1H-Pyrazolo[3,4-b]pyridines: Synthesis and Biomedical Applications

A Donaire-Arias, AM Montagut, R Puig de la Bellacasa… - Molecules, 2022 - mdpi.com
Pyrazolo [3, 4-b] pyridines are a group of heterocyclic compounds presenting two possible
tautomeric forms: the 1 H-and 2 H-isomers. More than 300,000 1 H-pyrazolo [3, 4-b] …

The application of click chemistry in the synthesis of agents with anticancer activity

N Ma, Y Wang, BX Zhao, WC Ye… - Drug design, development …, 2015 - Taylor & Francis
The copper (I)-catalyzed 1, 3-dipolar cycloaddition between alkynes and azides (click
chemistry) to form 1, 2, 3-triazoles is the most popular reaction due to its reliability …

Identification of GZD824 as an orally bioavailable inhibitor that targets phosphorylated and nonphosphorylated breakpoint cluster region–abelson (Bcr-Abl) kinase …

X Ren, X Pan, Z Zhang, D Wang, X Lu… - Journal of medicinal …, 2013 - ACS Publications
Bcr-AblT315I mutation-induced imatinib resistance remains a major challenge for clinical
management of chronic myelogenous leukemia (CML). Herein, we report GZD824 (10a) as …

Usnic acid enaminone-coupled 1, 2, 3-triazoles as antibacterial and antitubercular agents

PK Bangalore, SK Vagolu, RK Bollikanda… - Journal of natural …, 2019 - ACS Publications
(+)-Usnic acid, a product of secondary metabolism in lichens, has displayed a broad range
of biological properties such as antitumor, antimicrobial, antiviral, anti-inflammatory, and …

Discovery and Optimization of 3-(2-(Pyrazolo[1,5-a]pyrimidin-6-yl)ethynyl)benzamides as Novel Selective and Orally Bioavailable Discoidin Domain Receptor 1 …

M Gao, L Duan, J Luo, L Zhang, X Lu… - Journal of medicinal …, 2013 - ACS Publications
Discoidin domain receptor 1 (DDR1) is an emerging potential molecular target for new
anticancer drug discovery. We have discovered a series of 3-(2-(pyrazolo [1, 5-a] pyrimidin-6 …

Regioselective Annulation of 3(5)‐Aminopyrazole with Aryl Ketones or Aryl Alkynes Using N,N‐Dimethylethanolamine as a Single/Triple Carbon Synthon

X Zhang, J Chen, R Chen, L Wang… - Advanced Synthesis & …, 2024 - Wiley Online Library
An efficient and regioselective cyclization for construction of pyrazolo [3, 4‐b] pyridines and
methylene‐bridged bis (pyrazolo [1, 5‐a] pyrimidines) has been established. It involves a [3+ …

Research progress of DDR1 inhibitors in the treatment of multiple human diseases

M Liu, J Zhang, X Li, Y Wang - European Journal of Medicinal Chemistry, 2024 - Elsevier
Abstract Discoidin domain receptor 1 (DDR1) is a collagen-activated receptor tyrosine
kinase (RTK) and plays pivotal roles in regulating cellular functions such as proliferation …

Designing novel BCR-ABL inhibitors for chronic myeloid leukemia with improved cardiac safety

M Pandrala, AAN Bruyneel, AP Hnatiuk… - Journal of medicinal …, 2022 - ACS Publications
Development of tyrosine kinase inhibitors (TKIs) targeting the BCR-ABL oncogene
constitutes an effective approach for the treatment of chronic myeloid leukemia (CML) and/or …

Recent advances in 1, 2, 4-triazolo [1, 5-a] pyrimidine chemistry

G Fischer - Advances in Heterocyclic Chemistry, 2019 - Elsevier
The review deals with the pharmaceutically and agrochemically important group of 1, 2, 4-
triazolo [1, 5-a] pyrimidines (TPs) and covers relevant literature published from about 2006 …

Recent advances in the chemistry of pyrazolo [1, 5-a] pyrimidines

J Portilla - Advances in Heterocyclic Chemistry, 2024 - Elsevier
Abstract Pyrazolo [1, 5-a] pyrimidine-containing compounds are an important and strategic N-
heterocycle family because of their proven applicability and synthetic versatility in preparing …