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Lauroyl-CoA (Synonyms:月桂酰基辅酶A;Lauroyl Coenzyme A;Dodecanoyl-CoA)
Catalog No. : FM036 Purity : BR/95%以上 Brand : CHEMSOON Cas No. : 6244-92-4 PubChem Id : 165436
Lauroyl-CoA is a medium-chain fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of lauric (dodecanoic) acid. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a dodecanoic acid. It is a conjugate acid of a lauroyl-CoA(4-).;Lauroyl-CoA is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).;Lauroyl-coa is a natural product found in Homo sapiens with data available.;lauroyl-CoA is a metabolite found in or produced by Saccharomyces cerevisiae.
Lauroyl-CoA
Cas No. : 6244-92-4
Specification No. Purity Package Inventory Price
FM036-2mg BR/95%以上 2mg
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FM036-5mg BR/95%以上 5mg
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Product Name: Lauroyl-CoA
Other Names: 月桂酰基辅酶A;Lauroyl Coenzyme A;Dodecanoyl-CoA
CAS:6244-92-4
Structural Information
Molecular Formula C33H58N7O17P3S Molecular Weight 967.85
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.Effect of carbon chain length in acyl coenzyme A on the efficiency of enzymatic transformation of okadaic acid to 7-O-acyl okadaic acid. Furumochi, Sachie et al. Bioorganic & Medicinal Chemistry Letters, 26(13), 2992-2996; 2016

2.Biochemical and Structural Characterization of the trans-Enoyl-CoA Reductase from Treponema denticola. Bond-Watts, Brooks B. et al. Biochemistry, 51(34), 6827-6837; 2012

3.N-Acylation during Glidobactin Biosynthesis by the Tridomain Nonribosomal Peptide Synthetase Module GlbF. Imker, Heidi J. et al. Chemistry & Biology (Cambridge, MA, United States), 17(10), 1077-1083; 2010

4.Rv3389C from Mycobacterium tuberculosis, a member of the (R)-specific hydratase/dehydratase family. Sacco, Emmanuelle et al. Biochimica et Biophysica Acta, Proteins and Proteomics, 1774(2), 303-311; 2007

5.Promiscuous Fatty Acyl CoA Ligases Produce Acyl-CoA and Acyl-SNAC Precursors for Polyketide Biosynthesis. Arora, Pooja et al. Journal of the American Chemical Society, 127(26), 9388-9389; 2005