Azetidinecarboxylic Acid
Molecular Sequence Data
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
Heat-Shock Proteins
Amino Acid Sequence
Heat-Shock Response
Models, Molecular
Creatine Kinase
A transferase that catalyzes formation of PHOSPHOCREATINE from ATP + CREATINE. The reaction stores ATP energy as phosphocreatine. Three cytoplasmic ISOENZYMES have been identified in human tissues: the MM type from SKELETAL MUSCLE, the MB type from myocardial tissue and the BB type from nervous tissue as well as a mitochondrial isoenzyme. Macro-creatine kinase refers to creatine kinase complexed with other serum proteins.
Creatine
Rabbits
Stereoisomerism
Effect of L-azetidine-2-carboxylic acid on glycosylations of collagen in chick-embryo tendon cells. (1/140)
The glycosylations of hydroxylysine during collagen biosynthesis in isolated chick-embryo tendon cells were studied by using pulse-chase labelling experiments with [14C]-lysine. The hydroxylation of lysine and the glycosylations of hydroxylysine continued after a 5 min pulse label for up to about 10 min during the chase period. These data differ from those obtained previously in isolated chick-embryo cartilage cells, in which, after a similar 5 min pulse label, these reactions continued during the chase period for up to about 20 min. The collagen synthesized by the isolated chick-embryo tendon cells differed markedly from the type I collagen of adult tissues in its degree of hydroxylation of lysine residues and glycosylations of hydroxylysine residues. When the isolated tendon cells were incubated in the presence of L-azetidine-2-carboxylic acid, the degree of glycosylations of hydroxylysine during the first 10 min of the chase period was identical with that in cells incubated without thcarboxylic acid for at least 60 min, whereas no additional glycosylations took place in the control cells after the 10 min time-point. As a consequence, the collagen synthesized in the presence of this compound contained more carbohydrate than did the collagen synthesized by the control cells. Additional experiments indicated that azetidine-2-carboxylic acid did not increase the collagen glycosyltransferase activities in the tendon cells or the rate of glycosylation reactions when added directly to the enzyme incubation mixture. Control experiments with colchicine indicated that the delay in the rate of collagen secretion, which was observed in the presence of azetidine-2-carboxylic acid, did not in itself affect the degree of glycosylations of collagen. The results thus suggest that the increased glycosylations were due to inhibition of the collagen triple-helix formation, which is known to occur in the presence of azetidine-2-carboxylic acid. (+info)Intracellular retention of procollagen within the endoplasmic reticulum is mediated by prolyl 4-hydroxylase. (2/140)
The correct folding and assembly of proteins within the endoplasmic reticulum (ER) are prerequisites for subsequent transport from this organelle to the Golgi apparatus. The mechanisms underlying the ability of the cell to recognize and retain unassembled or malfolded proteins generally require binding to molecular chaperones within the ER. One classic example of this process occurs during the biosynthesis of procollagen. Here partially folded intermediates are retained and prevented from secretion, leading to a build up of unfolded chains within the cell. The accumulation of these partially folded intermediates occurs during vitamin C deficiency due to incomplete proline hydroxylation, as vitamin C is an essential co-factor of the enzyme prolyl 4-hydroxylase. In this report we show that this retention is tightly regulated with little or no secretion occurring under conditions preventing proline hydroxylation. We studied the molecular mechanism underlying retention by determining which proteins associate with partially folded procollagen intermediates within the ER. By using a combination of cross-linking and sucrose gradient analysis, we show that the major protein binding to procollagen during its biosynthesis is prolyl 4-hydroxylase, and no binding to other ER resident proteins including Hsp47 was detected. This binding is regulated by the folding status rather than the extent of hydroxylation of the chains demonstrating that this enzyme can recognize and retain unfolded procollagen chains and can release these chains for further transport once they have folded correctly. (+info)Activation of the unfolded protein response pathway induces human asparagine synthetase gene expression. (3/140)
The gene for the amino acid biosynthetic activity asparagine synthetase (AS) is induced by both amino acid and glucose deprivation of cells. The data reported here document that the human AS gene is induced following activation of the Unfolded Response Pathway (UPR), also known as the Endoplasmic Reticulum Stress Response (ERSR) in mammals. Increased AS transcription occurs in response to glucose deprivation, tunicamycin, or azetidine-2-carboxylate, all known to activate the UPR/ERSR pathway. Previously identified ERSR target genes contain multiple copies of a single highly conserved cis-element. In contrast, the human AS gene does not contain the ERSR element, as it has been described for other responsive genes. Instead, AS induction requires an Sp1-like sequence, a sequence previously shown to be associated with amino acid control of transcription, and possibly, a third region containing no consensus sequences for known transcription factors. Oligonucleotides covering each of these regions form DNA-protein complexes in vitro, and for some the amount of these complexes is greater when nuclear extracts from glucose-starved cells are tested. These results document that a wider range of metabolic activities are activated by the UPR/ERSR pathway than previously recognized and that genomic elements other than those already described can serve to enhance transcription of specific target genes. (+info)Upregulation of cytosolic chaperonin CCT subunits during recovery from chemical stress that causes accumulation of unfolded proteins. (4/140)
The chaperonin containing TCP-1 (CCT) is a molecular chaperone consisting of eight subunit species and assists in the folding of actin, tubulin and some other cytosolic proteins. We examined the stress response of CCT subunit proteins in mammalian cultured cells using chemical stressors that cause accumulation of unfolded proteins. Levels of CCT subunit proteins in HeLa cells were coordinately and transiently upregulated under continuous chemical stress with sodium arsenite. CCT subunit levels in several mammalian cell lines were also upregulated during recovery from chemical stress caused by sodium arsenite or a proline analogue, L-azetidine-2-carboxylic acid. Several unidentified proteins that were newly synthesized and associated with CCT were found to increase concomitantly with CCT subunits themselves and known substrates during recovery from the stress. These results suggest that CCT plays important roles in the recovery of cells from protein damage by assisting in the folding of proteins that are actively synthesized and/or renatured during this period. (+info)Saccharomyces cerevisiae sigma 1278b has novel genes of the N-acetyltransferase gene superfamily required for L-proline analogue resistance. (5/140)
We discovered on the chromosome of Saccharomyces cerevisiae Sigma 1278b novel genes involved in L-proline analogue L-azetidine-2-carboxylic acid resistance which are not present in the standard laboratory strains. The 5.4 kb-DNA fragment was cloned from the genomic library of the L-azetidine-2-carboxylic acid-resistant mutant derived from a cross between S. cerevisiae strains S288C and Sigma 1278b. The nucleotide sequence of a 4.5-kb segment exhibited no identity with the sequence in the genome project involving strain S288C. Deletion analysis indicated that one open reading frame encoding a predicted protein of 229 amino acids is indispensable for L-azetidine-2-carboxylic acid resistance. The protein sequence was found to be a member of the N-acetyltransferase superfamily. Genomic Southern analysis and gene disruption showed that two copies of the novel gene with one amino acid change at position 85 required for L-azetidine-2-carboxylic acid resistance were present on chromosomes X and XIV of Sigma 1278b background strains. When this novel MPR1 or MPR2 gene (sigma 1278b gene for L-proline analogue resistance) was introduced into the other S. cerevisiae strains, all of the recombinants were resistant to L-azetidine-2-carboxylic acid, indicating that both MPR1 and MPR2 are expressed and have a global function in S. cerevisiae. (+info)Induced activity of adenine phosphoribosyltransferase (APRT) in iron-deficiency barley roots: a possible role for phytosiderophore production. (6/140)
To isolate the genes involved in the response of graminaceous plants to Fe-deficient stress, a protein induced by Fe-deficiency treatment was isolated from barley (Hordeum vulgare L.) roots. Based on the partial amino acid sequence of this protein, a cDNA (HvAPT1) encoding adenine phosphoribosyltransferase (APRT: EC 2.4.2.7) was cloned from a cDNA library prepared from Fe-deficient barley roots. Southern analysis suggested that there were at least two genes encoding APRT in barley. Fe deficiency increased HvAPT1 expression in barley roots and resupplying Fe to the Fe-deficient plants rapidly negated the increase in HvAPT1 mRNA. Analysis of localization of HvAPT1-sGFP fusion proteins in tobacco BY-2 cells indicated that the protein from HvAPT1 was localized in the cytoplasm of cells. Consistent with the results of Northern analysis, the enzymatic activity of APRT in barley roots was remarkably increased by Fe deficiency. This induction of APRT activity by Fe deficiency was also observed in roots of other graminaceous plants such as rye, maize, and rice. In contrast, the induction was not observed to occur in the roots of a non-graminaceous plant, tobacco. Graminaceous plants generally synthesize the mugineic acid family phytosiderophores (MAs) in roots under Fe-deficient conditions. In this paper, a possible role of HvAPT1 in the biosynthesis of MAs related to adenine salvage in the methionine cycle is discussed. (+info)Hydroxylated phytosiderophore species possess an enhanced chelate stability and affinity for iron(III). (7/140)
Graminaceous plant species acquire soil iron by the release of phytosiderophores and subsequent uptake of iron(III)-phytosiderophore complexes. As plant species differ in their ability for phytosiderophore hydroxylation prior to release, an electrophoretic method was set up to determine whether hydroxylation affects the net charge of iron(III)-phytosiderophore complexes, and thus chelate stability. At pH 7.0, non-hydroxylated (deoxymugineic acid) and hydroxylated (mugineic acid; epi-hydroxymugineic acid) phytosiderophores form single negatively charged iron(III) complexes, in contrast to iron(III)-nicotianamine. As the degree of phytosiderophore hydroxylation increases, the corresponding iron(III) complex was found to be less readily protonated. Measured pKa values of the amino groups and calculated free iron(III) concentrations in presence of a 10-fold chelator excess were also found to decrease with increasing degree of hydroxylation, confirming that phytosiderophore hydroxylation protects against acid-induced protonation of the iron(III)-phytosiderophore complex. These effects are almost certainly associated with intramolecular hydrogen bonding between the hydroxyl and amino functions. We conclude that introduction of hydroxyl groups into the phytosiderophore skeleton increases iron(III)-chelate stability in acid environments such as those found in the rhizosphere or the root apoplasm and may contribute to an enhanced iron acquisition. (+info)Protein misfolding and temperature up-shift cause G1 arrest via a common mechanism dependent on heat shock factor in Saccharomycescerevisiae. (8/140)
Accumulation of misfolded proteins in the cell at high temperature may cause entry into a nonproliferating, heat-shocked state. The imino acid analog azetidine 2-carboxylic acid (AZC) is incorporated into cellular protein competitively with proline and can misfold proteins into which it is incorporated. AZC addition to budding yeast cells at concentrations sufficient to inhibit proliferation selectively activates heat shock factor (HSF). We find that AZC treatment fails to cause accumulation of glycogen and trehalose (Msn2/4-dependent processes) or to induce thermotolerance (a protein kinase C-dependent process). However, AZC-arrested cells can accumulate glycogen and trehalose and can acquire thermotolerance in response to a subsequent heat shock. We find that AZC treatment arrests cells in a viable state and that this arrest is reversible. We find that cells at high temperature or cells deficient in the ubiquitin-conjugating enzymes Ubc4 and Ubc5 are hypersensitive to AZC-induced proliferation arrest. We find that AZC treatment mimics temperature up-shift in arresting cells in G1 and represses expression of CLN1 and CLN2. Mutants with reduced G1 cyclin-Cdc28 activity are hypersensitive to AZC-induced proliferation arrest. Expression of the hyperstable Cln3-2 protein prevents G1 arrest upon AZC treatment and temperature up-shift. Finally, we find that the EXA3-1 mutation, encoding a defective HSF, prevents efficient G1 arrest in response to both temperature up-shift and AZC treatment. We conclude that nontoxic levels of misfolded proteins (induced by AZC treatment or by high temperature) selectively activate HSF, which is required for subsequent G1 arrest. (+info)
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Domain assignment for YHR166C from Saccharomyces cerevisiae Sigma1278b
Iron acquisition by phytosiderophores contributes to cadmium tolerance | AVESİS
Effect of nitrogen on root release of phytosiderophores and root uptake of Fe(III)-phytosiderophore in Fe-deficient wheat...
Early senescence of the oldest leaves of Fe-deficient barley plants may contribute to phytosiderophore release from the roots -...
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Identification of two novel phytosiderophores secreted by perennial grasses.
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List of MeSH codes (D12.125)
... imino acids MeSH D12.125.072.401.200 - azetidinecarboxylic acid MeSH D12.125.072.401.623 - proline MeSH D12.125.072.401.623.270 ... 2-aminoadipic acid MeSH D12.125.119.170 - aspartic acid MeSH D12.125.119.170.150 - d-aspartic acid MeSH D12.125.119.170.275 - ... aspartic acid MeSH D12.125.067.500.150 - d-aspartic acid MeSH D12.125.067.500.275 - isoaspartic acid MeSH D12.125.067.500.400 ... aspartic acid MeSH D12.125.427.300 - glutamic acid MeSH D12.125.481.100 - allylglycine MeSH D12.125.481.700 - n-substituted ...
List of MeSH codes (D03)
... azetidinecarboxylic acid MeSH D03.383.097.217 - aziridines MeSH D03.383.097.217.300 - carbazilquinone MeSH D03.383.097.217.900 ... pipemidic acid MeSH D03.383.725.547.650 - piromidic acid MeSH D03.383.725.547.900 - 3-pyridinecarboxylic acid, 1,4-dihydro-2,6- ... niflumic acid MeSH D03.066.515.635 - pipemidic acid MeSH D03.066.515.650 - piromidic acid MeSH D03.066.515.950 - xanthinol ... nalidixic acid MeSH D03.438.810.835.055.550 - nedocromil MeSH D03.438.810.835.055.580 - oxolinic acid MeSH D03.438.810.835.188 ...
2-Azetidinecarboxylic acid
Azetidinecarboxylic Acid | Harvard Catalyst Profiles | Harvard Catalyst
"Azetidinecarboxylic Acid" by people in Harvard Catalyst Profiles by year, and whether "Azetidinecarboxylic Acid" was a major or ... "Azetidinecarboxylic Acid" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical ... Below are the most recent publications written about "Azetidinecarboxylic Acid" by people in Profiles. ... Below are MeSH descriptors whose meaning is more general than "Azetidinecarboxylic Acid". ...
S)-(-)-2-Azetidinecarboxylic acid | 2133-34-8
2-Azetidinecarboxylic acid(2133-34-8). At last,(S)-(-)-2-Azetidinecarboxylic acid(2133-34-8) safety, risk, hazard and MSDS, CAS ... 2-Azetidinecarboxylic acid(2133-34-8) information like chemical properties,Structure,melting point,boiling point,density, ... S)-(-)-2-Azetidinecarboxylic acid structure CAS No.. 2133-34-8. Chemical Name:. (S)-(-)-2-Azetidinecarboxylic acid. Synonyms. H ... L-AZETIDINECARBOXYLIC ACID;azetidyl-2-carboxylic acid;l-azetidine-2-carboxylicaci;L-2-AZETIDINECARBOXYLIC ACID. CBNumber:. ...
3-Azetidinecarboxylic acid/36476-78-5-ChonTech
1-BOC-3-AZETIDINE CARBOXYLIC ACID Manufacturer,Supplier,Exporter
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886510-13-0,1-Azetidinecarboxylicacid, 3-hydroxy-, 9H-fluoren-9-ylmethyl ester
Category:Carboxylic acids - Wikimedia Commons
For the conjugate bases of carboxylic acids, RCO2−, see Category:Carboxylate ions. For salts of carboxylic acids, RCO2M, see ... Molecules containing such a functional group are also called carboxylic acids or organic acids, although there are other ... In chemistry, carboxylic acids are acids characterized by the presence of a carboxyl group. ... carboxylic acid-transporting ATPase activity (cargo),. carboxylic acid transmembrane transporter activity (cargo),. carboxylic ...
WAND Product and Services - Organic Acids
... acetic acid],2-Azetidinecarboxylic Acid,3,3,3-(Trioxo-1,3,5-triazinetriyl)tri(propionic Acid),3,4-Dimethoxyphthalic Acid, ... butyric Acid,(S)-Piperidine-2-carboxylic Acid,1,1-Ferrocenedicarboxylic Acid,1-Amino-4-bromo-9,10-dioxoanthracene-2-sulfonic ... WAND Categories > Chemicals, Organic>Organic Acids >. The WAND Organic Chemicals taxonomy includes the set of substances, ... 3,3,3-(Trioxo-1,3,5-triazinetriyl)tri(propionic Acid). [Display Results] ...
Boc-azetidine-3-carboxylic acid, 142253-552, suppliers and manufacturers
3-dicarboxylic acid mono-tert-butyl ester; 1-(tert-butoxycarbonyl)-3-azetidinecarboxylic acid ... Synonyms: N-Boc-azetidine-3-carboxylic acid; 1-(tert-butoxycarbonyl)azetidine-3-carboxylic acid; azetidine-1, ... Find manufacturers and suppliers for Boc-azetidine-3-carboxylic acid, 142253-552. ... N-Boc-azetidine-3-carboxylic acid; 1-(tert-butoxycarbonyl)azetidine-3-carboxylic acid; azetidine-1,3-dicarboxylic acid mono- ...
Combi-Blocks
... carboxylic acids, imidazoles, thiazoles, azoles, indoles, oxindoles, pyridines, heterocycles, bormides, fluoro compounds, ... 1-Methyl-3-azetidinecarboxylic acid. Purity: 95%. [875629-26-8], MFCD11520621. © 1997-2019 Combi-Blocks Inc. Phone: 1-858-635- ... 3-(Methylamino)propanoic acid HCl. Purity: 98%. [65845-56-9], MFCD03490507. ST-8874. 3-(Methylamino)propionic acid. Purity: 95% ... 3-(Methylamino)-4-nitrobenzoic acid. Purity: 98%. [214778-10-6], MFCD18826011. ST-1576. 4-(Methylamino)-3-nitrobenzoic acid. ...
CAS Number, CAS NO. Search, cas no. of chemicals Search,cas number database free -CasNo list - 1,178322-42-4,17791-80-9
1-Azetidinecarboxylic acid, 3-[4-(aminosulfonyl)-1-piperazinyl]-, 1,1-dimethylethyl ester. C12H24N4O4S. ... Benzoic acid, 4-[4,5-dihydro-3-methyl-5-oxo-4-(2-pyridinylmethylene)-1H-pyrazol-1-yl]-. C17H13N3O3. ... L-Aspartic acid, L-prolyl-L-arginyl-L-cysteinylglycyl-L-valyl-L-prolyl-. C30H50N10O10S. ... Heptanoic acid, 3,4,6-trihydroxy-2-methyl-6-(4-methyl-5-oxo-3-cyclohexen-1-yl)-. C15H24O6. ...
WO1992019593A1 - Novel immunosuppressive compounds
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Neurotrophic 2-azetidinecarboxylic acid derivatives, and related compositions and methods WO2001004091A1 (en) * 1999-07-09. ... Neurotrophic 2-azetidinecarboxylic acid derivatives, and related compositions and methods US6187784B1 (en) 1998-06-03. 2001-02- ... Neurotrophic 2-azetidinecarboxylic acid derivatives, and related compositions and methods US6734211B1 (en) 1999-07-09. 2004-05- ... Fatty acids such as oleic acid and its glyceride derivatives find use in the preparation of injectables, as do natural ...
CAS Number, CAS NO. Search, cas no. of chemicals Search,cas number database free -CasNo list - 1,169038-39-5,169453-31-0
Butanoic acid,4-[(4-amino-1,2,3,6-tetrahydro-1-methyl-2,6-dioxo-5-pyrimidinyl)amino]-4-oxo-. C9H12 N4 O5. ... 2-Azetidinecarboxylicacid, 3-(2-hydroxyethyl)-4-oxo-, (2S-trans)- (9CI). C6H9 N O4. ... Benzeneacetic acid, a-[[1-[[(1,1-dimethylethyl)amino]carbonyl]-2-methylpropyl]amino]-,methyl ester, [R-(R*,R*)]- (9CI). C18H28 ... Hexadecanoic acid,1,1-[(1R)-1-[(phosphonooxy)methyl]-1,2-ethanediyl] ester, sodium salt (1:1). C35H69 O8 P . Na. ...
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1-[[4-[(1E)-1-[[[4-Cyclohexyl-3-(trifluoromethyl)phenyl]methoxy]imino]ethyl]-2-ethylphenyl]methyl]-3-azetidinecarboxylic acid ( ... MAYZENT tablets contains siponimod, an S1P receptor modulator, as 2:1 co-crystal of siponimod and fumaric acid and has the ... 1 co-crystal of siponimod and fumaric acid, respectively. ...
David Valle - Research Output
- Johns Hopkins University
Mutant cell lines resistant to azetidine carboxylic acid: Quantitative and qualitative differences in pyrroline-5-carboxylate ... Mutant cell lines resistant to azetidine-2-carboxylic acid: Changes in the biosynthesis of proline from glutamic acid. Smith, R ... Mutant cell lines resistant to azetidine‐2‐carboxylic acid: Alterations in the synthesis of proline from glutamic acid. Lodato ... Defective imino acid metabolism in hypoglycin-treated rats. Goodman, S. I. & Valle, D., Feb 1984, In : Biochemical medicine. 31 ...
List of MeSH codes (D12.125) - Wikipedia
... imino acids MeSH D12.125.072.401.200 - azetidinecarboxylic acid MeSH D12.125.072.401.623 - proline MeSH D12.125.072.401.623.270 ... 2-aminoadipic acid MeSH D12.125.119.170 - aspartic acid MeSH D12.125.119.170.150 - d-aspartic acid MeSH D12.125.119.170.275 - ... aspartic acid MeSH D12.125.067.500.150 - d-aspartic acid MeSH D12.125.067.500.275 - isoaspartic acid MeSH D12.125.067.500.400 ... aspartic acid MeSH D12.125.427.300 - glutamic acid MeSH D12.125.481.100 - allylglycine MeSH D12.125.481.700 - n-substituted ...
US5990333A - Silyl-linked polyamidoamines and their preparation
- Google Patents
... azetidine, carboxylic acid anhydride, acryloxy, methacryloxy, acrylamido, methacrylamido, halide, and carboxylic acid halide ... butyric acid, valeric acid, caproic acid, caprylic acid, oleic acid, ortho-toluic acid, meta-toluic acid, and para-toluic acid ... 2-hydroxybenzoic acid (i.e., salicylic acid), 3-hydroxybenzoic acid, acetic acid, phenylacetic acid, propionic acid, ... orthomethoxybenzoic acid, meta-methoxybenzoic acid, and paramethoxybenzoic acid.. Monofunctional carboxylic acid esters which ...
Author K. Bláha | Collection of Czechoslovak Chemical Communications
Proton magnetic reasonance studies of cyclodipeptides containing pipecolic acid, proline and/or 2-azetidinecarboxylic acid. ... An alternative route to Nα-methylamino acid derivatives: Synthesis and conformation of some Nα-acetyl-Nα-methylamino acid ... Amino acids and peptides. CIII. Infrared spectra and conformations of methylamides of N-acylated amino acids with a hydroxyl ... Amino acids and peptides. LXXXVII. Optical rotatory dispersion of some β-aryl α-amino acids and model compounds. 1968, Vol. 33 ...
Conformationally Restricted Creatine Analogs and Substrate Specificity of Rabbit Muscle Creatine Kinase<...
2-iminoimidazolidine-4-carboxylic acid (11), and 2-imino-3-methylimidazolidine-4-carboxylic acid (12) did not show detectable ... 2-iminoimidazolidine-4-carboxylic acid (11), and 2-imino-3-methylimidazolidine-4-carboxylic acid (12) did not show detectable ... 2-iminoimidazolidine-4-carboxylic acid (11), and 2-imino-3-methylimidazolidine-4-carboxylic acid (12) did not show detectable ... 2-iminoimidazolidine-4-carboxylic acid (11), and 2-imino-3-methylimidazolidine-4-carboxylic acid (12) did not show detectable ...
HYBRID CHIMERA POLYPEPTIDES AS DUAL INHIBITORS OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR AND PLATELET-DERIVED GROWTH...
... azetidinecarboxylic acid, 2-aminoadipic acid, 3- aminoadipic acid, beta-alanine, aminopropionic acid, 2-aminobutyric acid, 4- ... aminobutyric acid, 6-aminocaproic acid, 2-aminoheptanoic acid, 2-aminoisobutyric acid, 3-aminoisbutyric acid, 2- aminopimelic ... aspartic acid- (beta-methyl ester), a modified amino acid of aspartic acid; N-ethylglycine, a modified amino acid of glycine; ... acid, tertiary-butylglycine, 2,4-diaminoisobutyric acid, desmosine, 2,2- diaminopimelic acid, 2,3-diaminopropionic acid, N- ...
Kuniki Kino - Research Output
- Waseda University
NRPSs and amide ligases producing homopoly(amino acid)s and homooligo(amino acid)s. Hamano, Y., Arai, T., Ashiuchi, M. & Kino, ... Poly-α-glutamic acid synthesis using a novel catalytic activity of Rimk from Escherichia coli K-12. Kino, K., Arai, T. & ... Effective production of Pro-Gly by mutagenesis of l-amino acid ligase. Kino, H., Nakajima, S., Arai, T. & Kino, K., 2016 Aug 1 ... Structure of RizA, an l-amino-acid ligase from Bacillus subtilis. Kagawa, W., Arai, T., Ishikura, S., Kino, K. & Kurumizaka, H ...
DeCS
3 azetidinecarboxylic Acid. 3-azetidinecarboxylic Acid. Azetidine 2 carboxylic Acid. Azetidine 3 carboxylic Acid. Azetidine-2- ... Azetidinecarboxylic Acid - Preferred Concept UI. M0002071. Scope note. A proline analog that acts as a stoichiometric ... carboxylic Acid. Azetidine-3-carboxylic Acid. Tree number(s):. D02.241.081.583.100. D02.491.485.100. D03.383.082.301.100. ... Azetidine-3-carboxylic Acid Entry term(s). 3 azetidinecarboxylic Acid 3-azetidinecarboxylic Acid Azetidine 3 carboxylic Acid ...
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2-aminoethanesulfonic acid - definition of 2-aminoethanesulfonic acid by The Free Dictionary
2-aminoethanesulfonic acid synonyms, 2-aminoethanesulfonic acid pronunciation, 2-aminoethanesulfonic acid translation, English ... n. An amino acid, C2H7NO3S, not found in proteins, that is synthesized in the liver from cysteine, is found in... ... dictionary definition of 2-aminoethanesulfonic acid. adj. Of, relating to, or resembling a bull. ... Taurine, also known as 2-aminoethanesulfonic acid, is a naturally occurring beta-amino acid (which has a sulphonic acid group ...
2-butanone - definition of 2-butanone by The Free Dictionary
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Intermediates
3-Azetidine carboxylic acid. 36476-78-5. 2-(2-(2,2,2-Trifluoroethoxy)phenoxy)-ethyl methanesulfonate. 160969-03-9. ... 4 Chloro Nicotinic Acid. 10177-29-4. 3-(2-chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one. 63234-80-0 ... 2-Butyrylamino Propionic acid. 59875-04-6. 2-(2-Ethoxy Phenyl)-5-methyl-7-propylimidazo(1-5-f)-(1,2,4)-triazin-4-(1H)-one. ... 2-Sulfamoyl-ethyl)-carbamic acid benzyl ester. 136027-17-3. 3-Ethyl-4-Methyl-2-Oxo-N(2-Phenyl ethyl)-2,5-Dihydro-1H-. 247098-18 ...
Carboxylic7
- ChEBI: The (S)-enantiomer of azetidine-2-carboxylic acid. (chemicalbook.com)
- On the other hand, the conformationally restricted creatine analogues N-[2-(4,5-dihydroimidazolyl)]sarcosine (10), 2-iminoimidazolidine-4-carboxylic acid (11), and 2-imino-3-methylimidazolidine-4-carboxylic acid (12) did not show detectable activity either as substrates or as inhibitors. (elsevier.com)
- Binding studies of the (R)-N-amidino-azetidine-2-carboxylic acid (7) and its corresponding S enantiomer 6 in dead-end complexes with MnADP and in an-ion-stabilized dead-end complexes revealed that the affinity of the enzyme for 7 was between one and two orders of magnitude greater than for its S enantiomer 6. (elsevier.com)
- Taurine, also known as 2-aminoethanesulfonic acid , is a naturally occurring beta-amino acid (which has a sulphonic acid group instead of carboxylic acid, differentiating it from other amino acids) yielded by methionine and cysteine metabolism in the liver. (thefreedictionary.com)
- 4-Fluoro-2-methyl benzonitrile 147754-12-9 C8H6NF Indole-2-carboxylic acid 1477-50-5 C9H7NO2 4-Methyl-3-nitro benzaldehyde 14753-51-6 C8H7NO3 3-Amino picolinic acid 1462-86-8. (twfta.com)
- In organic chemistry , Acyclic Acids (Ethanoic Acids) , as organic compounds are 2 carbon straight-chain saturated carboxylic acids , that have an open-chain molecular structures as opposed to ring-shaped structures. (wellnessadvocate.com)
- The Zolpidem Phenyl-4-carboxylic Acid Ethyl Ester n/a (Catalog # MBS6057623 ) is a Biochemical and is intended for research purposes only. (mybiosource.com)
Methionine and cysteine metabolism1
- Aminoethanesulfonic Acid is also a product of methionine and cysteine metabolism. (alphachemikaindia.com)
Peptides1
- Ensembling three multicomponent reactions for the synthesis of a novel category of pseudo-peptides containing dithiocarbamate and N , X -heterocyclic groups , Amino Acids 2018 . (uol.de)
Acyclic2
- In protein science , an Imino Acid (Secondary Amino Acid) is a molecule, related to amino acids (differing in the bonding to the nitrogen), that contains both an imino (>C=NH) and a carboxyl (-C(=O)-OH) functional group, which occurs as either an acyclic acid or a cyclic imino acid . (wellnessadvocate.com)
- In carbohydrate science , Sugar Acids , as an acyclic acid , are acidic sugars. (wellnessadvocate.com)
Proteins1
- An amino acid, C 2 H 7 NO 3 S, not found in proteins, that is synthesized in the liver from cysteine, is found in bile and other body fluids and tissues, and has a variety of physiological functions. (thefreedictionary.com)
Benzoic1
- aminotetrahydro- Boc-4-Methoxyphenylalanine Ethyl 2-(2-Aminothiazole-4-Yl)Acetate 2-Amino-5-Iodobenzoic acid 4-Iodo-3-Nitrotoluene 4-Bromo-3-Nitrotoluene 2-hydrazino-benzoic acid 6-Chloro Nicotinic Acid Benzoyl Isothiocyanate 2-Chloro-4-Methylsulfonyl Benzoic Acid Benzeneacetic acid , .alpha. (twfta.com)
Benzeneacetic1
- chloromethyl)- N , N'-Carbonyldiimidazole 3 , 5-Dimethoxy-4-Hydroxybenzoic Acid 4-Amino-6-Chloropyrimidine 4 , 6-Dichloro-5-Pyrimidine Carboxaldehyde 4-Fluoro-4'-Methylbenzophenone 3-Pyridinecarboxaldehyde , 6-methyl- 7alpha-Hydroxydehydroepiandrosterone Isoquinoline , 6-methoxy- DL-Tropic Acid 1H-Indazole , 1-[(3-fluorophenyl)methyl]-5-nitro- Benzeneacetic acid , 2-chloro-.alpha. (twfta.com)
Gallic Acid1
- The data also suggest CAS polyphenols might be oligomeric proanthocyanidins with gallic acid and ellagic acid. (labome.ru)
Chemicals1
- Our company is mainly engaged in R&D,contract manufacture and scale-up production of API,Advance Intermediates,Fine Chemicals,Bio Chemicals,Protect Amino Acids,Chiral compounds and Electronic Chemicals. (chembuyersguide.com)
Synthesis1
- S)-(-)-2-Azetidinecarboxylic acid is a four-membered ring analog of L-Proline, It is a useful intermediate in the synthesis of polypeptides,Used in synthesis of abnormally high molecular weight polypeptides. (chemicalbook.com)
Suppliers2
- Full List of Hyluronic Acid Suppliers & Hyluronic Acid manufacturers in European Global & USA Asian. (twfta.com)
- Full List of ' 2-fluoro-4-methyl-1-nitro- 2-nitro-5-fluoro toluene 4-amino-2-fluorobenzoic acid 4-chloro-2-fluorobenzoic acid 3- 2 ' Manufacturers& 2-fluoro-4-methyl-1-nitro- 2-nitro-5-fluoro toluene 4-amino-2-fluorobenzoic acid 4-chloro-2-fluorobenzoic acid 3- 2 Suppliers in European Global & USA Asian. (twfta.com)
Compounds1
- At our sound processing unit, we process this acid using high quality compounds, sourced from trusted vendors. (alphachemikaindia.com)
Dimethyl1
- amino-4-methoxy- 2 , 5-Dimethyl Benzoxazole Benzenamine , 3-fluoro-2-nitro- 1 , 12-Dodecanediol (R)-2-chloro-1-phenylethanol 2-Amino-4-Hydroxy-6-Phenylpyrimidine 5-Amino-2-Fluorobenzoic acid Z-Glu-OMe 4-(2-Methoxyethyl)Phenol Tryptophan , 5-hydroxy- Benzenepropanoic acid , .alpha. (twfta.com)
MeSH1
- Azetidinecarboxylic Acid" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (harvard.edu)
Residue1
- e) fifth block (B1 e) comprising from about 7-1 1 amino acid residues of PDGF-B, starting from residue 94-98 up to residue 104. (sumobrain.com)
Products1
- Our prime products are Acid, Mordant,Direct and Basic dyes. (twfta.com)
Type1
- identification of individual amino acids in platelet-derived growth factor that contribute to the specificity towards the beta-type receptor. (sumobrain.com)
Year1
- This graph shows the total number of publications written about "Azetidinecarboxylic Acid" by people in Harvard Catalyst Profiles by year, and whether "Azetidinecarboxylic Acid" was a major or minor topic of these publication. (harvard.edu)
Publications1
- Below are the most recent publications written about "Azetidinecarboxylic Acid" by people in Profiles. (harvard.edu)