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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1989-7-11
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pubmed:abstractText |
1-Imidazolylalkyl-substituted di- or tetrahydrobenzo[b]thiophenecarboxylic acid derivatives and related compounds were synthesized from tetrahydrobenzo[b]thiophene derivatives (1 or 4) in order to study the structure-activity relationships of the inhibition of thromboxane A2 synthetase in vitro. Sodium 2-(1-imidazolylmethyl)-4,5-dihydrobenzo[b]thiophene-6-carboxylate (26) and 2-(1-imidazolylmethyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-6-carbo xylic acid hydrochloride (28) showed the most potent and specific activity in vitro for thromboxane A2 synthetase inhibition.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
|
pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1265-72
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2724299-Animals,
pubmed-meshheading:2724299-Chemical Phenomena,
pubmed-meshheading:2724299-Chemistry,
pubmed-meshheading:2724299-Humans,
pubmed-meshheading:2724299-Male,
pubmed-meshheading:2724299-Microsomes,
pubmed-meshheading:2724299-Molecular Structure,
pubmed-meshheading:2724299-Rabbits,
pubmed-meshheading:2724299-Rats,
pubmed-meshheading:2724299-Rats, Inbred Strains,
pubmed-meshheading:2724299-Structure-Activity Relationship,
pubmed-meshheading:2724299-Thiophenes,
pubmed-meshheading:2724299-Thromboxane-A Synthase
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pubmed:year |
1989
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pubmed:articleTitle |
Synthesis and thromboxane synthetase inhibitory activity of di- or tetrahydrobenzo[b]thiophenecarboxylic acid derivatives.
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pubmed:affiliation |
Medicinal Chemistry Research Laboratories, Sankyo Co., Ltd., Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Comparative Study
|