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psoralens

A furanocoumarin with a 7H-furo[3,2-g]chromen-7-one skeleton and its substituted derivatives thereof.

ChEBI ID: 26369

Members (23)

MemberDefinitionRole
3-(3,5-dimethyl-7-oxo-6-furo[3,2-g][1]benzopyranyl)propanoic acid3-(3,5-dimethyl-7-oxo-6-furo[3,2-g][1]benzopyranyl)propanoic acid
3-carbethoxypsoralen3-(ethoxycarbonyl)psoralen
3-methyl-5-propyl-7-furo[3,2-g][1]benzopyranone3-methyl-5-propyl-7-furo[3,2-g][1]benzopyranone
4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one
5-(4-phenylbutoxy)psoralenA member of the class of psoralens that is psoralen substituted by a 4-phenylbutoxy group at position 5. It is a potent inhibitor of the voltage-gated potassium channel Kv1.3 (EC50 = 3 nM).psora 4
5-methoxypsoralenA 5-methoxyfurocoumarin that is psoralen substituted by a methoxy group at position 5.5-methoxypsoralen
6',7'-dihydroxybergamottin6',7'-Dihydroxybergamottin
9-(2,3-dihydroxy-3-methylbutoxy)-4-methoxy-7h-furo(3,2-g)(1)benzopyran-7-oneByakangelicin
acetic acid 2-(7-oxo-2,3-dihydrofuro[3,2-g][1]benzopyran-2-yl)propan-2-yl esteracetic acid 2-(7-oxo-2,3-dihydrofuro[3,2-g][1]benzopyran-2-yl)propan-2-yl ester
bergaptolbergaptol
byakangelicolByakangelicol
cnidilinCnidilin
epoxybergamottinEpoxybergamottin
ficusinThe simplest member of the class of psoralens that is 7H-furo[3,2-g]chromene having a keto group at position 7. It has been found in plants like Psoralea corylifolia and Ficus salicifolia.psoralen
imperatorinA member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor.imperatorin
isoimperatorinA member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 5. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor.isoimperatorin
isopimpinellinisopimpinellin
methoxsalenA member of the class of psoralens that is 7H-furo[3,2-g]chromen-7-one in which the 9 position is substituted by a methoxy group. It is a constituent of the fruits of Ammi majus. Like other psoralens, trioxsalen causes photosensitization of the skin. It is administered topically or orally in conjunction with UV-A for phototherapy treatment of vitiligo and severe psoriasis.methoxsalen
NeobyakangelicolNeobyakangelicol
oxypeucadanin(R)-Oxypeucedanin
phellopterinPhellopterin
rutamarinChalepin acetate
trioxsalen7H-Furo[3,2-g]chromen-7-one in which positions 2, 5, and 9 are substituted by methyl groups. Like other psoralens, trioxsalen causes photosensitization of the skin. It is administered orally in conjunction with UV-A for phototherapy treatment of vitiligo. After photoactivation it creates interstrand cross-links in DNA, inhibiting DNA synthesis and cell division, and can lead to cell injury; recovery from the cell injury may be followed by increased melanisation of the epidermis.trioxsalen

Research

Studies (4,097)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19901,666 (40.66)18.7374
1990's812 (19.82)18.2507
2000's670 (16.35)29.6817
2010's717 (17.50)24.3611
2020's232 (5.66)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials240 (4.62%)5.53%
Reviews202 (3.89%)6.00%
Case Studies203 (3.91%)4.05%
Observational1 (0.02%)0.25%
Other4,549 (87.56%)84.16%