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http://linked.open...gbank/description
| - Trioxsalen (trimethylpsoralen, trioxysalen or trisoralen) is a furanocoumarin and a psoralen derivative. It is obtained from several plants, mainly Psoralea corylifolia. Like other psoralens it causes photosensitization of the skin. It is administered either topically or orally in conjunction with UV-A (the least damaging form of ultraviolet light) for phototherapy treatment of vitiligo[1] and hand eczema.[2] After photoactivation it creates interstrand cross-links in DNA, which can cause programmed cell death unless repaired by cellular mechanisms. In research it can be conjugated to dyes for confocal microscopy and used to visualize sites of DNA damage.[3] The compound is also being explored for development of antisense oligonucleotides that can be cross-linked specifically to a mutant mRNA sequence without affecting normal transcripts differing at even a single base pair. (en)
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http://linked.open...generalReferences
| - # van Coevorden AM, Kamphof WG, van Sonderen E, Bruynzeel DP, Coenraads PJ: Comparison of oral psoralen-UV-A with a portable tanning unit at home vs hospital-administered bath psoralen-UV-A in patients with chronic hand eczema: an open-label randomized controlled trial of efficacy. Arch Dermatol. 2004 Dec;140(12):1463-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/15611423 # Thazhathveetil AK, Liu ST, Indig FE, Seidman MM: Psoralen conjugates for visualization of genomic interstrand cross-links localized by laser photoactivation. Bioconjug Chem. 2007 Mar-Apr;18(2):431-7. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17373769 # Higuchi M, Yamayoshi A, Kobori A, Yamaoka T, Murakami A: Synthesis and properties of photo-reactive antisense oligonucleotides containing 2'-O-psoralen-conjugated adenosine. Nucleic Acids Symp Ser (Oxf). 2005;(49):331-2. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17150768 (en)
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http://linked.open...gy/drugbank/group
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http://linked.open...ugbank/indication
| - Trioxsalen is a pigmenting photosensitizing agent used in conjunction with ultraviolet light in the treatment of vitiligo. (en)
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sameAs
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - After photoactivation it creates interstrand cross-links in DNA, which can cause programmed cell death. (en)
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http://linked.open.../drugbank/synonym
| - Trioxsalen (en)
- trimethylpsoralen (en)
- trioxysalen (en)
- trisoralen (en)
- 4,5',8-Trimethylpsoralen (en)
- 2',4,8-Trimethylpsoralen (en)
- 4,8,5'-Trimethylpsoralen (en)
- Trioxisaleno (en)
- Trioxysalene (en)
- Trioxysalenum (en)
- 6-Hydroxy-beta,2,7-trimethyl-5-benzofuranacrylic acid, delta-lactone (en)
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http://linked.open...k/foodInteraction
| - avoid eating limes, figs, parsley, parsnips, mustard, carrots, and celery while you are being treated with trioxsalen (en)
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foaf:page
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http://linked.open...ugbank/IUPAC-Name
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http://linked.open...gy/drugbank/InChI
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...noisotopic-Weight
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http://linked.open...y/drugbank/SMILES
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http://linked.open.../Water-Solubility
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http://linked.open...ogy/drugbank/logP
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http://linked.open...ogy/drugbank/logS
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http://linked.open...l/drug/hasATCCode
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http://linked.open...nd-Acceptor-Count
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http://linked.open...-Bond-Donor-Count
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http://linked.open...drugbank/InChIKey
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http://linked.open...urface-Area--PSA-
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http://linked.open...nk/Polarizability
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http://linked.open...bank/Refractivity
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http://linked.open...atable-Bond-Count
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http://linked.open...casRegistryNumber
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http://linked.open...drugbank/category
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http://linked.open...k/Bioavailability
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http://linked.open...bank/Ghose-Filter
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http://linked.open...nk/MDDR-Like-Rule
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http://linked.open...ank/Melting-Point
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http://linked.open...k/Number-of-Rings
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http://linked.open...siological-Charge
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http://linked.open...bank/Rule-of-Five
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http://linked.open...tional-IUPAC-Name
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http://linked.open...-strongest-basic-
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