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- Prodrugs of HIV protease inhibitors—saquinavir, indinavir and nelfinavir—derived from diglycerides or amino acids: synthesis, stability and anti-HIV activity. Bérangère Gaucher, Marielle Rouquayrol, Dominique Roche, Jacques Greiner, Anne-Marie Aubertin, Pierre Vierling
, Org. Biomol. Chem.
, 2004
, 2
, 345
- Reaching beyond HIV/HCV: nelfinavir as a potential starting point for broad-spectrum protease inhibitors against dengue and chikungunya virus. Soumendranath Bhakat, Leen Delang, Suzanne Kaptein, Johan Neyts, Pieter Leyssen, Venkatesan Jayaprakash
, RSC Adv.
, 2015
, 5
, 85938
- Consensus virtual screening of dark chemical matter and food chemicals uncover potential inhibitors of SARS-CoV-2 main protease. Marisa G. Santibáñez-Morán, Edgar López-López, Fernando D. Prieto-Martínez, Norberto Sánchez-Cruz, José L. Medina-Franco
, RSC Adv.
, 2020
, 10
, 25089
- Revealing the binding and drug resistance mechanism of amprenavir, indinavir, ritonavir, and nelfinavir complexed with HIV-1 protease due to double mutations G48T/L89M by molecular dynamics simulations and free energy analyses. Rui-Ge Wang, Hong-Xing Zhang, Qing-Chuan Zheng
, Phys. Chem. Chem. Phys.
, 2020
, 22
, 4464
- β-Blockers bearing hydroxyethylamine and hydroxyethylene as potential SARS-CoV-2 Mpro inhibitors: rational based design, in silico, in vitro, and SAR studies for lead optimization. Mohammed I. A. Hamed, Khaled M. Darwish, Raya Soltane, Amani Chrouda, Ahmed Mostafa, Noura M. Abo Shama, Sameh S. Elhady, Hamada S. Abulkhair, Ahmed E. Khodir, Ayman Abo Elmaaty, Ahmed A. Al-karmalawy
, RSC Adv.
, 2021
, 11
, 35536
- Biocatalytic routes to anti-viral agents and their synthetic intermediates. Sjoerd Slagman, Wolf-Dieter Fessner
, Chem. Soc. Rev.
, 2021
, 50
, 1968
- Potential role of medicinal plants and their constituents in the mitigation of SARS-CoV-2: identifying related therapeutic targets using network pharmacology and molecular docking analyses. Eman Shawky, Ahmed A. Nada, Reham S. Ibrahim
, RSC Adv.
, 2020
, 10
, 27961
- Design and synthesis of potent macrocyclic HIV-1 protease inhibitors involving P1–P2 ligands. Arun K. Ghosh, Gary E. Schiltz, Linah N. Rusere, Heather L. Osswald, D. Eric Walters, Masayuki Amano, Hiroaki Mitsuya
, Org. Biomol. Chem.
, 2014
, 12
, 6842
- Simultaneous fluorescence imaging of hydrogen peroxide in mitochondria and endoplasmic reticulum during apoptosis. Haibin Xiao, Ping Li, Xiufen Hu, Xiaohui Shi, Wen Zhang, Bo Tang
, Chem. Sci.
, 2016
, 7
, 6153
- Discovery of acylphloroglucinol-based meroterpenoid enantiomers as KSHV inhibitors from Hypericum japonicum. Linzhen Hu, Yanfei Liu, Yanxing Wang, Zhenzhen Wang, Jinfeng Huang, Yongbo Xue, Junjun Liu, Zhenming Liu, Yong Chen, Yonghui Zhang
, RSC Adv.
, 2018
, 8
, 24101