Discovery of a multipotent chaperone, 1-(2,6-Difluorobenzylamino)-3-(1,2,3,4-tetrahydrocarbazol-9-yl)-propan-2-ol with the inhibitory effects on the proliferation of prion, cancer as well as influenza virus

被引:6
|
作者
Yamashita, Satoshi [1 ]
Yamashitaa, Satoshi [1 ]
Honda, Ryo [1 ]
Fukuoka, Mayuko [1 ]
Kimura, Tsutomu [2 ]
Hosokawa-Muto, Junji [3 ]
Kuwata, Kazuo [1 ,4 ]
机构
[1] Gifu Univ, United Grad Sch Drug Discovery & Med Informat Sci, Yanagido 1-1, Gifu 5011193, Japan
[2] Tokyo Univ Sci, Fac Sci, Dept Chem, Div 2, Tokyo, Japan
[3] Natl Res Inst Police Sci, Dept Forsen Sci 1, Chiba, Japan
[4] Gifu Univ, Grad Sch Med, Dept Gene & Dev, Gifu, Japan
关键词
Chaperone; multipotent; stabilization; free energy; activation free energy; prion; cancer; influenza virus; anti-viral agent; carbazol; PROTEIN; BINDING; P53; IDENTIFICATION;
D O I
10.1080/19336896.2020.1714372
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We previously discovered three carbazole derivatives, GJP14 (1-piperidinylmethyl-2-(1-oxo-6-methyl-1,2,3,4-tetrahydrocarbazol-9-yl)-ethan-1-ol) with anti-prion activity, GJC29 (benzylamino-3-(1,2,3,4-tetrahydrocarbazol-9-yl)-propan-2-ol) with anti-cancer activity, and THC19 (1-piperidinylmethyl-2-(1,2,3,4-tetrahydrocarnazol-9-yl)-ethan-1-ol) with anti-influenza virus activity. During optimization of GJP14 for the anti-prion activity, we discovered a compound, 1-(2,6-difluorobenzylamino)-3-(1,2,3,4-tetrahydrocarbazol-9-yl)-propan-2-ol, termed 5Y, had the most strong anti-prion activity among a series of newly synthesized derivatives. Intriguingly, we noticed that 5Y had also the most strong anti-colon cancer as well as the anti-influenza virus activities among derivatives. No significant toxicity of 5Y was observed. These results demonstrate that 5Y is a multipotent lead compound with unusually wide spectrum, and may be applicable to therapeutics targeting multiple diseases.
引用
收藏
页码:42 / 46
页数:5
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