XEN723 is a potent thiazolylimidazolidinone inhibitor of Stearoyl-CoA Desaturase (SCD1) with IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively.

CAY10566是一种选择性硬脂酰辅酶 A 去饱和酶 1 (SCD1) 抑制剂，具有生物可利用性，常用于研究脂肪酸代谢调节和代谢性疾病。

PluriSln 1 is an inhibitor of cell pluripotency and stearoyl-coA desaturase (SCD1) that can induce ER stress and apoptosis in hPSCs.

MF-438 is an inhibitor of stearoyl-CoA desaturase 1 (SCD1) with EC50 of 2.3 nM for rSCD1.

SCD1 inhibitor-4 是一种选择性的脂肪酸去饱和酶 1 (SCD1) 抑制剂，对 SCD1 具有高亲和力。SCD1 inhibitor-4 主要用于脂肪代谢和代谢综合症的研究。

MK-8245 is a liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy.

A939572 是一种有效且具有口服活性的硬脂酰CoA 去饱和酶 1（SCD1）抑制剂，作用于 mSCD1 和 hSCD1 的 IC50 分别为 <4 nM 和 37 nM。

Aramchol is a conjugate of cholic acid and arachidic acid that could inhibit stearoyl coenzyme A desaturase 1 (SCD1) activity.

CVT-12012 is a potent and orally bioavailable stearoyl-coA desaturase (SCD) inhibitor, with IC50s of 38 nM, 6.1 nM for rat microsomal and human HEPG2, respectively.

SCD inhibitor 1 is an inhibitor of stearoyl-coa desaturase (SCD).