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新型苯甲酰基哌啶基硬脂酰辅酶 A 去饱和酶 1 抑制剂:6-[4-(2-甲基苯甲酰基)哌啶-1-基]哒嗪-3-羧酸(2-羟基-2-吡啶-3-基乙基)酰胺的鉴定及其在 Zucker 肥胖大鼠中的降低血浆甘油三酯作用。

Novel benzoylpiperidine-based stearoyl-CoA desaturase-1 inhibitors: Identification of 6-[4-(2-methylbenzoyl)piperidin-1-yl]pyridazine-3-carboxylic acid (2-hydroxy-2-pyridin-3-ylethyl)amide and its plasma triglyceride-lowering effects in Zucker fatty rats.

机构信息

Medicinal Chemistry Research Laboratories I, Daiichi Sankyo Co. Ltd, Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.

出版信息

Bioorg Med Chem Lett. 2010 Jan 1;20(1):341-5. doi: 10.1016/j.bmcl.2009.10.101. Epub 2009 Oct 29.

Abstract

Starting from a known piperazine-based SCD-1 inhibitor, we obtained more potent benzoylpiperidine analogs. Optimization of the structure of the benzoylpiperidine-based SCD-1 inhibitors resulted in the identification of 6-[4-(2-methylbenzoyl)piperidin-1-yl]pyridazine-3-carboxylic acid (2-hydroxy-2-pyridin-3-yl-ethyl)amide (24) which showed strong inhibitory activity against both human and murine SCD-1. In addition, this compound exhibited good oral bioavailability and demonstrated plasma triglyceride lowering effects in Zucker fatty rats in a dose-dependent manner after a 7-day oral administration (qd).

摘要

从已知的 SCD-1 抑制剂哌嗪出发,我们得到了更有效的苯甲酰哌啶类似物。对苯甲酰哌啶基 SCD-1 抑制剂的结构进行优化,得到了 6-[4-(2-甲基苯甲酰基)哌啶-1-基]哒嗪-3-羧酸(2-羟基-2-吡啶-3-基-乙基)酰胺(24),该化合物对人和鼠 SCD-1 均具有很强的抑制活性。此外,该化合物在 7 天口服给药后(qd),在 Zucker 肥胖大鼠中具有良好的口服生物利用度,并表现出剂量依赖性的降低血浆甘油三酯的作用。

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