Pallabi Halder, Anubhav Rai, Vishal Talukdar, Parthasarathi Das and Naga Rajiv Lakkaniga
RSC Med. Chem., 2024,15, 1452-1470
Abstract
Pyrazolopyridines have gained increasing attention in kinase-targeting anti-cancer drug discovery. This review analyzes the success stories wherein this bicycle was employed to address various challenges.
Karen Acosta-Quiroga, Claudio A. Jiménez, Kevin Cobos-Montes, Yeray A. Rodríguez-Núñez, Jhon López, Cristian Guerra, Deiber A. Calderón Orjuela, Margarita Gutierrez and Efraín Polo-Cuadrado
RSC Adv., 2026,16, 7648-7658
Abstract
The aldehyde-functionalized pyrazolo[3,4-b]pyridine derivative CJ129 was examined in the solid state for the first time using single-crystal X-ray diffraction.
Viktoria V. Viktorova, Dmitrii L. Obydennov, Alsu F. Mustafina, Maria V. Ulitko, Mikhail Y. Kornev and Vyacheslav Y. Sosnovskikh
Org. Biomol. Chem., 2025,23, 2206-2220
Abstract
A general and convenient approach for the synthesis of biologically important pyrazolo[4,3-c]pyridines has been developed via amination of 5-acyl-4-pyridones with hydrazines.
Munmee Goswami, Pooja Paul, Ridahunlang Nongkhlaw, Jyothi Kumari, Dharmarajan Sriram and Rishanlang Nongkhlaw
Green Chem., 2024,26, 9423-9432
Abstract
The synthesis of fused N-heterocycles under microwave irradiation using HKUST-1 and evaluation of their in vitro biological activities.
Efraín Polo-Cuadrado, Lorena López-Cuellar, Karen Acosta-Quiroga, Cristian Rojas-Peña, Iván Brito, Jonathan Cisterna, Jorge Trilleras, Joel B. Alderete, Yorley Duarte and Margarita Gutiérrez
RSC Adv., 2023,13, 30118-30128
Abstract
In this study, two pyrazolo[3,4-b]pyridine derivatives (4a and 4b) were grown using a slow evaporation solution growth technique and characterized by FT-IR, HRMS, 1H/13C NMR spectroscopy, and X-ray crystallography.