物质信息

ID:436

名称和标识
IUPAC标准名
9-methoxy-7H-furo[3,2-g]chromen-7-one
IUPAC传统名
methoxsalen
别名
Methoxsalen
商标名
ZanthotoxinOxsoralen LotionProralone-MopPuvalenPuvametXanthotoxinXanthoxinUltramop LotionMethoxalenNew-MeladininOxypsoralenXanthotoxineMethoxatenMeladoxenMeloxineMethoxa-DomeOxoralenOxsoralenUltra MopAmmoidinMeladinineOxsoralen-UltraPsoralen-MopUvadexAmmodinMeladinin
数据登录号
CAS号
PubChem CID
PubChem SID
化合物性质
理化性质
溶解度
0.0476 mg/mL at 30 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]
疏水性(logP)
1.7
描述信息
Drug Groups
approved
Description
A naturally occurring furocoumarin compound found in several species of plants, including Psoralea corylifolia. It is a photoactive substance that forms DNA adducts in the presence of ultraviolet A irradiation. [PubChem]
Indication
For the treatment of psoriasis and vitiligo
Pharmacology
Methoxsalen selectively inhibits the synthesis of deoxyribonucleic acid (DNA). The guanine and cytosine content correlates with the degree of Methoxsalen-induced cross-linking. At high concentrations of the drug, cellular RNA and protein synthesis are also suppressed.
Affected Organisms
Humans and other mammals
Half Life
Approximately 2 hours
Elimination
In both mice and man, methoxsalen is rapidly metabolized. Approximately 95% of the drug is excreted as a series of metabolites in the urine within 24 hours (Pathak et al. 1977).
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