The therapeutic voyage of pyrazole and its analogs: a review

MF Khan, MM Alam, G Verma, W Akhtar… - European journal of …, 2016 - Elsevier
Pyrazole, a five membered heteroaromatic ring with two nitrogen atoms is of immense
significance. Presence of this nucleus in the pharmacological agents of diverse therapeutic …

Acetyl-CoA carboxylase (ACC) as a therapeutic target for metabolic syndrome and recent developments in ACC1/2 inhibitors

L Chen, Y Duan, H Wei, H Ning, C Bi… - Expert Opinion on …, 2019 - Taylor & Francis
ABSTRACT Introduction: Acetyl-CoA Carboxylase (ACC) is an essential rate-limiting
enzyme in fatty acid metabolism. For many years, ACC inhibitors have gained great attention …

Decarboxylative N-alkylation of azoles through visible-light-mediated organophotoredox catalysis

R Kobayashi, S Shibutani, K Nagao, Z Ikeda… - Organic …, 2021 - ACS Publications
An organophotoredox-catalyzed decarboxylative cross-coupling between azole
nucleophiles and aliphatic carboxylic acid-derived redox-active esters is demonstrated. This …

A close look into the biological and synthetic aspects of fused pyrazole derivatives

MM Li, H Huang, Y Pu, W Tian, Y Deng, J Lu - European journal of …, 2022 - Elsevier
The fusion of pyrazole scaffold with other skeletons creates a class of attractive molecules,
demonstrating significant biological and chemical potentiality in the development of …

The Curtius rearrangement: applications in modern drug discovery and medicinal chemistry

AK Ghosh, M Brindisi, A Sarkar - ChemMedChem, 2018 - Wiley Online Library
The Curtius rearrangement is the thermal decomposition of an acyl azide derived from
carboxylic acid to produce an isocyanate as the initial product. The isocyanate can undergo …

Progress of the synthesis of condensed pyrazole derivatives (from 2010 to mid-2013)

M Li, BX Zhao - European Journal of Medicinal Chemistry, 2014 - Elsevier
Condensed pyrazole derivatives are important heterocyclic compounds due to their
excellent biological activities and have been widely applied in pharmaceutical and …

Design and synthesis of novel pyrazole-phenyl semicarbazone derivatives as potential α-glucosidase inhibitor: Kinetics and molecular dynamics simulation study

F Azimi, JB Ghasemi, H Azizian, M Najafi… - International Journal of …, 2021 - Elsevier
A series of novel pyrazole-phenyl semicarbazone derivatives were designed, synthesized,
and screened for in vitro α-glucosidase inhibitory activity. Given the importance of hydrogen …

Design, synthesis, biological evaluation, and molecular modeling studies of pyrazole-benzofuran hybrids as new α-glucosidase inhibitor

F Azimi, H Azizian, M Najafi, G Khodarahmi… - Scientific Reports, 2021 - nature.com
In this work, new derivatives of biphenyl pyrazole-benzofuran hybrids were designed,
synthesized and evaluated in vitro through enzymatic assay for inhibitory effect against α …

Pyrazole scaffold‐based derivatives: A glimpse of α‐glucosidase inhibitory activity, SAR, and route of synthesis

J Firdaus, N Siddiqui, O Alam, A Manaithiya… - Archiv der …, 2023 - Wiley Online Library
The α‐glucosidase is a validated target to develop drugs for treating type 2 diabetes
mellitus. The existing α‐glucosidase inhibitors have certain shortcomings related to side …

Recent Advances in the Development of Acetyl-CoA Carboxylase (ACC) Inhibitors for the Treatment of Metabolic Disease: Miniperspective

MP Bourbeau, MD Bartberger - Journal of medicinal chemistry, 2015 - ACS Publications
The development of acetyl-CoA carboxylase (ACC) inhibitors for the treatment of metabolic
disease has been pursued by the pharmaceutical industry for some time. A number of recent …