Natural products and synthetic analogues against HIV: A perspective to develop new potential anti-HIV drugs

J Popović-Djordjević, C Quispe, R Giordo… - European journal of …, 2022 - Elsevier
The human immunodeficiency virus (HIV) is responsible for acquired immune deficiency
syndrome (AIDS), one of the major pandemic diseases. Highly active antiretroviral therapy …

Therapeutic potential of indole derivatives as anti-HIV agents: A mini-review

Q Chen, C Wu, J Zhu, E Li, Z Xu - Current Topics in Medicinal …, 2022 - ingentaconnect.com
Acquired immunodeficiency syndrome (AIDS), caused by the human immunodeficiency
virus (HIV), is one of the leading causes of human deaths. The advent of different anti-HIV …

The antimalarial activity of indole alkaloids and hybrids

JY Li, XF Sun, JJ Li, F Yu, Y Zhang… - Archiv der …, 2020 - Wiley Online Library
Malaria, caused by the genus Plasmodium, remains a global public health concern. It is
estimated by the World Health Organization that over 40% of the world's population lives in …

Click chemistry‐based synthesis of new benzenesulfonamide derivatives bearing triazole ring as selective carbonic anhydrase II inhibitors

EF Ewies, E Sabry, MS Bekheit… - Drug Development …, 2022 - Wiley Online Library
Abstract A series of 1, 2, 3‐triazol‐1‐ylbenzenesulfonamide derivatives was designed,
synthesized and their ability to inhibit several carbonic anhydrase isoforms was evaluated …

4-Phenylcoumarin derivatives as new HIV-1 NNRTIs: Design, synthesis, biological activities, and computational studies

RZ Batran, A Sabt, MA Khedr, AK Allayeh… - Bioorganic …, 2023 - Elsevier
A series of 4-phenylcoumarin derivatives was synthesized and evaluated for their cellular
anti-HIV-1 and HIV-2 activities as well as their inhibitory effects against HIV-1 reverse …

A review of the therapeutic importance of indole scaffold in drug discovery

N Teraiya, K Agrawal, TM Patel, A Patel… - Current Drug …, 2023 - ingentaconnect.com
Indole is known as a versatile heterocyclic building block for its multiple pharmacological
activities and has a high probability of success in the race for drug candidates. Many natural …

[HTML][HTML] Current scenario on non-nucleoside reverse transcriptase inhibitors (2018-present)

C Deng, H Yan, J Wang, K Liu, B Liu, Y Shi - Arabian Journal of Chemistry, 2022 - Elsevier
Acquired immune deficiency syndrome (AIDS) mainly caused by human immunodeficiency
virus (HIV) type 1 (HIV-1) is a deadliest infectious disease, in which the immune system …

The Molecular Diversity of 1H-Indole-3-Carbaldehyde Derivatives and Their Role in Multicomponent Reactions

G Mohammadi Ziarani, S Hasani, F Mohajer… - Topics in Current …, 2022 - Springer
Abstract 1 H-Indole-3-carbaldehyde and related members of the indole family are ideal
precursors for the synthesis of active molecules. 1 H-Indole-3-carbaldehyde and its …

Farnesyl pyrophosphate synthase inhibitors with antiosteoporosis efficacy in ovariectomized rats: A mixed binding approach beyond bisphosphonates

NF El-Sayed, M El-Hussieny, ST Mansour… - European Journal of …, 2024 - Elsevier
The primary focus of bisphosphonate medications is on targeting human farnesyl
pyrophosphate synthase (hFPPS), an essential regulator of mammalian isoprenoids. Yet …

Design, synthesis, biological evaluation, and molecular docking of new benzofuran and indole derivatives as tubulin polymerization inhibitors

NF El‐Sayed, M El‐Hussieny, EF Ewies… - Drug Development …, 2022 - Wiley Online Library
Microtubules and the mitotic spindle have become an important target for cancer treatment
due to their critical role in cell division. In this work, a novel series of benzofuran and indole …