CAS 66-97-7
:Psoralen
Description:
Psoralen is a naturally occurring compound found in various plants, particularly in the seeds of the Psoralea genus. It belongs to the class of furanocoumarins and is characterized by its ability to absorb ultraviolet (UV) light, which allows it to form covalent bonds with DNA. This property makes psoralen useful in phototherapy, particularly for treating skin conditions such as psoriasis and vitiligo, as it enhances the effects of UV light on affected skin. Chemically, psoralen has a molecular formula that includes carbon, hydrogen, and oxygen, and it typically appears as a colorless to pale yellow crystalline solid. It is soluble in organic solvents but has limited solubility in water. Psoralen can also exhibit mutagenic properties due to its interaction with DNA, necessitating careful handling and consideration of its effects in therapeutic applications. Additionally, it has been studied for its potential roles in cancer research and as a photosensitizer in various photochemical reactions.
Formula:C11H6O3
InChI:InChI=1S/C11H6O3/c12-11-2-1-7-5-8-3-4-13-9(8)6-10(7)14-11/h1-6H
InChI key:InChIKey=ZCCUUQDIBDJBTK-UHFFFAOYSA-N
SMILES:O=C1OC2=C(C=C3C(=C2)OC=C3)C=C1
Synonyms:- 2-Propenoic acid, 3-(6-hydroxy-5-benzofuranyl)-, δ-lactone
- 6,7-Furanocoumarin
- 7H-Furo[3,2-g][1]benzopyran-7-on
- 7H-furo[3,2-g][1]benzopirano-7-ona
- 7H-furo[3,2-g][1]benzopyran-7-one
- 7H-furo[3,2-g][1]benzopyranne-7-one
- 7H-furo[3,2-g]chromen-7-one
- Ficusin
- Furo[2',3':7,6]coumarin
- Furo[2′,3′:7,6]coumarin
- Furo[4',5':6,7]coumarin
- Furo[4′,5′:6,7]coumarin
- Furocoumarin
- Nsc 404562
- Prosuler
- Psoralen 90%
- Psoralene
- See more synonyms
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Found 16 products.
Psoralen
CAS:Formula:C11H6O3Purity:>99.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:186.17Psoralen, 97%
CAS:<p>Intercalates into DNA; photochemical reagent for the investigation of nucleic acid structure</p>Formula:C11H6O3Purity:97%Molecular weight:186.16Psoralen
CAS:Psoralen analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C11H6O3Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:186.177H-Furo[3,2-g]chromen-7-one
CAS:Formula:C11H6O3Purity:98%Color and Shape:SolidMolecular weight:186.1635Psoralen
CAS:Psoralen crosslinking between human immunodeficiency virus type 1 RNA and primer tRNA3(Lys).Formula:C11H6O3Purity:95%~99%Color and Shape:PowderMolecular weight:186.166Psoralen
CAS:<p>Psoralen (Ficusin) is a furocoumarin that intercalates with DNA, inhibiting DNA synthesis and cell division.</p>Formula:C11H6O3Purity:99.3% - 99.87%Color and Shape:Crystals From Ether Crystalline SolidMolecular weight:186.16Psoralen
CAS:Formula:C11H6O3Purity:≥ 98.0%Color and Shape:White to light-yellow powderMolecular weight:186.16Psoralen
CAS:LactoneFormula:C11H6O3Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:186.17Psoralen
CAS:Controlled Product<p>Applications Psoralens are phytoalexins; they are used by plants in a defensive response to attacks by fungi and insects. They have also shown photosensitizing and phototoxic effects in animals and humans and have been used in photochemotherapy for management of vitiligo, psoriasis, and mycosis fungoides. Used as photochemical probe in biological systems.<br>References Parsons, B.J., et al.: Photochem. Photobiol., 32, 813 (1980),<br></p>Formula:C11H6O3Color and Shape:Off White PowderMolecular weight:186.16Psoralen
CAS:<p>Psoralen is a naturally occurring furocoumarin compound, which is derived from various plants, including those in the Apiaceae family, such as parsley and celery. Its mode of action involves intercalating into DNA and forming covalent cross-links when activated by ultraviolet A (UVA) light. This photoreactivity enables it to modify the biological activity of nucleic acids, making it a valuable tool in both therapeutic and experimental settings.</p>Formula:C11H6O3Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:186.16 g/mol















