Design, synthesis, antiproliferative and antibacterial evaluation of quinazolinone derivatives-Reference-Cited by-同舟云学术

Design, synthesis, antiproliferative and antibacterial evaluation of quinazolinone derivatives

Published:2018-12-26 Issue:2 Volume:28 Page:203-214
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Wang Hai-Xin,Liu Hai-Ying,Li Wei,Zhang Shuai,Wu Zheng,Li Xin,Li Cai-Wen,Liu Yu-Ming,Chen Bao-Quan

Funder

National Natural Science Foundation of China

Tianjin Municipal Natural Science Foundation

Training Project of Innovation Team of Colleges and Universities in Tianjin

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/article/10.1007/s00044-018-2276-8/fulltext.html

Reference25 articles.

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2. Alegaon SG, Parchure P, Araujo LD, Salve PS, Alagawadi KR, Jalalpure SS, Kumbaret VM (2017) Quinoline-azetidinone hybrids: synthesis and in vitro antiproliferation activity against Hep G2 and Hep 3B human cell lines. Bioorg Med Chem Lett 27:1566–1571

3. Al-Salem HS, Hegazy GH, El-Taher KE, El-Messery SM, Al-Obaid AM, El-Subbagh HI (2015) Synthesis, anticonvulsant activity and molecular modeling study of some new hydrazinecar-bothioamide, benzenesulfonohydrazide, and phenacylacetohydrazide analogues of 4(3H)-quinazolinone. Bioorg Med Chem Lett 25:1490–1499

4. Amir M, Ali I, Hassan MZ (2014) Design, synthesis and anticonvulsant activity of some newer 3H-quinazolin-4-one derivatives. Indian J Chem 53:597–604

5. Gaowa A, Horibe T, Kohno M, Tabata Y, Harada H, Hiraoka M, Kawakami K (2015) Enhancement of anti-tumor activity of hybrid peptide in conjugation with carboxymethyl dextran via disulfide linkers. Eur J Pharm Biopharm 92:228–236

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