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重要文件

5.30151

Sigma-Aldrich

ATGL Inhibitor, Atglistatin

同義詞:

ATGL Inhibitor, Atglistatin, 3-(4ʹ-(Dimethylamino)biphenyl-3-yl)-1,1-dimethylurea, Adipose Triglyceride Lipase Inhibitor

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About This Item

經驗公式(希爾表示法):
C17H21N3O
CAS號碼:
分子量::
283.37
MDL號碼:
分類程式碼代碼:
51111800
NACRES:
NA.77

化驗

≥97% (HPLC)

品質等級

形狀

powder

效力

700 nM IC50
355 nM Ki

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

beige

溶解度

DMSO: 100 mg/mL

儲存溫度

2-8°C

SMILES 字串

N(C)(C)c1ccc(cc1)c2cc(ccc2)NC(=O)N(C)C

InChI

1S/C17H21N3O/c1-19(2)16-10-8-13(9-11-16)14-6-5-7-15(12-14)18-17(21)20(3)4/h5-12H,1-4H3,(H,18,21)

InChI 密鑰

AWOPBSAJHCUSAS-UHFFFAOYSA-N

一般說明

A cell-permeable biphenyldimethyl urea compound that inhibits adipose triglyceride lipase (ATGL) activity (IC50 = 700 nM; [Substrate] = [Triolein] = 165 µM) in a substrate-competitive (Ki = 355 nM) and highly selective manner, exhibiting little potency against hormone-sensitive lipase (HSL), monoglyceride lipase (MGL), pancreatic lipase, lipoprotein lipase, or lysophospholipases PNPLA6/7 even at concentrations as high as 100 µM. Shown to effectively suppress FA/glycerol productions from adipocytes (ICmax = 50 to 100 µM in 3T3-L1-differentiated adipocytes or primary murine white adipose tissue/WAT cultures) in vitro and in blood of mice in vivo via either oral or intraperitoneal administration (EDmax = 200 µmol/kg) without affecting plasma glucose, total cholesterol, insulin, or β-hydroxybutyrate (beta-HB) level. Significant cytotoxicity is reported at concentrations >50 µM in AML-12 murine hepatocyte cultures. Although ATGL deficiency causes cardiomyopathy in human and ATGL-ko animals due to severe triacylglycerol (TG) accumulation in cardiac muscle, significant atglistatin level (>0.2 nmol/g tissue) is only seen in liver, white and brown adipose tissues, and detectable TG accumulation is only observed in liver tissue in wt mice 8 h post single 200 µmol/kg oral dosage.

生化/生理作用

Cell permeable: yes
Primary Target
ATGL
Reversible: yes

包裝

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

重構

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

其他說明

Mayer, N., et al. 2013. Nat. Chem. Biol.9, 785.
Produced under the license of University of Graz/Graz University of Technology

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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