Literature DB >> 9719600

Tipranavir (PNU-140690): a potent, orally bioavailable nonpeptidic HIV protease inhibitor of the 5,6-dihydro-4-hydroxy-2-pyrone sulfonamide class.

S R Turner1, J W Strohbach, R A Tommasi, P A Aristoff, P D Johnson, H I Skulnick, L A Dolak, E P Seest, P K Tomich, M J Bohanon, M M Horng, J C Lynn, K T Chong, R R Hinshaw, K D Watenpaugh, M N Janakiraman, S Thaisrivongs.   

Abstract

A broad screening program previously identified phenprocoumon (1) as a small molecule template for inhibition of HIV protease. Subsequent modification of this lead through iterative cycles of structure-based design led to the activity enhancements of pyrone and dihydropyrone ring systems (II and V) and amide-based substitution (III). Incorporation of sulfonamide substitution within the dihydropyrone template provided a series of highly potent HIV protease inhibitors, with structure-activity relationships described in this paper. Crystallographic studies provided further information on important binding interactions responsible for high enzymatic binding. These studies culminated in compound VI, which inhibits HIV protease with a Ki value of 8 pM and shows an IC90 value of 100 nM in antiviral cell culture. Clinical trials of this compound (PNU-140690, Tipranavir) for treatment of HIV infection are currently underway.

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Year:  1998        PMID: 9719600     DOI: 10.1021/jm9802158

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  34 in total

1.  Evaluating the substrate-envelope hypothesis: structural analysis of novel HIV-1 protease inhibitors designed to be robust against drug resistance.

Authors:  Madhavi N L Nalam; Akbar Ali; Michael D Altman; G S Kiran Kumar Reddy; Sripriya Chellappan; Visvaldas Kairys; Aysegül Ozen; Hong Cao; Michael K Gilson; Bruce Tidor; Tariq M Rana; Celia A Schiffer
Journal:  J Virol       Date:  2010-03-17       Impact factor: 5.103

2.  HIV-1 protease inhibitors from inverse design in the substrate envelope exhibit subnanomolar binding to drug-resistant variants.

Authors:  Michael D Altman; Akbar Ali; G S Kiran Kumar Reddy; Madhavi N L Nalam; Saima Ghafoor Anjum; Hong Cao; Sripriya Chellappan; Visvaldas Kairys; Miguel X Fernandes; Michael K Gilson; Celia A Schiffer; Tariq M Rana; Bruce Tidor
Journal:  J Am Chem Soc       Date:  2008-04-16       Impact factor: 15.419

3.  Interaction of ritonavir-boosted tipranavir with loperamide does not result in loperamide-associated neurologic side effects in healthy volunteers.

Authors:  Geoffrey Mukwaya; Thomas MacGregor; David Hoelscher; Thomas Heming; Daniel Legg; Kelli Kavanaugh; Phillip Johnson; John P Sabo; Scott McCallister
Journal:  Antimicrob Agents Chemother       Date:  2005-12       Impact factor: 5.191

Review 4.  Tetrahydrofuran, tetrahydropyran, triazoles and related heterocyclic derivatives as HIV protease inhibitors.

Authors:  Arun K Ghosh; David D Anderson
Journal:  Future Med Chem       Date:  2011-07       Impact factor: 3.808

5.  Role of tipranavir in treatment of patients with multidrug-resistant HIV.

Authors:  Joshua D Courter; Colleen J Teevan; Michael H Li; Jennifer E Girotto; Juan C Salazar
Journal:  Ther Clin Risk Manag       Date:  2010-10-05       Impact factor: 2.423

6.  Tipranavir (TPV) genotypic inhibitory quotient predicts virological response at 48 weeks to TPV-based salvage regimens.

Authors:  Daniel Gonzalez de Requena; Stefano Bonora; Andrea Calcagno; Antonio D'Avolio; Marco Siccardi; Silvia Fontana; Maria Grazia Milia; Mauro Sciandra; Silvia Garazzino; Antonio Di Garbo; Lorena Baietto; Laura Trentini; Giovanni Di Perri
Journal:  Antimicrob Agents Chemother       Date:  2007-12-26       Impact factor: 5.191

7.  Steady-state disposition of the nonpeptidic protease inhibitor tipranavir when coadministered with ritonavir.

Authors:  Linzhi Chen; John P Sabo; Elsy Philip; Yanping Mao; Stephen H Norris; Thomas R MacGregor; Jan M Wruck; Sandra Garfinkel; Mark Castles; Amy Brinkman; Hernan Valdez
Journal:  Antimicrob Agents Chemother       Date:  2007-05-07       Impact factor: 5.191

8.  Prediction of potency of protease inhibitors using free energy simulations with polarizable quantum mechanics-based ligand charges and a hybrid water model.

Authors:  Debananda Das; Yasuhiro Koh; Yasushi Tojo; Arun K Ghosh; Hiroaki Mitsuya
Journal:  J Chem Inf Model       Date:  2009-12       Impact factor: 4.956

9.  P2' benzene carboxylic acid moiety is associated with decrease in cellular uptake: evaluation of novel nonpeptidic HIV-1 protease inhibitors containing P2 bis-tetrahydrofuran moiety.

Authors:  Ravikiran S Yedidi; Kenji Maeda; W Sean Fyvie; Melinda Steffey; David A Davis; Ira Palmer; Manabu Aoki; Joshua D Kaufman; Stephen J Stahl; Harisha Garimella; Debananda Das; Paul T Wingfield; Arun K Ghosh; Hiroaki Mitsuya
Journal:  Antimicrob Agents Chemother       Date:  2013-07-22       Impact factor: 5.191

10.  Crystal structure of lysine sulfonamide inhibitor reveals the displacement of the conserved flap water molecule in human immunodeficiency virus type 1 protease.

Authors:  Madhavi N L Nalam; Anik Peeters; Tim H M Jonckers; Inge Dierynck; Celia A Schiffer
Journal:  J Virol       Date:  2007-06-27       Impact factor: 5.103

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