Literature DB >> 9311554

Synthesis, cytotoxicity and SAR of simple geiparvarin analogues.

P Valenti1, A Rampa, M Recanatini, A Bisi, F Belluti, P Da Re, M Carrara, L Cima.   

Abstract

Some simple geiparvarin analogues, in which the coumarin moiety has been replaced with an X-substituted benzene ring, are described. The compounds were tested on LoVo cells (human colon carcinoma cell line) and some of them show a cytotoxicity comparable with that of the prototype. A QSAR analysis was also attempted, but it did not provide satisfactory results, mainly because of the limited range of variation of the biological activity.

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Year:  1997        PMID: 9311554

Source DB:  PubMed          Journal:  Anticancer Drug Des        ISSN: 0266-9536


  2 in total

1.  An improved synthesis of 4-chlorocoumarin-3-sulfonyl chloride and its reactions with different bidentate nucleophiles to give pyrido[1',2':2,3]- and thiazino[3',2':2,3]-1,2,4-thiadiazino[6,5-c]benzopyran-6-one 7,7-dioxides.

Authors:  Ahmed Jashari; Evamarie Hey-Hawkins; Bozhana Mikhova; Gerald Draeger; Emil Popovski
Journal:  Molecules       Date:  2007-08-22       Impact factor: 4.411

2.  BF3·Et2O Catalysed 4-Aryl-3-phenyl-benzopyrones, Pro-SERMs, and Their Characterization.

Authors:  Ambika Srivastava; Pooja Singh; Rajesh Kumar
Journal:  Adv Pharmacol Sci       Date:  2015-09-01
  2 in total

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