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两种 C75 对映异构体的药效差异:(+)-C75 是一种强烈的食欲抑制剂;(-)-C75 具有抗肿瘤活性。

Differential pharmacologic properties of the two C75 enantiomers: (+)-C75 is a strong anorectic drug; (-)-C75 has antitumor activity.

机构信息

Department of Biochemistry and Molecular Biology, Facultat de Farmàcia, Universitat de Barcelona, E-08028 Barcelona, Spain.

出版信息

Chirality. 2013 May;25(5):281-7. doi: 10.1002/chir.22139.

Abstract

C75 is a synthetic compound described as having antitumoral properties. It produces hypophagia and weight loss in rodents, limiting its use in cancer therapy but identifying it as a potential anti-obesity drug. C75 is a fatty acid synthase (FAS) inhibitor and, through its coenzyme A (CoA) derivative, it acts as a carnitine palmitoyltransferase (CPT) 1 inhibitor. Racemic mixtures of C75 have been used in all the previous studies; however, the potential different biological activities of C75 enantiomers have not been examined yet. To address this question we synthesized the two C75 enantiomers separately. Our results showed that (-)-C75 inhibits FAS activity in vitro and has a cytotoxic effect on tumor cell lines, without affecting food consumption. (+)-C75 inhibits CPT1 and its administration produces anorexia, suggesting that central inhibition of CPT1 is essential for the anorectic effect of C75. The differential activity of C75 enantiomers may lead to the development of potential new specific drugs for cancer and obesity.

摘要

C75 是一种合成化合物,具有抗肿瘤特性。它会引起啮齿动物的食欲减退和体重减轻,限制了其在癌症治疗中的应用,但将其鉴定为一种有潜力的抗肥胖药物。C75 是脂肪酸合酶 (FAS) 抑制剂,通过其辅酶 A (CoA) 衍生物,它充当肉碱棕榈酰转移酶 (CPT) 1 抑制剂。以前的所有研究都使用了 C75 的外消旋混合物;然而,尚未研究 C75 对映异构体的潜在不同生物学活性。为了解决这个问题,我们分别合成了两种 C75 对映异构体。我们的结果表明,(-)-C75 在体外抑制 FAS 活性,并对肿瘤细胞系具有细胞毒性作用,而不影响食物消耗。(+)-C75 抑制 CPT1,其给药会引起厌食症,表明 CPT1 的中枢抑制对于 C75 的厌食作用是必要的。C75 对映异构体的差异活性可能会导致开发出针对癌症和肥胖症的潜在新的特异性药物。

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