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Propionyl-CoA (Synonyms:丙酰辅酶A;opionyl-coenzyme A; n-Propionyl CoA)
目录号 : FM020 纯度 : BR/95%以上 品牌 : CHEMSOON Cas No. : 317-66-8 PubChem Id : 92753
Propionyl-CoA is an acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of propionic acid. It has a role as a metabolite, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a coenzyme A and a propionic acid. It is a conjugate acid of a propionyl-CoA(4-).;Propionyl-CoA is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).;propionyl-CoA is a natural product found in Streptomyces peucetius, Saccharomyces cerevisiae, and Homo sapiens with data available.;propionyl-CoA is a metabolite found in or produced by Saccharomyces cerevisiae.
Propionyl-CoA
Cas No. : 317-66-8
规格编号 纯度 包装 库存 价格 拼团价
FM020-2mg BR/95%以上 2mg
面议
FM020-5mg BR/95%以上 5mg
面议

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产品名称: Propionyl-CoA
其他名称: 丙酰辅酶A;opionyl-coenzyme A; n-Propionyl CoA
CAS:317-66-8
结构信息
分子式 C24H40N7O17P3S 分子量 823.6
IUPAC Name  S-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] 3-hydroxy-2-methylbutanethioate
InChIKey  PEKYNTFSOBAABV-UHFFFAOYSA-N
InChI  InChI=1S/C26H44N7O18P3S/c1-13(14(2)34)25(39)55-8-7-28-16(35)5-6-29-23(38)20(37)26(3,4)10-48-54(45,46)51-53(43,44)47-9-15-19(50-52(40,41)42)18(36)24(49-15)33-12-32-17-21(27)30-11-31-22(17)33/h11-15,18-20,24,34,36-37H,5-10H2,1-4H3,(H,28,35)(H,29,38)(H,43,44)(H,45,46)(H2,27,30,31)(H2,40,41,42)
SMILES  CC(C(C)O)C(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)O
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1.Identification of an α-Oxoamine Synthase and a One-Pot Two-Step Enzymatic Synthesis of α-Amino Ketones. Zhou, Ting et al. Organic Letters, 23(1), 37-41; 2021

2.Drosophila melanogaster nonribosomal peptide synthetase Ebony encodes an atypical condensation domain. IzorA, Thierry et al. Proceedings of the National Academy of Sciences of the United States of America, 116(8), 2913-2918; 2019

3.Identification of 3-sulfinopropionyl coenzyme A (CoA) desulfinases within the acyl-CoA dehydrogenase superfamily. Schuermann, Marc et al. Journal of Bacteriology, 196(4), 882-893, 13 pp.; 2014

4.On the thermodynamic equilibrium between (R)-2-hydroxyacyl-CoA and 2-enoyl-CoA. Parthasarathy, Anutthaman et al. FEBS Journal, 277(7), 1738-1746; 2010

5.Point Mutations (Q19P and N23K) Increase the Operational Solubility of a 2α-O-Benzoyltransferase that Conveys Various Acyl Groups from CoA to a Taxane Acceptor. Nawarathne, Irosha N. and Walker, Kevin D.. Journal of Natural Products, 73(2), 151-159; 2010

6.Thioester hydrolysis and C-C bond formation by carboxymethylproline synthase from the crotonase superfamily. Batchelar, Edward T. et al. Angewandte Chemie, International Edition, 47(48), 9322-9325; 2008

7.Metabolic pathway engineering for complex polyketide biosynthesis in Saccharomyces cerevisiae. Mutka, Sarah C. et al. FEMS Yeast Research, 6(1), 40-47; 2006