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Succinyl-CoA (Synonyms:Succinyl-coenzyme A;S-Succinoyl-CoA)
目录号 : FM016 纯度 : BR/95%以上 品牌 : CHEMSOON Cas No. : 604-98-8 PubChem Id : 92133
Succinyl-CoA is an omega-carboxyacyl-CoA having succinoyl as the S-acyl component. It has a role as an inhibitor, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a coenzyme A. It is a conjugate acid of a succinyl-CoA(5-).;Succinyl-CoA is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).;Succinyl-coenzyme A is a natural product found in Homo sapiens with data available.;Succinyl-CoA is a metabolite found in or produced by Saccharomyces cerevisiae.
Succinyl-CoA
Cas No. : 604-98-8
规格编号 纯度 包装 库存 价格 拼团价
FM016-2mg BR/95%以上 2mg
¥11600.00
FM016-5mg BR/95%以上 5mg
面议

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产品名称: Succinyl-CoA
其他名称: Succinyl-coenzyme A;S-Succinoyl-CoA
CAS:604-98-8
结构信息
分子式 C25H40N7O19P3S 分子量 867.61
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
相关文献

1.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

2.Elucidating the stereochemistry of enzymatic benzylsuccinate synthesis with chirally labeled toluene. Seyhan, Deniz et al. Angewandte Chemie, International Edition, 55(38), 11664-11667; 2016

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

4.6-Deoxyerythronolide B Analogue Production in Escherichia coli through Metabolic Pathway Engineering. Kennedy, Jonathan et al. Biochemistry, 42(48), 14342-14348; 2003

5.A new method of specific acylation of thiols. Application to coenzyme A. Le Goffic, F. et al. Tetrahedron Letters, (33), 2845-7; 1976