Chemical Structure : TIPP-204
货号: PC-23874Not For Human Use, Lab Use Only.
TIPP-204 is a potent, selective PPARδ agonist with EC50 of 0.91 nM, >250-fold selective PPARα and PPARγ.
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TIPP-204 is a potent, selective PPARδ agonist with EC50 of 0.91 nM, >250-fold selective PPARα and PPARγ.
TIPP-204 exhibits extremely potent PPARδ transactivation activity, comparable with or somewhat superior to that of the known PPARδ-selective agonist GW-501516.
TIPP-204 does not significantly activate VDR, PPARγ, LXRα, RARα or RXRα at concentrations up to 300 nM.
TIPP-204 regulated the expression of genes involved in lipid and glucose homeostasis.
分子量 | 469.48 | |
分子式 | C24H27F4NO4 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Kasuga J, et al. Bioorg Med Chem. 2007 Aug 1;15(15):5177-90.
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