CAS 298-81-7
:8-Methoxypsoralen
Description:
8-Methoxypsoralen, also known as 8-MOP, is a naturally occurring compound belonging to the class of furanocoumarins. It is primarily derived from the seeds of the plant Psoralea corylifolia. This substance is characterized by its ability to absorb ultraviolet (UV) light, which makes it useful in photochemotherapy, particularly for treating skin conditions such as psoriasis and vitiligo. 8-Methoxypsoralen acts as a photosensitizer, enhancing the effects of UVA radiation on affected skin. Chemically, it features a methoxy group (-OCH3) at the 8-position of the psoralen structure, contributing to its biological activity. The compound is typically a white to off-white crystalline solid and is soluble in organic solvents like ethanol and dimethyl sulfoxide, but has limited solubility in water. Due to its photosensitizing properties, caution is advised when handling 8-Methoxypsoralen, as it can increase the risk of skin reactions upon exposure to sunlight. Additionally, it has been studied for its potential effects on DNA and cellular processes, highlighting its significance in both therapeutic and research contexts.
Formula:C12H8O4
InChI:InChI=1/C12H8O4/c1-14-12-10-8(4-5-15-10)6-7-2-3-9(13)16-11(7)12/h2-6H,1H3
InChI key:InChIKey=QXKHYNVANLEOEG-UHFFFAOYSA-N
SMILES:O(C)C=1C2=C(C=C3C1OC=C3)C=CC(=O)O2
Synonyms:- 5-Benzofuranacrylic acid, 6-hydroxy-7-methoxy-, δ-lactone
- 5-Demethoxyisoimpinellin
- 6-Hydroxy-7-Methoxy-5-Benzofuranacrylic Acid Delta-Lactone
- 6-Hydroxy-7-methoxy-5-benzofuranacrylic acid-γ-lactone
- 7-Furocoumarin
- 7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-
- 8-Methoxy
- 8-Methoxy-2',3',6,7-Furocoumarin
- 8-Methoxy-4',5':6,7-furocoumarin
- 8-Methoxy-6,7-furanocoumarin
- 8-Methoxy[furano-3',2':6,7-coumarin]
- 8-Methoxy[furano-3′,2′:6,7-coumarin]
- 8-Methoxyfuranocoumarin
- 8-Methoxypsoralen
- 8-Methoxypsoralene
- 8-Mop
- 8-Mp
- 9-Methoxy-7H-furo[3,2-g] [1]benzopyran-7-one
- 9-Methoxyfuro[3,2-G]Chromen-7-One
- 9-Methoxyfuro[3,2-G]Chromene-7-One
- 9-Methoxyfuro[3,2-g]chromen-7-on
- 9-Methoxypsoralen
- 9-Metoxifuro[3,2-G]Cromen-7-Ona
- 9-methoxy-7H-furo(3,2-g)benzopyran-7-one
- 9-methoxy-7H-furo[3,2-g]chromen-7-one
- Ammodin
- Ammoidin
- Deltapsoralen
- Geroxalen
- MOP
- Meladinin
- Meladinine
- Meladoxen
- Meloxine
- Methoxa-Dome
- Methoxalen
- Methoxsalene
- New-Meladinin
- Nsc 45923
- Oxsoralen
- Oxsoralen Lotion
- Oxsoralen Ultra
- Oxypsoralen
- Proralone-Mop
- Psoralen-Mop
- Psoralon-MOP
- Puvalen
- Puvamet
- Uvadex
- Vitpso
- Xanthotoxin
- Xanthotoxine
- Xanthoxin
- Zanthotoxin
- 2-g)(1)benzopyran-7-one,9-methoxy-7h-furo(
- 6-Hydroxy-7-methoxy-5-benzofuranacrylic acid gamma-lactone
- 6-hydroxy-7-methoxy-5-benzofuranacrylicacidelta-lactone
- AKOS 214-64
- 5-Benzofuranacrylic acid, 6-hydroxy-7-methoxy-, delta-lactone
- 6-hydroxy-7-methoxy-5-benzofuranacrylicaciddelta-lactone
- 5-Benzofuranacrylicacid,6-hydroxy-7-methoxy-,δ-lactone
- 2-g][1]benzopyran-7-one,9-methoxy-7h-furo[
- 9-METHOXYFURO[3,2-G][1]BENZOPYRAN-7-ONE
- METHOXSALEN
- See more synonyms
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Found 19 products.
Xanthotoxin
CAS:Formula:C12H8O4Purity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:216.198-Methoxypsoralen, 98%
CAS:<p>8-Methoxypsoralen, is used in Photochemotherapy (methoxsalen with long wave ultraviolet radiation) is indicated for the repigmentation of idiopathic vitiligo. It is also used in Photopheresis (methoxsalen with long wave ultraviolet radiation of white blood cells) is indicated for use with the UVAR </p>Formula:C12H8O4Purity:98%Color and Shape:White to pale cream or pale yellow, Crystals or powder or crystalline powderMolecular weight:216.19Xanthotoxin
CAS:Xanthotoxin analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C12H8O4Purity:(HPLC) ≥90%Color and Shape:PowderMolecular weight:216.19Methoxsalen
CAS:<p>Aromatic lactones used as drugs</p>Formula:C12H8O4Color and Shape:Off-White PowderMolecular weight:216.042269-methoxy-2H-furo[3,2-g]chromen-2-one
CAS:Formula:C12H8O4Purity:98%Color and Shape:SolidMolecular weight:216.1895Methoxsalen
CAS:<p>Methoxsalen (NCI-C55903) is a Photoactivated Radical Generator and Psoralen. The mechanism of action of methoxsalen is as a Photoabsorption. The physiologic effect of methoxsalen is by means of Photosensitizing Activity.</p>Formula:C12H8O4Purity:99.47% - 99.86%Color and Shape:Silky Needles From Hot Water Or Benzene + Petroleum Ether Tingling Sensation (Ntp 1992)Molecular weight:216.19Xanthotoxin
CAS:Formula:C12H8O4Purity:≥ 98.0%Color and Shape:White to yellow powder or crystalsMolecular weight:216.209-Methoxy-7H-furo[3,2-g]chromen-7-one
CAS:Purity:95.0%Color and Shape:Solid, White to pale yellowMolecular weight:216.19200134277344Methoxsalen
CAS:Controlled ProductFormula:C12H8O4Color and Shape:Light Yellow SolidMolecular weight:216.19Xanthotoxin
CAS:LactoneFormula:C12H8O4Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:216.198-Methoxy Psoralen
CAS:Controlled Product<p>Applications Naturally occurring analog of Psoralen (P839800). Use in treatment of psoriasis and mycosis fungoides.<br>References Loutfy, M.A., et al.: Anal. Profiles Drug Subs., 9, 427 (1980), Parrish, J.A., et al.: Int. J. Dermatol., 19, 379 (1980),<br></p>Formula:C12H8O4Color and Shape:NeatMolecular weight:216.198-Methoxypsoralen
CAS:<p>8-Methoxypsoralen is a furocoumarin compound, which is derived from natural plant sources such as the seeds of the Ammi majus plant. Its primary mode of action involves intercalation into DNA strands and the formation of covalent bonds with pyrimidine bases upon exposure to ultraviolet A (UVA) light. This interaction results in the inhibition of DNA synthesis and cell proliferation.</p>Formula:C12H8O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:216.19 g/mol


















