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诺卡地霉素G、H和I,来自新星诺卡氏菌JCM 6044的具有毒蕈碱M3受体结合抑制活性的铁载体。

Nocardimicins G, H and I, siderophores with muscarinic M3 receptor binding inhibitory activity from Nocardia nova JCM 6044.

作者信息

Ikeda Yoshitaka, Furumai Tamotsu, Igarashi Yasuhiro

机构信息

Pharmaceuticals Research Unit, Mitsubishi Pharma Corporation, 1000, Kamoshida-cho, Aoba-ku, Yokohama, Kanagawa 227-0033, Japan.

出版信息

J Antibiot (Tokyo). 2005 Sep;58(9):566-72. doi: 10.1038/ja.2005.77.

Abstract

In the screening for muscarinic M3 receptor binding inhibitors from microbial secondary metabolites, the extract of Nocardia nova JCM 6044 was found to be highly active. Bioassay-guided isolation led to the identification of three siderophores, nocardimicins G (1), H (2) and I (3). Their chemical structures were determined by spectroscopic analysis using NMR and MS. 1 and 2 inhibited the binding of tritium-labeled N-methylscopolamine to the muscarinic M3 receptor with Ki values of 0.44 microM and 0.37 microM, respectively, whereas 3 showed no inhibition at 10 microM. 1 and 2 also showed weak binding inhibitory activity to the M5 receptor but not to the M1, M2 and M4 receptors at 10 microM.

摘要

在从微生物次级代谢产物中筛选毒蕈碱M3受体结合抑制剂的过程中,发现新星诺卡氏菌JCM 6044的提取物具有高活性。通过生物活性导向分离鉴定出三种铁载体,即诺卡菌素G(1)、H(2)和I(3)。利用核磁共振(NMR)和质谱(MS)通过光谱分析确定了它们的化学结构。化合物1和2抑制氚标记的N-甲基东莨菪碱与毒蕈碱M3受体的结合,其抑制常数(Ki)值分别为0.44微摩尔和0.37微摩尔,而化合物3在10微摩尔浓度下未表现出抑制作用。在10微摩尔浓度下,化合物1和2对M5受体也表现出较弱的结合抑制活性,但对M1、M2和M4受体无抑制作用。

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