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新型二氢吡喃酮衍生物,由土曲霉 FKI-3864 产生的哺乳动物细胞三酰基甘油合成的有效抑制剂。

New dinapinone derivatives, potent inhibitors of triacylglycerol synthesis in mammalian cells, produced by Talaromyces pinophilus FKI-3864.

机构信息

Graduate School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.

出版信息

J Antibiot (Tokyo). 2013 Mar;66(3):179-89. doi: 10.1038/ja.2012.127.

Abstract

Eight new dinapinones, AB1, AB2, AC1, AC2, AD1, AD2, AE1 and AE2, were isolated from the culture broth of Talaromyces pinophilus FKI-3864. The structures of these dinapinones were elucidated by various NMR experiments. All these dinapinones possessed the same biaryl dihydronaphthopyranone skeleton consisting of a heterodimer with one monapinone A and one different monapinone. Dinapinones AB1 and AB2, consisting of monapinones A and B, were atropisomers. Similarly, dinapinones AC1 and AC2, consisting of monapinones A and C, dinapinones AD1 and AD2, consisting of monapinones A and D, and dinapinones AE1 and AE2, consisting of monapinones A and E, were atropisomers. Dinapinone AB2 showed potent inhibition of triacylglycerol (TG) synthesis in intact mammalian cells with an IC50 value of 1.17 μM, whereas the other dinapinones showed weak inhibition of TG synthesis.

摘要

从土曲霉 FKI-3864 的发酵液中分离得到了 8 个新的二萘并吡喃酮,分别为 AB1、AB2、AC1、AC2、AD1、AD2、AE1 和 AE2。通过各种 NMR 实验阐明了这些二萘并吡喃酮的结构。所有这些二萘并吡喃酮都具有相同的双芳基二氢萘并吡喃酮骨架,由一个杂二聚体组成,其中一个是单萘并吡喃酮 A,另一个是不同的单萘并吡喃酮。由单萘并吡喃酮 A 和 B 组成的二萘并吡喃酮 AB1 和 AB2 是对映异构体。同样,由单萘并吡喃酮 A 和 C 组成的二萘并吡喃酮 AC1 和 AC2、由单萘并吡喃酮 A 和 D 组成的二萘并吡喃酮 AD1 和 AD2、由单萘并吡喃酮 A 和 E 组成的二萘并吡喃酮 AE1 和 AE2 也是对映异构体。二萘并吡喃酮 AB2 对完整哺乳动物细胞中三酰基甘油 (TG) 的合成具有很强的抑制作用,IC50 值为 1.17 μM,而其他二萘并吡喃酮对 TG 合成的抑制作用较弱。

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