| Weight | 186.166 g/mol |
|---|---|
| Formula | C11H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
Psoralen (66-97-7)
Ficusin · Psoralene
Score:
#1055 in Biochemistry
,
#2736 in Biology
,
#3431 in Chemistry
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- Malignant Melanoma in Patients Treated for Psoriasis with Methoxsalen (Psoralen) and Ultraviolet A Radiation (PUVA) (The New England Journal of Medicine, 1997)
- Photochemical inactivation of viruses and bacteria in platelet concentrates by use of a novel psoralen and long-wavelength ultraviolet light (Transfusion, 1997)
- Light-induced cross-linking of DNA in the presence of a furocoumarin (psoralen). Studies with phage lambda, Escherichia coli, and mouse leukemia cells. (Biochimica et Biophysica Acta, 1970)
- Synthesis and characterization of new psoralen derivatives with superior photoreactivity with DNA and RNA. (Biochemistry, 1977)
- Treatment of Vitiligo With UV-B Radiation vs Topical Psoralen Plus UV-A (Archives of Dermatology, 1997)
- Lipid nanoparticles as vehicles for topical psoralen delivery: solid lipid nanoparticles (SLN) versus nanostructured lipid carriers (NLC). (European Journal of Pharmaceutics and Biopharmaceutics, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ficusin
- Psoralene
-
SMILESC1=CC(=O)OC2=CC3=C(C=CO3)C=C21
-
InChIKeyZCCUUQDIBDJBTK-UHFFFAOYSA-N
- Pubchem - Psoralen
- Wikipedia - psoralen
Psoralen (also called psoralene) is the parent compound in a family of natural products known as furocoumarins. It is structurally related to coumarin by the addition of a fused furan ring, and may be considered as a derivative of umbelliferone. Psoralen occurs naturally in the seeds of Psoralea corylifolia, as well as in the common fig, celery, parsley, West Indian satinwood and in all citrus fruits.
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Psoralen
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