Probing the Anticancer Activity of Nucleoside Analogues: A QSAR Model Approach Using an Internally Consistent Training Set-Reference-Cited by-同舟云学术

Probing the Anticancer Activity of Nucleoside Analogues: A QSAR Model Approach Using an Internally Consistent Training Set

Published:2007-03-07 Issue:7 Volume:50 Page:1537-1545
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Morales Helguera Aliuska¹,Rodríguez-Borges J. E.¹,García-Mera Xerardo¹,Fernández Franco¹,Cordeiro M. Natália D. S.¹

Affiliation:

1. REQUIMTE and CIQ, Department of Chemistry, University of Porto, Rua do Campo Alegre 687, 4169-007 Porto, Portugal, CBQ and Department of Chemistry, Central University of Las Villas, Santa Clara, 54830, Villa Clara, Cuba, and Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, 15706 Santiago de Compostela, Spain

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm061445m

Reference76 articles.

1. Simons, C.Carbocyclic Nucleosides; Gordon & Breach Science Publisher: Reading, UK, 2001; Vol. 3, pp 137−153.

2. Drug Resistance to Cytotoxic Nucleoside Analogues

3. Role of thymidine kinase in the inhibitory activity of 5-substituted-2'-deoxyuridines on the growth of human and murine tumor cell lines

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