A critical review on recent trends on pharmacological applications of pyrazolone endowed derivatives

G Mustafa, M Zia-ur-Rehman, SH Sumrra… - Journal of Molecular …, 2022 - Elsevier
Pyrazolone is a well-known influential synthon for the synthesis of many molecules which
hold remarkable potential in the advancement of functional materials, coordination …

Pyrazole scaffold: a remarkable tool in the development of anticancer agents

H Kumar, D Saini, S Jain, N Jain - European Journal of Medicinal Chemistry, 2013 - Elsevier
Pyrazole has been the topic of interest for thousands of researchers across the world
because of its wide spectrum pharmacological activities. Various structural modifications of …

Development of combretastatins as potent tubulin polymerization inhibitors

SNA Bukhari, GB Kumar, HM Revankar, HL Qin - Bioorganic chemistry, 2017 - Elsevier
The combretastatins are isolated from South African tree combretum caffrum kuntze. The
lead compound combretastatin A-4 has displayed remarkable cytotoxic effect in a wide …

Dihydropyrazole derivatives act as potent α-amylase inhibitors and free radical scavengers: synthesis, bioactivity evaluation, structure–activity relationship, ADMET …

A Ali, MIA Shah, C Fu, Z Hussain, MN Qureshi… - ACS …, 2023 - ACS Publications
Dihydropyrazole (1–22) derivatives were synthesized from already synthesized chalcones.
The structures of all of the synthesized compounds were confirmed by elemental analysis …

sea urchin embryo model as a reliable in vivo phenotypic screen to characterize selective antimitotic molecules. Comparative evaluation of combretapyrazoles …

MN Semenova, DV Demchuk… - ACS Combinatorial …, 2018 - ACS Publications
A series of both novel and reported combretastatin analogues, including diarylpyrazoles,-
isoxazoles,-1, 2, 3-triazoles, and-pyrroles, were synthesized via improved protocols to …

Tubulin inhibitors binding to colchicine-site: a review from 2015 to 2019

LY **a, YL Zhang, R Yang, ZC Wang… - Current medicinal …, 2020 - ingentaconnect.com
Due to the three domains of the colchicine-site which is conducive to the combination with
small molecule compounds, colchicine-site on the tubulin has become a common target for …

Synthesis and antiproliferative activity of conformationally restricted 1, 2, 3-triazole analogues of combretastatins in the sea urchin embryo model and against human …

DV Demchuk, AV Samet, NB Chernysheva… - Bioorganic & medicinal …, 2014 - Elsevier
Abstract A series of 1, 5-diaryl-and 4, 5-diaryl-1, 2, 3-triazole derivatives of combretastatin A4
were synthesized and evaluated as antimitotic microtubule destabilizing agents using the …

Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers

H Rajak, P Kumar Dewangan, V Patel… - Current …, 2013 - ingentaconnect.com
Tubulin protein is a highly imperative and feasible goal for anticancer drug discovery.
Hundreds of naturally occurring, semi synthetic and synthetic antitubulin agents have been …

Anticancer effects of new dibenzenesulfonamides by inducing apoptosis and autophagy pathways and their carbonic anhydrase inhibitory effects on hCA I, hCA II …

HI Gul, C Yamali, M Bulbuller, PB Kirmizibayrak… - Bioorganic …, 2018 - Elsevier
In this study, new dibenzensulfonamides, 7–9, having the chemical structure 4, 4′-(5′-
chloro-3′-methyl-5-aryl-3, 4-dihydro-1′ H, H-[3, 4′-bipyrazole]-1′, 2-diyl) …

[HTML][HTML] Approaches for chemical synthesis and diverse pharmacological significance of pyrazolone derivatives: a review

M Asif, M Imran, A Husain - Journal of the Chilean Chemical Society, 2021 - SciELO Chile
Pyrazolone is a five-membered lactam ring containing two Nitrogens and one ketonic group
in its structure. Numerous pyrazolone derivatives were exhibited with diverse biological …