Source:http://linkedlifedata.com/resource/pubmed/id/15603940
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2004-12-17
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pubmed:abstractText |
We have synthesized 3,4-dihydroquinazoline derivatives for the potent and selective T-type Ca(2+) channel blockers and evaluated for their inhibitory activities against two subtypes T-type Ca(2+) channels and N-type Ca(2+) channels. Among them, 5b (KYS05044, IC(50)=0.56+/-0.10 microM) was identified as potent T-type Ca(2+) channel blocker with in vitro selectivity profile at meaningful level (T/N-type, SI=>100).
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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 |
Jan
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
17
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
283-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15603940-Calcium Channel Blockers,
pubmed-meshheading:15603940-Calcium Channels, N-Type,
pubmed-meshheading:15603940-Calcium Channels, T-Type,
pubmed-meshheading:15603940-Cell Line,
pubmed-meshheading:15603940-Inhibitory Concentration 50,
pubmed-meshheading:15603940-Molecular Structure,
pubmed-meshheading:15603940-Oocytes,
pubmed-meshheading:15603940-Quinazolines
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pubmed:year |
2005
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pubmed:articleTitle |
Synthesis and biological activity of 3,4-dihydroquinazolines for selective T-type Ca2+ channel blockers.
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pubmed:affiliation |
Life Sciences Division, Korea Institute of Science & Technology, PO Box 131, Cheongryang, Seoul 130-650, Republic of Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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