Literature DB >> 30393404

Syntheses of FDA Approved HIV Protease Inhibitors.

Arun K Ghosh1, Geoffrey Bilcer1, Gary Schiltz1.   

Abstract

The treatment of HIV and AIDS was revolutionized by the introduction of peptidomimetic aspartyl protease inhibitors. One of the major limitations of this type of therapy is that higher therapeutic doses are necessary because of the presence of 'peptide-like' features in the drugs. Therefore, adequate supplies and cost effective syntheses of these drugs are of utmost importance. To date, there are six protease inhibitors approved by the United States Food and Drug Administration (FDA) for the treatment of HIV and AIDS. This review focuses on the published syntheses of currently FDA approved HIV protease inhibitor drugs, their isosteres and ligands.

Entities:  

Keywords:  HIV; inhibitor; isostere; protease; synthesis

Year:  2001        PMID: 30393404      PMCID: PMC6211199          DOI: 10.1055/s-2001-18434

Source DB:  PubMed          Journal:  Synthesis (Stuttg)        ISSN: 0039-7881            Impact factor:   3.157


  32 in total

1.  Solid phase synthesis of indinavir and its analogues.

Authors:  Y Cheng; Z Lu; K T Chapman; J R Tata
Journal:  J Comb Chem       Date:  2000 Sep-Oct

2.  A Concise Formal Synthesis of the Potent HIV Protease Inhibitor Nelfinavir Mesylate.

Authors:  Dale L. Rieger
Journal:  J Org Chem       Date:  1997-11-28       Impact factor: 4.354

3.  Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: enantioselective synthesis of the core unit of ritonavir.

Authors:  Arun K Ghosh; Dongwoo Shin; Packiarajan Mathivanan
Journal:  Chem Commun (Camb)       Date:  1999       Impact factor: 6.222

4.  The gag gene products of human immunodeficiency virus type 1: alignment within the gag open reading frame, identification of posttranslational modifications, and evidence for alternative gag precursors.

Authors:  R J Mervis; N Ahmad; E P Lillehoj; M G Raum; F H Salazar; H W Chan; S Venkatesan
Journal:  J Virol       Date:  1988-11       Impact factor: 5.103

5.  Potent HIV-1 Protease Inhibitors: Stereoselective Synthesis of a Dipeptide Mimic.

Authors:  Arun K Ghosh; Sean P McKee; Wayne J Thompson; Paul L Darke; Joan C Zugay
Journal:  J Org Chem       Date:  1993-02       Impact factor: 4.354

Review 6.  HIV protease as an inhibitor target for the treatment of AIDS.

Authors:  P L Darke; J R Huff
Journal:  Adv Pharmacol       Date:  1994

7.  Hydroxyethylene isostere inhibitors of human immunodeficiency virus-1 protease: structure-activity analysis using enzyme kinetics, X-ray crystallography, and infected T-cell assays.

Authors:  G B Dreyer; D M Lambert; T D Meek; T J Carr; T A Tomaszek; A V Fernandez; H Bartus; E Cacciavillani; A M Hassell; M Minnich
Journal:  Biochemistry       Date:  1992-07-28       Impact factor: 3.162

Review 8.  Current knowledge and future prospects for the use of HIV protease inhibitors.

Authors:  G Moyle; B Gazzard
Journal:  Drugs       Date:  1996-05       Impact factor: 9.546

9.  Rational design of peptide-based HIV proteinase inhibitors.

Authors:  N A Roberts; J A Martin; D Kinchington; A V Broadhurst; J C Craig; I B Duncan; S A Galpin; B K Handa; J Kay; A Kröhn
Journal:  Science       Date:  1990-04-20       Impact factor: 47.728

10.  L-735,524: the design of a potent and orally bioavailable HIV protease inhibitor.

Authors:  B D Dorsey; R B Levin; S L McDaniel; J P Vacca; J P Guare; P L Darke; J A Zugay; E A Emini; W A Schleif; J C Quintero
Journal:  J Med Chem       Date:  1994-10-14       Impact factor: 7.446

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  8 in total

1.  Synthesis of Novel C-Pivot Lariat 18-Crown-6 Ethers and their Efficient Purification.

Authors:  Susovan Jana; Vallabh Suresh; Salvatore D Lepore
Journal:  Synlett       Date:  2015-07-29       Impact factor: 2.454

2.  Nature Inspired Molecular Design: Stereoselective Synthesis of Bicyclic and Polycyclic Ethers for Potent HIV-1 Protease Inhibitors.

Authors:  Arun K Ghosh; Margherita Brindisi
Journal:  Asian J Org Chem       Date:  2018-06-08       Impact factor: 3.319

3.  Diastereoselective Synthesis of Substituted Tetrahydropyrans by Copper(II)-Bisphosphine-Catalyzed Olefin Migration and Prins Cyclization.

Authors:  Arun K Ghosh; Jorden Kass; Daniel R Nicponski; Chad Keyes
Journal:  Synthesis (Stuttg)       Date:  2012-12       Impact factor: 3.157

4.  Highly Stereoselective Asymmetric Aldol Routes to tert-Butyl-2-(3,5-difluorophenyl)-1-oxiran-2-yl)ethyl)carbamates: Building Blocks for Novel Protease Inhibitors.

Authors:  Arun K Ghosh; Emilio L Cárdenas; Margherita Brindisi
Journal:  Tetrahedron Lett       Date:  2017-09-14       Impact factor: 2.415

5.  A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative.

Authors:  Nimalini Devi Moirangthem; Warjeet Singh Laitonjam
Journal:  Beilstein J Org Chem       Date:  2010-11-09       Impact factor: 2.883

Review 6.  Organic carbamates in drug design and medicinal chemistry.

Authors:  Arun K Ghosh; Margherita Brindisi
Journal:  J Med Chem       Date:  2015-01-07       Impact factor: 7.446

7.  Synthesis and Application of 1,2-Aminoalcohols with Neoisopulegol-Based Octahydrobenzofuran Core.

Authors:  Fatima Zahra Bamou; Tam Minh Le; Bettina Volford; András Szekeres; Zsolt Szakonyi
Journal:  Molecules       Date:  2019-12-19       Impact factor: 4.411

Review 8.  A comprehensive update on the structure and synthesis of potential drug targets for combating the coronavirus pandemic caused by SARS-CoV-2.

Authors:  Prerna Malik; Sonika Jain; Pankaj Jain; Jyoti Kumawat; Jaya Dwivedi; Dharma Kishore
Journal:  Arch Pharm (Weinheim)       Date:  2022-01-17       Impact factor: 4.613

  8 in total

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