Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo [2, 1-b][1, 3, 4] thiadiazoles as highly potent acetylcholinesterase and non …

S Askin, H Tahtaci, C Türkeş, Y Demir, A Ece… - Bioorganic …, 2021 - Elsevier
Imidazole and thiadiazole derivatives display an extensive application in pharmaceutical
chemistry, and they have been investigated as bioactive molecules for medicinal chemistry …

Novel spiroindoline derivatives targeting aldose reductase against diabetic complications: bioactivity, cytotoxicity, and molecular modeling studies

Ö Güleç, C Türkeş, M Arslan, Y Demir, B Dincer… - Bioorganic …, 2024 - Elsevier
Despite significant developments in therapeutic strategies, Diabetes Mellitus remains an
increasing concern, leading to various complications, eg, cataracts, neuropathy, retinopathy …

Comprehensive study on potent and selective carbonic anhydrase inhibitors: Synthesis, bioactivities and molecular modelling studies of 4-(3-(2-arylidenehydrazine-1 …

C Yamali, H Sakagami, Y Uesawa, K Kurosaki… - European journal of …, 2021 - Elsevier
In this research, rational design, synthesis, carbonic anhydrases (CAs) inhibitory effects, and
cytotoxicities of the 4-(3-(2-arylidenehydrazine-1-carbonyl)-5-(thiophen-2-yl)-1 H-pyrazole-1 …

Novel imidazo[2,1‐b]thiazole‐based anticancer agents as potential focal adhesion kinase inhibitors: Synthesis, in silico and in vitro evaluation

F Başoğlu, N Ulusoy‐Güzeldemirci… - Chemical Biology & …, 2021 - Wiley Online Library
The purpose of this study was to synthesize imidazo [2, 1‐b] thiazole derivatives,
characterize them with spectroscopical techniques and investigate for cytotoxic and …

Computational medicinal chemistry applications to target Asian-prevalent strain of hepatitis C virus

R Hussain, Z Haider, H Khalid, MQ Fatmi, S Carradori… - RSC …, 2023 - pubs.rsc.org
Hepatitis C Virus (HCV), affecting millions of people worldwide, is the leading cause of liver
disorder, cirrhosis, and hepatocellular carcinoma. HCV is genetically diverse having eight …

Synthesis, Biological Evaluation, Molecular Docking, and Acid Dissociation Constant of New Bis‐1, 2, 3‐triazole Compounds

Y Nural, S Ozdemir, MS Yalcin, B Demir… - …, 2021 - Wiley Online Library
In this study, new bis‐1, 2, 3‐triazole derivatives, N, N′‐(1, 3‐phenylene) bis (2‐(4‐R‐1H‐
1, 2, 3‐triazol‐1‐yl) acetamide), were synthesized by copper‐catalyzed azide‐alkyne …

Copper-Catalyzed Asymmetric Borylacylation of Styrene and Indene Derivatives

Z Yang, P Li, H Lu, G Li - The Journal of Organic Chemistry, 2021 - ACS Publications
The enantioselective copper-catalyzed borylacylation of aryl olefins with acyl chlorides and
bis-(pinacolato) diboron is reported. This three-component reaction involves an …

Rhodium-Catalyzed Asymmetric Annulation of Unactivated Alkynes with 3-(ortho-Boronated Aryl) Conjugated Enones: Enantioselective Synthesis of 2,3-Disubstituted …

Y Sun, J Pan, X Wang, X Bu, M Ma… - The Journal of Organic …, 2023 - ACS Publications
A rhodium-catalyzed tandem arylation/cyclization reaction of 3-(ortho-boronated aryl)
conjugated enones with unactivated alkynes is reported. By using a rhodium (I)/chiral-diene …

[HTML][HTML] Design, synthesis and biological evaluation of a novel bioactive indane scaffold 2-(diphenylmethylene) c-2, 3-dihydro-1H-inden-1-one with potential …

T Zhang, V Bandero, C Corcoran, I Obaidi… - European Journal of …, 2023 - Elsevier
Over the past decades, designing of privileged structures has emerged as a useful approach
to the discovery and optimisation of novel biologically active molecules, and many have …

Design, Synthesis and Late‐Stage Modification of Indane‐Based Peptides via [2+ 2+ 2] Cyclotrimerization

S Kotha, N Kumar Gupta, G Sreevani… - Chemistry–An Asian …, 2021 - Wiley Online Library
Here, we prepared several dipeptides containing 2‐aminoindane‐2‐carboxylic acid (Aic)
and carried out further synthetic transformations. Synthesis and purification of modified …