Answers are grounded in this paper and cite their sources.
Review reveals the synthetic versatility and diverse bioactivities of beta-carboline scaffolds across disease models, highlighting their potential for drug development.
Abstract β ‐Carboline, a prominent framework (within the alkaloid family) has gained significant attention for their synthetic and biological potential owing to their diverse pharmacological and synthetic characteristics. β ‐Carbolines work as versatile intermediates in organic synthesis and their structural properties make them beneficial for the development of new molecules with specific activities; including abecarnil, cipargamin, and tadalafil. Due to the significant pharmacological relevance of β ‐carboline derivatives, they demonstrate a varied roles and spark interest in their potential therapeutic applications. In this context, 1(3)‐formyl‐9 H ‐ β ‐carbolines serve as promising AXB3s that offer alternative routes for the diversity‐oriented synthesis of β ‐carboline scaffolds. These derivatives exhibited remarkable pharmaceutical properties such as osteoprotective, antimicrobial, anticancer, antileishmanial, AChE inhibitor, APN inhibitor, antiproliferative, and antiplasmodial. This review article provides a comprehensive summary (from 2017 to 2024) of the synthetic potential and the biological potential of β ‐carboline and its derivatives.
No takes yet. Share an insight, caveat, or question.
Vaishali et al. (2025) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: