HRID1634857

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO

HCID6251

未命名化合物

HCID23672064

Monosodium phosphate

H2NaO4P

HCID54670067

L-Ascorbic acid

C6H8O6

结构：CC(C)(COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O)[C@@H](O)C(=O)NCCC(=O)NCCS.CC(C)=O

HCID86758803

未命名化合物

PRODUCTS

生成物

结构：CC(C)(COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O)[C@@H](O)C(=O)NCCC(=O)NCCS

HCID87642

Coenzyme A

C21H36N7O16P3S

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID962

Water

H2O

PROCEDURE

实验过程

750 ml salt-free water were added to 500,000 units of CoA acetone powder, then 25 g Vitamin C, 25 g sodium dihydrogen phosphate and 25 g mannitol were added in turn, the mixture was stirred to dissolve and lyophilized.

WORKUP

后处理

dissolutionto dissolve

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0f1d064d047d41c4b85ae8859a7252c2
来源数据集: uspto-grants-2003_01
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06509035B1
来源说明: uspto-grants-2003_01

反应 SMILES

CC(C)=O.[C@@H:5]1([N:43]2[C:52]3[N:51]=[CH:50][N:49]=[C:47]([NH2:48])[C:46]=3[N:45]=[CH:44]2)[O:42][C@H:14]([CH2:15][O:16][P:17]([O:20][P:21]([O:24][CH2:25][C:26]([C@H:29]([C:31]([NH:33][CH2:34][CH2:35][C:36]([NH:38][CH2:39][CH2:40][SH:41])=[O:37])=[O:32])[OH:30])([CH3:28])[CH3:27])([OH:23])=[O:22])([OH:19])=[O:18])[C@@H:8]([O:9][P:10]([OH:13])([OH:12])=[O:11])[C@H:6]1[OH:7].OC1[C@@H]([C@@H](O)CO)OC(=O)C=1O.P([O-])(O)(O)=O.[Na+].C(O)[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O>O>[CH3:28][C:26]([C@@H:29]([OH:30])[C:31]([NH:33][CH2:34][CH2:35][C:36]([NH:38][CH2:39][CH2:40][SH:41])=[O:37])=[O:32])([CH2:25][O:24][P:21]([O:20][P:17]([O:16][CH2:15][C@H:14]1[O:42][C@@H:5]([N:43]2[C:52]3[N:51]=[CH:50][N:49]=[C:47]([NH2:48])[C:46]=3[N:45]=[CH:44]2)[C@H:6]([OH:7])[C@@H:8]1[O:9][P:10]([OH:13])([OH:12])=[O:11])([OH:19])=[O:18])([OH:23])=[O:22])[CH3:27]