Source:http://linkedlifedata.com/resource/pubmed/id/20739104
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2010-10-11
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pubmed:abstractText |
Simple synthetic strategies for the hitherto unreported [1,2,4]triazolo[4,3-a]pyrido[4,3-d]pyrimidines 8 and [1,2,4]triazolo[4',3':1,2]pyrimido[4,5-b][1,6]naphthyridine-5-one 15 are described based on reaction of thione 3 and 12 with hydrazonoyl chloride 1a-h, respectively. The structures of products 8 and 15 were confirmed by spectroscopic and X-ray crystallographic analyses. Also, the mechanism of such reactions was discussed. In addition, reaction of compound 12 with bromoacetic acid and hydrazine hydrate was investigated. Compounds were screened against 5?-reductase and showed activities with good LD(50) and LD(90) for all compounds.
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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 |
Nov
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pubmed:issn |
1768-3254
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Masson SAS. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4838-44
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pubmed:meshHeading |
pubmed-meshheading:20739104-3-Oxo-5-alpha-Steroid 4-Dehydrogenase,
pubmed-meshheading:20739104-5-alpha Reductase Inhibitors,
pubmed-meshheading:20739104-Animals,
pubmed-meshheading:20739104-Crystallography, X-Ray,
pubmed-meshheading:20739104-Heterocyclic Compounds,
pubmed-meshheading:20739104-Magnetic Resonance Spectroscopy,
pubmed-meshheading:20739104-Male,
pubmed-meshheading:20739104-Models, Molecular,
pubmed-meshheading:20739104-Rats,
pubmed-meshheading:20739104-Rats, Sprague-Dawley,
pubmed-meshheading:20739104-Spectrophotometry, Infrared
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pubmed:year |
2010
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pubmed:articleTitle |
Synthesis of bioactive polyheterocyclic ring systems as 5?-reductase inhibitors.
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pubmed:affiliation |
Department of Applied Organic Chemistry, National Research Center, Dokki, Cairo, Egypt.
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pubmed:publicationType |
Journal Article
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