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Christophe Pannecouque

Showing results (61-70 of 426) with videos related to

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Medicinal Chemistry (Shariqah (United Arab Emirates))|July 6, 2012
Substituted naphthalen-1-yl-acetic acid hydrazides: synthesis, antimicrobial evaluation and QSAR analysisRakesh Narang, Balasubramanian Narasimhan, Sunil Sharma, et al.
Bioorganic Chemistry|August 18, 2023
Development of novel HEPT analogs featuring significantly improved anti-resistance potency against HIV-1 through chemical space exploration of the tolerant region IRuo-Lan Zhou, Christophe Pannecouque, Erik De Clercq, et al.
Acta Pharmaceutica Sinica. B|July 31, 2023
Picomolar inhibitor of reverse transcriptase featuring significantly improved metabolic stabilityYa-Li Sang, Christophe Pannecouque, Erik De Clercq, et al.
European Journal of Medicinal Chemistry|January 17, 2018
New findings on the d(TGGGAG) sequence: Surprising anti-HIV-1 activityValeria Romanucci, Armando Zarrelli, Sandra Liekens, et al.
Bioorganic & Medicinal Chemistry|March 14, 2007
Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3-thiazolidin-4-one analogues as anti-HIV-1 agentsRavindra K Rawal, Rajkamal Tripathi, S B Katti, et al.
The Journal of Organic Chemistry|October 27, 2022
Conformationally Locked Carbocyclic Nucleosides Built on a 4'-Hydroxymethyl-3'-hydroxybicyclo[4.1.0]heptane Template. Stereoselective Synthesis and Antiviral ActivitySergio Jurado, Ona Illa, Angel Álvarez-Larena, et al.
European Journal of Medicinal Chemistry|June 9, 2022
Expansion of the S-CN-DABO scaffold to exploit the impact on inhibitory activities against the non-nucleoside HIV-1 reverse transcriptaseXu Ling, Qing-Qing Hao, Christophe Pannecouque, et al.
RSC Medicinal Chemistry|October 18, 2024
Rapid identification of novel indolylarylsulfone derivatives as potent HIV-1 NNRTIs <i>via</i> miniaturized CuAAC click-chemistry-based combinatorial librariesPing Gao, Shu Song, Christophe Pannecouque, et al.
European Journal of Medicinal Chemistry|July 12, 2024
Structure-based discovery of novel piperidine-biphenyl-DAPY derivatives as non-nucleoside reverse transcriptase inhibitors featuring improved potency, safety, and selectivity: From piperazine-biphenyl-DAPYs to piperidine-biphenyl-DAPYsWen-Juan Huang, Christophe Pannecouque, Erik De Clercq, et al.
Acta Pharmaceutica Sinica. B|December 4, 2023
Structure-based design of novel heterocycle-substituted ATDP analogs as non-nucleoside reverse transcriptase inhibitors with improved selectivity and solubilityLi-Min Zhao, Christophe Pannecouque, Erik De Clercq, et al.
Pageof 43

Showing results (61-70 of 426) with videos related to

Sort By:
Pageof 43
Medicinal Chemistry (Shariqah (United Arab Emirates))|July 6, 2012
Substituted naphthalen-1-yl-acetic acid hydrazides: synthesis, antimicrobial evaluation and QSAR analysisRakesh Narang, Balasubramanian Narasimhan, Sunil Sharma, et al.
Bioorganic Chemistry|August 18, 2023
Development of novel HEPT analogs featuring significantly improved anti-resistance potency against HIV-1 through chemical space exploration of the tolerant region IRuo-Lan Zhou, Christophe Pannecouque, Erik De Clercq, et al.
Acta Pharmaceutica Sinica. B|July 31, 2023
Picomolar inhibitor of reverse transcriptase featuring significantly improved metabolic stabilityYa-Li Sang, Christophe Pannecouque, Erik De Clercq, et al.
European Journal of Medicinal Chemistry|January 17, 2018
New findings on the d(TGGGAG) sequence: Surprising anti-HIV-1 activityValeria Romanucci, Armando Zarrelli, Sandra Liekens, et al.
Bioorganic & Medicinal Chemistry|March 14, 2007
Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3-thiazolidin-4-one analogues as anti-HIV-1 agentsRavindra K Rawal, Rajkamal Tripathi, S B Katti, et al.
The Journal of Organic Chemistry|October 27, 2022
Conformationally Locked Carbocyclic Nucleosides Built on a 4'-Hydroxymethyl-3'-hydroxybicyclo[4.1.0]heptane Template. Stereoselective Synthesis and Antiviral ActivitySergio Jurado, Ona Illa, Angel Álvarez-Larena, et al.
European Journal of Medicinal Chemistry|June 9, 2022
Expansion of the S-CN-DABO scaffold to exploit the impact on inhibitory activities against the non-nucleoside HIV-1 reverse transcriptaseXu Ling, Qing-Qing Hao, Christophe Pannecouque, et al.
RSC Medicinal Chemistry|October 18, 2024
Rapid identification of novel indolylarylsulfone derivatives as potent HIV-1 NNRTIs <i>via</i> miniaturized CuAAC click-chemistry-based combinatorial librariesPing Gao, Shu Song, Christophe Pannecouque, et al.
European Journal of Medicinal Chemistry|July 12, 2024
Structure-based discovery of novel piperidine-biphenyl-DAPY derivatives as non-nucleoside reverse transcriptase inhibitors featuring improved potency, safety, and selectivity: From piperazine-biphenyl-DAPYs to piperidine-biphenyl-DAPYsWen-Juan Huang, Christophe Pannecouque, Erik De Clercq, et al.
Acta Pharmaceutica Sinica. B|December 4, 2023
Structure-based design of novel heterocycle-substituted ATDP analogs as non-nucleoside reverse transcriptase inhibitors with improved selectivity and solubilityLi-Min Zhao, Christophe Pannecouque, Erik De Clercq, et al.
Pageof 43