Triazole derivatives and their anti-tubercular activity

S Zhang, Z Xu, C Gao, QC Ren, L Chang, ZS Lv… - European journal of …, 2017 - Elsevier
Tuberculosis (TB) remains one of the most widespread and leading deadliest diseases,
threats one-third of the world's population. Although numerous efforts have been undertaken …

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 …

Synthesis of pyrazolo [3, 4-d] pyrimidin-4 (5H)-ones tethered to 1, 2, 3-triazoles and their evaluation as potential anticancer agents

M Allam, AKD Bhavani, A Mudiraj, N Ranjan… - European Journal of …, 2018 - Elsevier
A series of hybrid aza heterocycles containing pyrazolo [3, 4-d] pyrimidin-4 (5 H)-ones
tethered to 1, 2, 3-triazole scaffold were synthesized from 1, 3-dipolar cycloaddition reaction …

Design, synthesis and chemoinformatic studies of new thiazolopyrimidine derivatives as potent anticancer agents via phosphodiesterase-5 inhibition and apoptotic …

MTM Nemr, M Teleb, AM AboulMagd… - Journal of Molecular …, 2023 - Elsevier
Abstract Inhibition of phosphodiesterase-5 (PDE5) has been validated as possible new
therapeutic approach for cancer. To further explore this concept, three series of …

New pyrazolo [3, 4-d] pyrimidine derivatives as EGFR-TK inhibitors: design, green synthesis, potential anti-proliferative activity and P-glycoprotein inhibition

AI Hassaballah, AM AboulMagd, MM Hemdan… - RSC …, 2024 - pubs.rsc.org
In this study, four series of new pyrazolo [3, 4-d] pyrimidine derivatives were designed and
synthesized with both green and conventional methods. All the synthesized candidates were …

A new insight into the synthesis and biological activities of pyrazole based derivatives

S Mor, M Khatri, R Punia, S Nagoria… - Mini-Reviews in …, 2022 - ingentaconnect.com
This review aims to collate literature work reported by researchers (from 1994 to 2021) to
provide an overview of the available methodologies for the synthesis and diverse …

N-and s-substituted Pyrazolopyrimidines: A promising new class of potent c-Src kinase inhibitors with prominent antitumor activity

AA Awaji, WAZ El Zaloa, MA Seleem, M Alswah… - Bioorganic …, 2024 - Elsevier
In this work, readily achievable synthetic pathways were utilized for construction of a library
of N/S analogues based on the pyrazolopyrimidine scaffold with terminal alkyl or aryl …

Synthesis, cyclooxygenase inhibition, anti-inflammatory evaluation and ulcerogenic liability of new 1-phenylpyrazolo[3,4-d]pyrimidine derivatives

RB Bakr, AA Azouz, KRA Abdellatif - Journal of enzyme inhibition …, 2016 - Taylor & Francis
A new group of 1-phenylpyrazolo [3, 4-d] pyrimidine derivatives 14a–d–21 were synthesized
from 2-(6-methyl-1-phenyl-1 H-pyrazolo [3, 4-d] pyrimidin-4-yloxy) acetohydrazide (12). All …

Design and synthesis of pyrazolo [3, 4-d] pyrimidines: Nitric oxide releasing compounds targeting hepatocellular carcinoma

YAMM Elshaier, MA Shaaban, MK Abd El Hamid… - Bioorganic & Medicinal …, 2017 - Elsevier
A new series of pyrazolo [3, 4-d] pyrimidines tethered with nitric oxide (NO) producing
functionality was designed and synthesized. Sulforhodamine B (SRB) protein assay …

Design and synthesis of novel pyrazolo [3, 4-d] pyrimidin-4-one bearing quinoline scaffold as potent dual PDE5 inhibitors and apoptotic inducers for cancer therapy

TS Ibrahim, MM Hawwas, ES Taher, NA Alhakamy… - Bioorganic …, 2020 - Elsevier
PDE5 targeting represents a new and promising strategy for apoptosis induction and
inhibition of tumor cell growth due to its over-expression in diverse types of human …