INT 131

Pricing Availability   Qty
说明: PPARγ partial agonist
化学名: 2,4-Dichloro-N-[3,5-dichloro-4-(3-quinolinyloxy)phenyl]benzenesulfonamide
纯度: ≥98% (HPLC)
说明书
引用文献
评论

生物活性 for INT 131

INT 131 is a potent and selective PPARγ partial agonist (EC50 = 4 nM; Ki = 3.7 nM). It has a 20-fold higher affinity for PPARγ compared with that of Rosiglitazone (Cat. No. 5325). INT 131 improves glucose tolerance in a rodent model of diabetes without inducing hemodynamic and cardiovascular effects. Antidiabetic agent.

技术数据 for INT 131

分子量 514.21
公式 C21H12Cl4N2O3S
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 315224-26-1
PubChem ID 10229498
InChI Key NMRWDFUZLLQSBN-UHFFFAOYSA-N
Smiles O=S(=O)(NC1=CC(Cl)=C(OC2=CN=C3C=CC=CC3=C2)C(Cl)=C1)C4=CC=C(Cl)C=C4Cl

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for INT 131

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 2.57 5
ethanol 2.57 5

制备储备液 for INT 131

以下数据基于产品分子量 514.21。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.05 mM 38.89 mL 194.47 mL 388.95 mL
0.25 mM 7.78 mL 38.89 mL 77.79 mL
0.5 mM 3.89 mL 19.45 mL 38.89 mL
2.5 mM 0.78 mL 3.89 mL 7.78 mL

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参考文献 for INT 131

参考文献是支持产品生物活性的出版物。

Frkic et al (2017) Structure-activity relationship of 2,4-Dichloro-N-(3,5-dichloro-4-(quinolin-3-yloxy)phenyl)benzenesulfonamide (INT131) analogs for PPARγ-targeted antidiabetics. J.Med.Chem. 60 4584 PMID: 28485590

Motani et al (2009) INT131: a selective modulator of PPARγ. J.Mol.Biol. 386 1301 PMID: 19452630


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关键词: INT 131, INT 131 supplier, INT131, PPARγ, PPARgamma, partial, agonists, antidiabetics, agent, Peroxisome, Proliferator-activating, Receptors, in, vivo, diabetes, 7423, Tocris Bioscience

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