Literature DB >> 15242246

Purine nucleoside antimetabolites in development for the treatment of cancer.

William B Parker1, John A Secrist, William R Waud.   

Abstract

Purine nucleoside analogs are an important class of drugs that are used in the treatment of cancer. Five purine analogs have been approved by the FDA (mercaptopurine, thioguanine, fludarabine monophosphate, deoxycoformycin and cladribine) and four compounds are currently being evaluated clinically (clofarabine, immucillin-H, nelarabine and 8-chloroadenosine). In addition, two gene therapy approaches are being evaluated that are based on the selective activation of purine nucleoside analogs (ganciclovir, fludarabine monophosphate and others) in tumor cells. Even though nucleoside analogs have been extensively evaluated over the last 50 years, the development of these new compounds demonstrates that there is still much promise in identifying new anticancer drugs from this class of compounds.

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Year:  2004        PMID: 15242246

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  15 in total

Review 1.  Polymeric nanogel formulations of nucleoside analogs.

Authors:  Serguei V Vinogradov
Journal:  Expert Opin Drug Deliv       Date:  2007-01       Impact factor: 6.648

Review 2.  How were new medicines discovered?

Authors:  David C Swinney; Jason Anthony
Journal:  Nat Rev Drug Discov       Date:  2011-06-24       Impact factor: 84.694

3.  The discovery of medicines for rare diseases.

Authors:  David C Swinney; Shuangluo Xia
Journal:  Future Med Chem       Date:  2014-06       Impact factor: 3.808

4.  Forodesine, an inhibitor of purine nucleoside phosphorylase, induces apoptosis in chronic lymphocytic leukemia cells.

Authors:  Kumudha Balakrishnan; Ramadevi Nimmanapalli; Farhad Ravandi; Michael J Keating; Varsha Gandhi
Journal:  Blood       Date:  2006-06-15       Impact factor: 22.113

5.  Deoxycytidine kinase modulates the impact of the ABC transporter ABCG2 on clofarabine cytotoxicity.

Authors:  Shinjiro Nagai; Kazumasa Takenaka; Deepa Nachagari; Charles Rose; Kali Domoney; Daxi Sun; Alex Sparreboom; John D Schuetz
Journal:  Cancer Res       Date:  2011-01-18       Impact factor: 12.701

Review 6.  The therapeutic implications of clinically applied modifiers of heat shock protein 70 (Hsp70) expression by tumor cells.

Authors:  Mathias Gehrmann; Jürgen Radons; Michael Molls; Gabriele Multhoff
Journal:  Cell Stress Chaperones       Date:  2008-02-05       Impact factor: 3.667

7.  Identification of Purine-Scaffold Small-Molecule Inhibitors of Stat3 Activation by QSAR Studies.

Authors:  Vijay M Shahani; Peibin Yue; Sina Haftchenary; Wei Zhao; Julie L Lukkarila; Xiaolei Zhang; Daniel Ball; Christina Nona; Patrick T Gunning; James Turkson
Journal:  ACS Med Chem Lett       Date:  2010-10-25       Impact factor: 4.345

8.  Synthesis of cyclic N (1)-pentylinosine phosphate, a new structurally reduced cADPR analogue with calcium-mobilizing activity on PC12 cells.

Authors:  Ahmed Mahal; Stefano D'Errico; Nicola Borbone; Brunella Pinto; Agnese Secondo; Valeria Costantino; Valentina Tedeschi; Giorgia Oliviero; Vincenzo Piccialli; Gennaro Piccialli
Journal:  Beilstein J Org Chem       Date:  2015-12-22       Impact factor: 2.883

9.  Amide-controlled, one-pot synthesis of tri-substituted purines generates structural diversity and analogues with trypanocidal activity.

Authors:  Maria J Pineda de las Infantas y Villatoro; Juan D Unciti-Broceta; Rafael Contreras-Montoya; Jose A Garcia-Salcedo; Miguel A Gallo Mezo; Asier Unciti-Broceta; Juan J Diaz-Mochon
Journal:  Sci Rep       Date:  2015-03-16       Impact factor: 4.379

10.  Versatile synthesis and biological evaluation of novel 3'-fluorinated purine nucleosides.

Authors:  Hang Ren; Haoyun An; Paul J Hatala; William C Stevens; Jingchao Tao; Baicheng He
Journal:  Beilstein J Org Chem       Date:  2015-12-09       Impact factor: 2.883

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