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Structural Modifications of Diarylpyrimidine-quinolone Hybrids as Potent HIV-1 NNRTIs with an Improved Drug Resistance Profile

Current pharmaceutical design, 2016-12, Vol.22 (46), p.6982

2016

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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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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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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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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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Phenylpropanoids from Brachybotrys paridiformis Maxim. ex Oliv. and their anti-HBV activities

Phytochemistry (Oxford), 2022-05, Vol.197, p.113114-113114, Article 113114

2022

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Phenylpropanoids from Brachybotrys paridiformis maxim. Ex oliv. And their anti-HBV activities (II)

Phytochemistry (Oxford), 2022-11, Vol.203, p.113364-113364, Article 113364

2022

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Anti-HIV diarylpyrimidine–quinolone hybrids and their mode of action

Bioorganic & medicinal chemistry, 2015-07, Vol.23 (13), p.3860-3868

2015

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Synthesis and biological evaluation of DAPY–DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase

Bioorganic & medicinal chemistry, 2015-02, Vol.23 (3), p.624-631

2015

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Development of an Efficient Process for the Decomposition of the Borate Complexes Formed during the Large-Scale Synthesis of (S)‑1,2,4-Butanetriol

Organic process research & development, 2013-12, Vol.17 (12), p.1540-1542

2013

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Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2014-06, Vol.22 (12), p.3220-3226

2014

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Hybrid diarylbenzopyrimidine non-nucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy

Bioorganic & medicinal chemistry, 2010-07, Vol.18 (14), p.5039-5047

2010

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An efficient enantioselective synthesis of florfenicol via a vanadium-catalyzed asymmetric epoxidation

Tetrahedron: asymmetry, 2011-06, Vol.22 (12), p.1337-1341

2011

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Docking-based CoMFA and CoMSIA studies on naphthyl-substituted diarylpyrimidines as NNRTIs

SAR and QSAR in environmental research, 2014-10, Vol.25 (10), p.761-775

2014

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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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Towards new C6-rigid S-DABO HIV-1 reverse transcriptase inhibitors: Synthesis, biological investigation and molecular modeling studies

Bioorganic & medicinal chemistry, 2013-11, Vol.21 (21), p.6477-6483

2013

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Synthesis and biological evaluation of 5-fluoroquinolone-3-carboxylic acids as potential HIV-1 integrase inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2013-08, Vol.28 (4), p.671-676

2013

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Structural modifications of CH(OH)-DAPYs as new HIV-1 non-nucleoside reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2014-04, Vol.22 (8), p.2535-2541

2014

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Synthesis and anti-HIV activity of 2-naphthyl substituted DAPY analogues as non-nucleoside reverse transcriptase inhibitors

Bioorganic & medicinal chemistry, 2010-07, Vol.18 (13), p.4601-4605

2010

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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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Synthesis and biological evaluation of new conformationally restricted S-DABO hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase

MedChemComm, 2014, Vol.5 (4), p.468

2014

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Structural Modifications of Diarylpyrimidine-quinolone Hybrids as Potent HIV-1 NNRTIs with an Improved Drug Resistance Profile

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

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

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

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

Phenylpropanoids from Brachybotrys paridiformis Maxim. ex Oliv. and their anti-HBV activities

Phenylpropanoids from Brachybotrys paridiformis maxim. Ex oliv. And their anti-HBV activities (II)

Anti-HIV diarylpyrimidine–quinolone hybrids and their mode of action

Synthesis and biological evaluation of DAPY–DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase

Development of an Efficient Process for the Decomposition of the Borate Complexes Formed during the Large-Scale Synthesis of (S)‑1,2,4-Butanetriol

Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors

Hybrid diarylbenzopyrimidine non-nucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy

An efficient enantioselective synthesis of florfenicol via a vanadium-catalyzed asymmetric epoxidation

Docking-based CoMFA and CoMSIA studies on naphthyl-substituted diarylpyrimidines as NNRTIs

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

Towards new C6-rigid S-DABO HIV-1 reverse transcriptase inhibitors: Synthesis, biological investigation and molecular modeling studies

Synthesis and biological evaluation of 5-fluoroquinolone-3-carboxylic acids as potential HIV-1 integrase inhibitors

Structural modifications of CH(OH)-DAPYs as new HIV-1 non-nucleoside reverse transcriptase inhibitors

Synthesis and anti-HIV activity of 2-naphthyl substituted DAPY analogues as non-nucleoside 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

Synthesis and biological evaluation of new conformationally restricted S-DABO hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase

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