Synthesis and primary cytotoxicity evaluation of arylmethylenenaphthofuranones derivatives-Reference-Cited by-同舟云学术

Synthesis and primary cytotoxicity evaluation of arylmethylenenaphthofuranones derivatives

Published:2006-01-01 Issue:3 Volume:21 Page:313-325
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Lardic Morgane¹,Patry Cedric¹,Duflos Muriel¹,Guillon Jean²,Massip Stephane²,Cruzalegui Francisco³,Edmonds Thomas³,Giraudet Stephanie³,Marini Laetitia³,Leonce Stephane³

Affiliation:

1. Nantes University, Nantes Atlantique Universities, Faculty of Pharmacy, Department of Pharmacochemistry, BioCiT, UPRES EA 1155, 1 rue Gaston Veil, Nantes, F-44000, France

2. Victor Segalen Bordeaux 2 University, EA 2962 - Pharmacochemistry, Faculty of Pharmacy, 146 rue Léo Saignat, 33076, Bordeaux Cedex, France

3. Institut de Recherches Servier, 125 chemin de ronde, F-78290, Croissy sur Seine, France

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756360600741834

Reference20 articles.

1. From oncogene to drug: development of small molecule tyrosine kinase inhibitors as anti-tumor and anti-angiogenic agents

2. Potential Inhibitors of Angiogenesis. Part II: 3-(Azolylmethylene)-2,3-dihydrobenzo[b]furan-2-ones

3. Synthesis and Biological Evaluations of 3-Substituted Indolin-2-ones: A Novel Class of Tyrosine Kinase Inhibitors That Exhibit Selectivity toward Particular Receptor Tyrosine Kinases

4. Potential Inhibitors of Angiogenesis. Part I: 3-(Imidazol-4(5)-ylmethylene)indolin-2-ones

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