[HTML][HTML] Synthesis of biologically active molecules through multicomponent reactions

D Insuasty, J Castillo, D Becerra, H Rojas, R Abonia - Molecules, 2020 - mdpi.com
Focusing on the literature progress since 2002, the present review explores the highly
significant role that multicomponent reactions (MCRs) have played as a very important tool …

Emerging approaches for the identification of protein targets of small molecules-a practitioners' perspective

KM Comess, SM McLoughlin, JA Oyer… - Journal of medicinal …, 2018 - ACS Publications
Small-molecule (SM) leads in the early drug discovery pipeline are progressed primarily
based on potency against the intended target (s) and selectivity against a very narrow slice …

Quinoline‐based thiazolidinone derivatives as potent cytotoxic and apoptosis‐inducing agents through EGFR inhibition

MS Nafie, SM Kishk, S Mahgoub… - Chemical Biology & …, 2022 - Wiley Online Library
Quinoline‐based thiazolidinone heterocycles exhibited potent activity in the field of cancer
therapy. Hence, ten quinoline‐based thiazolidinone derivatives were evaluated for their …

[HTML][HTML] An update of label-free protein target identification methods for natural active products

Z Cui, C Li, P Chen, H Yang - Theranostics, 2022 - ncbi.nlm.nih.gov
Natural active products (NAPs) are derived from chemical substances found in nature that
have biological activity and medicinal potential. Screening and revealing the protein targets …

Tuning Potency of Bioactive Molecules via Polymorphic Modifications: A Case Study

A Kumar, J Chauhan, KD Dubey, S Sen… - Molecular …, 2022 - ACS Publications
Polymorphism in drugs and bioactive molecules is not uncommon, and it has remained as
one of the critical issues in drug development processes. While improving physicochemical …

[HTML][HTML] 3-Amino-5-(indol-3-yl) methylene-4-oxo-2-thioxothiazolidine derivatives as antimicrobial agents: Synthesis, computational and biological evaluation

V Horishny, V Kartsev, V Matiychuk, A Geronikaki… - Pharmaceuticals, 2020 - mdpi.com
Herein we report the design, synthesis, computational, and experimental evaluation of the
antimicrobial activity of fourteen new 3-amino-5-(indol-3-yl) methylene-4-oxo-2 …

Synthesis of some 5‐arylidene‐2‐(4‐acetamidophenylimino)‐thiazolidin‐4‐one derivatives and exploring their breast anticancer activity

HMA Abumelha, A Saeed - Journal of Heterocyclic Chemistry, 2020 - Wiley Online Library
Abstract Ten 2‐(4‐acetamidophenylimino)‐5‐arylidenethiazolidin‐4‐one derivatives 6a‐k
were synthesized and evaluated for their anticancer activity against MCF‐7 cell line (breast …

Leucettamine B analogs and their carborane derivative as potential anti-cancer agents: Design, synthesis, and biological evaluation

MH Hsu, CY Hsieh, M Kapoor, JH Chang, HL Chu… - Bioorganic …, 2020 - Elsevier
Leucettamine B is a natural product found in marine sponge Leucetta microraphis. Several
of analogs of its family, such as aplysinopsine and clathridine, are medicinally active …

Identification of protein binding partners of small molecules using label-free methods

C Saxena - Expert Opinion on Drug Discovery, 2016 - Taylor & Francis
Introduction: Drug discovery efforts across the globe are chasing new drug targets and novel
mechanisms of action. To support the identification of novel mechanisms of action …

Tetrahydrocarbazoles incorporating 5-arylidene-4-thiazolinones as potential antileukemia and antilymphoma targeting tyrosine kinase and tubulin polymerase …

BS Ali, AF Mohammed, BM Kariuki, R El-Awady… - Bioorganic …, 2024 - Elsevier
Finding effective and selective anticancer agents is a top medical priority due to high clinical
treatment demand. However, current anticancer agents have serious side effects and …