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新型抗肿瘤药物 I:合成 1,5-双(4-羟基-3-甲氧基苯基)-1,4-戊二烯-3-酮及其衍生物的体外抗癌活性和体内急性毒性。

New antitumoral agents I: In vitro anticancer activity and in vivo acute toxicity of synthetic 1,5-bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one and derivatives.

机构信息

Laboratory of Organic Synthesis, Universidade Bandeirante de São Paulo (UNIBAN), São Paulo, Brazil.

出版信息

Bioorg Med Chem. 2010 Sep 1;18(17):6275-81. doi: 10.1016/j.bmc.2010.07.026. Epub 2010 Jul 16.

Abstract

This paper describes a new method for the preparation of 1,5-bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one 1 and its derivatives 2-5. This set of synthetic compounds exhibited high antitumoral activities regarding in vitro screening against several human tumor cell lines as lung carcinoma NCI-460, melanoma UACC-62, breast MCF-7, colon HT-29, renal 786-O, ovarian OVCAR-03 and ovarian expressing the resistance phenotype for adriamycin NCI-ADR/RES, prostate PC-3, and leukemia K-562. Compounds were also tested against murine tumor cell line B16F10 melanoma and lymphocytic leukemia L1210 as well as to their effect toward normal macrophages. Specific activity against colon cancer cells HT-29 was observed for all tested compounds and suggests further studies with models of colon cancer. Compounds 1, 2, and 4 showed significant cytotoxic activity with IC(50) values 2.3 microM for all human cancer cell lines. Intraperitoneal acute administration of compound 1 and 2 showed very low toxicity rate.

摘要

本文描述了一种新的方法来制备 1,5-双(4-羟基-3-甲氧基苯基)-1,4-戊二烯-3-酮 1 及其衍生物 2-5。这组合成化合物在体外筛选对多种人类肿瘤细胞系(肺癌 NCI-460、黑色素瘤 UACC-62、乳腺癌 MCF-7、结肠 HT-29、肾 786-O、卵巢 OVCAR-03 和表达多柔比星耐药表型的卵巢 NCI-ADR/RES、前列腺 PC-3 和白血病 K-562)表现出高抗肿瘤活性。化合物还针对鼠肿瘤细胞系 B16F10 黑色素瘤和淋巴细胞白血病 L1210 进行了测试,并对其对正常巨噬细胞的影响进行了测试。所有测试的化合物对结肠癌细胞 HT-29 均表现出特异性活性,提示对结肠癌模型进行进一步研究。化合物 1、2 和 4 对所有人类癌细胞系的 IC(50) 值均为 2.3 μM,表现出显著的细胞毒性活性。化合物 1 和 2 的腹腔内急性给药显示出非常低的毒性率。

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