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Synthesis, Characterization, and Anticancer Activity of Benzothiazole Aniline Derivatives and Their Platinum (II) Complexes as New Chemotherapy Agents.
Islam, Md Kamrul; Baek, Ah-Rum; Sung, Bokyung; Yang, Byeong-Woo; Choi, Garam; Park, Hyun-Jin; Kim, Yeoun-Hee; Kim, Minsup; Ha, Seongmin; Lee, Gang-Ho; Kim, Hee-Kyung; Chang, Yongmin.
Affiliation
  • Islam MK; Institute of Biomedical Engineering Research, Kyungpook National University, 680, Gukchaebosang-ro, Jung-gu, Daegu 41944, Korea.
  • Baek AR; Department of Medical & Biological Engineering, Kyungpook National University, 80, Daehak-ro, Buk-gu, Daegu 41566, Korea.
  • Sung B; Department of Medical & Biological Engineering, Kyungpook National University, 80, Daehak-ro, Buk-gu, Daegu 41566, Korea.
  • Yang BW; Department of Medical & Biological Engineering, Kyungpook National University, 80, Daehak-ro, Buk-gu, Daegu 41566, Korea.
  • Choi G; R&D Center, Mirae BioPharm. Co., 124, Sagimakgol-ro, Jungwon-gu, Seongnam-si 13207, Korea.
  • Park HJ; R&D Center, Mirae BioPharm. Co., 124, Sagimakgol-ro, Jungwon-gu, Seongnam-si 13207, Korea.
  • Kim YH; R&D Center, Mirae BioPharm. Co., 124, Sagimakgol-ro, Jungwon-gu, Seongnam-si 13207, Korea.
  • Kim M; InCerebro Drug Discovery Institute, Seoul 01811, Korea.
  • Ha S; Department of Biomedical Science, School of Medicine, Kyungpook National University, 680, Gukchaebosang-ro, Jung-gu, Daegu 41944, Korea.
  • Lee GH; Department of Chemistry, Kyungpook National University, 80, Daehak-ro, Buk-gu, Daegu 41566, Korea.
  • Kim HK; Laboratory Animal Center, the Daegu-Gyeongbuk Medical Innovation Foundation, 88 Dongnae-ro, Dong-gu, Daegu 41061, Korea.
  • Chang Y; Department of Medical & Biological Engineering, Kyungpook National University, 80, Daehak-ro, Buk-gu, Daegu 41566, Korea.
Pharmaceuticals (Basel) ; 14(8)2021 Aug 23.
Article in En | MEDLINE | ID: mdl-34451928
ABSTRACT
We describe the synthesis, characterization, molecular modeling, and in vitro anticancer activity of three benzothiazole aniline (BTA) ligands and their corresponding platinum (II) complexes. We designed the compounds based on the selective antitumor properties of BTA, along with three types of metallic centers, aiming to take advantage of the distinctive and synergistic activity of the complexes to develop anticancer agents. The compounds were characterized using nuclear magnetic resonance spectrometry, Fourier transform infrared spectroscopy, mass spectrometry, elemental analysis, and tested for antiproliferative activity against multiple normal and cancerous cell lines. L1, L2, and L1Pt had better cytotoxicity in the liver, breast, lung, prostate, kidney, and brain cells than clinically used cisplatin. Especially, L1 and L1Pt demonstrated selective inhibitory activities against liver cancer cells. Therefore, these compounds can be a promising alternative to the present chemotherapy drugs.
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