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Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents

Bioorganic & medicinal chemistry, 2022-02, Vol.55, p.116597-116597, Article 116597

2022

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Advances in the development of HIV integrase strand transfer inhibitors

European journal of medicinal chemistry, 2021-12, Vol.225, p.113787-113787, Article 113787

2021

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Anticancer activity evaluation of indazolyl-substituted piperidin-4-yl-aminopyrimidines

Medicinal chemistry research, 2020-05, Vol.29 (5), p.910-915

2020

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Chiral resolution, absolute configuration assignment and biological activity of racemic diarylpyrimidine CH(OH)-DAPY as potent nonnucleoside HIV-1 reverse transcriptase inhibitors

European journal of medicinal chemistry, 2012-07, Vol.53, p.229-234

2012

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Advances in rationally designed dual inhibitors of HIV-1 reverse transcriptase and integrase

Bioorganic & medicinal chemistry, 2016-11, Vol.24 (21), p.5007-5016

2016

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Advances in diarylpyrimidines and related analogues as HIV-1 nonnucleoside reverse transcriptase inhibitors

European journal of medicinal chemistry, 2018-10, Vol.158, p.371-392

2018

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Recent progress in HIV-1 inhibitors targeting the entrance channel of HIV-1 non-nucleoside reverse transcriptase inhibitor binding pocket

European journal of medicinal chemistry, 2019-07, Vol.174, p.277-291

2019

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Synthesis and Anti-HIV Activity of Aryl-2-[(4-cyanophenyl)amino]-4-pyrimidinone hydrazones as Potent Non-nucleoside Reverse Transcriptase Inhibitors

ChemMedChem, 2011-12, Vol.6 (12), p.2225-2232

2011

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Hybrids of delavirdine and piperdin-4-yl-aminopyrimidines (DPAPYs) as potent HIV-1 NNRTIs: Design, synthesis and biological activities

European journal of medicinal chemistry, 2023-02, Vol.248, p.115114-115114, Article 115114

2023

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Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2011-07, Vol.19 (14), p.4220-4226

2011

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Indazolyl-substituted piperidin-4-yl-aminopyrimidines as HIV-1 NNRTIs: Design, synthesis and biological activities

European journal of medicinal chemistry, 2020-01, Vol.186, p.111864-111864, Article 111864

2020

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Structural modifications of diarylpyrimidines (DAPYs) as HIV-1 NNRTIs: Synthesis, anti-HIV activities and SAR

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (8), p.2491-2497

2017

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Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2011-08, Vol.19 (16), p.4704-4709

2011

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A novel family of diarylpyrimidines (DAPYs) featuring a diatomic linker: Design, synthesis and anti-HIV activities

Bioorganic & medicinal chemistry, 2015-10, Vol.23 (20), p.6587-6593

2015

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Design and synthesis of hybrids of diarylpyrimidines and diketo acids as HIV-1 inhibitors

Bioorganic & medicinal chemistry letters, 2017-04, Vol.27 (8), p.1640-1643

2017

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Virtual Screening and Optimization of Novel mTOR Inhibitors for Radiosensitization of Hepatocellular Carcinoma

Drug design, development and therapy, 2020-01, Vol.14, p.1779-1798

2020

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Synthesis and structure–activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIs

Bioorganic & medicinal chemistry, 2011-09, Vol.19 (17), p.5117-5124

2011

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Structural modification of diarylpyrimidine derivatives as HIV-1 reverse transcriptase inhibitors

Medicinal chemistry research, 2015-01, Vol.24 (1), p.220-225

2015

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Design, synthesis and biological evaluation of cycloalkyl arylpyrimidines (CAPYs) as HIV-1 NNRTIs

Bioorganic & medicinal chemistry, 2011-12, Vol.19 (23), p.7093-7099

2011

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Synthesis and biological activity of naphthyl-substituted (B-ring) benzophenone derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2011-08, Vol.19 (15), p.4601-4607

2011

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Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity

Bioorganic & medicinal chemistry, 2011-08, Vol.19 (16), p.5039-5045

2011

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Synthesis, structure–activity relationships, and docking studies of N-phenylarylformamide derivatives (PAFAs) as non-nucleoside HIV reverse transcriptase inhibitors

European journal of medicinal chemistry, 2012-12, Vol.58, p.504-512

2012

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Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitors

Bioorganic & medicinal chemistry, 2011-09, Vol.19 (18), p.5553-5558

2011

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Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents

Advances in the development of HIV integrase strand transfer inhibitors

Anticancer activity evaluation of indazolyl-substituted piperidin-4-yl-aminopyrimidines

Chiral resolution, absolute configuration assignment and biological activity of racemic diarylpyrimidine CH(OH)-DAPY as potent nonnucleoside HIV-1 reverse transcriptase inhibitors

Advances in rationally designed dual inhibitors of HIV-1 reverse transcriptase and integrase

Advances in diarylpyrimidines and related analogues as HIV-1 nonnucleoside reverse transcriptase inhibitors

Recent progress in HIV-1 inhibitors targeting the entrance channel of HIV-1 non-nucleoside reverse transcriptase inhibitor binding pocket

Synthesis and Anti-HIV Activity of Aryl-2-[(4-cyanophenyl)amino]-4-pyrimidinone hydrazones as Potent Non-nucleoside Reverse Transcriptase Inhibitors

Hybrids of delavirdine and piperdin-4-yl-aminopyrimidines (DPAPYs) as potent HIV-1 NNRTIs: Design, synthesis and biological activities

Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitors

Indazolyl-substituted piperidin-4-yl-aminopyrimidines as HIV-1 NNRTIs: Design, synthesis and biological activities

Structural modifications of diarylpyrimidines (DAPYs) as HIV-1 NNRTIs: Synthesis, anti-HIV activities and SAR

Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors

A novel family of diarylpyrimidines (DAPYs) featuring a diatomic linker: Design, synthesis and anti-HIV activities

Design and synthesis of hybrids of diarylpyrimidines and diketo acids as HIV-1 inhibitors

Virtual Screening and Optimization of Novel mTOR Inhibitors for Radiosensitization of Hepatocellular Carcinoma

Synthesis and structure–activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIs

Structural modification of diarylpyrimidine derivatives as HIV-1 reverse transcriptase inhibitors

Design, synthesis and biological evaluation of cycloalkyl arylpyrimidines (CAPYs) as HIV-1 NNRTIs

Synthesis and biological activity of naphthyl-substituted (B-ring) benzophenone derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity

Synthesis, structure–activity relationships, and docking studies of N-phenylarylformamide derivatives (PAFAs) as non-nucleoside HIV reverse transcriptase inhibitors

Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitors

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