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Cetilistat  (Synonyms: 新利司他; ATL-962)

目录号: HY-14471 纯度: ≥98.0%
COA 产品使用指南

摩尔计算器

Cetilistat (ATL-962) 是一种胰腺脂肪酶 (pancreatic lipase) 抑制剂，可作为有效的抗肥胖药。Cetilistat 抑制大鼠和人胰脂肪酶活性，IC50 分别为 54.8 nM 和 5.95 nM。

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Cetilistat Chemical Structure

Cetilistat Chemical Structure

CAS No. : 282526-98-1

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Customer Review

Cetilistat 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Cetilistat (ATL-962), an inhibitor of pancreatic lipase, acts as an effective anti-obesity agent. Cetilistat inhibits rat and human pancreatic lipase activity with IC50s of 54.8 nM, and 5.95 nM, respectively[1].

IC50 & Target

IC50: 54.8 nM (rat pancreatic lipase), 5.95 nM (human pancreatic lipase)[1]
体外研究
(In Vitro)

Cetilistat inhibits rat pancreatic lipase activity with an IC50 of 54.8 nM. Also, Cetilistat inhibits human pancreatic lipase activity with an IC50 of 5.95 nM, which is 9.2 times more potent than for rat pancreatic lipase[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cetilistat 相关抗体:
体内研究
(In Vivo)

Cetilistat (3, 10, 30, or 100 mg/kg) reduces intestinal fat absorption by inhibiting pancreatic lipase activity in male SD rats[1].
Cetilistat (4.9, 14.9, or 50.7 mg/kg; mixed into powdered high-fat diet; once a day; for three weeks) shows anti-obesity and antihyperlipidemic effects on DIO F344 rats by reducing intestinal fat absorption[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Fifty male SD rats (eight weeks of age)[1]
Dosage: 3, 10, 30, or 100 mg/kg
Administration: Orally administered; prepared in 0.5 % methylcellulose (MC) suspension
Result: Dose-dependently reduced AUC 0-6 h of plasma triglyceride induced by oral loading of Intrafat 20%. The effect was statistically significant at 3 mg/kg, reaching 45% reduction, while an almost 90 % reduction was achieved at 100 mg/kg.
Animal Model: Male diet-induced obesity (DIO) F344 rats (five weeks of age)[1]
Dosage: 4.9, 14.9, or 50.7 mg/kg
Administration: Administered as food admixture in a high-fat diet; once a day; for three weeks
Result: Significantly and dose-dependently reduced body weight gain compared with control.
Clinical Trial
分子量

401.58

Formula

C25H39NO3
CAS 号
性状

固体

颜色

White to off-white

中文名称

新利司他；西替利斯他；赛利司他；西替利斯塔
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
溶解性数据
In Vitro: 

DMSO 中的溶解度 : < 1 mg/mL (insoluble or slightly soluble)

H2O 中的溶解度 : < 0.1 mg/mL (insoluble)

*Cetilistat is usually formulated as a suspension.

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息：

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

只
由于实验过程有损耗，建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

Cetilistat 相关分类

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Cetilistat282526-98-1ATL-962新利司他西替利斯他赛利司他西替利斯塔ATL962ATL 962Othershigh-fat dietcholesterolpancreaticlipaseanti-obesityInhibitorinhibitorinhibit

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目录号：
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