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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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Quinolines and isoquinolines as HIV-1 inhibitors: Chemical structures, action targets, and biological activities

Bioorganic chemistry, 2023-07, Vol.136, p.106549-106549, Article 106549

2023

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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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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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Non-peptidic inhibitors targeting SARS-CoV-2 main protease: A review

Bioorganic chemistry, 2024-06, Vol.147, p.107380-107380, Article 107380

2024

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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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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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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 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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Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris

Genome research, 2005-06, Vol.15 (6), p.757

2005

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Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells

Genome research, 2000-10, Vol.10 (10), p.1546

2000

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

Quinolines and isoquinolines as HIV-1 inhibitors: Chemical structures, action targets, and biological activities

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

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

Non-peptidic inhibitors targeting SARS-CoV-2 main protease: A review

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

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

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

Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris

Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells

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