[HTML][HTML] The anti-HIV potential of imidazole, oxazole and thiazole hybrids: A mini-review

C Deng, H Yan, J Wang, B Liu, K Liu, Y Shi - Arabian Journal of Chemistry, 2022 - Elsevier
Human immunodeficiency virus (HIV) especially HIV-1 infection and its progression to
acquired immune deficiency syndrome (AIDS) remains a significant global health challenge …

[HTML][HTML] HIV-1 Reverse Transcriptase/Integrase dual inhibitors: A review of recent advances and structure-activity relationship studies

M Mahboubi-Rabbani, M Abbasi… - Iranian Journal of …, 2021 - ncbi.nlm.nih.gov
The significant threat to humanity is HIV infection, and it is uncertain whether a definitive
treatment or a safe HIV vaccine is. HIV-1 is continually evolving and resistant to commonly …

Continuous-flow Hofmann rearrangement using trichloroisocyanuric acid for the preparation of 2-benzoxazolinone

G Gambacorta, IR Baxendale - Organic Process Research & …, 2022 - ACS Publications
A continuous-flow preparation of 2-benzoxazolinone via the Hofmann rearrangement of
salicylamide has been implemented employing trichloroisocyanuric acid as the stable and …

1, 2-Dibenzoylhydrazine as a multi-inhibitor compound: A morphological and docking study

V Patamia, G Floresta, C Zagni, V Pistarà… - International Journal of …, 2023 - mdpi.com
In the framework of the multitarget inhibitor study, we report an in silico analysis of 1, 2-
dibenzoylhydrazine (DBH) with respect to three essential receptors such as the ecdysone …

Visible-Light-Induced Intramolecular C(sp2)–H Amination and Aziridination of Azidoformates via a Triplet Nitrene Pathway

Y Zhang, X Dong, Y Wu, G Li, H Lu - Organic letters, 2018 - ACS Publications
Catalytic intramolecular C–H amination and aziridination reactions of o-allylphenyl
azidoformates have been achieved under visible-light irradiation, providing a mild, clean …

Synthesis, DFT calculations, and molecular docking study of acetohydrazide‐based sulfonamide derivatives as paraoxonase 1 inhibitors

G Arslan, B Gökçe, MT Muhammed, Ö Albayrak… - …, 2023 - Wiley Online Library
Abstract Paraoxonase 1 (PON1), an esterase linked to high‐density lipoprotein (HDL), is
known to have strong antioxidant and anti‐cardiovascular properties. In this study, eleven …

Design, synthesis, molecular modeling and anti-HIV assay of novel quinazolinone incorporated coumarin derivatives

M Safakish, Z Hajimahdi, MR Aghasadeghi… - Current HIV …, 2020 - ingentaconnect.com
Background: The emergence of drug-resistant viral strains has created the need for the
development of novel anti-HIV agents with a diverse structure that targets key enzymes in …

Design, synthesis, antiproliferative and antimicrobial evaluation of a new class of disulfides containing 1, 3, 4-thiadiazole units

R Zhang, B Li, C Chi, Y Liu, X Liu, J Li, W Li… - Medicinal Chemistry …, 2022 - Springer
In the present study, 24 kinds of 2-arylamino-5-substituteddisulfanyl-1, 3, 4-thiadiazoles
were prepared through multistep synthesis. The structures of synthesized compounds were …

[HTML][HTML] Design, synthesis, molecular modeling, in silico ADME studies and anti-HIV-1 assay of new diazocoumarin derivatives

ZA Livani, M Safakish, Z Hajimahdi… - Iranian Journal of …, 2018 - ncbi.nlm.nih.gov
Design, Synthesis, Molecular Modeling, In Silico ADME Studies and Anti-HIV-1 Assay of New
Diazocoumarin Derivatives - PMC Back to Top Skip to main content NIH NLM Logo Access keys …

[HTML][HTML] Molecular docking and QSAR study of 2-benzoxazolinone, quinazoline and diazocoumarin derivatives as anti-HIV-1 agents

K Faghihi, M Safakish, T Zebardast… - Iranian Journal of …, 2019 - ncbi.nlm.nih.gov
A series of 2-benzoxazolinone, diazocoumarin and quinazoline derivatives have been
shown to inhibit HIV replication in cell culture. To understand the pharmacophore properties …