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Cetilistat(ATL-962)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Cetilistat(ATL-962)图片
CAS NO:282526-98-1
规格:≥98%
包装与价格:
包装价格(元)
500mg电议
1g电议
2g电议
5g电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 401.58
Formula C25H39NO3
CAS No. 282526-98-1
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 3 mg/mL (7.5 mM)
Water: < 1 mg/mL
Ethanol: 9 mg/mL (20 mM)
Solubility (In vivo)
Synonyms ATL962; ATL-962; ATL 962
SMILES Code CC1=CC=C(N=C(OCCCCCCCCCCCCCCCC)OC2=O)C2=C1
实验参考方法
In Vitro

In vitro activity: Cetilistat inhibits rat and human pancreatic lipase activity with IC50 of 54.8 nM and 5.95 nM, respectively.


Kinase Assay:


Cell Assay:

In VivoCetilistat reduces intestinal fat absorption in rats and decreases energy intake without CNS side effects. Cetilistat ameliorates obesity and hyperlipidemia in DIO rats, a plausible animal model of the most common type of human obesity.
Animal modelMale nine-week-old SD rats
Formulation & DosageFormulated in 0.5 % methylcellulose suspension; 3, 10, 30, or 100 mg/kg; P.O.
References Horm Metab Res. 2008 Aug;40(8):539-43.