Antiproliferative novel isoxazoles: Modeling, virtual screening, synthesis, and bioactivity evaluation-Reference-Cited by-同舟云学术

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Antiproliferative novel isoxazoles: Modeling, virtual screening, synthesis, and bioactivity evaluation

Published:2014-06 Issue: Volume:81 Page:139-149
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Tzanetou Evangelia,Liekens Sandra,Kasiotis Konstantinos M.,Melagraki Georgia,Afantitis Antreas,Fokialakis Nikolas,Haroutounian Serkos A.

Funder

Chemical Approaches to Targeting Drug Resistance in Cancer Stem Cells

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference29 articles.

1. The thymidine phosphorylase inhibitor 5′-O-tritylinosine (KIN59) is an antiangiogenic multitarget fibroblast growth factor-2 antagonist;Liekens;Mol. Cancer Ther.,2012

2. Hallmarks of cancer: the next generation;Hanahan;Cell,2011

3. The identification, synthesis, protein crystal structure and in vitro biochemical evaluation of a new 3,4-diarylpyrazole class of Hsp90 inhibitors;Cheung;Bioorg. Med. Chem. Lett.,2005

4. Inhibition of the ras-net (Elk-3) pathway by a novel pyrazole that affects microtubules;Wasylyk;Cancer Res.,2008

5. Anti-cancer therapeutic approaches based on intracellular and extracellular heat shock proteins;Didelot;Curr. Med. Chem.,2007

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