In vitro seintransduksie meganisme uitgeoefen deur 2-etiel-3-O-sulphamoyl-estra-1,3,5(10),15-tetraen-3-ol-17-een in kombinasie met ‘n dichloro-asetielsuur op die bors adenokarsinoom (MCF-7) en bors nie-tumorigene (MCF-12A) selle

X. X. Stander, A. Stander, A. Joubert
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Abstract

2-Etiel-3-O-sulphamoyl-estra-1,3,5(10),15-tetraen-3-ol-17 (C9) is ‘n nuwe,in silico-ontwerpte, antimitotiese 17-beta-estradiolderivaat. Dichloro-asetielsuur (DCA) inhibeer pirovaat dehydrogenase kinase ensiem aktiwiteit wat die vorming en vervoer van asetiel-KoA in die mitochondria inhibeer. Dit veroorsaak dat fermentasie prosesse, wat in kankerselle bevoordeel word, onderdruk word.
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体外浓缩机制由2-乙基-3-O-磺酰基-雌二醇-1,3,5(10),15-四烯-3-醇-17-酮与“二氯asetyl管”联合作用于乳腺腺癌细胞(MCF-7)和乳腺非肿瘤细胞(MCF-12A)来确定
2-埃塞俄比亚-3-O-氨磺酰基-雌二醇-1,3,5(10),15-四烯-3-醇-17(C9)是“新的、在计算机上开发的抗有丝分裂的17β-雌二醇衍生物”。二氯asetyle管(DCA)抑制焦酸脱氢酶激酶以及抑制线粒体中asetyle-coA形成和输出的活性。这就是为什么系统托盘中有序的发酵过程被抑制的原因。
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