丙酮酸脱羧酶结构式
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常用名 | 丙酮酸脱羧酶 | 英文名 | (R)-Mandelonitrile lyase |
|---|---|---|---|---|
| CAS号 | 9024-43-5 | 分子量 | 2526.5 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C132H116F12N14O23S | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | N/A |
丙酮酸脱羧酶用途(R) -曼德拉裂合酶(Mandelonitrile lyase)是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。 |
| 中文名 | 丙酮酸脱羧酶 |
|---|---|
| 英文名 | EC 4.1.1.1 |
| 英文别名 | 更多 |
| 分子式 | C132H116F12N14O23S |
|---|---|
| 分子量 | 2526.5 |
| 精确质量 | 2525.7900400 |
| InChIKey | WIXYSENSXLKJOG-UHFFFAOYSA-N |
| SMILES | CC1=NN=C(C=C1)N2C(C(=C(C3=CC=C(C=C3)CC(C)C)O)C(=O)C2=O)C4=CC=C(C=C4)OC(F)(F)F.CC1=NN=C(C=C1)N2C(C(=C(C3=CC=C(C=C3)C(C)C)O)C(=O)C2=O)C4=CC=C(C=C4)S(=O)(=O)C.CC1=CN=C(C=N1)N2C(C(=C(C3=CC=C(C=C3)C(C)C)O)C(=O)C2=O)C4=CC=C(C=C4)OC(F)(F)F.CC(C)C1=CC=C(C=C1)C(=C2C(N(C(=O)C2=O)C3=NN=C(C=C3)OC)C4=CC=C(C=C4)OC(F)(F)F)O.CC(C)C1=CC=C(C=C1)C(=C2C(N(C(=O)C2=O)C3=CC=CN(C3=O)C)C4=CC=C(C=C4)OC(F)(F)F)O |
| 储存条件 | 2-8°C |
| 个人防护装备 | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
|---|---|
| 危害码 (欧洲) | Xn |
| 风险声明 (欧洲) | 42-42/43 |
| 安全声明 (欧洲) | 23-45-36/37-22 |
| 危险品运输编码 | NONH for all modes of transport |
| WGK德国 | 3 |
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Investigation of the microheterogeneity and aglycone specificity-conferring residues of black cherry prunasin hydrolases.
Plant Physiol. 129(3) , 1252-64, (2002) In black cherry (Prunus serotina Ehrh.) seed homogenates, (R)-amygdalin is degraded to HCN, benzaldehyde, and glucose by the sequential action of amygdalin hydrolase (AH), prunasin hydrolase (PH), and... |
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Catalytic mechanism of hydroxynitrile lyase from Hevea brasiliensis: a theoretical investigation.
J. Phys. Chem. B 114(29) , 9622-8, (2010) Density functional theory (DFT) calculations using the hybrid functional B3LYP have been performed to investigate the catalytic mechanism of hydroxynitrile lyase from Hevea brasiliensis (Hb-HNL). This... |
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(R)-oxynitrilase-catalysed synthesis of chiral silicon-containing aliphatic (R)-ketone-cyanohydrins.
Biotechnol. Lett. 25(3) , 219-22, (2003) Optically active 2-trimethylsilyl-2-hydroxyl-ethylcyanide was prepared by enzymatic enantioselective transcyanation of acetyltrimethylsilane with acetone cyanohydrin in a biphasic system at 35 degrees... |
| EINECS 232-780-5 |