Butaprost is a selective prostaglandin E receptor (EP2) agonist with an EC50 of 33 nM and a Ki of 2.4 µM for murine EP2 receptor. Butaprost is less activity against murine EP1, EP3 and EP4 receptors. Butaprost attenuates fibrosis by hampering TGF-beta/Smad2 signalling[1][2][3].
Molecular Weight:
408.57
Purity:
99.2
CAS Number:
[69685-22-9]
Formula:
C24H40O5
Target:
Prostaglandin Receptor,TGF-beta/Smad
Application Notes:
MCE Product type: Reference compound1
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