Source:http://linkedlifedata.com/resource/pubmed/id/14506915
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-9-24
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pubmed:abstractText |
The synthesis and pharmacological evaluation of new 3-(imidazol-4(5)-ylmethylene)indolin-2-ones, analogues of SU-5416, are reported. The final compounds 20-51 were obtained by Knoevenagel coupling between the substituted indolin-2-ones 1-15 and either the formylimidazole derivatives 16-18 or 2-formyl-3,5-dimethylpyrrole 19. Methylation at the nitrogen atom of the indolin-2-one and/or imidazole moities was carried out in the presence of the couple NaH/DMF. A Mannich reaction afforded the 1-dimethylaminomethyl derivatives 43 and 48. The antiangiogenic activity of these compounds was evaluated in a three dimensional in vitro rat aortic ring assay. In this test, compound 20 induced a decrease of angiogenesis comparable to that observed with SU-5416; the vascular density indexes at 1 microM were 30 +/- 18 and 22 +/- 4% of control, respectively. The compounds were also evaluated, in an independent manner, as inhibitors of the human EGF-receptor tyrosine kinase activity. As expected, only minor activities were observed with four compounds, out of thirty-one, exerting inhibitory effects in the range of 40-55% at 10 microM concentration.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Angiogenesis Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrogen,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/SU 5416
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1475-6366
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
243-52
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:14506915-Angiogenesis Inhibitors,
pubmed-meshheading:14506915-Animals,
pubmed-meshheading:14506915-Aorta,
pubmed-meshheading:14506915-Cells, Cultured,
pubmed-meshheading:14506915-Endothelium, Vascular,
pubmed-meshheading:14506915-Humans,
pubmed-meshheading:14506915-Indoles,
pubmed-meshheading:14506915-Male,
pubmed-meshheading:14506915-Methylation,
pubmed-meshheading:14506915-Models, Chemical,
pubmed-meshheading:14506915-Nitrogen,
pubmed-meshheading:14506915-Protein-Tyrosine Kinases,
pubmed-meshheading:14506915-Pyrroles,
pubmed-meshheading:14506915-Rats,
pubmed-meshheading:14506915-Rats, Inbred F344,
pubmed-meshheading:14506915-Receptor, Epidermal Growth Factor
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pubmed:year |
2003
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pubmed:articleTitle |
Potential inhibitors of angiogenesis. Part I: 3-(imidazol-4(5)-ylmethylene)indolin-2-ones.
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pubmed:affiliation |
Laboratoire de Chimie Organique et de Chimie Thérapeutique, UPRES EA 1155, Faculté de Pharmacie, 1 rue Gaston Veil, F-44035 Nantes, France.
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pubmed:publicationType |
Journal Article
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