Propionyl-CoA - CAS:317-66-8

Specification No.	Purity	Package	Inventory	Price
FM020-2mg	BR/95%以上	2mg		Discuss Personally
FM020-5mg	BR/95%以上	5mg		Discuss Personally

Specification No.

Purity

Package

Inventory

Price

FM020-2mg

BR/95%以上

2mg

Discuss Personally

FM020-5mg

BR/95%以上

5mg

Discuss Personally

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Product Name：	Propionyl-CoA
Alias：	opionyl-coenzyme A; n-Propionyl CoA
CAS No.：	317-66-8

Product Name：

Propionyl-CoA

Alias：

opionyl-coenzyme A; n-Propionyl CoA

CAS No.：

317-66-8

Product Name： Propionyl-CoA
Other Names： 丙酰辅酶A;opionyl-coenzyme A; n-Propionyl CoA
CAS：317-66-8

Structural Information

Molecular Formula	C24H40N7O17P3S	Molecular Weight	823.6
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.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.Drosophila melanogaster nonribosomal peptide synthetase Ebony encodes an atypical condensation domain. IzorA, Thierry et al. Proceedings of the National Academy of Sciences of the United States of America, 116(8), 2913-2918; 2019

3.Identification of 3-sulfinopropionyl coenzyme A (CoA) desulfinases within the acyl-CoA dehydrogenase superfamily. Schuermann, Marc et al. Journal of Bacteriology, 196(4), 882-893, 13 pp.; 2014

4.On the thermodynamic equilibrium between (R)-2-hydroxyacyl-CoA and 2-enoyl-CoA. Parthasarathy, Anutthaman et al. FEBS Journal, 277(7), 1738-1746; 2010

5.Point Mutations (Q19P and N23K) Increase the Operational Solubility of a 2α-O-Benzoyltransferase that Conveys Various Acyl Groups from CoA to a Taxane Acceptor. Nawarathne, Irosha N. and Walker, Kevin D.. Journal of Natural Products, 73(2), 151-159; 2010

6.Thioester hydrolysis and C-C bond formation by carboxymethylproline synthase from the crotonase superfamily. Batchelar, Edward T. et al. Angewandte Chemie, International Edition, 47(48), 9322-9325; 2008

7.Metabolic pathway engineering for complex polyketide biosynthesis in Saccharomyces cerevisiae. Mutka, Sarah C. et al. FEMS Yeast Research, 6(1), 40-47; 2006

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