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Organic Carbamates in Drug Design and Medicinal Chemistry

Journal of medicinal chemistry, 2015-04, Vol.58 (7), p.2895-2940

2015

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BACE1 (β-secretase) inhibitors for the treatment of Alzheimer's disease

Chemical Society reviews, 2014-10, Vol.43 (19), p.6765-6813

2014

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Recent Progress in the Development of HIV‑1 Protease Inhibitors for the Treatment of HIV/AIDS

Journal of medicinal chemistry, 2016-06, Vol.59 (11), p.5172-5208

2016

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Drug Development and Medicinal Chemistry Efforts toward SARS‐Coronavirus and Covid‐19 Therapeutics

ChemMedChem, 2020-06, Vol.15 (11), p.907-932

2020

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The Curtius rearrangement: mechanistic insight and recent applications in natural product syntheses

Organic & biomolecular chemistry, 2018, Vol.16 (12), p.26-227

2018

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The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry

ChemMedChem, 2018-11, Vol.13 (22), p.2351-2373

2018

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Achmatowicz reaction and its application in the syntheses of bioactive molecules

RSC advances, 2016-01, Vol.6 (112), p.111564-111598

2016

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Beyond darunavir: recent development of next generation HIV-1 protease inhibitors to combat drug resistance

Chemical communications (Cambridge, England), 2022-10, Vol.58 (84), p.11762-11782

2022

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Urea Derivatives in Modern Drug Discovery and Medicinal Chemistry

Journal of medicinal chemistry, 2020-03, Vol.63 (6), p.2751-2788

2020

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A small molecule compound with an indole moiety inhibits the main protease of SARS-CoV-2 and blocks virus replication

Nature communications, 2021-01, Vol.12 (1), p.668-12, Article 668

2021

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BACE1 inhibitor drugs for the treatment of Alzheimer's disease: Lessons learned, challenges to overcome, and future prospects

Global health & medicine, 2024-06, Vol.6 (3), p.164-169, Article 2024.01033

Ghosh, Arun K.

2024

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Total Syntheses of the Proposed Structure of Iriomoteolide-1a, -1b and Synthesis of Three Derivatives for Structural Studies

Marine drugs, 2022-09, Vol.20 (10), p.587

2022

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Four decades of continuing innovations in the development of antiretroviral therapy for HIV/AIDS: Progress to date and future challenges

Global health & medicine, 2023-08, Vol.5 (4), p.194-198, Article 2023.01013

Ghosh, Arun K.

2023

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Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitors

Nature communications, 2021-07, Vol.12 (1), p.4491-4491, Article 4491

2021

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Enantioselective Total Synthesis of (−)-Zampanolide, a Potent Microtubule-Stabilizing Agent

Organic letters, 2011-08, Vol.13 (15), p.4108-4111

2011

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Enhancing Protein Backbone Binding-A Fruitful Concept for Combating Drug-Resistant HIV

Angewandte Chemie International Edition, 2012-02, Vol.51 (8), p.1778-1802

International ed. in English, 2012

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Enantioselective Syntheses of FR901464 and Spliceostatin A: Potent Inhibitors of Spliceosome

Organic letters, 2013-10, Vol.15 (19), p.5088-5091

2013

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Evaluation of darunavir-derived HIV-1 protease inhibitors incorporating P2′ amide-derivatives: Synthesis, biological evaluation and structural studies

Bioorganic & medicinal chemistry letters, 2023-03, Vol.83 (C), p.129168-129168, Article 129168

2023

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Enantioselective Syntheses of (-)-Alloyohimbane and (-)-Yohimbane by an Efficient Enzymatic Desymmetrization Process

European journal of organic chemistry, 2016-12, Vol.2016 (36), p.6001-6009

2016

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GRL-0920, an Indole Chloropyridinyl Ester, Completely Blocks SARS-CoV-2 Infection

mBio, 2020-08, Vol.11 (4)

2020

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noncovalent class of papain-like protease/deubiquitinase inhibitors blocks SARS virus replication

Proceedings of the National Academy of Sciences - PNAS, 2008-10, Vol.105 (42), p.16119-16124

2008

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Deubiquitinating and Interferon Antagonism Activities of Coronavirus Papain-Like Proteases

Journal of Virology, 2010-05, Vol.84 (9), p.4619-4629

2010

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Enantioselective Total Synthesis of (+)-Largazole, a Potent Inhibitor of Histone Deacetylase

Organic letters, 2008-09, Vol.10 (17), p.3907-3909

2008

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U2 snRNA structure is influenced by SF3A and SF3B proteins but not by SF3B inhibitors

PloS one, 2021-10, Vol.16 (10), p.e0258551-e0258551

2021

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An enantioselective enzymatic desymmetrization route to hexahydro-4H-furopyranol, a high-affinity ligand for HIV-1 protease inhibitors

Tetrahedron letters, 2017-08, Vol.58 (33), p.3230-3233

2017

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Organic Carbamates in Drug Design and Medicinal Chemistry

BACE1 (β-secretase) inhibitors for the treatment of Alzheimer's disease

Recent Progress in the Development of HIV‑1 Protease Inhibitors for the Treatment of HIV/AIDS

Drug Development and Medicinal Chemistry Efforts toward SARS‐Coronavirus and Covid‐19 Therapeutics

The Curtius rearrangement: mechanistic insight and recent applications in natural product syntheses

The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry

Achmatowicz reaction and its application in the syntheses of bioactive molecules

Beyond darunavir: recent development of next generation HIV-1 protease inhibitors to combat drug resistance

Urea Derivatives in Modern Drug Discovery and Medicinal Chemistry

A small molecule compound with an indole moiety inhibits the main protease of SARS-CoV-2 and blocks virus replication

BACE1 inhibitor drugs for the treatment of Alzheimer's disease: Lessons learned, challenges to overcome, and future prospects

Total Syntheses of the Proposed Structure of Iriomoteolide-1a, -1b and Synthesis of Three Derivatives for Structural Studies

Four decades of continuing innovations in the development of antiretroviral therapy for HIV/AIDS: Progress to date and future challenges

Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitors

Enantioselective Total Synthesis of (−)-Zampanolide, a Potent Microtubule-Stabilizing Agent

Enhancing Protein Backbone Binding-A Fruitful Concept for Combating Drug-Resistant HIV

Enantioselective Syntheses of FR901464 and Spliceostatin A: Potent Inhibitors of Spliceosome

Evaluation of darunavir-derived HIV-1 protease inhibitors incorporating P2′ amide-derivatives: Synthesis, biological evaluation and structural studies

Enantioselective Syntheses of (-)-Alloyohimbane and (-)-Yohimbane by an Efficient Enzymatic Desymmetrization Process

GRL-0920, an Indole Chloropyridinyl Ester, Completely Blocks SARS-CoV-2 Infection

noncovalent class of papain-like protease/deubiquitinase inhibitors blocks SARS virus replication

Deubiquitinating and Interferon Antagonism Activities of Coronavirus Papain-Like Proteases

Enantioselective Total Synthesis of (+)-Largazole, a Potent Inhibitor of Histone Deacetylase

U2 snRNA structure is influenced by SF3A and SF3B proteins but not by SF3B inhibitors

An enantioselective enzymatic desymmetrization route to hexahydro-4H-furopyranol, a high-affinity ligand for HIV-1 protease inhibitors

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