Source:http://linkedlifedata.com/resource/pubmed/id/17085054
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2006-11-20
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pubmed:abstractText |
Recently, we discovered a novel class of anticancer compounds with remarkable potency in a panel of cancer cell lines. A prototype compound, SC144, showed significant in vivo efficacy in mice xenograft models of human breast cancer cells. Herein, we report on a new synthetic route to SC144 and the synthesis of several of its analogues in order to understand required features for activity. A one-step coupling of 7-fluoro-4-chloropyrrolo[1,2-a]quinoxaline with pyrazin-2-carbohydrazide improved the yield significantly. Although several of the analogues showed significant activities, modification of the heteroacyl moiety had a dramatic effect on potency.
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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 |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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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 |
288-94
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pubmed:meshHeading |
pubmed-meshheading:17085054-Antineoplastic Agents,
pubmed-meshheading:17085054-Cell Line, Tumor,
pubmed-meshheading:17085054-Dose-Response Relationship, Drug,
pubmed-meshheading:17085054-Drug Design,
pubmed-meshheading:17085054-Drug Screening Assays, Antitumor,
pubmed-meshheading:17085054-Humans,
pubmed-meshheading:17085054-Hydrazines,
pubmed-meshheading:17085054-Molecular Structure,
pubmed-meshheading:17085054-Quinoxalines,
pubmed-meshheading:17085054-Stereoisomerism,
pubmed-meshheading:17085054-Structure-Activity Relationship
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pubmed:year |
2007
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pubmed:articleTitle |
Synthesis and antitumor activities of a series of novel quinoxalinhydrazides.
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pubmed:affiliation |
Dipartimento di Scienze Farmaceutiche, Università della Calabria, 87036 Arcavacata di Rende (Cs), Italy.
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pubmed:publicationType |
Journal Article
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