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Acetoacetyl-CoA (Synonyms:乙酰乙酰辅酶A;Acetoacetylcoenzyme A;S-Acetoacetyl-CoA)
Catalog No. : FM024 Purity : BR/95%以上 Brand : CHEMSOON Cas No. : 1420-36-6 PubChem Id : 92153
Acetoacetyl-CoA is a 3-oxoacyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of acetoacetic acid. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a butyryl-CoA and an acetoacetic acid. It is a conjugate acid of an acetoacetyl-CoA(4-).;Acetoacetyl-CoA is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).;acetoacetyl-CoA is a natural product found in Homo sapiens and Bos taurus with data available.;acetoacetyl-CoA is a metabolite found in or produced by Saccharomyces cerevisiae.
Acetoacetyl-CoA
Cas No. : 1420-36-6
Specification No. Purity Package Inventory Price
FM024-2mg BR/95%以上 2mg
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Product Name: Acetoacetyl-CoA
Other Names: 乙酰乙酰辅酶A;Acetoacetylcoenzyme A;S-Acetoacetyl-CoA
CAS:1420-36-6
Structural Information
Molecular Formula C25H40N7O18P3S Molecular Weight 851.61
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
Literature

1.De novo biosynthesis of alpha-zingiberene from glucose in Escherichia coli. Zhang, Suping et al. Biochemical Engineering Journal, 176, 108188; 2021

2.Metabolic engineering of Clostridium acetobutylicum for the production of butyl butyrate. Noh, Hyeon Ji et al. Applied Microbiology and Biotechnology, 102(19), 8319-8327; 2018

3.NADPH supply for poly(3-hydroxybutyrate) synthesis concomitant with enzymatic oxidation of phosphite. Miyahara, Yuki et al. Journal of Bioscience and Bioengineering, 126(6), 764-768; 2018

4.A hybrid synthetic pathway for butanol production by a hyperthermophilic microbe. Keller, Matthew W. et al. Metabolic Engineering, 27, 101-106; 2015

5.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

6.A novel Acyl-CoA beta-transaminase characterized from a metagenome. Perret, Alain et al. PLoS One, 6(8), e22918; 2011