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头孢菌素C锌盐
生物活性靶点体外研究
| 中文名称 | 头孢菌素C锌盐 |
|---|---|
| 中文同义词 | 头孢霉素C钠盐;7-(D-5-氨基-5-羧基戊酰胺基)头孢霉烷酸锌盐;头孢菌素C锌盐;-(D-5-氨基-5-羧基戊酰胺基)头孢霉烷酸锌盐;(6R,7R)-3-(乙酰氧基甲基)-7 - ((R)-5-氨基-5- 羧基戊酰胺)-8-氧代-5-硫杂-1-氮杂双环[4.2.0]辛-2-烯-2-羧酸锌(II);PERFEMIKER]CEPHALOSPORINCZINCSALT,98%;(6R,7R)-3-(乙酰氧基甲基)-7-[(R)-5-氨基-5-羧基戊酰氨基]-8-氧代-5-硫杂-1-氮杂双环[4.2.0]辛-2-烯-2-甲酸锌(II) |
| 英文名称 | CEPHALOSPORIN C ZINC SALT |
| 英文同义词 | (6R,7R)-3-[(Acetyloxy)Methyl]-7-[[(5R)-5-aMino-5-carboxy-1-oxopentyl]aMino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Zinc Salt;[6R-[6α,7β(R*)]]-3-[(Acetyloxy)Methyl]-7-[(5-aMino-5-carboxy-1-oxopentyl)aMino]-8-oxo-5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Zinc Salt;5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-((acetyloxy)methyl)-7-((5-amino-5-carboxy-1-oxopentyl)amino)-8-oxo-, zinc salt (1:1), (6R-(6alpha,7beta(R*)))-;Einecs 261-624-9;Zinc (6R-(6alpha,7beta(R*)))-3-(acetoxymethyl)-7-((5-amino-5-carboxylato-1-oxopentyl)amino)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylate;CEPHALOSPORIN C ZINC SALT;zinc [6R-[6alpha,7beta(R*)]]-3-(acetoxymethyl)-7-[(5-amino-5-carboxylato-1-oxopentyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate;Zinc(II) (6R,7R)-3-(acetoxymethyl)-7-((R)-5-amino-5-carboxylatopentanamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate |
| CAS号 | 59143-60-1 |
| 分子式 | C16H21N3O8S.Zn |
| 分子量 | 480.82 |
| EINECS号 | 261-624-9 |
| 相关类别 | 酶类;抗生素及抗病毒;抗生素;抗生素类;通用生化试剂-抗生素;Intermediates & Fine Chemicals;Pharmaceuticals;A - KAntibiotics;Antibacterial;Antibiotics A to;Antibiotics A-FAntibiotics;Chemical Structure Class;Pharmaceutical Intermediates;Interferes with Cell Wall SynthesisAntibiotics;Mechanism of Action;Penicillins and Cephalosporins (beta-Lactams);Spectrum of Activity;Amines;Chiral Reagents;Heterocycles |
| Mol文件 | 59143-60-1.mol |
| 结构式 |  |
头孢菌素C锌盐 性质
| 熔点 | 240-242°C |
|---|---|
| 储存条件 | Keep in dark place,Inert atmosphere,2-8°C |
| 溶解度 | 酸水溶液（微溶） |
| 形态 | 结晶固体 |
| 颜色 | 白色至米白色 |
头孢菌素C锌盐 用途与合成方法
生物活性
Cephalosporin C zinc salt 是一种有效的 SAMHD1 抑制剂，IC50 值为 1.1 μM。
靶点
IC50: 1.1 μM (SAMHD1)
体外研究
Cephalosporin C zinc salt is a potent inhibitor of SAMHD1 with an IC 50 of 1.1 ± 0.1 μM, 200-fold more potent than Na + salt form of Cephalosporin C (ICC 50 CC-Na = 213 ± 30 μM).
安全信息
| 危险品标志 | Xn |
|---|---|
| 危险类别码 | 42/43 |
| 安全说明 | 22-45 |
| WGK Germany | 3 |
| F | 8 |
MSDS信息
| 提供商 | 语言 |
|---|---|
SigmaAldrich | 英文 |
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