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PBI-4050 sodium salt(Setogepram(sodium salt))
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。
PBI-4050 sodium salt(Setogepram(sodium salt))图片
CAS NO:1254472-97-3
规格:98%
分子量:228.26
包装与价格:
包装价格(元)
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PBI-4050用作GPR40激动剂和GPR84拮抗剂或反向激动剂。
CAS:1254472-97-3
分子式:C13H17NaO2
分子量:228.26
纯度:98%
存储:Store at -20°C

Background:

PBI-4050 acts as an agonist for GPR40 and as an antagonist or inverse agonist for GPR84.



PBI-4050, a synthetic analogue of a medium-chain length fatty acid, binds to FFA receptor 1 (FFAR1/GPR40) and GPR84. To determine the potential role of PBI-4050 on diabetic kidney disease, The accelerated model of type 2 diabetic nephropathy, eNOS-/- db/db mice are utilized. Mice are treated with either vehicle or PBI-4050 (100 mg/kg) by daily gavage from 8-20 weeks of age. eNOS-/- db/db mice are moderately hypertensive, and PBI-4050 has no effect on blood pressure. Furthermore, compared with vehicle-treated mice, which exhibit a decrease in glomerular filtration rate (GFR) from 8-20 weeks, PBI-4050 preserves GFR. Podocyte number per glomerulus section markedly decreases from 8-20 weeks of age in vehicle-treated mice, while PBI-4050 treatment significantly slows this loss[1].


[1]. Li Y, et al. Fatty acid receptor modulator PBI-4050 inhibits kidney fibrosis and improves glycemic control. JCI Insight. 2018 May 17;3(10). pii: 120365.


 
 
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