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HRID1492683

反应详情

EQUATION

反应方程式

HRID 1492683 的结构方程式

REACTANTS

反应物

8
结构：O=Cc1ccccc1
HCID240

Benzaldehyde

C7H6O

结构：CCC=O
HCID527

Propanal

C3H6O

结构：CCN(CC)C(=S)SSC(=S)N(CC)CC
HCID3117

Tetraethylthiuram disulfide

C10H20N2S4

结构：Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O
HCID5789

Thymidine

C10H14N2O5

结构：NC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](OP(=O)(O)O)[C@@H]3O)[C@@H](O)[C@H]2O)c1
HCID5886

Adenosine 5′-(trihydrogen diphosphate), 2′-(dihydrogen phosphate), P′→5′-ester with 3-(aminocarbonyl)-1-β-D-ribofuranosylpyridinium

C21H29N7O17P3+

结构：C=CC=O
HCID7847

Acrolein

C3H4O

结构：O=S(=O)(O)CCN1CCN(CCO)CC1
HCID23831

(4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acid

C8H18N2O4S

结构：NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
HCID439153

Adenosine 5'-(trihydrogen diphosphate), P'→5'-ester with 1,4-dihydro-1-.beta.-D-ribofuranosyl-3-pyridinecarboxamide

C21H29N7O14P2

PRODUCTS

生成物

1
结构：CCc1ccc(C=O)c(N)c1CC
HCID54482978

未命名化合物

PROCEDURE

实验过程

Materials: SDA was prepared by acid hydrolysis of the corresponding bioacetal supplied by the Department of Pharmaceutical Development at our Institute. [3H]-Thymidine was purchased from New England Nuclear, Boston, Mass. Concanavalin A, horse serum, RPMI-1640 and HEPES were from Gibco, Grand Island, N.Y. NAD and NADP were purchased from Boehringer, Mannheim. Acrolein and disulfiram were obtained from Aldrich Chemical Co., Milwaukee, Wis. Propionaldehyde and benzaldehyde were from Eastman Kodak Chemical Co., Rochester, N.Y. Diethyl aminobenzaldehyde (DEAB) was kindly provided by Dr. John Hilton, Johns Hopkins School of Medicine, Baltimore, Md.

WORKUP

后处理

  1. customMaterials: SDA was prepared by acid hydrolysis of the corresponding bioacetal