Recent applications of hydantoin and thiohydantoin in medicinal chemistry
SH Cho, SH Kim, D Shin - European journal of medicinal chemistry, 2019 - Elsevier
Abstract Hydantoin, imidazolidine-2, 4-dione, is a non-aromatic five-membered heterocycle,
which is considered a valuable, privileged scaffold in medicinal chemistry. The importance …
which is considered a valuable, privileged scaffold in medicinal chemistry. The importance …
Voltage gated sodium channel inhibitors as anticonvulsant drugs: A systematic review on recent developments and structure activity relationship studies
Voltage-gated sodium channel blockers are one of the vital targets for the management of
several central nervous system diseases, including epilepsy, chronic pain, psychiatric …
several central nervous system diseases, including epilepsy, chronic pain, psychiatric …
Synthesis of a novel phenytoin derivative: crystal structure, Hirshfeld surface analysis and DFT calculations
Hydantoin compounds are important heterocyclic scaffolds and a class of well-known
bioactive molecules with a broad spectrum of pharmacological properties. Consequently …
bioactive molecules with a broad spectrum of pharmacological properties. Consequently …
Solvent free synthesis, anti-inflammatory and anticancer activity evaluation of tricyclic and tetracyclic benzimidazole derivatives
Heterocyclic benzimidazole derivatives 3a–h, 5a–c and 7a–d have been synthesized by
condensation of succinic acid (1) homophthalic acid (4) and 2, 3-pyrazinedicarboxlic acid (6) …
condensation of succinic acid (1) homophthalic acid (4) and 2, 3-pyrazinedicarboxlic acid (6) …
[PDF][PDF] Amidines: Their synthesis, reactivity, and applications in heterocycle synthesis
The reactivity of amidines makes them valuable as building blocks for the synthesis of
heterocyclic motifs of biological relevance, for functional materials, for organo-catalysts and …
heterocyclic motifs of biological relevance, for functional materials, for organo-catalysts and …
Organocatalytic cascade nucleophilic/aza-Michael addition reactions: metal-free catalytic strategy for the synthesis of hydantoins
L **e, L Sun, P Wu, Z Wang, C Zhao, L Wu… - Organic & …, 2023 - pubs.rsc.org
Lewis base-catalyzed cascade nucleophilic/aza-Michael addition reaction of N-alkoxy β-oxo-
acrylamides with isocyanates has been developed to afford various highly functionalized …
acrylamides with isocyanates has been developed to afford various highly functionalized …
Catalyst-Free, Three-Component Synthesis of Amidinomaleimides
WR Swift-Ramirez, LA Whalen… - The Journal of …, 2024 - ACS Publications
Maleimide and amidine functionalities often appear in medicinal and natural product targets.
We describe a catalyst-free, three-component coupling reaction for the synthesis of …
We describe a catalyst-free, three-component coupling reaction for the synthesis of …
Anticonvulsant Classes and Possible Mechanism of Actions
Epilepsy is considered one of the most common neurological disorders worldwide; it needs
long-term or life-long treatment. Despite the presence of several novel antiepileptic drugs …
long-term or life-long treatment. Despite the presence of several novel antiepileptic drugs …
Synthesis and antimicrobial activity of thiazolyl pyrazoles and isoxazoles
SS Basha, K Divya, A Padmaja… - Research on Chemical …, 2015 - Springer
Thiazolyl pyrazoles and isoxazoles were prepared and their antimicrobial activity studied.
Chloro-and nitro-substituted thiazolyl isoxazoles were potential antibacterial agents against …
Chloro-and nitro-substituted thiazolyl isoxazoles were potential antibacterial agents against …
Novel synthesis of pyran, thiophene, and pyridine derivatives incorporating thiazole ring and their antitumor evaluation
RM Mohareb, EM Khalil, AE Mayhoub… - Journal of …, 2020 - Wiley Online Library
This study aims to design and synthesize a number of novel pyran, thiophene, and pyridine
derivatives incorporating thiazole ring and evaluate their antitumor inhibition (μM) as …
derivatives incorporating thiazole ring and evaluate their antitumor inhibition (μM) as …