Medicinal attributes of pyrazolo [3, 4-d] pyrimidines: a review

M Chauhan, R Kumar - Bioorganic & medicinal chemistry, 2013 - Elsevier
Pyrazolopyrimidines are the fused heterocyclic ring systems which structurally resemble
purines which prompted biological investigations to assess their potential therapeutic …

[HTML][HTML] Substituted pyrazoles and their heteroannulated analogs—recent syntheses and biological activities

M Ramadan, AA Aly, LEA El-Haleem, MB Alshammari… - Molecules, 2021 - mdpi.com
Pyrazoles are considered privileged scaffolds in medicinal chemistry. Previous reviews have
discussed the importance of pyrazoles and their biological activities; however, few have …

Synthesis of N-aryl-5-amino-4-cyanopyrazole derivatives as potent xanthine oxidase inhibitors

S Gupta, LM Rodrigues, AP Esteves… - European journal of …, 2008 - Elsevier
Some pyrazolo [3, 4-d] pyrimidines, structurally related with allopurinol, a well known
xanthine oxidase inhibitor, clinically used in the therapy of gout, have also been reported as …

Novel pyrazolo [3, 4-d] pyrimidine with 4-(1H-benzimidazol-2-yl)-phenylamine as broad spectrum anticancer agents: Synthesis, cell based assay, topoisomerase …

P Singla, V Luxami, R Singh, V Tandon… - European journal of …, 2017 - Elsevier
A series of new pyrazolo [3, 4-d] pyrimidine possessing 4-(1H-benzimidazol-2-yl)-
phenylamine moiety at C4 position and primary as well as secondary amines at C6 position …

New pyrazolopyrimidine derivatives with anticancer activity: Design, synthesis, PIM-1 inhibition, molecular docking study and molecular dynamics

JN Philoppes, MA Khedr, MHA Hassan, G Kamel… - Bioorganic …, 2020 - Elsevier
In this study, new pyrazolopyrimidine derivatives were designed and evaluated for
anticancer activity. PIM-1 inhibitiory activity were measured for the most potent compounds …

Pyrazolo[3,4‐d]pyrimidine scaffold: A review on synthetic approaches and EGFR and VEGFR inhibitory activities

AE Kassab - Archiv der Pharmazie, 2023 - Wiley Online Library
Abstract The pyrazolo [3, 4‐d] pyrimidine core has received a lot of interest from the
medicinal chemistry community as a promising framework for drug design and discovery. It …

Synthesis and Antimicrobial Activity of Some New Pyrazoles, Fused Pyrazolo[3,4-d]-pyrimidine and 1,2-Dihydroimidazo-[2,1-c][1,2,4]triazin-6-one Derivatives

SM Gomha, HME Hassaneen - Molecules, 2011 - mdpi.com
A novel series of 7, 7-diphenyl-1, 2-dihydroimidazo [2, 1-c][1, 2, 4] triazin-6 (7 H)-one 6a–h,
were easily prepared via reactions of novel 2-hydrazinyl-4, 4-diphenyl-1 H-imidazol-5 (4 H) …

Synthesis, structural elucidation, and in vitro antitumor activities of some pyrazolopyrimidines and Schiff bases derived from 5-amino-3-(arylamino)-1H-pyrazole-4 …

TS Hafez, SA Osman, HAA Yosef… - Scientia …, 2013 - pmc.ncbi.nlm.nih.gov
The reaction of 5-amino-3-(arylamino)-1H-pyrazole-4-carboxamides 1a, b with
acetylacetone 2 and arylidenemalononitriles 5a–c yielded the pyrazolo [1, 5-a]-pyrimidine …

Synthesis, characterization and biological studies of some novel thieno [2, 3-d] pyrimidines

KM Al-Taisan, HMA Al-Hazimi, SS Al-Shihry - Molecules, 2010 - mdpi.com
Several 2-unsubstituted thieno [2, 3-d] pyrimidines have been prepared from 2-
aminothiophene-3-carboxylic acid esters and their carbonitrile analogs. Some triazolo …

Synthesis and in vitro antibacterial evaluation of 6-substituted 4-amino-pyrazolo[3,4-d]pyrimidines

H Beyzaei, M Moghaddam-Manesh, R Aryan… - Chemical Papers, 2017 - Springer
Abstract Pyrazolo [3, 4-d] pyrimidines are one of the most important classes of fused
heterocyclic compounds which exhibit a broad range of biological and medicinal properties …