Design, synthesis and cytotoxic evaluation of a novel series of benzo[d]thiazole-2-carboxamide derivatives as potential EGFR inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis and cytotoxic evaluation of a novel series of benzo[d]thiazole-2-carboxamide derivatives as potential EGFR inhibitors

Published:2017-05-29 Issue:9 Volume:26 Page:2180-2189
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Zhang Lan,Deng Xin-Shan,Zhang Chao,Meng Guang-Peng,Wu Jiao-Feng,Li Xue-Song,Zhao Qing-Chun,Hu Chun

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/article/10.1007/s00044-017-1925-7/fulltext.html

Reference20 articles.

1. Al-Ghorbani M, Pavankumar GS, Naveen P, Thirusangu P, Prabhakar BT, Khanum SA (2016) Synthesis and an angiolytic role of novel piperazine–benzothiazole analogues on neovascularization, a chief tumoral parameter in neoplastic development. Bioorg Chem 65:110–117

2. Chen LJ, She XD, Wang T (2015) Overcoming acquired drug resistance in colorectal cancer cells by targeted delivery of 5-FU with EGF grafted hollow mesoporous silica nanoparticles. Nanoscale 7:14080–14092

3. Cheng YF, Peng HJ, Chen WX, Ni NT, Ke BW, Dai CF, Wang BH (2013) Rapid and specific post-synthesis modification of DNA through a biocompatible condensation of 1,2-aminothiols with 2-cyanobenzothiazole. Chem Eur J 19:4036–4042

4. Ciuffreda P, Casati S, Meroni G, Santaniello E (2013) A new synthesis of dehydroluciferin [2-(60-hydroxy-20-benzothiazolyl)-thiazole-4-carboxylic acid] from 1,4-benzoquinone. Tetrahedron 69:5893–5897

5. Ismail MAH, Tratrat C, Haroun MG (2013) Molecular modelling design, synthesis and cytotoxic evaluation of certain substituted 2-(3,4,5-triacetoxybenzoylamino)benzo[d]thiazole and 2-(galloylamino)benzo[d]thiazole derivatives having potential topoisomerase-I inhibitory activity. J Enzyme Inhib Med Chem 28:1331–1345

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