[HTML][HTML] Synthesis and pharmacological activities of pyrazole derivatives: A review

K Karrouchi, S Radi, Y Ramli, J Taoufik, YN Mabkhot… - Molecules, 2018 - mdpi.com
Pyrazole and its derivatives are considered a pharmacologically important active scaffold
that possesses almost all types of pharmacological activities. The presence of this nucleus in …

Overview of recent developments of pyrazole derivatives as an anticancer agent in different cell line

FE Bennani, L Doudach, Y Cherrah, Y Ramli… - Bioorganic …, 2020 - Elsevier
Pyrazole is a five-membered aromatic heterocyclic ring with two adjacent nitrogen atoms C 3
H 3 N 2 H. The presence of this nucleus in pharmacological agents of various therapeutic …

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 …

Pharmaceutical significance of azepane based motifs for drug discovery: A critical review

GF Zha, KP Rakesh, HM Manukumar… - European Journal of …, 2019 - Elsevier
Azepane-based compounds showed a variety of pharmacological properties, and its
derivatives possess a high degree of structural diversity, and it is useful for the discovery of …

Design and synthesis of novel quinazolinone-pyrazole derivatives as potential α-glucosidase inhibitors: Structure-activity relationship, molecular modeling and kinetic …

F Azimi, H Azizian, M Najafi, F Hassanzadeh… - Bioorganic …, 2021 - Elsevier
In this study, a new series of quinazolinone-pyrazole hybrids were designed, synthesized
and screened for their α-glucosidase inhibitory activity. The results of the in vitro screening …

Design, synthesis, cytotoxicity, HuTopoIIα inhibitory activity and molecular docking studies of pyrazole derivatives as potential anticancer agents

R Alam, D Wahi, R Singh, D Sinha, V Tandon… - Bioorganic …, 2016 - Elsevier
In an attempt to find potential anticancer agents, a series of novel ethyl 4-(3-(aryl)-1-phenyl-
1H-pyrazol-4-yl)-2-oxo-6-(pyridin-3-yl) cyclohex-3-enecarboxylates 5a-i and 5-(3-(4 …

Analysis and prediction of drug–drug interaction by minimum redundancy maximum relevance and incremental feature selection

L Liu, L Chen, YH Zhang, L Wei, S Cheng… - Journal of …, 2017 - Taylor & Francis
Drug–drug interaction (DDI) defines a situation in which one drug affects the activity of
another when both are administered together. DDI is a common cause of adverse drug …

Design, synthesis, and biological evaluation of pyrimidine dihydroquinoxalinone derivatives as tubulin colchicine site-binding agents that displayed potent anticancer …

S Pochampally, KL Hartman, R Wang… - ACS Pharmacology & …, 2023 - ACS Publications
Polymerization of tubulin dimers to form microtubules is one of the key events in cell
proliferation. The inhibition of this event has long been recognized as a potential treatment …

Synthesis of 1, 3, 5-trisubstituted pyrazole-4-carboxylates through 1, 3-dipolar cycloaddition of nitrilimines with allenoates

Y Wang, C Xiong, J Zhong, Q Zhou - Tetrahedron, 2022 - Elsevier
Abstract A strategy for the 1, 3-dipolar cycloaddition of nitrilimines to δ-allenoates has been
developed to provide various 1, 3, 5-trisubstituted pyrazole-4-carboxylates and pyrazole-4 …

Design, synthesis, and evaluation of some novel heterocycles bearing pyrazole moiety as potential anticancer agents

N Abdelgawad, MF Ismail, MH Hekal… - Journal of …, 2019 - Wiley Online Library
1, 3‐Diphenylpyrazole‐4‐carboxylaldehyde and o‐hydroxyacetophenone were exploited as
starting materials for the synthesis of novel substituted chalconated pyrazole derivative. The …