FMO-guided design of darunavir analogs as HIV-1 protease inhibitors
The prevalence of HIV-1 infection continues to pose a significant global public health issue, highlighting the need for antiretroviral drugs that target viral proteins to reduce viral replication. One such target is HIV-1 protease (PR), responsible for cleaving viral polyproteins, leading to the mat...
Saved in:
Main Authors: | Chuntakaruk, Hathaichanok, Hengphasatporn, Kowit, Shigeta, Yasuteru, Aonbangkhen, Chanat, Lee, Vannajan Sanghiran, Khotavivattana, Tanatorn, Rungrotmongkol, Thanyada, Hannongbua, Supot |
---|---|
Format: | Article |
Published: |
Nature Research
2024
|
Subjects: | |
Online Access: | http://eprints.um.edu.my/45628/ https://doi.org/10.1038/s41598-024-53940-1 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Computational study on peptidomimetic inhibitors against SARS-CoV-2 main protease
by: Somboon, Tuanjai, et al.
Published: (2021) -
Identification of repurposing therapeutics toward SARS-CoV-2 main protease by virtual screening
by: Sanachai, Kamonpan, et al.
Published: (2022) -
Structural Basis of Specific Glucoimidazole and Mannoimidazole Binding by Os3BGlu7
by: Nutho, Bodee, et al.
Published: (2020) -
Binding hotspot and activation mechanism of maltitol and lactitol toward the Human Sweet Taste Receptor
by: Mahalapbutr, Panupong, et al.
Published: (2020) -
Designed antiviral ankyrin – A computational approach to combat HIV-1 via intracellular pathway by targeting the viral capsid of HIV-1
by: Karim, Hana Atiqah Abdul, et al.
Published: (2019)