Related Experiment Video
Updated: Oct 16, 2026

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
Quinoxaline Derivatives (2020-2025): Emerging Therapeutic Applications and Opportunities for Drug Repurposing
Patricia Piris1, Manon Carré1, Omar Khoumeri2
1Centre de Recherche en Cancérologie de Marseille (CRCM), Inserm UMR1068, CNRS UMR7258, Aix-Marseille Université UM105, Institut Paoli Calmettes - Faculté de Pharmacie, Marseille, France.
Abstract:
Quinoxaline derivatives, formed by the fusion of two aromatic rings, benzene and pyrazine, possess a broad spectrum of pharmacological activities including antimicrobial, anticancer, anti-inflammatory, neuroprotective, antiparasitic and antidiabetic effects, which have attracted considerable attention in the field of medicinal chemistry. This review aims to present recent advances (2020-2025) in the pharmacological potential of the quinoxaline scaffold and to highlight its emerging role in drug-repurposing strategies. A comprehensive literature review was conducted across major databases to identify publications describing the chemical synthesis, biological evaluation, mechanisms of action, and pharmacokinetic properties of quinoxaline derivatives. The collected data were analyzed to identify the key Structure- Activity Relationships (SARs), therapeutic trends, and existing translational challenges. Despite their promising biological properties, quinoxaline derivatives possess important limitations, such as poor aqueous solubility, variable bioavailability, and potential toxicity. These challenges have been partially addressed, and their therapeutic potential has been expanded by recent advances in structural optimization, nanocarrier-based delivery systems, and computational drug design. Compared with other heterocyclic scaffolds, such as indole, pyrazole, benzothiazole, and quinoline, quinoxalines provide an advantageous balance between structural versatility, pharmacological diversity, and modifiability. These characteristics make them attractive scaffolds for drug repurposing.
Related Concept Videos
Prescription, Nonprescription and Orphan Drugs
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
Pharmacogenomics: Identification of New Drug Targets
Direct-Acting Cholinergic Agonists: Therapeutic Uses
Sedatives and Hypnotics Drugs: Miscellaneous Agents
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Cholinergic Antagonists: Therapeutic Uses
Respiratory Tract: Ipratropium, aclidinium, and tiotropium treat asthma, chronic bronchitis, and chronic obstructive pulmonary disease (COPD). They protect against bronchoconstriction caused by irritants like cigarette smoke, sulfur dioxide, and ozone. They also help reduce nasopharyngeal secretions in common...
Targets for Drug Action: Overview
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
