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(E)-Cinnamoyl-coA (Synonyms:(E)-肉桂酰辅酶A;cinnamoyl-coenzyme A)
Catalog No. : FM295 Purity : BR/95%以上 Brand : CHEMSOON Cas No. : 76109-04-1 PubChem Id : 6444037
Cinnamoyl-CoA is an acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of cinnamic acid. It is functionally related to a coenzyme A. It is a conjugate acid of a cinnamoyl-CoA(4-).;Cinnamoyl-coa is a natural product found in Streptomyces venezuelae with data available.
(E)-Cinnamoyl-coA
Cas No. : 76109-04-1
Specification No. Purity Package Inventory Price
FM295-2mg BR/95%以上 2mg
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FM295-5mg BR/95%以上 5mg
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Product Name:(E)-Cinnamoyl-coA
Other Names:(E)-肉桂酰辅酶A;cinnamoyl-coenzyme A
 CAS:76109-04-1
Structural Information
Molecular Formula  C30H42N7O17P3S Molecular Weight   897.677580000001
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-(4-hydroxyphenyl)prop-2-enethioate
InChIKey  DMZOKBALNZWDKI-UHFFFAOYSA-N
InChI  InChI=1S/C30H42N7O18P3S/c1-30(2,25(42)28(43)33-10-9-20(39)32-11-12-59-21(40)8-5-17-3-6-18(38)7-4-17)14-52-58(49,50)55-57(47,48)51-13-19-24(54-56(44,45)46)23(41)29(53-19)37-16-36-22-26(31)34-15-35-27(22)37/h3-8,15-16,19,23-25,29,38,41-42H,9-14H2,1-2H3,(H,32,39)(H,33,43)(H,47,48)(H,49,50)(H2,31,34,35)(H2,44,45,46)
SMILES  CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)C=CC4=CC=C(C=C4)O)O
Product Pictures

 Light yellow crystalline

Description of properties
1) Recommended to dissolve and use directly
2) Store away from light in a -20 degree refrigerator
Spectral Information
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Literature
1.Chemoenzymatic Synthesis of Acyl Coenzyme A Substrates Enables in Situ Labeling of Small Molecules and Proteins. Agarwal, Vinayak et al. Organic Letters, 17(18), 4452-4455; 2015

2.Synthesis of coenzyme A thioesters using methyl acyl phosphates in an aqueous medium. Pal, Mohan and Bearne, Stephen L.. Organic & Biomolecular Chemistry, 12(48), 9760-9763; 2014

3.Multiplexing of Combinatorial Chemistry in Antimycin Biosynthesis: Expansion of Molecular Diversity and Utility. Yan, Yan et al. Angewandte Chemie, International Edition, 52(47), 12308-12312; 2013