hormone sensitive lipase

HSL-IN-1 是一种具有口服活性和高效性的激素敏感脂肪酶 (HSL) 抑制剂 ，显著降低了活性代谢物负荷，能减少储存脂肪中游离脂肪酸的释放。

HSL-IN-3 (HSL inhibitor 3) 是激素敏感性脂肪酶的抑制剂，是一种硼酸衍生物。

Orlistat-d3 is intended for use as an internal standard for the quantification of orlistat by GC- or LC-MS. Orlistat is a digestive lipase inhibitor. It inhibits diacylglycerol lipase α (DAGLα), DAGLβ, α β-hydrolase domain-containing protein 12 (ABHD12), ABHD16A, and platelet-activating factor acetylhydrolase (PAF-AH; IC50s = 0.06, 0.1, 0.08, 0.03, and 0.05 µM, respectively), as well as pancreatic lipase and hormone-sensitive lipase (IC50s = 0.65 and 2.1 µg ml, respectively) but does not inhibit fatty acid amide hydrolase (FAAH) or KIAA1363 (IC50s = >100 µM for both). Orlistat decreases ionomycin-induced production of the endocannabinoid 2-arachidonoyl glycerol (2-AG) in N18TG2 murine neuroblastoma cells when used at a concentration of 1 µM. It also inhibits fatty acid synthase (FASN; Kiapp = ~0.1 µM for the human enzyme) and the proliferation of PC3 prostate cancer cells in a concentration-dependent manner. Orlistat (10 mg kg) decreases serum cholesterol levels and total bod......

HSL-IN-2 is a selective inhibitor of Hormone Sensitive Lipase (HSL; IC50: 0.023 μM).

Lys-γ3-MSH(human) TFA是源自POMC片段C端的黑素皮质素肽，具备增强大鼠肾上腺对促肾上腺皮质激素(ACTH)的类固醇生成反应的能力。该化合物作为一种有效的脂解激活剂，其表观EC50值为3.56 nM，能够激活激素敏感脂肪酶(HSL)和紫苏脂素A，进而促进脂解。

Hi 76-0079 (NNC0076-0079) 是一种激素敏感性脂肪酶 (HSL) 抑制剂，其 IC50 为 184 nM。Hi 76-0079 是研究和预防肥胖和糖尿病的潜在化合物。

HSL-IN-5 (Example 21) 作为一种有效的激素敏感性脂肪酶 (HSL) 抑制剂，其半抑制浓度 (IC50) 为0.25 μM。该化合物广泛应用于糖尿病的相关研究中。