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An insight into the medicinal perspective of synthetic analogs of indole: A review

European journal of medicinal chemistry, 2019-10, Vol.180, p.562-612

2019

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The Journey of HIV‑1 Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) from Lab to Clinic

Journal of medicinal chemistry, 2019-05, Vol.62 (10), p.4851-4883

2019

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1,2,3-Triazoles as Amide Bioisosteres: Discovery of a New Class of Potent HIV‑1 Vif Antagonists

Journal of medicinal chemistry, 2016-08, Vol.59 (16), p.7677-7682

2016

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Design, Synthesis, and Evaluation of Thiophene[3,2‑d]pyrimidine Derivatives as HIV‑1 Non-nucleoside Reverse Transcriptase Inhibitors with Significantly Improved Drug Resistance Profiles

Journal of medicinal chemistry, 2016-09, Vol.59 (17), p.7991-8007

2016

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Identification of Dihydrofuro[3,4‑d]pyrimidine Derivatives as Novel HIV‑1 Non-Nucleoside Reverse Transcriptase Inhibitors with Promising Antiviral Activities and Desirable Physicochemical Properties

Journal of medicinal chemistry, 2019-02, Vol.62 (3), p.1484-1501

2019

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T‐Cell‐Mimicking Nanoparticles Can Neutralize HIV Infectivity

Advanced materials (Weinheim), 2018-11, Vol.30 (45), p.e1802233-n/a

2018

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In Vitro Antiretroviral Properties of S/GSK1349572, a Next-Generation HIV Integrase Inhibitor

Antimicrobial Agents and Chemotherapy, 2011-02, Vol.55 (2), p.813-821

2011

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Design, synthesis and structure-activity relationships of 4-phenyl-1H-1,2,3-triazole phenylalanine derivatives as novel HIV-1 capsid inhibitors with promising antiviral activities

European journal of medicinal chemistry, 2020-03, Vol.190, p.112085-112085, Article 112085

2020

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Design, Synthesis, and Mechanism Study of Benzenesulfonamide-Containing Phenylalanine Derivatives as Novel HIV‑1 Capsid Inhibitors with Improved Antiviral Activities

Journal of medicinal chemistry, 2020-05, Vol.63 (9), p.4790-4810

2020

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Dendritic Cell Lectin-Targeting Sentinel-like Unimolecular Glycoconjugates To Release an Anti-HIV Drug

Journal of the American Chemical Society, 2014-03, Vol.136 (11), p.4325-4332

2014

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Discovery of Novel Dihydrothiopyrano[4,3‑d]pyrimidine Derivatives as Potent HIV‑1 NNRTIs with Significantly Reduced hERG Inhibitory Activity and Improved Resistance Profiles

Journal of medicinal chemistry, 2021-09, Vol.64 (18), p.13658-13675

2021

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Betulinic acid and its derivatives: a review on their biological properties

Current medicinal chemistry, 2005-01, Vol.12 (6), p.657-666

2005

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Development of Novel Dihydrofuro[3,4‑d]pyrimidine Derivatives as HIV‑1 NNRTIs to Overcome the Highly Resistant Mutant Strains F227L/V106A and K103N/Y181C

Journal of medicinal chemistry, 2022-02, Vol.65 (3), p.2458-2470

2022

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Core-structure-inspired asymmetric addition reactions: enantioselective synthesis of dihydrobenzoxazinone- and dihydroquinazolinone-based anti-HIV agents

Chemical Society reviews, 2015-11, Vol.44 (21), p.7439-7448

2015

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Synthesis, Binding and Antiviral Properties of Potent Core-Extended Naphthalene Diimides Targeting the HIV‑1 Long Terminal Repeat Promoter G‑Quadruplexes

Journal of medicinal chemistry, 2015-12, Vol.58 (24), p.9639-9652

2015

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2,4,5-Trisubstituted Pyrimidines as Potent HIV‑1 NNRTIs: Rational Design, Synthesis, Activity Evaluation, and Crystallographic Studies

Journal of medicinal chemistry, 2021-04, Vol.64 (7), p.4239-4256

2021

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Hydrogen-Bond-Directed Enantioselective Decarboxylative Mannich Reaction of β-Ketoacids with Ketimines: Application to the Synthesis of Anti-HIV Drug DPC 083

Angewandte Chemie (International ed.), 2013-04, Vol.52 (14), p.3869-3873

2013

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Catalytic enantioselective 1,6-conjugate additions of propargyl and allyl groups

Nature (London), 2016-09, Vol.537 (7620), p.387-393

2016

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Topology of a DNA G‑Quadruplex Structure Formed in the HIV‑1 Promoter: A Potential Target for Anti-HIV Drug Development

Journal of the American Chemical Society, 2014-04, Vol.136 (14), p.5249-5252

2014

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Discovery of phenylalanine derivatives as potent HIV-1 capsid inhibitors from click chemistry-based compound library

European journal of medicinal chemistry, 2018-10, Vol.158, p.478-492

2018

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Synthesis and bioevaluation of substituted chalcones, coumaranones and other flavonoids as anti-HIV agents

Bioorganic & medicinal chemistry, 2016-06, Vol.24 (12), p.2768-2776

2016

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Rhodium(II) acetate-catalyzed stereoselective synthesis, SAR and anti-HIV activity of novel oxindoles bearing cyclopropane ring

European journal of medicinal chemistry, 2011-04, Vol.46 (4), p.1181-1188

2011

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Design, synthesis, and structure activity relationship analysis of new betulinic acid derivatives as potent HIV inhibitors

European journal of medicinal chemistry, 2021-04, Vol.215, p.113287-113287, Article 113287

2021

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Discovery of Novel Aryl Triazolone Dihydropyridines (ATDPs) Targeting Highly Conserved Residue W229 as Promising HIV‑1 NNRTIs

Journal of medicinal chemistry, 2024-04, Vol.67 (8), p.6570-6584

2024

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Unlocking the Drug Potential of the Bryostatin Family: Recent Advances in Product Synthesis and Biomedical Applications

Chemistry : a European journal, 2020-01, Vol.26 (6), p.1166-1195

2020

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An insight into the medicinal perspective of synthetic analogs of indole: A review

The Journey of HIV‑1 Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) from Lab to Clinic

1,2,3-Triazoles as Amide Bioisosteres: Discovery of a New Class of Potent HIV‑1 Vif Antagonists

Design, Synthesis, and Evaluation of Thiophene[3,2‑d]pyrimidine Derivatives as HIV‑1 Non-nucleoside Reverse Transcriptase Inhibitors with Significantly Improved Drug Resistance Profiles

Identification of Dihydrofuro[3,4‑d]pyrimidine Derivatives as Novel HIV‑1 Non-Nucleoside Reverse Transcriptase Inhibitors with Promising Antiviral Activities and Desirable Physicochemical Properties

T‐Cell‐Mimicking Nanoparticles Can Neutralize HIV Infectivity

In Vitro Antiretroviral Properties of S/GSK1349572, a Next-Generation HIV Integrase Inhibitor

Design, synthesis and structure-activity relationships of 4-phenyl-1H-1,2,3-triazole phenylalanine derivatives as novel HIV-1 capsid inhibitors with promising antiviral activities

Design, Synthesis, and Mechanism Study of Benzenesulfonamide-Containing Phenylalanine Derivatives as Novel HIV‑1 Capsid Inhibitors with Improved Antiviral Activities

Dendritic Cell Lectin-Targeting Sentinel-like Unimolecular Glycoconjugates To Release an Anti-HIV Drug

Discovery of Novel Dihydrothiopyrano[4,3‑d]pyrimidine Derivatives as Potent HIV‑1 NNRTIs with Significantly Reduced hERG Inhibitory Activity and Improved Resistance Profiles

Betulinic acid and its derivatives: a review on their biological properties

Development of Novel Dihydrofuro[3,4‑d]pyrimidine Derivatives as HIV‑1 NNRTIs to Overcome the Highly Resistant Mutant Strains F227L/V106A and K103N/Y181C

Core-structure-inspired asymmetric addition reactions: enantioselective synthesis of dihydrobenzoxazinone- and dihydroquinazolinone-based anti-HIV agents

Synthesis, Binding and Antiviral Properties of Potent Core-Extended Naphthalene Diimides Targeting the HIV‑1 Long Terminal Repeat Promoter G‑Quadruplexes

2,4,5-Trisubstituted Pyrimidines as Potent HIV‑1 NNRTIs: Rational Design, Synthesis, Activity Evaluation, and Crystallographic Studies

Hydrogen-Bond-Directed Enantioselective Decarboxylative Mannich Reaction of β-Ketoacids with Ketimines: Application to the Synthesis of Anti-HIV Drug DPC 083

Catalytic enantioselective 1,6-conjugate additions of propargyl and allyl groups

Topology of a DNA G‑Quadruplex Structure Formed in the HIV‑1 Promoter: A Potential Target for Anti-HIV Drug Development

Discovery of phenylalanine derivatives as potent HIV-1 capsid inhibitors from click chemistry-based compound library

Synthesis and bioevaluation of substituted chalcones, coumaranones and other flavonoids as anti-HIV agents

Rhodium(II) acetate-catalyzed stereoselective synthesis, SAR and anti-HIV activity of novel oxindoles bearing cyclopropane ring

Design, synthesis, and structure activity relationship analysis of new betulinic acid derivatives as potent HIV inhibitors

Discovery of Novel Aryl Triazolone Dihydropyridines (ATDPs) Targeting Highly Conserved Residue W229 as Promising HIV‑1 NNRTIs

Unlocking the Drug Potential of the Bryostatin Family: Recent Advances in Product Synthesis and Biomedical Applications

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