disodium [(2R,3S,4R,5R)-5-(3-carbamoyl-1,4-dihydropyridin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl ({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)phosphonate

• ChemBase编号: 174901
• 分子式: C21H27N7Na2O14P2
• 平均质量: 709.404642
• 单一同位素质量: 709.0886604
• SMILES: C([C@@H]1[C@@H](O)[C@@H](O)[C@@H](O1)n1c2c(nc1)c(ncn2)N)OP(=O)(OP(=O)(OC[C@@H]1[C@H]([C@H]([C@@H](O1)N1C=C(CC=C1)C(=O)N)O)O)[O-])[O-].[Na+].[Na+]
• Canonical SMILES: O[C@@H]1[C@H](O)[C@H](O[C@H]1N1C=CCC(=C1)C(=O)N)COP(=O)(OP(=O)(OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2N)[O-])[O-].[Na+].[Na+]
• InChI: InChI=1S/C21H29N7O14P2.2Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33;;/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25);;/q;2*+1/p-2/t10-,11-,13-,14-,15-,16-,20-,21-;;/m1../s1
• InChIKey: QRGNQKGQENGQSE-WUEGHLCSSA-L

名称和登记号

名称

• IUPAC标准名: disodium [(2R,3S,4R,5R)-5-(3-carbamoyl-1,4-dihydropyridin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl ({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)phosphonate
• IUPAC传统名: disodium nadh dianion
• 别名: Adenosine 5'-(Trihydrogen diphosphate) P'→5'-ester 1,4-Dihydro-1-β-D-ribofuranosylnicotinamide Sodium Salt; 1,4-Dihydronicotinamide Adenine Dinucleotide Disodium; Codehydrase I Reduced; Codehydrogenase I Reduced; Coenzyme I Reduced; Cozymase I Reduced; DPNH; Dihydrocodehydrogenase I; Dihydrocozymase Disodium; Dihydronicotinamide Adenine Dinucleotide Disodium; ENADA; N 8129; NADH; NADH2; Reduced Codehydrogenase I; Reduced Diphosphopyridine Nucleotide; Reduced Ncotinamide Adenine Diphosphate; β-DPNH Disodium Salt; β-NADH Disodium Salt

登记号

• CAS号: 606-68-8
• PubChem SID: 164230811
• PubChem CID: 2724710

理论计算性质

• 质子受体: 16
• 质子供体: 6
• LogD (pH = 5.5): -8.287103
• LogD (pH = 7.4): -8.577429
• Log P: -6.6937027
• 摩尔折射率: 140.7563 cm^3
• 极化性: 56.47071 Å^3
• 极化表面积: 323.28 Å^2
• 可自由旋转的化学键: 11
• 里宾斯基五规则: false
• Acid pKa: -5.4450006

详细说明

Toronto Research Chemicals - N201480

One of the biologically active forms of nicotinic acid. Serves as a coenzyme of hydrogenases and dehydrogenases. NAD usually acts as a hydrogen acceptor, forming NADH which then serves as a hydrogen donor in the respiratory chain. Present in living cells

参考文献

• Bartlett, G.R., et al.: J. Biol. Chem., 234, 449 (1959)
• Dixon, M., et al.: Science, 132, 1548 (1959)
• Heyes, D., et al.: Biochemistry, 43, 8265 (1959)
• Dietzek, B., et al.: Chem. Phys. Chem., 7, 1727 (1959)