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Chloroxine

产品号 DB01243 公司名称 DrugBank
CAS号 773-76-2 公司网站 http://www.ualberta.ca/
分子式 C9H5Cl2NO 电 话 (780) 492-3111
分子量 214.0481 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 1112

产品价格信息

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产品别名

标题
Chloroxine
IUPAC标准名
5,7-dichloroquinolin-8-ol
IUPAC传统名
chloroxine
商标名
Endiaron
Quixalin
Capitrol
Quinolor
Chlofucid
Clofuzid
Quesyl
别名
Dichlorohydroxyquinoline
Dikhloroskin
CHQ
Dichloroquinolinol
Dichloroxin
Chloroxyquinoline
Chlorquinol

产品登记号

PubChem SID 46508620
PubChem CID 2722
CAS号 773-76-2

产品性质

疏水性(logP) 3

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Chloroxine is a synthetic antibacterial compound. Chloroxine is a compound used in some shampoos for the treatment of dandruff and seborrheic dermatitis of the scalp.
Indication Used in the treatment of dandruff and mild to moderately severe seborrheic dermatitis of the scalp.
Pharmacology Chloroxine has an antibacterial action, inhibiting the growth of gram-positive as well as some gram-negative organisms. Also, chloroxine has shown some antifungal activity against certain dermatophytes and yeasts.
Toxicity The toxicological properties of this material have not been investigated.
Affected Organisms
Humans and other mammals
References
Malaveille C, Brun G, Bartsch H: Genotoxicity of ochratoxin A and structurally related compounds in Escherichia coli strains: studies on their mode of action. IARC Sci Publ. 1991;(115):261-6. [Pubmed]
Malaveille C, Brun G, Bartsch H: Structure-activity studies in E. coli strains on ochratoxin A (OTA) and its analogues implicate a genotoxic free radical and a cytotoxic thiol derivative as reactive metabolites. Mutat Res. 1994 May 1;307(1):141-7. [Pubmed]
External Links
Drugs.com

参考文献

  • Malaveille C, Brun G, Bartsch H: Genotoxicity of ochratoxin A and structurally related compounds in Escherichia coli strains: studies on their mode of action. IARC Sci Publ. 1991;(115):261-6. Pubmed
  • Malaveille C, Brun G, Bartsch H: Structure-activity studies in E. coli strains on ochratoxin A (OTA) and its analogues implicate a genotoxic free radical and a cytotoxic thiol derivative as reactive metabolites. Mutat Res. 1994 May 1;307(1):141-7. Pubmed