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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SOME HYBRID LINKER MODE C-2-SYMMETRICAL 1,3,5-TRIAZINE DERIVATIVES AND THEIR BIOLOGICAL EVALUATION
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SOME HYBRID LINKER MODE C-2-SYMMETRICAL 1,3,5-TRIAZINE DERIVATIVES AND THEIR BIOLOGICAL EVALUATION

机译:一些杂交接头模式C-2对称1,3,5-三嗪衍生物及其生物学评估

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We report the preparation of some new C-2-symmetrical multivalent hybrid-type molecules having a methylene linker group and 1,3,5-triazine (TAZ) recognition moieties in the molecule and we also report the results of biological evaluation of their anti-herpes simplex virus type 1 (anti-HSV-1) activity and cytotoxic activity against Vero cells. All mid-size C-2-symmetrical multivalent hybrid-type molecules (3a-2, 3a-4, 3b-2, 3b-3, 3b-4) showed considerably high levels of anti-HSV-1 activity (EC50 = 7.6 similar to 95.6 mu M) with low levels of cytotoxicity (CC50 > 200 mu M) against Vero cells. Among the tested compounds, the hybrid-type C-2-symmetrical multivalent molecule (3a-4) seems to be an interesting new lead in the search for new hybrid-type multivalent mid-size antiviral compounds.
机译:我们报告了在分子中具有亚甲基接头组和1,3,5-三嗪(TAZ)识别部分的一些新的C-2对称多价杂化型分子的制备,我们还报告了对其抗的生物学评估结果 -herpes单纯x病毒类型1(抗HSV-1)活性和对Vero细胞的细胞毒性活性。 所有中等尺寸的C-2对称多价杂化分子(3A-2,3A-4,3B-2,3B-3,3B-4)显示出大量高水平的抗HSV-1活性(EC50 = 7.6 类似于95.6μm),具有较低水平的细胞毒性(CC50>200μm)对Vero细胞。 在测试的化合物中,杂化型C-2-对称多元分子(3A-4)似乎是在寻找新的杂化式多价中型抗病毒化合物中的有趣新铅。

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