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3-Methylcrotonyl-CoA (Synonyms:3-methylbut-2-enoyl-CoA；Dimethylacryloyl-CoA；DMA-CoA；)
目录号 : FM076 纯度 : BR/95%以上 品牌 : CHEMSOON Cas No. : 6712-03-4 PubChem Id : 9549326
3-methylbut-2-enoyl-CoA is an unsaturated fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of 3-methylbut-2-enoic acid. It has a role as a mouse metabolite. It is a short-chain fatty acyl-CoA, a methyl-branched fatty acyl-CoA, a 2-enoyl-CoA and a monounsaturated fatty acyl-CoA. It is functionally related to a but-2-enoyl-CoA and a 3-methylbut-2-enoic acid. It is a conjugate acid of a 3-methylbut-2-enoyl-CoA(4-).;3-Methylcrotonyl-CoA is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).;3-methylbut-2-enoyl-CoA is a natural product found in Homo sapiens with data available.
3-Methylcrotonyl-CoA
Cas No. : 6712-03-4
规格编号 纯度 包装 库存 价格 拼团价
FM076-2mg BR/95%以上 2mg
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FM076-5mg BR/95%以上 5mg
面议
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产品详情
产品名称： 3-Methylcrotonyl-CoA
其他名称： 3-methylbut-2-enoyl-CoA；Dimethylacryloyl-CoA；DMA-CoA；
CAS：6712-03-4
结构信息
分子式 C26H42N7O17P3S 分子量 849.63
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.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.Screening and Engineering the Synthetic Potential of Carboxylating Reductases from Central Metabolism and Polyketide Biosynthesis. Peter, Dominik M. et al. Angewandte Chemie, International Edition, 54(45), 13457-13461; 2015

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