盐酸头孢卡品酯
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- CAS号:
- 147816-23-7
- 英文名:
- Cefcapene Pivoxil Hydrochloride
- 英文别名:
- Cefcapinaxil hydrochloride;(6R,7R)-(Pivaloyloxy)methyl 7-((Z)-2-(2-aminothiazol-4-yl)pent-2-enamido)-3-((carbamoyloxy)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrochloride;5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-(((aminocarbonyl)oxy)methyl)-7-(((2Z)-2-(2-amino-4-thiazolyl)-1-oxo-2-pentenyl)amino)-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, (6R,7R)-;5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-(((aminocarbonyl)oxy)methyl)-7-((2-(2-amino-4-thiazolyl)-1-oxo-2-pentenyl)amino)-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, (6R-(6alpha,7beta(Z)))-
- 中文名:
- 盐酸头孢卡品酯
- 中文别名:
- 盐酸头孢卡培萘酯
- CBNumber:
- CB62130363
- 分子式:
- C23H30ClN5O8S2
- 分子量:
- 604.096
- MOL File:
- 147816-23-7.mol
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盐酸头孢卡品酯化学性质
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熔点:
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158-164°C
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储存条件:
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Inert atmosphere,Store in freezer, under -20°C
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溶解度:
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DMSO (Slightly), Methanol (Slightly), Water (Sparingly)
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形态:
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Solid
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颜色:
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White to Pale Beige
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盐酸头孢卡品酯性质、用途与生产工艺
Cefcapene pivoxil hydrochloride，一种抗生素，具有口服活性的第三代头孢菌素，具有广谱的抗菌 (anti-bacterial) 活性。Cefcapene pivoxil hydrochloride 可用于脓疱病 (PPP) 的研究。
Cefcapene pivoxil hydrochloride (oral administration; 100mg/kg; 4 days) is effective against invasive BLNAR strains in mice lung, stimates peak antibiotic concentrations of 1 to 2 μg/ml in the blood of mice from 30 to 120 min after intragastric administration.
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Animal Model:
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Four-week-old female C57BL/6J mice with bacterial suspension in BSG (1×10
9
CFU)
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Dosage:
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100 mg/kg
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Administration:
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Oral administration; 100mg/kg; 4 days
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Result:
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Was against
H. influenzae
colonization in mouse lung.
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盐酸头孢卡品酯
上下游产品信息
上游原料
下游产品
147816-23-7, 盐酸头孢卡品酯 相关搜索:
- Sulfur & Selenium Compounds
- Pharmaceuticals
- Intermediates & Fine Chemicals
- Chiral Reagents
- Chiral Reagents, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
- 盐酸头孢卡培萘酯
- 147816-23-7
- Cefcapinaxil hydrochloride
- (6R,7R)-(Pivaloyloxy)methyl 7-((Z)-2-(2-aminothiazol-4-yl)pent-2-enamido)-3-((carbamoyloxy)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrochloride
- 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-(((aminocarbonyl)oxy)methyl)-7-((2-(2-amino-4-thiazolyl)-1-oxo-2-pentenyl)amino)-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, (6R-(6alpha,7beta(Z)))-
- 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-(((aminocarbonyl)oxy)methyl)-7-(((2Z)-2-(2-amino-4-thiazolyl)-1-oxo-2-pentenyl)amino)-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, (6R,7R)-