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Myristyl-CoA (Synonyms:肉豆蔻酰辅酶A;Myristoyl Coenzyme A;NSC97420)
Catalog No. : FM029 Purity : BR/95%以上 Brand : CHEMSOON Cas No. : 3130-72-1 PubChem Id : 11966124
Tetradecanoyl-CoA is a metabolite found in or produced by Saccharomyces cerevisiae.
Myristyl-CoA
Cas No. : 3130-72-1
Specification No. Purity Package Inventory Price
FM029-2mg BR/95%以上 2mg
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FM029-5mg BR/95%以上 5mg
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Product Name: Myristyl-CoA
Other Names: 肉豆蔻酰辅酶A;Myristoyl Coenzyme A;NSC97420
CAS:3130-72-1
Structural Information
Molecular Formula C35H62N7O17P3S Molecular Weight 977.89
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.A KAS-III Heterodimer in Lipstatin Biosynthesis Nondecarboxylatively Condenses C8 and C14 Fatty Acyl-CoA Substrates by a Variable Mechanism during the Establishment of a C22 Aliphatic Skeleton. Zhang, Daozhong et al. Journal of the American Chemical Society, 141(9), 3993-4001; 2019

2.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

3.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

4.New Molecular Markers for Prostate Tumor Imaging: A Study on 2-Methylene Substituted Fatty Acids as New AMACR Inhibitors. Morgenroth, Agnieszka et al. Chemistry - A European Journal, 17(36), 10144-10150, S10144/1-S10144/32; 2011