Recent advances on biologically active coumarin-based hybrid compounds

M Yildirim, S Poyraz, M Ersatir - Medicinal Chemistry Research, 2023 - Springer
Coumarin hybrids have been designed and synthesized as an important new strategy in the
field of medicinal chemistry. Coumarin core has been shown to form various compounds to …

Recent insights about pyrrolidine core skeletons in pharmacology

S Poyraz, HA Döndaş, NY Döndaş… - Frontiers in …, 2023 - frontiersin.org
To overcome numerous health disorders, heterocyclic structures of synthetic or natural origin
are utilized, and notably, the emergence of various side effects of existing drugs used for …

A review on biological and medicinal significance of thiazoles

PM Jadhav, S Kantevari, AB Tekale… - … , Sulfur, and Silicon …, 2021 - Taylor & Francis
Thiazole, a five-membered heterocyclic compound constitutes the skeleton of various
commercially marketed drug candidates and the heart-core in a diverse range of entities of …

Green chemistry approaches for thiazole containing compounds as a potential scaffold for cancer therapy

D Sharma, V Sharma, A Sharma, R Goyal… - Sustainable Chemistry …, 2021 - Elsevier
The exhaustive exploration of the conventional synthetic approaches for the synthesis of
nitrogen and sulphur containing heterocyclic moieties has diverted the attention of …

Thiazole‐substituted benzoylpiperazine derivatives as acetylcholinesterase inhibitors

Z Sahin, M Ertas, C Bender, EF Bülbül… - Drug Development …, 2018 - Wiley Online Library
Hit, Lead & Candidate Discovery After acetylcholine is released into the synaptic cleft, it is
reabsorbed or deactivated by acetylcholinesterase (AChE). Studies on Alzheimer's disease …

Design, synthesis, biological evaluation and docking analysis of pyrrolidine-benzenesulfonamides as carbonic anhydrase or acetylcholinesterase inhibitors and …

S Poyraz, HA Döndaş, C Yamali… - Journal of …, 2024 - Taylor & Francis
The synthesis and biological assessment of novel multi-functionalized pyrrolidine-containing
benzenesulfonamides were reported along with their antimicrobial, antifungal, CAs …

Synthesis and evaluation of 3-substituted-4-(quinoxalin-6-yl) pyrazoles as TGF-β type I receptor kinase inhibitors

LM Zhao, Z Guo, YJ Xue, JZ Min, WJ Zhu, XY Li… - Molecules, 2018 - mdpi.com
The transforming growth factor-β (TGF-β), in which overexpression has been associated with
various diseases, has become an attractive molecular target for the treatment of cancers …

N-Benzoylthiourea-pyrrolidine carboxylic acid derivatives bearing an imidazole moiety: Synthesis, characterization, crystal structure, in vitro ChEs inhibition, and …

S Poyraz, HA Döndaş, JM Sansano, S Belveren… - Journal of Molecular …, 2023 - Elsevier
A series of novel N-benzoylthiourea-pyrrolidine carboxylic acid derivatives bearing an
imidazole moiety has been prepared and their various biological activities are evaluated …

An efficient, one-pot, regioselective synthesis of 2-aryl/hetaryl-4-methyl-5-acylthiazoles under solvent-free conditions

R Aggarwal, M Hooda, N Jain, D Sanz… - Journal of Sulfur …, 2022 - Taylor & Francis
In this article, we present an efficient, one-pot regioselective approach towards the synthesis
of 2-aryl/hetaryl-4-methyl-5-acylthiazoles obtained during the reaction of α-bromo-1, 3 …

One-pot four-component synthesis of polysubstituted thiazoles via cascade Ugi/Wittig cyclization starting from odorless Isocyano (triphenylphosphoranylidene) …

ZR Guan, ZM Liu, Q Wan, MW Ding - Tetrahedron, 2020 - Elsevier
A new one-pot four-component preparation of polysubstituted thiazoles by a cascade
Ugi/Wittig cyclization has been developed. The four-component reactions of the odorless …