Trypanocidal Activity of 2,5-Diphenyloxazoles Isolated from the Roots of Oxytropis lanata

被引:27
作者
Banzragchgarav, Orkhon [1 ]
Murata, Toshihiro [1 ]
Odontuya, Gendaram [2 ]
Buyankhishig, Buyanmandakh [3 ]
Suganuma, Keisuke [4 ,5 ]
Davaapurev, Bekh-Ochir [3 ]
Inoue, Noboru [6 ]
Batkhuu, Javzan [3 ]
Sasaki, Kenroh [1 ]
机构
[1] Tohoku Med & Pharmaceut Univ, Dept Pharmacognosy, Aoba Ku, 4-1 Komatsushima 4 Chome, Sendai, Miyagi 9818558, Japan
[2] Mongolian Acad Sci, Inst Chem & Chem Technol, Nat Prod Chem Lab, 13330 Peace Ave,4th Bldg MAS, Ulaanbaatar, Mongolia
[3] Natl Univ Mongolia, Sch Engn & Appl Sci, POB 617, Ulaanbaatar 46A, Mongolia
[4] Obihiro Univ Agr & Vet Med, Natl Res Ctr Protozoan Dis, Obihiro, Hokkaido 0808555, Japan
[5] Obihiro Univ Agr & Vet Med, Res Ctr Global Agromed, Obihiro, Hokkaido 0808555, Japan
[6] Obihiro Univ Agr & Vet Med, Obihiro, Hokkaido 0808555, Japan
来源
JOURNAL OF NATURAL PRODUCTS | 2016年 / 79卷 / 11期
关键词
2,5-DISUBSTITUTED OXAZOLES; ISOFLAVONOIDS; CULTIVATION;
D O I
10.1021/acs.jnatprod.6b00778
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Eleven 2,5-diphenyloxazole derivatives (1-11), together with six known isoflavonoid derivatives, were isolated from the roots of Oxytropis lanata. The 2,5-diphenyloxazole (1) obtained proved to be identical to a standard sample used as a scintillator and liquid laser dye. The other oxazole derivatives isolated were found to have one to four hydroxy and/or O-methyl groups in their phenyl rings. Seven of the oxazole derivatives obtained are new (3-9). The inhibitory activity of the isolated compounds was evaluated against Trypanosoma congolense, the causative agent of African trypanosomosis in animals. Oxazoles with di- and tribsydroxy groups showed trypanocidal activity, and 2(2',3' -dihydroxyphenyl)-5-(2"-hydro xyph enyl) oxazole (4) exhibited the most potent inhibitory activity (IC50 1.0 mu M).
引用
收藏
页码:2933 / 2940
页数:8
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