Chalcones
Millettia
Luciferases, Renilla
Molecular Structure
Structure-Activity Relationship
Agrochemicals
Dictionaries as Topic
Biopharmaceutics
Pinus sylvestris
Pinus
Acyltransferases
Gymnosperms
Gymnosperms are a group of vascular plants whose seeds are not enclosed by a ripened ovary (fruit), in contrast to ANGIOSPERMS whose seeds are surrounded by an ovary wall. The seeds of many gymnosperms (literally, "naked seed") are borne in cones and are not visible. Taxonomists now recognize four distinct divisions of extant gymnospermous plants (CONIFEROPHYTA; CYCADOPHYTA; GINKGOPHYTA; and GNETOPHYTA).
Trees
Antioxidants
Selective effect of 2',6'-dihydroxy-4'-methoxychalcone isolated from Piper aduncum on Leishmania amazonensis. (1/302)
2',6'-Dihydroxy-4'-methoxychalcone (DMC) was purified from the dichloromethane extract of Piper aduncum inflorescences. DMC showed significant activity in vitro against promastigotes and intracellular amastigotes of Leishmania amazonensis, with 50% effective doses of 0.5 and 24 micrograms/ml, respectively. Its inhibitory effect on amastigotes is apparently a direct effect on the parasites and is not due to activation of the nitrogen oxidative metabolism of macrophages, since the production of nitric oxide by both unstimulated and recombinant gamma interferon-stimulated macrophages was decreased rather than increased with DMC. The phagocytic activity of macrophages was functioning normally even with DMC concentrations as high as 80 micrograms/ml, as seen by electron microscopy and by the uptake of fluorescein isothiocyanate-labeled beads. Ultrastructural studies also showed that in the presence of DMC the mitochondria of promastigotes were enlarged and disorganized. Despite destruction of intracellular amastigotes, no disarrangement of macrophage organelles were observed, even at 80 micrograms of DMC/ml. These observations suggest that DMC is selectively toxic to the parasites. Its simple structure may well enable it to serve as a new lead compound for the synthesis of novel antileishmanial drugs. (+info)Improvement of in vitro and in vivo antileishmanial activities of 2', 6'-dihydroxy-4'-methoxychalcone by entrapment in poly(D,L-lactide) nanoparticles. (2/302)
The inhibition of intracellular Leishmania amazonensis growth by 2', 6'-dihydroxy-4'-methoxychalcone (DMC) isolated from Piper aduncum was further enhanced after encapsulation of DMC in polymeric nanoparticles. Encapsulated DMC also showed increased antileishmanial activity in infected BALB/c mice, as evidenced by significantly smaller lesions and fewer parasites in the lesions. (+info)Epoxide hydrolases regulate epoxyeicosatrienoic acid incorporation into coronary endothelial phospholipids. (3/302)
Cytochrome P-450-derived epoxyeicosatrienoic acids (EETs) are avidly incorporated into and released from endothelial phospholipids, a process that results in potentiation of endothelium-dependent relaxation. EETs are also rapidly converted by epoxide hydrolases to dihydroxyeicosatrienoic acid (DHETs), which are incorporated into phospholipids to a lesser extent than EETs. We hypothesized that epoxide hydrolases functionally regulate EET incorporation into endothelial phospholipids. Porcine coronary artery endothelial cells were treated with an epoxide hydrolase inhibitor, 4-phenylchalcone oxide (4-PCO, 20 micromol/l), before being incubated with (3)H-labeled 14,15-EET (14,15-[(3)H]EET). 4-PCO blocked conversion of 14,15-[(3)H]EET to 14,15-[(3)H]DHET and doubled the amount of radiolabeled products incorporated into cell lipids, with >80% contained in phospholipids. Moreover, pretreatment with 4-PCO before incubation with 14,15-[(3)H]EET enhanced A-23187-induced release of radiolabeled products into the medium. In contrast, 4-PCO did not alter uptake, distribution, or release of [(3)H]arachidonic acid. In porcine coronary arteries, 4-PCO augmented 14,15-EET-induced potentiation of endothelium-dependent relaxation to bradykinin. These data suggest that epoxide hydrolases may play a role in regulating EET incorporation into phospholipids, thereby modulating endothelial function in the coronary vasculature. (+info)2'-hydroxychalcone inhibits nuclear factor-kappaB and blocks tumor necrosis factor-alpha- and lipopolysaccharide-induced adhesion of neutrophils to human umbilical vein endothelial cells. (4/302)
Inhibition of expression of cell adhesion molecules (CAM), including intercellular CAM-1 (ICAM-1), vascular CAM-1 (VCAM-1), and E-selectin, has been shown to be important in controlling various inflammatory diseases. The cell adhesion proteins are induced by various inflammatory cytokines, such as tumor necrosis factor-alpha, interleukin-1, and bacterial lipopolysaccharide. The induction process primarily takes place at the level of transcription, where nuclear factor-kappaB (NF-kappaB) plays a major role. We demonstrate here that 2'-hydroxychalcone inhibits the adhesion of peripheral neutrophils to the endothelial cell monolayers by inhibiting the expression of ICAM-1, VCAM-1, and E-selectin in a concentration-dependent manner. The inhibition by 2'-hydroxychalcone is reversible. 2'-hydroxychalcone inhibits the induction of steady-state transcript levels of ICAM-1, VCAM-1, and E-selectin by tumor necrosis factor-alpha as determined by reverse transcription-polymerase chain reaction, and therefore it may interfere with the transcription of their genes. Because NF-kappaB is a major transcription factor involved in CAM expression, we studied its status in the 2'-hydroxychalcone treated cells. We demonstrate that 2'-hydroxychalcone inhibits the activation of NF-kappaB. These results have implications for using NF-kappaB inhibitors for the treatment of various inflammatory diseases. (+info)Neohesperidin dihydrochalcone is not a taste enhancer in aqueous sucrose solutions. (5/302)
Neohesperidin dihydrochalcone (NHDC) is an intensive sweetener, obtained by alkaline hydrogenation of neohesperidin. In this investigation a supposed taste enhancing effect of this substance was tested. A three-step procedure was used. In the first experiment, using a pool of 31 subjects, NHDC and sucrose detection thresholds were measured. In the second experiment, psychophysical functions for both tastants were determined. Then, 15 participants closest to the group threshold who, in addition, had produced monotonic psychophysical taste functions were selected to participate in the next two experiments. In the third experiment, taste enhancement was tested. Three psychophysical sucrose functions were constructed, one with a near-threshold amount of NHDC added to each of seven sucrose concentrations, one with a near-threshold amount of sucrose added (control 1) and one without any addition (control 2). No difference was found between the NHDC-enriched sucrose function and the sucrose-enriched sucrose function. Finally, in experiment 4, differential threshold functions were constructed with either NHDC or sucrose added. Neither the overall shape of the functions nor a comparison of the points of subjective equality showed enhancement. It was concluded that weak NHDC does not enhance the taste of aqueous sucrose solutions. (+info)Flavonoids inhibit cell growth and induce apoptosis in B16 melanoma 4A5 cells. (6/302)
We investigated the growth inhibitory activity of several flavonoids, including apigenin, luteolin, kaempherol, quercetin, butein, isoliquiritigenin, naringenin, genistein, and daizein against B16 mouse melanoma 4A5 cells. Isoliquiritigenin and butein, belonging to the chalcone group, markedly suppressed the growth of B16 melanoma cells and induced cell death. The other flavonoids tested showed little growth inhibitory activity and scarcely caused cell death. In cells treated with isoliquiritigenin or butein, condensation of nuclei and fragmentation of nuclear DNA, which are typical phenomena of apoptosis, were observed by Hoechst 33258 staining and by agarose gel electrophoresis of DNA. Flowcytometric analysis showed that isoliquiritigenin and butein increased the proportion of hypodiploid cells in the population of B16 melanoma cells. These results demonstrate that isoliquiritigenin and butein inhibit cell proliferation and induce apoptosis in B16 melanoma cells. Extracellular glucose decreased the proportion of hypodiploid cells that appeared as a result of isoliquiritigenin treatment. p53 was not detected in cells treated with either of these chalcones, however, protein of the Bcl-2 family were detected. The level of expression of Bax in cells treated with either of these chalcones was markedly elevated and the level of Bcl-XL decreased slightly. Isoliquiritigenin did not affect Bcl-2 expression, but butein down-regulated Bcl-2 expression. From these results, it seems that the pathway by which the chalcones induce apoptosis may be independent of p53 and dependent on proteins of the Bcl-2 family. It was supposed that isoliquiritigenin induces apoptosis in B16 cells by a mechanism involving inhibition of glucose transmembrane transport and promotion of Bax expression. On the other hand, it was suggested that butein induces apoptosis via down-regulation of Bcl-2 expression and promotion of Bax expression. This mechanism differs from the isoliquiritigenin induction pathway. (+info)PROP (6-n-Propylthiouracil) tasting and sensory responses to caffeine,sucrose, neohesperidin dihydrochalcone and chocolate. (7/302)
The genetically determined ability to taste 6-n-propylthiouracil (PROP) has been linked with lowered acceptance of some bitter foods. Fifty-four women, aged 18-30 years, tasted and rated PROP-impregnated filter paper and seven solutions of PROP. Summed bitterness intensity ratings for PROP solutions determined PROP taster status. Respondents also tasted five sucrose and seven caffeine solutions, as well as seven solutions each of caffeine and PROP that had been sweetened with 0.3 mmol/l neohesperidin dihydrochalcone (NHDC). Respondents also rated three kinds of chocolate using 9-point category scales. PROP tasters rated caffeine solutions as more bitter than did non-tasters and liked them less. PROP tasters did not rate either sucrose or NHDC as more sweet. The addition of NHDC to PROP and caffeine solutions suppressed bitterness intensity more effectively for tasters than for non-tasters and improved hedonic ratings among both groups. PROP tasters and non-tasters showed the same hedonic response to sweetened caffeine solutions and did not differ in their sensory responses to chocolate. Genetic taste markers may have only a minor impact on the consumption of such foods as sweetened coffee or chocolate. (+info)Dibenzoylmethane modulates aryl hydrocarbon receptor function and expression of cytochromes P50 1A1, 1A2, and 1B1. (8/302)
The phytochemical dibenzoylmethane (DBM) has been shown to prevent polycyclic aromatic hydrocarbon (PAH)-induced tumorigenesis in rodents. However, the biochemical basis of this activity is unclear. We have therefore investigated the effects of DBM on the activity and expression of carcinogen-activating enzymes, the cytochromes P450 (CYP) 1A1, 1A2, and 1B1. Oral administration of DBM to female Sprague Dawley rats inhibited the increase in hepatic enzyme activity and mRNA levels of CYP1A1, 1A2, and 1B1 caused by the PAH 7,12-dimethylbenz[a]anthracene (DMBA). However, DBM administration alone caused an increase in both activity and expression in the liver, albeit to levels much lower than that induced by DMBA. To characterize the molecular mechanisms involved in this dual action of DBM, we examined the effects of DBM in vitro. In HepG2 human hepatoma cells, DBM inhibited DMBA- and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced enzyme activity and CYP1A1, 1A2, and 1B1 mRNA levels, whereas DBM itself induced activity and mRNA expression. Modulation of CYP1A1 expression by DBM occurred at the transcriptional level, as transient transfection assays demonstrated. Because the transcription of CYP1A1 is regulated by the aryl hydrocarbon receptor (AhR), we investigated the effect of DBM on AhR activation. DBM inhibited TCCD-induced DNA-binding of the AhR to the xenobiotic-responsive element (XRE) of CYP1A1 as measured by electrophoretic mobility shift assay. These data suggest that the chemopreventive activity of DBM results from its ability to affect Phase 1 enzyme expression by modulation of AhR function. (+info)
Photoprotective compositions comprising photosensitive 1,3,5-triazine compounds, dibenzoylmethane compounds and siliceous s...
Synthesis, Antioxidant and Antimicrobial Activities of a Novel Series of Chalcones, Pyrazolic Chalcones, and Allylic Chalcones
Synthesis, Antioxidant and Antimicrobial Activities of a Novel Series of Chalcones, Pyrazolic Chalcones, and Allylic Chalcones
Our previous research show that chalcones display potent antileishmanial and antimalarial - Extracellular ATP inhibits chloride...
Chalcones as Scavengers of HOCl and Inhibitors of Oxidative Burst: Structure-Activity Relationship Studies | Bentham Science
Most recent papers with the keyword indole hydroxylation | Read by QxMD
Two existing drugs can block cell death in mice with neurodegeneration | AberdareOnline
Molecules | Free Full-Text | Structure of Dihydrochalcones and Related Derivatives and Their Scavenging and Antioxidant...
Biological evaluation and synthesis of new pyrimidine-2(1H)-ol/-thiol derivatives derived from chalcones using the solid phase...
淡江大學機構典藏:Item 987654321/112966
Dietary chalcones with chemopreventive and chemotherapeutic potential | Genes & Nutrition | Full Text
Chalcones - Natural Products
Desiging of the Style sheet
chalcones (CHEBI:23086)
Synthèse de dérivés coumariniques dintérêts biologiques et antioxydants - Université de Lorraine
KEGG PATHWAY: Flavonoid biosynthesis - Vitis vinifera (wine grape)
KEGG PATHWAY: map00941
Isoliquiritigenin | CAS# 961-29-5 | 2528 | BioVision, Inc.
Isoliquiritigenin triggers developmental toxicity and oxidative stressemediated apoptosis in zebrafish embryos/larvae via Nrf2...
Isoliquiritigenin reduces oxidative damage and alleviates
Naringenin and some of its useful pharmakinetics - AnabolicMinds.com
Academic Journals
Butein|Protein kinase inhibitor|CAS# 487-52-5
ılgın Resimleri - Ilgın Haberler - Son Dakika Ilgın Haberleri
GFT505 was well tolerated.
Computer-aided Design of Chalcone Derivatives as Lead Compounds Targeting Acetylcholinesterase - E-JURNAL
HPLC of flavanones and chalcones in different species and clones of Salix. - Semantic Scholar
Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis...
Anti-Proliferative Activity and Apoptosis Induction of an Ethanolic Extract of Boesenbergia pandurata (Roxb.) Schlecht. against...
The chalcone butein from Rhus verniciflua Stokes inhibits clonogenic growth of human breast cancer cells co-cultured with...
Dietary compound isoliquiritigenin, an antioxidant from licorice, suppresses triple-negative breast tumor growth via apoptotic...
2-Hydroxychalcone | Anticancer Agent | MedChemExpress
Second Harmonic Generation in Some Donor-Acceptor Substituted Chalcone Derivatives
Methoxyphenyl chalcone sensitizes aggressive epithelial cancer to cisplatin through apoptosis induction and cancer stem cell...
Targets
Flavonoid biosynthesis - Wikipedia
Determination of phenolic compounds and evaluation of antioxidant capacity of Campomanesia adamantium leaves
A Convergent Approach for the Synthesis of New Pyrazolyl Bipyridinyl Substituted Coumarin Derivatives as Antimicrobials
Isoliquiritigenin alleviates early brain injury after experimental intracerebral hemorrhage via suppressing ROS- and/or NF-κB...
Naringin Dihydrochalcone - Changsha Staherb Natural Ingredients Co., Ltd - ecplaza.net
Licochalcone A inhibiting proliferation of bladder cancer T24 cells by inducing reactive oxygen species production - IOS Press
Sci. Pharm. | Free Full-Text | Gene Regulatory Effects of Sappan lignum Extract in a Cell Model of Joint Inflammation
Navegando por assunto 2-quinolinonas
China 100% Natural Plant Extract Cardamom Extract Cardamonin 98% Photos & Pictures - Made-in-china.com
Plus it
MetNet - plant pathway - flavonoid biosynthesis
Army Air Forces Western Technical Training Command, 214th Mobile Training Unit B-29, Southern California, 1945 :: Dick...
Research Journal of Science and Technology
Efficient Reaction Between Substituted 2-Acetyl-1-Naphthol/2-Acetyl-1-Naphthol and Different Substituted Benz Aldehydes -...
BioNews - Liquorice could lower female fertility
DBD::DBM(3pm) - libdbi-perl - Debian testing - Debian Manpages
Forex russia gft
PJS | Imaging Proteolysis by Living Human Breast Cancer Cells
International Legal Group (ILG), Kuwait - Company Information, Key People, Latest News and Contact Details - ZAWYA MENA Edition
Prêmios | GFT Brazil
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Frizieru Piederumi - GLOBElife ☎ - Halonis - Produkti matiem, B.trend - Migliori prodotti PARRUCCHIERI | migliori marche...
阿伏苯宗 - 維基百科,自由的百科全書
4'-Methoxychalcone</span>
Chalco, NE: escorts - Sahra Escort
Synthesis and Characterization of Some New Pyrazoline Compounds Derived from Azo Chalcones
... was reacted with differently substituted benzaldehyde to obtain azo-chalcone (Ch1-Ch6). These chalcones were reacted with ... Ch6). These chalcones were reacted with hydrazine hydrate to yield azo-pyrazoline compounds (Py1-Py6). The. structures of ... "Synthesis and Characterization of Some New Pyrazoline Compounds Derived from Azo Chalcones". Journal of Garmian University, 6, ... Synthesis and Characterization of Some New Pyrazoline Compounds Derived from Azo Chalcones. Journal of Garmian University, 2019 ...
Hesperidin Methyl Chalcone - Citrus Extract to Support Venous Health
Hesperidin Methyl Chalcone (HMC) is a powerful antioxidant, protecting the cardiovascular system from oxidative attack and ... Hesperidin Methyl Chalcone Supplement - Supports Venous Health. Hesperidin methyl chalcone (HMC) supplement is an extract of ... What is Hesperidin Methyl Chalcone?. Hesperidin methyl chalcone (HMC) is a methylated derivative of the flavonoid compound ... With a long history of popular use in Asia, hesperidin methyl chalcone has now made a grand entrance in Europe. Drawing on ...
Asymmetric total synthesis and biological evaluation of proapoptotic natural myrcene-derived cyclohexenyl chalcones | CEBA
View of Synthesis and characterization of new Oxazine , Thiazine and Pyrazol derived from chalcones
Antirougeurs CALM Soothing Mask
Charcone | GreenMedInfo | Substance | Natural Medicine | Alternative
Unusual regiochemical control of the reactivity of some organometallics with chalcone<...
N2 - A series of α-thio- and seleno-alkyl-lithiums add to chalcone mainly at the C-3 site in tetrahydrofuran (THF) and quite ... AB - A series of α-thio- and seleno-alkyl-lithiums add to chalcone mainly at the C-3 site in tetrahydrofuran (THF) and quite ... A series of α-thio- and seleno-alkyl-lithiums add to chalcone mainly at the C-3 site in tetrahydrofuran (THF) and quite ... Dumont, W. ; Lucchetti, J. ; Krief, A. / Unusual regiochemical control of the reactivity of some organometallics with chalcone ...
New peripherally and non-peripherally tetra-substituted metal-free, magnesium(II) and zinc(II) phthalocyanine derivatives fused...
Since chalcones and their derivatives show a broad range of biological and pharmaceutical activities, these products are ... Chalcone containing new peripherally and non-peripherally tetra-substituted metal-free and metallophthalo-cyanine derivatives ... Moreover; the chalcone fused magnesium(II) and zinc(II) phthalocyanines also showed excellent fluorescence properties. ... Specifically, the new non-peripheral zinc(II) and magnesium(II) chalcone-phthalocyanines have the remarkable potential to be ...
Publications | Max Planck Institute of Colloids and Interfaces
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Iraqi Academic Scientific Journals - IASJ
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Hamilton, V.<...
Battaglia, Z. O., Kersten, J. T., Nicol, E. M., Whitworth, P., Wheeler, K. A., Hall, C. L., Potticary, J., Hamilton, V., Hall, S. R., DAmbruoso, G., Matsumoto, M., Warren, S. D. & Cremens, M. E., 25 Aug 2020, (Accepted/In press) In: Acta Crystallographica Section E: Crystallographic Communications. E76, p. 1496-1502 7 p.. Research output: Contribution to journal › Article (Academic Journal) › peer-review ...
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PDF) Synthesis of Chalcones by grindstone chemistry as Chalcones: an update on utility we have synthesized chalcones by ... chalcones synthesis by grinding stone technique. chalcones synthesis by grinding stone technique spitseu. chalcones synthesis ... chalcones synthesis by grinding stone technique. chalcones synthesis by grinding stone technique. chalcones synthesis by ... chalcones synthesis by grinding stone technique. chalcones synthesis by grinding stone technique- chalcones synthesis by ...
Parapharmaceuticals
Ep.45: Raise Your Vibe with Dr. Cowan's Garden | GreenSmoothieGirl
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Ukubulala izinambuzane emakhaya
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Chemical Reagent
Cypermethrin
Synergist
Methyl8
- Hesperidin methyl chalcone (HMC) supplement is an extract of Citrus aurentium standardised to 98% hesperidin methyl chalcone delivered in vegetarian capsules, to support venous health and improve circulation, now available to buy at Supersmart. (supersmart.com)
- Hesperidin methyl chalcone (HMC) is a methylated derivative of the flavonoid compound hesperidin . (supersmart.com)
- What are the benefits associated with Hesperidin Methyl Chalcone? (supersmart.com)
- With a long history of popular use in Asia, hesperidin methyl chalcone has now made a 'grand entrance' in Europe. (supersmart.com)
- What do studies show about Hesperidin methyl chalcone (HMC)? (supersmart.com)
- Buy Hesperidin Methyl Chalcone capsules for benefits to circulation and venous support. (supersmart.com)
- Varitonin by Douglas Laboratories provides a blend of vitamin C, hesperidin methyl chalcone, and standardized extracts of horse chestnut, butcher's broom, and gotu kola for comprehensive vascular support. (covenanthealthproducts.com)
- combination of 3 active molecules: hesperidin methyl chalcones, dipeptide VW and lipo peptide Pal-GQPBR. (glombeauty.com)
Derivatives5
- Chalcone and curcumin derivatives: a way ahead for malarial treatment. (greenmedinfo.com)
- Chalcone containing new peripherally and non-peripherally tetra-substituted metal-free and metallophthalo-cyanine derivatives were designed and synthesized (Schemes 1 and 2). (ktu.edu.tr)
- Since chalcones and their derivatives show a broad range of biological and pharmaceutical activities, these products are promising candidates for various applications, particularly as photosensitizers for photodynamic therapy in combination with fluorescence imaging. (ktu.edu.tr)
- Chalcone derivative were synthesized by reaction of some benzaldehyde derivatives with acetophenone or substituted. (iasj.net)
- In this study, we examined the potential of licochalcone A (a natural chalcone) and five synthetic derivatives (LM compounds) for inhibiting Tau misfolding, scavenging reactive oxygen species (ROS) and providing neuroprotection in human cells expressing proaggregant ΔK280 Tau RD -DsRed. (ntnu.edu.tw)
Flavonoids1
- The medicinal property of mulethi is mainly because of the presence of powerful phytochemicals namely flavonoids, chalcones, saponins and xenoestrogens. (jaydhanvantari.com)
Synthesis3
- 2019). 'Synthesis and Characterization of Some New Pyrazoline Compounds Derived from Azo Chalcones', Journal of Garmian University , 6(SCAPAS Conferance), pp. 18-25. (edu.krd)
- An efficient and operationally simple synthesis of some new pdf n efficient and operationally simple synthesis of some new chalcones by using grinding technique friendly method for synthesis of chalcones by grinding technique. (hotelcityderendingen.ch)
- The synthesis and properties of new chalcone ligand 4I-L ((2E)-1-[4-(1H-imidazol-1-yl)phenyl]-3-(4-iodophenyl)prop-2-en-1-one) and tetracoordinate Co(II) complex [Co(4I-L)(2)Cl-2], (1a), are reported in this article. (vutbr.cz)
Compounds1
- These chalcones were reacted with hydrazine hydrate to yield azo-pyrazoline compounds (Py1-Py6). (edu.krd)
Solvent free1
- chalcones into novel cyclohexenones under solvent-free conditions. (inlib.in)
Yellowish1
- Japanese scientists have discovered that its yellowish sap - Chalcone possesses valuable carcinostatic, antithrombotic and ulcer preventive abilities. (aceashitaba.com)
Reaction1
- yield by milling the reaction mixture of dimedone, chalcone and. (hotelcityderendingen.ch)
Unique1
- When mature, these plants are found to contain the unique chalcones of xanthoangelol and 4-hydroxyderricin . (aceashitaba.com)
Properties1
- the chalcone fused magnesium(II) and zinc(II) phthalocyanines also showed excellent fluorescence properties. (ktu.edu.tr)
Potential1
- Specifically, the new non-peripheral zinc(II) and magnesium(II) chalcone-phthalocyanines have the remarkable potential to be used as Type II photosensitizers for the treatment of cancer in PDT owing to their good singlet oxygen and appropriate photodegradation quantum yields. (ktu.edu.tr)