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Synthesis of some steroidal mitocans of nanomolar cytotoxicity acting by apoptosis

机译:细胞凋亡作用作用的纳米摩尔细胞毒性的一些甾体系系的合成

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Several steroids (abiraterone, prednisone, testosterone, cholesterol) and the BCL-2 inhibitor bexarotene were used as starting materials to synthesize iperazinyl-spacered rhodamine B conjugates. The conjugates were screened for their cytotoxicity in SRB assays against several human tumor cell lines and found to be active in a low mu M to nM range. The conjugate derived from testosterone held an EC50 = 59 nM against MCF-7 tumor cells and acted mainly by necrosis. The prednisone conjugate, however, was less cytotoxic but acted mainly by apoptosis and held a moderate selectivity against MCF-7 tumor cells. (C) 2020 Elsevier Masson SAS. All rights reserved.
机译:使用几种类固醇(AbiraTerone,泼尼松,睾酮,胆固醇)和Bcl-2抑制剂苯甲酰基作为原料,以合成Iperazinyl-kcodamery罗丹明B缀合物。 将缀合物筛选在SRB测定中筛选其对几种人肿瘤细胞系的细胞毒性,并发现在低mu m至nm范围内是活性的。 衍生自睾酮的缀合物对抗MCF-7肿瘤细胞的EC50 = 59nm,并主要通过坏死作用。 然而,泼尼松缀合物的细胞毒性较少,但主要通过细胞凋亡作用,并对MCF-7肿瘤细胞保持着中等的选择性。 (c)2020 Elsevier Masson SAS。 版权所有。

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