rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
6
|
pubmed:dateCreated |
1991-8-6
|
pubmed:abstractText |
The design, synthesis, and in vitro pharmacology of a new class of compounds exerting both thromboxane receptor antagonist and thromboxane synthase inhibitory activities is described. [(3-Pyridinyl)bicycloheptyl] alkanoic acid 9 and its analogues, designed with the help of molecular modeling, were synthesized and found to be inhibitors of thromboxane A2 (TxA2) biosynthesis in a human platelet microsomal preparation. The compounds were also found to antagonize both platelet and vascular TxA2 receptors. The compounds inhibited the U 46619 induced aggregation of human washed platelets and platelet-rich plasma and the U 46619 induced contraction of the dog saphenous vein.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0022-2623
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
34
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1790-7
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1829485-Bicyclo Compounds,
pubmed-meshheading:1829485-Blood Platelets,
pubmed-meshheading:1829485-Carboxylic Acids,
pubmed-meshheading:1829485-Humans,
pubmed-meshheading:1829485-Microsomes,
pubmed-meshheading:1829485-Models, Molecular,
pubmed-meshheading:1829485-Pyridines,
pubmed-meshheading:1829485-Receptors, Prostaglandin,
pubmed-meshheading:1829485-Receptors, Thromboxane,
pubmed-meshheading:1829485-Thromboxane-A Synthase,
pubmed-meshheading:1829485-Thromboxanes,
pubmed-meshheading:1829485-X-Ray Diffraction
|
pubmed:year |
1991
|
pubmed:articleTitle |
Thromboxane receptor antagonism combined with thromboxane synthase inhibition. 1. (+/-)-(3-pyridinylbicycloheptyl)alkanoic acids.
|
pubmed:affiliation |
Research Department, CIBA-GEIGY Corporation, Summit, New Jersey 07901.
|
pubmed:publicationType |
Journal Article,
In Vitro
|