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The evaluation of novel natural products as inhibitors of human glutathione transferase P1-1

机译:新型天然产物作为人谷胱甘肽转移酶P1-1抑制剂的评估

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Glutathione transferase P1-1 is over expressed in some cancer cells and contributes to detoxification of anticancer drugs, leading to drug-resistant tumors. The inhibition of human recombinant GSTP1-1 by natural plant products was investigated using 10 compounds isolated from plants indigenous to Southern and Central Africa. Monochlorobimane and 1-chloro-2,4-dinitrobenzene were used to determine GST activity. Each test compound was screened at 33 and 100 μM. Isofuranonapthoquinone (1) (from Bulbine frutescens) showed 68% inhibition at 33 μM, and sesquiterpene lactone (2) (from Dicoma anomala) showed 75% inhibition at 33 μM. The IC50 value of 1 was 6.8 μM. The mode of inhibition was mixed, partial (G site) and noncompetitive (H site) with Ki values of 8.8 and 0.21 μM, respectively. Sesquiterpene 2 did not inhibit the CDNB reaction. Therefore, isofuranonapthoquinone 1 needs further investigations in vivo because of its potent inhibition of GSTP1-1 in vitro.
机译:谷胱甘肽转移酶P1-1在某些癌细胞中过度表达,并且有助于抗癌药物的解毒,从而导致耐药性肿瘤。使用从南部和中部非洲土著植物中分离的10种化合物研究了天然植物产品对人重组GSTP1-1的抑制作用。一氯二苯胺和1-氯-2,4-二硝基苯用于测定GST活性。每种测试化合物的筛选浓度分别为33和100μM。异富拉农萘醌(1)(来自Bulbine frutescens)在33μM时显示68%的抑制作用,倍半萜内酯(2)(来自Dicoma anomala)在33μM时显示75%的抑制率。 IC 50 的值为1,为6.8μM。抑制方式为混合的,部分的(G位点)和非竞争的(H位点),K 值分别为8.8和0.21μM。倍半萜烯2没有抑制CDNB反应。因此,由于在体外有效地抑制了GSTP1-1,因此异氟醚萘醌1在体内需要进一步研究。

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