Linked Life Data

3491788

Source:http://linkedlifedata.com/resource/pubmed/id/3491788

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
70
pubmed:dateCreated
1987-2-10
pubmed:abstractText
The main products of the photoreaction of 3-carbethoxypsoralen and 8-methoxypsoralen with 2'-deoxyribonucleosides have been isolated and characterized by various spectroscopic measurements involving proton nuclear magnetic resonance and mass spectrometry (fast atom bombardment and 252Cf plasma desorption techniques). Near ultraviolet photolysis of frozen aqueous solutions of thymidine containing 3-carbethoxypsoralen gives rise to two furan-side photocycloadducts having cis-syn stereochemistry. The corresponding thymine mean value of 3-carbethoxy-psoralen monoadduct has been shown to be the major photoproduct in DNA. The main cis-syn diastereoisomeric [2+2] photocycloadducts which arise from the photoreaction of 8-methoxypsoralen and thymidine in frozen aqueous solutions were shown to involve either the 4',5' furan ring or the 3,4 pyrone moiety and the 5,6-pyrimidine bond. Photobinding of 8-methoxypsoralen to 2'-deoxyadenosine also occurs, with covalent bond formation between carbon 3 or 4 of the pyrone ring and the sugar moiety of the nucleoside.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0300-5038
pubmed:author
pubmed:issnType
Print
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
247-51
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1986
pubmed:articleTitle
Isolation and characterization of psoralen photoadducts to DNA and related model compounds.
pubmed:publicationType
Journal Article, In Vitro