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Mefloquine

产品号 DB00358 公司名称 DrugBank
CAS号 53230-10-7 公司网站 http://www.ualberta.ca/
分子式 C17H16F6N2O 电 话 (780) 492-3111
分子量 378.3121592 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 242

产品价格信息

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产品别名

标题
Mefloquine
IUPAC标准名
[2,8-bis(trifluoromethyl)quinolin-4-yl](piperidin-2-yl)methanol
IUPAC传统名
mefloquin
商标名
Lariam
别名
Mefloquinone
Mefloquine HCL

产品登记号

CAS号 53230-10-7
PubChem CID 4046
PubChem SID 46505610

产品性质

疏水性(logP) 3.9
溶解度 5000 mg/L (HCl salt)

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description A phospholipid-interacting antimalarial drug (antimalarials). It is very effective against plasmodium falciparum with very few side effects. [PubChem]
Indication For the treatment of mild to moderate acute malaria caused by Mefloquineuine-susceptible strains of Plasmodium falciparum (both chloroquine-susceptible and resistant strains) or by Plasmodium vivax. Also for the prophylaxis of Plasmodium falciparum and Plasmodium vivax malaria infections, including prophylaxis of chloroquine-resistant strains of Plasmodium falciparum.
Pharmacology Mefloquine is an antimalarial agent which acts as a blood schizonticide. Mefloquine is active against the erythrocytic stages of Plasmodium species. However, the drug has no effect against the exoerythrocytic (hepatic) stages of the parasite. Mefloquine is effective against malaria parasites resistant to chloroquine. Mefloquine is a chiral molecule. According to some research, the (+) enantiomer is more effective in treating malaria, and the (-) enantiomer specifically binds to adenosine receptors in the central nervous system, which may explain some of its psychotropic effects.
Toxicity Oral, rat: LD50 = 880 mg/kg. Symptoms of overdose include nausea, vomiting, and weight loss.
Affected Organisms
Plasmodium
Biotransformation Hepatic. Two metabolites have been identified in humans. The main metabolite, 2,8-bis-trifluoromethyl-4-quinoline carboxylic acid, is inactive against Plasmodium falciparum. The second metabolite, an alcohol, is present in minute quantities.
Absorption Well absorbed from the gastrointestinal tract. The presence of food significantly enhances the rate and extent of absorption.
Half Life 2 to 4 weeks
Protein Binding 98%
Elimination There is evidence that mefloquine is excreted mainly in the bile and feces. Urinary excretion of unchanged mefloquine and its main metabolite under steady-state condition accounted for about 9% and 4% of the dose, respectively.
Distribution * 20 L/kg [healthy adults]
Clearance * 30 mL/min
External Links
Wikipedia
RxList
Drugs.com

参考文献