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Ambenonium

产品号 DB01122 公司名称 DrugBank
CAS号 7648-98-8 公司网站 http://www.ualberta.ca/
分子式 C28H42Cl2N4O2++ 电 话 (780) 492-3111
分子量 537.56468 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 993

产品价格信息

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产品别名

标题
Ambenonium
IUPAC标准名
[(2-chlorophenyl)methyl](2-{[(2-{[(2-chlorophenyl)methyl]diethylazaniumyl}ethyl)carbamoyl]formamido}ethyl)diethylazanium
IUPAC传统名
mytelase
商标名
Mytelase
别名
Ambenonum

产品登记号

PubChem SID 46508143
PubChem CID 2131
CAS号 7648-98-8

产品性质

溶解度 Soluble

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Ambenonium is a cholinesterase inhibitor used in the management of myasthenia gravis. [Wikipedia]
Indication Ambenonium is used to treat muscle weakness due to muscle disease (myasthenia gravis).
Pharmacology Ambenonium, similar to pyridostigmine and neostigmine, is used for the treatment of muscle weakness and fatigue in people with myasthenia gravis. It is postulated to exert its therapeutic effect by enhancing cholinergic function through the inhibition of the acetylcholine hydrolysis by acetylcholinesterase. Increased levels of acetylcholine has peripheral effects, as acetylcholine is also used in the brain, where it tends to cause excitatory actions. The glands that receive impulses from the parasympathetic part of the autonomic nervous system are also stimulated in the same way. This is why an increase in acetylcholine causes a decreased heart rate and increased production of saliva. Ambenonium is used less commonly than neostigmine or pyridostigmine but may be preferred in patients hypersensitive to the bromide ion. Ambenonium produces fewer muscarinic side effects than neostigmine, but more than pyridostigmine.
Toxicity LD50=150±44 mg/kg (orally in mice). Symptoms of overdose include muscle twitching, weakness and paralysis of voluntary muscles including the tongue, shoulders, neck and arms, blood pressure increase (with or without a slowing of heart rate), a sensation of internal trembling, severe anxiety, and panic. Death may occur rapidly if untreated.
Affected Organisms
Humans and other mammals
Biotransformation Plasma and hepatic
Absorption Oral - poorly absorbed from the gastrointestinal tract.
External Links
Wikipedia
Drugs.com

参考文献