benzoyl-CoA(4-)

Summary

benzoyl-CoA(4-) is a group of stereoisomers^[1].

Key Facts

• benzoyl-CoA(4-)'s instance of is recorded as group of stereoisomers^[2].
• benzoyl-CoA(4-)'s canonical SMILES is recorded as CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)([O-])[O-])C(C(=O)NCCC(=O)NCCSC(=O)C4=CC=CC=C4)O^[3].
• benzoyl-CoA(4-)'s InChI is recorded as InChI=1S/C28H40N7O17P3S/c1-28(2,22(38)25(39)31-9-8-18(36)30-10-11-56-27(40)16-6-4-3-5-7-16)13-49-55(46,47)52-54(44,45)48-12-17-21(51-53(41,42)43)20(37)26(50-17)35-15-34-19-23(29)32-14-33-24(19)35/h3-7,14-15,17,20-22,26,37-38H,8-13H2,1-2H3,(H,30,36)(H,31,39)(H,44,45)(H,46,47)(H2,29,32,33)(H2,41,42,43)/p-4/t17-,20-,21-,22+,26-/m1/s1^[4].
• benzoyl-CoA(4-)'s InChIKey is recorded as VEVJTUNLALKRNO-TYHXJLICSA-J^[5].
• benzoyl-CoA(4-)'s chemical formula is recorded as C₂₈H₃₆N₇O₁₇P₃S⁴⁻^[6].
• benzoyl-CoA(4-)'s subclass of is recorded as chemical compound^[7].
• benzoyl-CoA(4-)'s part of is recorded as benzoate-CoA ligase activity^[8].
• benzoyl-CoA(4-)'s part of is recorded as biphenyl synthase activity^[9].
• benzoyl-CoA(4-)'s part of is recorded as benzoyl-CoA 3-monooxygenase activity^[10].
• benzoyl-CoA(4-)'s part of is recorded as phenylglyoxylate dehydrogenase (acylating) activity^[11].
• benzoyl-CoA(4-)'s part of is recorded as anthranilate N-benzoyltransferase activity^[12].
• benzoyl-CoA(4-)'s part of is recorded as glycine N-benzoyltransferase activity^[13].
• benzoyl-CoA(4-)'s part of is recorded as ornithine N-benzoyltransferase activity^[14].
• benzoyl-CoA(4-)'s part of is recorded as 2-alpha-hydroxytaxane 2-O-benzoyltransferase activity^[15].
• benzoyl-CoA(4-)'s part of is recorded as trihydroxybenzophenone synthase activity^[16].
• benzoyl-CoA(4-)'s part of is recorded as 4-hydroxybenzoyl-CoA reductase activity^[17].
• benzoyl-CoA(4-)'s part of is recorded as 3'-N-debenzoyl-2'-deoxytaxol N-benzoyltransferase activity^[18].
• benzoyl-CoA(4-)'s part of is recorded as benzoyl-CoA reductase activity^[19].
• benzoyl-CoA(4-)'s part of is recorded as benzoyl-CoA metabolic process^[20].
• benzoyl-CoA(4-)'s part of is recorded as benzoyl-CoA catabolic process^[21].
• benzoyl-CoA(4-)'s part of is recorded as benzoyl-CoA biosynthetic process^[22].
• benzoyl-CoA(4-)'s ChemSpider ID is recorded as 26330742^[23].
• benzoyl-CoA(4-)'s PubChem CID is recorded as 45266596^[24].
• benzoyl-CoA(4-)'s ChEBI ID is recorded as 57369^[25].
• benzoyl-CoA(4-)'s isomeric SMILES is recorded as CC(C)(COP(=O)([O-])OP(=O)([O-])OC[C@@H]1C@HOP(=O)([O-])[O-])C@HO^{C@HOP(=O)([O-])[O-])C@HO">[26]}.