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首页-小分子抑制剂&激动剂-GPCR-GPR119-PSN632408
PSN632408

Chemical Structure : PSN632408

CAS No.: 857652-30-3

PSN632408 (PSN 632408)

货号: PC-20444Not For Human Use, Lab Use Only.

PSN632408 (PSN 632408) is a selective small-molecule GPR119 agonist with cAMP EC50 of 7.9 and 5.6 uM for mouse and human GPR119 receptor, respectively.

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5 mg ¥780 In stock
10 mg ¥1180 In stock
25 mg ¥2180 In stock
50 mg ¥3680 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

PSN632408 (PSN 632408) is a selective small-molecule GPR119 agonist with cAMP EC50 of 7.9 and 5.6 uM for mouse and human GPR119 receptor, respectively.
PSN632408 is selective for GPR119, shows no acitvities against cannabinoid receptors CB1 and CB2, PPARα, PPARγ, as well as a set of 107 targets comprising GPCRs, ligand-gated ion channels, other receptors.
PSN632408 (30-100 mg/kg, i.p.) acutely reduce food intake in freely feeding male Sprague-Dawley rats, did not significantly alter locomotor activity.
PSN632408 (100 mg, Oral) reduces body weight gain and white adipose tissue deposition upon subchronic oral administration to high-fat-fed rats.

物理化学性质&存储条件

分子量 360.41
分子式 C18H24N4O4
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

tert-butyl 4-((3-(pyridin-4-yl)-1,2,4-oxadiazol-5-yl)methoxy)piperidine-1-carboxylate

参考文献

1. Overton HA,, et al. Cell Metab. 2006 Mar;3(3):167-75.

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