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Benzoyl-CoA (Synonyms:苯甲酰辅酶A;Benzoyl coenzyme A;Benzoyl CoA)
目录号 : FM044 纯度 : BR/95%以上 品牌 : CHEMSOON Cas No. : 6756-74-7 PubChem Id : 122174
Benzoyl-CoA is the simplest member of the class of benzoyl-CoAs that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of benzoic acid. It has a role as a mouse metabolite. It is functionally related to a benzoic acid. It is a conjugate acid of a benzoyl-CoA(4-).;Benzoyl-coa is a natural product found in Streptomyces maritimus with data available.
Benzoyl-CoA
Cas No. : 6756-74-7
规格编号 纯度 包装 库存 价格 拼团价
FM044-2mg BR/95%以上 2mg
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FM044-5mg BR/95%以上 5mg
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产品名称: Benzoyl-CoA
其他名称: 苯甲酰辅酶A;Benzoyl coenzyme A;Benzoyl CoA
CAS:6756-74-7
结构信息
分子式 C28H40N7O17P3S 分子量 871.64
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] 4-hydroxybenzenecarbothioate
InChIKey  LTVXPVBFJBTNIJ-UHFFFAOYSA-N
InChI  InChI=1S/C28H40N7O18P3S/c1-28(2,22(39)25(40)31-8-7-18(37)30-9-10-57-27(41)15-3-5-16(36)6-4-15)12-50-56(47,48)53-55(45,46)49-11-17-21(52-54(42,43)44)20(38)26(51-17)35-14-34-19-23(29)32-13-33-24(19)35/h3-6,13-14,17,20-22,26,36,38-39H,7-12H2,1-2H3,(H,30,37)(H,31,40)(H,45,46)(H,47,48)(H2,29,32,33)(H2,42,43,44)
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)C4=CC=C(C=C4)O)O
相关文献

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.Enediyne Antitumor Antibiotic Maduropeptin Biosynthesis Featuring a C-Methyltransferase That Acts on a CoA-Tethered Aromatic Substrate. Ling, Jianya et al. Journal of the American Chemical Society, 132(36), 12534-12536; 2010

3.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

4.An N-Aroyltransferase of the BAHD Superfamily Has Broad Aroyl CoA Specificity in Vitro with Analogues of N-Dearoylpaclitaxel. Nevarez, Danielle M. et al. Journal of the American Chemical Society, 131(16), 5994-6002; 2009

5.Preferential Hydrolysis of Aberrant Intermediates by the Type II Thioesterase in Escherichia coli Nonribosomal Enterobactin Synthesis: Substrate Specificities and Mutagenic Studies on the Active-Site Residues. Guo, Zu-Feng et al. Biochemistry, 48(8), 1712-1722; 2009