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86393-32-0

中文名称 盐酸环丙沙星(一水物)
英文名称 Ciprofloxacin hydrochloride hydrate
CAS 86393-32-0
分子式 C17H21ClFN3O4
MDL 编号 MFCD00079044
分子量 385.82
MOL 文件 86393-32-0.mol
更新日期 2024/04/26 20:45:09
86393-32-0 结构式 86393-32-0 结构式

基本信息

中文别名
盐酸环丙沙星欧洲药典标准品
环丙沙星盐酸
环丙沙星HCL
1-环丙基-6-氟-1,4-二氢-4-氧代-7-(1-哌嗪基)-3-喹啉羧酸盐酸盐一水物
盐酸环丙沙星(一水物)
英文别名
3-QUINOLINECARBOXYLIC ACID HYDROCHLORIDE
CIPROFLOXACIN HCL
CIPROFLOXACIN HYDROCHLORIDE
CIPROFLOXACIN HCL/ CIPROFLOXACIN MONOHYDROCHLORIDE
CIPROFLOXACIN HCL USP
CIPROFLOXACINHYDROCHLORIDE,USP
1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride hydrate
Ciprofloxacin hydrochloride hydrate
1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride monohydrate

物理化学性质

外观性状白色或微黄色结晶粉末。易溶于水,微溶于甲醇,难溶于乙醇。
熔点318-320 °C
RTECS号VB1993800
储存条件0-6°C
溶解度Soluble in water, slightly soluble in methanol, very slightly soluble in anhydrous ethanol, practically insoluble in acetone, in ethyl acetate and in methylene chloride.
形态neat
PH值pH (25g/l, 25℃) 3.0~4.5
水溶解性Soluble in water (35mg/ml).
Merck2314
InChIKeyDIOIOSKKIYDRIQ-UHFFFAOYSA-N

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
WGK Germany3
危险等级IRRITANT
海关编码2933595960

应用领域

用途一
该品为广谱抗生素。通过抑制细菌DNA旋转酶,使DNA合成和复制受阻而导致细菌死亡。对大肠杆菌、克雷白杆菌和其他肠杆菌属有较强抗菌活性;对绿脓杆菌、金黄色葡萄球菌和肺炎链球菌的抗菌作用优于诺氟沙星和培氟沙星。用于敏感菌所致的中耳炎、外耳道炎和鼓膜炎等。偶有中耳痛及瘙痒感。
用途二
该品味广谱抗生素。通过抑制细菌DNA旋转酶,使DNA合成和复制受阻而导致细菌死亡。对大肠杆菌,克雷白杆菌和其他肠杆菌属有较强抗菌活性、对绿脓杆菌、金黄色葡萄球菌和肺炎链球菌的抗菌作用优于诺氟沙星和培氟沙星。用于敏感菌所致的中耳炎,外耳道炎和骨膜炎等。偶有中耳痛及瘙痒感。
盐酸环丙沙星(一水物)价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/01/16C2227环丙沙星盐酸盐一水合物
Ciprofloxacin Hydrochloride  Monohydrate
86393-32-05G200元
2024/01/16C2227环丙沙星盐酸盐一水合物
Ciprofloxacin Hydrochloride  Monohydrate
86393-32-025G330元
2024/01/16C2227环丙沙星盐酸盐 一水合物
Ciprofloxacin Hydrochloride Monohydrate
86393-32-0100g990元

常见问题列表

生物活性
Ciprofloxacin Hydrochloride (Ciloxan, Ceprimax, Oftacilox) 是ciprofloxacin的盐酸盐形式,ciprofloxacin是一种抗生素,用于治疗一些细菌感染疾病。
体外研究

Ciprofloxacin (hydrochloride monohydrate) is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity. Ciprofloxacin (hydrochloride monohydrate) (CIP) shows potent activity against Y. pestis with MIC 90 of 0.03 μg/mL.

体内研究

Ciprofloxacin (hydrochloride monohydrate) (1 mg/L) induces glutathione-S-transferase (GST) activity, in contrast with inhibited GST and Catalase (CAT) of larvae exposed to enrofloxacin. Ciprofloxacin (hydrochloride monohydrate) (≥10 μg/L) is ecotoxic for development, growth, detoxifying, and oxidative stress enzymes in anuran amphibian larvae. In a murine model of pneumonic plague, Ciprofloxacin (hydrochloride monohydrate) (30 mg/kg, i.p.) results in a drug exposure which is similar to the drug exposure observed in human following a 500 mg dose of oral Ciprofloxacin (hydrochloride monohydrate). Intraperitoneal Ciprofloxacin (hydrochloride monohydrate) reduces the lung bacterial load compare to controls treated with intraperitoneal PBS.

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