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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 2024/07/29 08:09:55
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
所属类别
原料药:其它抗生素类药

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
颜色White to Light yellow
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
2024/04/30C2227环丙沙星盐酸盐一水合物
Ciprofloxacin Hydrochloride  Monohydrate
86393-32-05G200元
2024/04/30C2227环丙沙星盐酸盐一水合物
Ciprofloxacin Hydrochloride  Monohydrate
86393-32-025G330元
2024/04/30S5208盐酸环丙沙星(一水物)
Ciprofloxacin hydrochloride hydrate
86393-32-025mg794.83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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