosides from Eurya japonica. Li Ming Yang Kuo, Li Jie Zhang, Hung Tse Huang, Zhi Hu Lin, ... Antioxidant lignans and chromone glycosides from Eurya japonica. / Yang Kuo, Li Ming; Zhang, Li Jie; Huang, Hung Tse; Lin, Zhi ... Antioxidant lignans and chromone glycosides from Eurya japonica. Journal of Natural Products. 2013 4月 26;76(4):580-587. https ... title = "Antioxidant lignans and chromone glycosides from Eurya japonica",. abstract = "Four new 8,8′,7,2′-lignans, (+)- ...
- Derivatives of chromone are collectively known as chromones. (wikipedia.org)
- Reactions of chromone derivatives 1 - 4 with N -substituted hydrazines were described. (springer.com)
- Four New Chromone Derivatives from Mangrove Endophytic Fungus Phomopsis sp. (mdpi.com)
- Four new chromone derivatives, phomopsichins A-D ( 1 - 4 ), along with a known compound, phomoxanthone A ( 5 ), were isolated from the fermentation products of mangrove endophytic fungus Phomopsis sp. (mdpi.com)
- This thesis comprises the design and synthesis of chalcone and chromone derivatives and their use in various biological applications, particularly as anticancer agents (targeting proteins associated with cancer pathogenesis) and as potential fluorophores for live-cell imaging. (dissertations.se)
- Structural diversity was accomplished by using palladium-mediated reactions for the incorporation of suitable substituents for the generation of chromone derivatives that possess different biological activities. (dissertations.se)
- Structural-based design and extensive synthesis provided chromone-based derivatives that target two different MAP kinases (p38␣ and MEK1), involved in essential cellular signal transduction pathways. (dissertations.se)
- Furthermore, molecular docking was used to study potential structural modifications on the chromone structure in order to obtain highly potent derivatives that selectively target the allosteric pocket on MEK1. (dissertations.se)
- Initial studies provided a first generation of non-ATP- competitive chromone derivatives that prevents the activation of MEK1 with micromolar activities. (dissertations.se)
- A series of novel chromone/aza-chromone fused α-aminophosphonate derivatives were synthesized in good yields using silica chloride as the catalyst. (niscair.res.in)
- The direct C-H bond activation or functionalization on these heterocyclic backbones provides highly powerful tools for the rapid accesses to densely functionalized chromone and flavone derivatives. (ccspublishing.org.cn)
- Discovery and Optimization of Chromone Derivatives as Novel Selective Phosphodiesterase 10 Inhibitors. (physiciansweekly.com)
- Synthesis, characterization, DNA-binding studies and acetylcholinesterase inhibition activity of new 3-formyl chromone derivatives. (semanticscholar.org)
- The aloes consist of free anthraquinones and their derivatives: Barbaloin, lsobarbaloin, Anthrone-C-glycosides and chromones. (ispub.com)
- Chromone derivatives have been extensively studied recently because of to their promising biological activities. (pubmedcentralcanada.ca)
- The novel 7-fluoro-4-chromone-3-sulfur compounds 5-12 were synthesized from the sulfinic acid 4, which can be obtained from the enaminone 3 and thionyl chloride. (uni-regensburg.de)
- Synthesis of diversely functionalized chromones and flavones constitutes significant research contents of the modern synthetic science because abundant molecular libraries of such types are crucial in providing candidate compounds for the discovery of new pharmaceuticals and functional materials. (ccspublishing.org.cn)
- Considering the importance of the functionalized chromone and flavone compounds as well as the notable advances in the synthesis of such products by direct C-H activation or functionalization, we review herein the research advances in the C-H bond activation and functionalization reactions of chromone and flavones, in hope of showing the current states and promise of the research domain. (ccspublishing.org.cn)
- 7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-acetic acid, also known as 5-(carboxymethyl)-7-hydroxy-2-methylchromone, belongs to the class of organic compounds known as chromones. (hmdb.ca)
- Chromones are compounds containing a benzopyran-4-one moiety. (hmdb.ca)
- belongs to the class of organic compounds known as chromones. (hmdb.ca)
- The study resulted in a series of highly selective ATP-competitive chromone-based p38␣ inhibitors with IC50 values in the nanomolar range. (dissertations.se)
- Different synthetic strategies were used to obtain an easily accessible chromone scaffold with appropriate handles that allows regioselective introduction of various substituents. (dissertations.se)
- Chromone (or 1,4-benzopyrone) is a derivative of benzopyran with a substituted keto group on the pyran ring. (wikipedia.org)
- Phosphorohydrazone of 3-formylchromone 8a and hydrazone of 2-amino-3-chromone derivative 11e showed appreciable cytotoxicity. (springer.com)
- A novel chromone derivative with anti-inflammatory property via inhibition of ROS-dependent activation of TRAF6-ASK1-p38 pathway. (sigmaaldrich.com)
- In the present study, we show that a novel chromone derivative, DCO-6, significantly reduced lipopolysaccharide (LPS)-induced production of nitric oxide, IL-1β and IL-6, decreased the levels of iNOS, IL-1β and IL-6 mRNA expression in both RAW264.7 cells and mouse primary peritoneal macrophages, and inhibited LPS-induced activation of p38 MAPK but not of JNK, ERK. (sigmaaldrich.com)
- Eugenitin is a chromone derivative, a type of phenolic compound found in cloves. (wikipedia.org)
- Chromone is a bicyclic compound consisting of a 1-benzopyran, which bears a ketone group at the 4-position. (hmdb.ca)
- Synthetic chromone precursors, i.e. chalcones, and related dienones were evaluated as antiproliferative agents that interfere with the tubulin-microtubule equilibrium, crucial for cellular mitosis. (dissertations.se)
- The present work deals with the validation of radical scavenging behavior of two identical chromones: 4′,5,7 trihydroxy isoflavone dihydrogenistein (DGT) and 4′,6,7 trihydroxy isoflavone demethyltexasin (DMT) through structural activity analysis to study the influence of H atom on the radical scavenging behavior. (springer.com)
- 6 i, Scheme 2), it was recognized that the chromone heterocycle represents major classes of natural products and is a key component for a plethora of bioactive molecules, commercial drugs, and agrochemicals. (docme.ru)
- Aza-chromone compound showed Src kinase inhibition with an IC 50 value of 15.8 µM. (niscair.res.in)
- Fitton AO, Frost JR, Suschitzky H (1975) Addition reactions of N-(chromone-3-ylidene)anilines. (springer.com)
- Addition reactions of 3-(aryliminoethyl)chromones. (springer.com)
- 1 Domino reactions of 2-methyl chromones containing an electron withdrawing group with chromone-fused dienes Jian Gong, Fuchun Xie, Wenming Ren, Hong Chen and Youhong Hu* State Key Laboratory of Drug Research, Shanghi Institute of Materia Medica, Chinese Academy of Sciences, 555 Zu Chong Zhi Road, Shanghai, , China Supporting Information List of contents Experiment procedures. (sciencedocbox.com)
- Paper II Polyunsaturated fatty acid-derived chromones exhibiting potent antioxidant activity. (uio.no)
- The chromone ring ( A ) is connected to the thia-zole ring ( C ) though a carboxamide spacer ( B ). The compound crystallizes with two different morphologies and the structural analysis revealed the presence of packing polymorphism. (pubmedcentralcanada.ca)
- Coumarin - a structural isomer Furanochromones Eucryphin, a new chromone rhamnoside from the bark of Eucryphia cordifolia. (wikipedia.org)
- Structural optimization and thermochemical calculations for the studied chromones is supported by DFT under the correlation functional B3LYP and M062X under 6-311G(d,p) basis set using Gaussian 09 package. (springer.com)
- Chromones" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (sickkids.ca)
- A chromone complex that acts by inhibiting the release of chemical mediators from sensitized mast cells. (umassmed.edu)
- Synthesis and biological activities of 3-[n-(4-oxo-2-substituted-3-quinazolinyl) formimidoyl] chromones. (ijpsonline.com)
- This commentary elaborates on the pharmacological rationale of repositioning the mast cell stabilizer chromones as an adjunctive treatment for SARS‐CoV‐2 infection, and proposes their practical clinical testing as an early, safe, and cost-effective anti-inflammatory intervention in COVID-19 to limit the eventual secondary progression toward life-threatening respiratory complications. (frontiersin.org)
- Resumen en inglés The development of state-of-the-art technologies for the preparation of cytostatics acquires special interest owing to both the low selectivity of these drugs and their high toxicity. (worldwidescience.org)
- Resumen en inglés Malignant glioma cell cultures have been done for studying the biology of the tumors, the efficiency of antineoplasic drugs, and for determining the differential sensitivity to cytostatics. (worldwidescience.org)
- S-4'-hydroxywarfarin belongs to the family of Chromones. (hmdb.ca)
- These are homoisoflavonoids with a structure based on the chromone system. (hmdb.ca)
- Synthesis of chromone 3-carboxamide 5 i and 8-carboxamide 6 i. gave us impetus to extend these initial studies. (docme.ru)
- This graph shows the total number of publications written about "Chromones" by people in this website by year, and whether "Chromones" was a major or minor topic of these publications. (sickkids.ca)
- Complications with the 1,2-addition of LDA to unhindered 2008 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2127 Zuschriften Table 1: Synthesis of chromone 3-carboxamides 5 a,c-k and 8-carboxamides 6 a,c-f,h-j. (docme.ru)
- Below are the most recent publications written about "Chromones" by people in Profiles. (sickkids.ca)
- Chromone and flavone are both central backbones of natural products and clinical medicines. (ccspublishing.org.cn)
- A series of 3-(4-fluorophenyl)-2-(4-pyridyl)-chromone derivs. (diva-portal.org)