|
Original Artikel |
Datum |
Titel |
Autoren Alle Autoren |
1 |
[GO] |
2025―Feb―23 |
An evaluation of spirooxindoles as blocking agents of SARS-CoV-2 spike/ACE2 interaction: synthesis, biological evaluation and computational analysis |
Albert Enama Ehinak, Maloba M. M. Lobe, Donatus B. Eni, Conrad V. Simoben, Ian Tietjen, Mathieu J. Mbenga Tjegbe, et al. (+6) Joel Cassel, Joseph M. Salvino, Luis J. Montaner, Wolfgang Sippl, Simon M. N. Efange, Fidele Ntie-Kang |
2 |
[GO] |
2024―Nov―14 |
Inhibition of SARS-CoV-2 replication in cells by G-quadruplex ligands |
Dehua Luo, Chenxi Liu, Elishiba Muturi, Zhe Hu, Wei Hong, Chao Gao, et al. (+4) Junhua Li, Hongping Wei, Dengguo Wei, Hang Yang |
3 |
[GO] |
2024―Jul―14 |
Potential therapeutic effects of ester derivatives of Ribavirin against SARS-CoV-2 |
Aaminat Qureshi, Samina Bano |
4 |
[GO] |
2024―Jun―26 |
Design and synthesis of diphenyl-1H-imidazole analogs targeting Mpro/3CLpro enzyme of SARS-CoV-2 |
Ashish M. Kanhed, Amisha Vora, Ami Thakkar, Gudepalya Renukaiah Rudramurthy, Radha Krishan Shandil, Rajappa Harisha, et al. (+2) Mayas Singh, Shridhar Narayanan |
5 |
[GO] |
2024―Mai―28 |
Exploring nucleoside analogs: key targets in the viral life cycle - advancing strategies against SARS-CoV-2 |
Roopal Garg, Raveen Kumar, Ritika Srivastava, Richa Srivastava |
6 |
[GO] |
2024―Mrz―05 |
Design, synthesis, and biochemical and computational screening of novel oxindole derivatives as inhibitors of Aurora A kinase and SARS-CoV-2 spike/host ACE2 interaction |
Donatus B. Eni, Joel Cassel, Cyril T. Namba-Nzanguim, Conrad V. Simoben, Ian Tietjen, Ravikumar Akunuri, et al. (+2) Joseph M. Salvino, Fidele Ntie-Kang |
7 |
[GO] |
2023―Dez―11 |
Computer-aided design, synthesis and evaluation of new SARS-CoV-2 Mpro inhibitors based on 1,5,6,7-tetrahydro-4H-indazol-4-one scaffold |
Yuri A. Piven, Veronica G. Zinovich, Dmitriy N. Shcherbakov, Varvara Yu. Chirkova, Svetlana V. Belenkaya, Raman M. Puzanau, et al. (+2) Tatyana S. Khlebnicova, Fedor A. Lakhvich |
8 |
[GO] |
2023―Aug―10 |
Synthesis of indole-based ferulic acid derivatives and in vitro evaluation of antiviral activity against SARS-CoV-2 |
Marina Mol S. A. Verzola, Daisymara Priscila de Almeida Marques, Elany Barbosa da Silva, Mateus Sá Magalhães Serafim, Rafaela Salgado Ferreira, Pavla Fajtová, et al. (+5) Markus Kohlhoff, Anthony John O’Donoghue, Vinícius Gonçalves Maltarollo, Jordana Grazziela Alves Coelho-dos-Reis, Renata Barbosa de Oliveira |
9 |
[GO] |
2023―Jul―05 |
SARS-CoV-2 3CL-protease inhibitors derived from ML300: investigation of P1 and replacements of the 1,2,3-benzotriazole |
Alice Hooper, Jonathan D. Macdonald, Brenna Reilly, Joshua Maw, Aidan P. Wirrick, Sang Hoon Han, et al. (+6) A. Abigail Lindsey, Emma G. Rico, Todd Romigh, Christopher M. Goins, Nancy S. Wang, Shaun R. Stauffer |
10 |
[GO] |
2022―Aug―30 |
The history, mechanism, and perspectives of nirmatrelvir (PF-07321332): an orally bioavailable main protease inhibitor used in combination with ritonavir to reduce COVID-19-related hospitalizations |
Ryan P. Joyce, Vivian W. Hu, Jun Wang |
11 |
[GO] |
2022―Mai―12 |
Invalidation of dieckol and 1,2,3,4,6-pentagalloylglucose (PGG) as SARS-CoV-2 main protease inhibitors and the discovery of PGG as a papain-like protease inhibitor |
Haozhou Tan, Chunlong Ma, Jun Wang |
12 |
[GO] |
2022―Jan―03 |
Review on molnupiravir as a promising oral drug for the treatment of COVID-19 |
Elham Zarenezhad, Mahrokh Marzi |
13 |
[GO] |
2021―Dez―02 |
A review of natural products, their effects on SARS-CoV-2 and their utility as lead compounds in the discovery of drugs for the treatment of COVID-19 |
Robert L. Chapman, Shridhar V. Andurkar |
14 |
[GO] |
2021―Feb―05 |
Structural modeling and analysis of the SARS-CoV-2 cell entry inhibitor camostat bound to the trypsin-like protease TMPRSS2 |
Diego E. Escalante, David M. Ferguson |
15 |
[GO] |
2020―Sep―10 |
What are the drugs having potential against COVID-19? |
Kaan Kucukoglu, Nagihan Faydalı, Dilek Bul |
16 |
[GO] |
2020―Jul―31 |
Genomics insights of SARS-CoV-2 (COVID-19) into target-based drug discovery |
P. Chellapandi, S. Saranya |