Synthesis and Pharmacological Evaluation of 3-propyl-2-substitutedamino-3H-quinazolin-4-ones as Analgesic and Anti-Inflammatory Agents-Reference-Cited by-同舟云学术

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Synthesis and Pharmacological Evaluation of 3-propyl-2-substitutedamino-3H-quinazolin-4-ones as Analgesic and Anti-Inflammatory Agents

Published:2016-06-28 Issue:5 Volume:53 Page:1371-1377
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Sheorey R. V.¹,Thangathiruppathy A.²,Alagarsamy V.³

Affiliation:

1. Research Scholar, Department of Pharmacy; Karpagam University, Eachanari Post; Coimbatore 641 021 Tamil Nadu India

2. Department of Pharmacology; SB College of Pharmacy; Sivakasi 626 130 Tamil Nadu India

3. Medicinal Chemistry Research Laboratory; MNR College of Pharmacy; Sangareddy Gr. Hyderabad 502 294 Andhra Pradesh India

Publisher

Wiley

Subject

Organic Chemistry

Reference16 articles.

1. New insights into the mode of action of anti-inflammatory drugs

2. COX-2 Selectivity and Inflammatory Processes

3. Inhibition of Prostaglandin Synthesis as a Mechanism of Action for Aspirin-like Drugs

4. Nonsteroidal Antiinflammatory Drugs: A New Generation of Cyclooxygenase Inhibitors

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of 2-phenyl- and 2-benzyl derivatives of 4(3Н)-quinazolinone with analgesic activity;Pharmacy & Pharmacology;2023-04-30

2. Green Catalyst‐ and Additive‐Free Three‐Component Deamination Cyclization Synthesis of 3‐Substituted‐4‐ oxo‐2‐quinazolinonyl Sulfides;ChemistrySelect;2021-11-10

3. Mechanistic evaluation of a novel cyclohexenone derivative’s functionality against nociception and inflammation: An in-vitro, in-vivo and in-silico approach;European Journal of Pharmacology;2021-07

4. Synthesis of bioactive quinazolin-4(3H)-one derivatives via microwave activation tailored by phase-transfer catalysis;Acta Pharmaceutica;2020-01-16

5. Synthesis of (1′ S *,2 R *,3 R *)‐ and (1′ S *,2 R *,3 S *)‐ N ‐arylsulfonyl‐2‐(1′‐halogenethyl)‐3‐methylindolines and their selective toxicity against SH‐SY5Y cell line;Journal of Heterocyclic Chemistry;2020-01-08

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