首页> 外国专利> Antitüberküloz aktif dogal bilesiklerin eldesi ve yapi tayinleri.

Antitüberküloz aktif dogal bilesiklerin eldesi ve yapi tayinleri.

机译:抗结核活性天然化合物的获取和结构测定。

摘要

According to invention, 7 diterpene consisting of 6 abietic and 1 primary structures have been extracted from the acetone extract of the roots of an sage tea species, Salvia Multicaulis, their formations have been determined by spectroscopic methods (TR, UV, IH and 13C NMR and MS) and referred as multicaulis (1), 12-dimethyl multicaulis (2), multiorthoquinone (3), 12-dimethylmultiorthoquinone (4), 12-methyl-5-dehydrohorminone (5), 12-methyl-5-dehydro-acetylhorminone (6) and salvipimarone (7). They have been thought to be active in formation and detected to have higher activity as a result of anti-tuberculosis test against Mycobacterium tuberculosis by liquid micro dilution method and three of these compounds (2, 4 and 6) have been found to be more active than the medication used in tuberculosis treatment like streptomycin, kanamycin, p-aminosalicylic acid (PAS) and isonicotinic acid hydracids (INH).
机译:根据本发明,从鼠尾草茶丹参多酚的根的丙酮提取物中提取了由6种松香和1种一级结构组成的7个二萜,并通过分光光度法(TR,UV,IH和13C NMR)确定了它们的形成。和MS),并称为多元酚(1),12-二甲基多元酚(2),多邻醌(3),12-二甲基多邻醌(4),12-甲基-5-脱氢激素(5),12-甲基-5-脱氢-乙酰激素(6)和沙维马酮(7)。通过液体微量稀释法对结核分枝杆菌进行抗结核试验,人们认为它们的形成具有活性,并被发现具有更高的活性,并且发现其中的三种化合物(2、4和6)更具活性。而非链球菌素,卡那霉素,对氨基水杨酸(PAS)和异烟酸水合酸(INH)等结核病治疗药物。

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