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Mechlorethamine

产品号 DB00888 公司名称 DrugBank
CAS号 51-75-2 公司网站 http://www.ualberta.ca/
分子式 C5H11Cl2N 电 话 (780) 492-3111
分子量 156.05354 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 765

产品价格信息

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产品别名

标题
Mechlorethamine
IUPAC标准名
bis(2-chloroethyl)(methyl)amine
IUPAC传统名
mechlorethamine
商标名
Mutagen
Cloramin
Caryolysine
Caryolysin
Dichloren
Embichin
Mustargen
别名
Chlormethine
HN2
MBA
Mechloroethamine
Mecloretamina
Nitrogen mustard
Chlorethazine
Mustine

产品登记号

CAS号 51-75-2
PubChem CID 4033
PubChem SID 46505784

产品性质

疏水性(logP) 1.6
溶解度 1.2E+004 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description A vesicant and necrotizing irritant destructive to mucous membranes. It was formerly used as a war gas. The hydrochloride is used as an antineoplastic in Hodgkin's disease and lymphomas. It causes severe gastrointestinal and bone marrow damage. [PubChem]
Indication For the palliative treatment of Hodgkin's disease (Stages III and IV), lymphosarcoma, chronic myelocytic or chronic lymphocytic leukemia, polycythemia vera, mycosis fungoides, and bronchogenic carcinoma. Also for the palliative treatment of metastatic carcinoma resulting in effusion.
Pharmacology Mechlorethamine also known as mustine, nitrogen mustard, and HN2, is the prototype anticancer chemotherapeutic drug. Successful clinical use of mechlorethamine gave birth to the field of anticancer chemotherapy. The drug is an analogue of mustard gas and was derived from toxic gas warfare research. It belongs to the group of nitrogen mustard alkylating agents. Alkylating agents work by three different mechanisms all of which achieve the same end result - disruption of DNA function and cell death.
Toxicity Symptoms of overexposure include severe leukopenia, anemia, thrombocytopenia, and a hemorrhagic diathesis with subsequent delayed bleeding may develop. Death may follow. The intravenous LD50 is 2 mg/kg and 1.6 mg/kg in mouse and rat, respectively.
Affected Organisms
Humans and other mammals
Biotransformation Undergoes rapid chemical transformation and combines with water or reactive compounds of cells, so that the drug is no longer present in active form a few minutes after administration.
Absorption Partially absorbed following intracavitary administration, most likely due to rapid deactivation by body fluids.
Half Life 15 minutes
External Links
Wikipedia
RxList
Drugs.com

参考文献