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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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 (D02)
... azetidinecarboxylic acid MeSH D02.241.081.583.400 - technetium tc 99m diethyl-iminodiacetic acid MeSH D02.241.081.583.450 - ... quinic acid MeSH D02.241.511.852 - shikimic acid MeSH D02.241.511.902 - sugar acids MeSH D02.241.511.902.107 - ascorbic acid ... azetidinecarboxylic acid MeSH D02.491.485.400 - technetium tc 99m diethyl-iminodiacetic acid MeSH D02.491.485.450 - technetium ... edetic acid MeSH D02.241.081.038.455 - egtazic acid MeSH D02.241.081.038.581 - iodoacetic acid MeSH D02.241.081.038.581.400 - ...
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 ...
1-Azetidinecarboxylic acid,2-oxo-4-phenyl-3-[[tris(1-methylethyl)silyl]oxy]-, 1,1-dimethylethyl ester,(3R,4S)-| CAS:#172213-23...
1-Azetidinecarboxylic acid,2-oxo-4-phenyl-3-[[tris(1-methylethyl)silyl]oxy]-, 1,1-dimethylethyl ester,(3R,4S)- CAS:172213-23-9, ... 1-Azetidinecarboxylic acid,2-oxo-4-phenyl-3-[[tris(1-methylethyl)silyl]oxy]-, 1,1-dimethylethyl ester,(3R,4S)- related products ... 1-Azetidinecarboxylic acid,2-oxo-4-phenyl-3-[[tris(1-methylethyl)silyl]oxy]-, 1,1-dimethylethyl ester,(3R,4S)-. *Product Name: ... 1-Azetidinecarboxylic acid,2-oxo-4-phenyl-3-[[tris(1-methylethyl)silyl]oxy]-, 1,1-dimethylethyl ester,(3R,4S)-. ...
Azetidines | Harvard Catalyst Profiles | Harvard Catalyst
Fmoc-azetidine-3-carboxylic acid | CAS 193693-64-0 | P212121 Store
Cas 193269-78-2,1-Boc-3-(Amino)azetidine | lookchem
Synonyms: 1-Azetidinecarboxylic acid, 3-amino-, 1,1-dimethylethyl ester;1-Boc-3-aminoazetidine ,97%;1-Boc-azetidin-3-amine;1- ... 3-AMino-1-azetidinecarboxylic Acid 1,1-DiMethylethyl Ester;tert-Butyl 3-AMino-1-azetidinecarboxylate ... 193269-94-2 (S)-3-((S)-2-AMino-propionylaMino)-pyrrolidine-1-carboxylic acid tert-butyl ester ... 193269-79-3 (S)-3-(2-AMino-acetylaMino)-pyrrolidine-1-carboxylic acid tert-butyl ester ...
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 ...
1,2,4-oxadiazoles (including Hydrogenated) Patents and Patent Applications (Class 548/131) - Justia Patents Search
3-azetidinecarboxylic acid (formula A). Also disclosed in the present invention are a preparation method for the salt form or ... Abstract: The present invention relates to crystalline forms of 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]-benzoic acid, ... Crystalline forms of 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]-benzoic acid for the treatment of disease ... Abstract: Novel 1,2,4-oxadiazole benzoic acid compounds, methods of using and pharmaceutical compositions comprising an 1,2,4- ...
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1016731-24-0 | MFCD07772065 | 1-Cbz-3-(aminomethyl)azetidine
1-Azetidinecarboxylic acid, 3-(aminomethyl)-, phenylmethyl ester 112257-20-2 3-aminomethyl-azetidine-1-carboxylic acid benzyl ... Boronic Acids. Iodos. Thiazoles. Bromides. Nitro Compounds. Other Heterocycles. Carboxes. Quinolines. Other Building Blocks. ... 102245-65-8 , 4-(tert-Butyl-dimethyl-silanyloxy)-but-2-ynoic acid , AA0006Y3 , MFCD06658386 ... 113467-97-3 , 2-Butenoic acid, 4-(cyclohexylamino)-4-oxo-, (E)- (9CI) , AA0008M7 , MFCD00086001 ...
CAS 128117-22-6 Four Membered Heterocyclic Compounds 1-Cbz-3-Hydroxyazetidine
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ß-N-Acetylhexosaminidase inhibition by an azetidine ADMDP-acetamide analogue is compared to an azetidine carboxylic acid amide ... 3-Hydroxyazetidine carboxylic acids: non-proteinogenic amino acids for medicinal chemists. Glawar, Andreas F G; Jenkinson, ... 4-iminoribonic acid is the first chemical synthesis of unprotected 3-hydroxyazetidine carboxylic acids. The long-term stability ... The structure of N,3-O-dibenzyl-2,4-dideoxy-2,4-imino-D-ribonic acid was established by X-ray crystallographic analysis. An N- ...
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... of the aldol reaction of benzaldehyde with acetone catalyzed by various proline derivatives and 2-azetidine carboxylic acid ... several parameters were tested on the industrial model reaction between 2-bromonaphthalene and phenylboronic acid catalyzed by ... features an unprecendented intramolecular cyclization reaction involving a carboxylic acid activated by tosyl chloride and an ... and intermolecular aldol reactions as well as Mannich reactions and oxyaminations catalyzed by proline and other amino acids, ...
DeCS
Azetidinecarboxylic Acid [D02.241.081.583.100] Azetidinecarboxylic Acid * Technetium Tc 99m Diethyl iminodiacetic Acid [D02.241 ... Acids, Imino. Acids, Secondary Amino. Amino Acids, Secondary. Secondary Amino Acids. Tree number(s):. D02.241.081.583. D02.491. ... do not confuse with AMINO ACIDS. Allowable Qualifiers:. AD administration & dosage. AE adverse effects. AG agonists. AI ... Carboxylic acids that contain an imino group (C=NH).. Annotation:. ...
CAS # 778646-92-7, 8-Oxo-5-azaspiro[3.5]nonane-5-carboxylic acid tert-butyl ester - chemBlink
... nonane-5-carboxylic acid tert-butyl ester. An open source of chemical information available to the public online since 2005. ... 4-Oxo-2-azetidinecarboxylic acid 3-Oxo-1-azetidinecarboxylic acid 2-propen-1-yl ester beta-Oxo-1-azetidinepropanenitrile ... 3-Oxo-4-aza-5-methoxy-5alpha-androst-1-ene-17beta-carboxylic acid methyl ester 7-Oxo-2-azaspiro[4.5]decane-2-carboxylic acid 1, ... heptane-1-carboxylic acid 1,1-dimethylethyl ester 6-Oxo-2-azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester 2-Oxo-6- ...
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CSC -Products
3R,4S)-2-Oxo-4-phenyl-3-[(triethylsilyl)oxy]-1-azetidinecarboxylic acid 1,1-dimethylethyl ester ... Kainic Acid Abscisic Acid(S-ABA) D-2-Amino-5-phosphonvaleric acid(D-AP5) L(+)-Quisqualic acid Ponasterone A. ... 1-Azetidinecarboxylic acid, 3-(1-ethoxyethoxy)-2-oxo-4-phenyl-, 1,1-dimethylethyl ester ... 4S,5R)-3-Benzoyl-2- (4-methoxyphenyl) -4-phenyl-5-oxazolidinecarboxylic acid ...
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DeCS 2016 - June 12, 2016 version
3 azetidinecarboxylic Acid use Azetidinecarboxylic Acid 3 Benzylchroman 4 Ones use Isoflavones ... 1-hydroxyethylene)diphosphonic acid, Tetrapotassium Salt use Etidronic Acid (1-hydroxyethylene)diphosphonic acid use Etidronic ... 2,4-Dichlorophenoxyacetic Acid, Ammonium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Lithium Salt ... 2,4-Dichlorophenoxyacetic Acid, Potassium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Sodium Salt ...
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DeCS 2016 - June 12, 2016 version
3 azetidinecarboxylic Acid use Azetidinecarboxylic Acid 3 Benzylchroman 4 Ones use Isoflavones ... 1-hydroxyethylene)diphosphonic acid, Tetrapotassium Salt use Etidronic Acid (1-hydroxyethylene)diphosphonic acid use Etidronic ... 2,4-Dichlorophenoxyacetic Acid, Ammonium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Lithium Salt ... 2,4-Dichlorophenoxyacetic Acid, Potassium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Sodium Salt ...
DeCS 2016 - June 12, 2016 version
3 azetidinecarboxylic Acid use Azetidinecarboxylic Acid 3 Benzylchroman 4 Ones use Isoflavones ... 1-hydroxyethylene)diphosphonic acid, Tetrapotassium Salt use Etidronic Acid (1-hydroxyethylene)diphosphonic acid use Etidronic ... 2,4-Dichlorophenoxyacetic Acid, Ammonium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Lithium Salt ... 2,4-Dichlorophenoxyacetic Acid, Potassium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Sodium Salt ...
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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. ...
DailyMed - MAYZENT- siponimod tablet, film coated
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. ...
DailyMed - MAYZENT- siponimod tablet, film coated
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. ...
MeSH Browser
Amino Acids [D12.125] * Amino Acids, Cyclic [D12.125.072] * Imino Acids [D12.125.072.401] * Azetidinecarboxylic Acid [D12.125. ... Carboxylic Acids [D02.241] * Acids, Acyclic [D02.241.081] * Imino Acids [D02.241.081.583] * Azetidinecarboxylic Acid [D02.241. ... Imino Acids [D02.491.485] * Azetidinecarboxylic Acid [D02.491.485.100] * Technetium Tc 99m Diethyl-iminodiacetic Acid [D02.491. ... 3-azetidinecarboxylic Acid Azetidine-2-carboxylic Acid Azetidine-3-carboxylic Acid Registry Number. 5GZ3E0L9ZU. Related Numbers ...
MeSH Browser
Amino Acids [D12.125] * Amino Acids, Cyclic [D12.125.072] * Imino Acids [D12.125.072.401] * Azetidinecarboxylic Acid [D12.125. ... Carboxylic Acids [D02.241] * Acids, Acyclic [D02.241.081] * Imino Acids [D02.241.081.583] * Azetidinecarboxylic Acid [D02.241. ... Imino Acids [D02.491.485] * Azetidinecarboxylic Acid [D02.491.485.100] * Technetium Tc 99m Diethyl-iminodiacetic Acid [D02.491. ... 3-azetidinecarboxylic Acid Azetidine-2-carboxylic Acid Azetidine-3-carboxylic Acid Registry Number. 5GZ3E0L9ZU. Related Numbers ...
Leustek, T.<...
रासायनिक अभिकर्मक -चेमवाट | रसायन और जीवविज्ञान का डेटाबेस
NDF-RT Code NDF-RT Name
Azauridine N0000006287 azelaic acid N0000006136 azelastine N0000007872 Azepines N0000170256 Azetidinecarboxylic Acid ... Neutral N0000006806 Amino Acids N0000011372 Amino Acids, Acidic N0000011248 Amino Acids, Aromatic N0000011332 Amino Acids, ... Acyclic N0000008269 Acids, Aldehydic N0000007628 Acids, Carbocyclic N0000007629 Acids, Heterocyclic N0000007630 Acids, ... Fatty Acid Synthases N0000169742 Fatty Acid Transport Proteins N0000193067 Fatty Acid-Binding Protein 7 N0000169572 Fatty Acid- ...
2-ethoxy-1-phenylethanone - 14869-39-7, C10H12O2, density, melting point, boiling point, structural formula, synthesis
Polyoxins
Technetium Tc 99m Lidofenin | Colorado PROFILES
22 March | Article about 22 March by The Free Dictionary
DeCS 2020 - June 23, 2020 version
3 azetidinecarboxylic Acid use Azetidinecarboxylic Acid 3 Benzylchroman 4 Ones use Isoflavones ... 1-hydroxyethylene)diphosphonic acid, Tetrapotassium Salt use Etidronic Acid (1-hydroxyethylene)diphosphonic acid use Etidronic ... 2,4-Dichlorophenoxyacetic Acid, Ammonium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Lithium Salt ... 2,4-Dichlorophenoxyacetic Acid, Potassium Salt use 2,4-Dichlorophenoxyacetic Acid 2,4-Dichlorophenoxyacetic Acid, Sodium Salt ...
CAS # 126938-14-5, 4-Methyl-7-[(6-O-sulfo-beta-D-galactopyranosyl)oxy]-2H-1-benzopyran-2-one
... benzoic acid 4-Methylsulfonylaniline 1-(Methylsulfonyl)-3-azetidinecarboxylic acid ... acetic acid 3-Methylsulfinylphenylboronic acid 2-[3-(Methylsulfinyl)propyl]-1H-isoindole-1,3(2H)-dione 2-(Methylsulfinyl)-5-( ... benzeneacetic acid [1-[2-[(Methylsulfonyl)amino]ethyl]-4-piperidinyl]methyl 5-fluoro-2-methoxy-1H-indole-3-carboxylate 1-N-( ... benzoic acid Methyl sulfone 4-[4-[1-[[S(R)]-S-Methylsulfonimidoyl]cyclopropyl]-6-[(3R)-3-methyl-4-morpholinyl]-2-pyrimidinyl]- ...
Temat: 'Triticum' - OpacWWW - Prolib Integro
µ
... s azeserine azeserines azetepa azetidin azetidine azetidinecarboxylic acid azetidinecarboxylic acids azetidines azetidinone ... acid radical acid radicals acid reaction acid reactions acid-resistance acid-resistant acidrine acids acid salt acid salts acid ... acid-base equilibria acid-base equilibrium acid bath acid baths acidbinding acid binding acid-binding acid cell acid cells acid ... acid fast acid-fast acid fast bacilli acid-fast bacilli acid fast bacillus acid-fast bacillus acidfastness acid fastness acid- ...
T000001A 23187
Azetidine-2-carboxylic T004051Azetidine 2 carboxylic Acid T004051Azetidine-2-carboxylic Acid T004052Acid, Azetidinecarboxylic ... Amino Acid T001797Amino Acid Sequences T001798Sequence, Amino Acid T001799Sequences, Amino Acid T001800Amino Acid Sequence ... Amino Acid T001786Activations, Amino Acid T001786Amino Acid Activation T001786Amino Acid Activations T001787Amino Acid ... D-Amino Acid T010491D Amino Acid Oxidase T010491D-Amino-Acid Oxidase T010491Oxidase, D-Amino-Acid T010492Acid Oxidase, dextro- ...
µ
... s azeserine azeserines azetepa azetidin azetidine azetidinecarboxylic acid azetidinecarboxylic acids azetidines azetidinone ... acid radical acid radicals acid reaction acid reactions acid-resistance acid-resistant acidrine acids acid salt acid salts acid ... acid-base equilibria acid-base equilibrium acid bath acid baths acidbinding acid binding acid-binding acid cell acid cells acid ... acid fast acid-fast acid fast bacilli acid-fast bacilli acid fast bacillus acid-fast bacillus acidfastness acid fastness acid- ...
TERM
Azetidinecarboxylic Acid Azetidines Azetines Azides Azinphosmethyl Aziridines Azirines Azithromycin Azlocillin Azo Compounds ... Amino Acids Amino Acids, Acidic Amino Acids, Aromatic Amino Acids, Basic Amino Acids, Branched-Chain Amino Acids, Cyclic Amino ... Acid Ceramidase Acid Etching, Dental Acid Phosphatase Acid Rain Acid Sensing Ion Channel Blockers Acid Sensing Ion Channels ... Acids Acids, Acyclic Acids, Aldehydic Acids, Carbocyclic Acids, Heterocyclic Acids, Noncarboxylic Acidulated Phosphate Fluoride ...
Carboxylic3
- Click the button below to add the Fmoc-azetidine-3-carboxylic acid 1 g to your wish list. (p212121.com)
- The mechanism, investigated through DFT calculations, features an unprecendented intramolecular cyclization reaction involving a carboxylic acid activated by tosyl chloride and an electron-poor pyridinic nitrogen. (hes-so.ch)
- Carboxylic acids that contain an imino group (C=NH). (bvsalud.org)
Amino1
- A non-essential amino acid that is synthesized from GLUTAMIC ACID. (jefferson.edu)