tcsc1135 Purmorphamine

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Product Description

Purmorphamine is a smoothened receptor agonist with an EC50 of 1 μM.

IC50 & Target: IC50: 1.5 μM (Smoothened)

In Vitro: Purmorphamine (10, 20 μM) in combination with sirolimus significantly decreases cell numbers according to the MTT assay. Purmorphamine induces up-regulation of alkaline phosphatase activity and expression of RUNX-2 at day 14. Up-regulation of osteocalcin is detected at the 3 and 5 μM doses of purmorphamine on day 14 post-induction. Matrix mineralization remains unchanged in the presence or absence of purmorphamine[1]. Purmorphamine induces STAT3 phosphorylation in mouse ES cell line ES14 and mesenchymal stem cell line C3H10T1/2[2]. Purmorphamine up-regulates the expressionof markers of the osteoblast phenotype-ALP activity and bone-like nodule formationd-in human bonemarrow mesenchymal cells[3].

Information

CAS No483367-10-8
FormulaC31H32N6O2
Clinical Informationclinicalinformation
PathwayStem Cell/Wnt
Autophagy
TargetSmo
Autophagy

Specifications

Purity / Grade>98%
Solubility10 mM in DMSO
Smilessmiles

Misc Information

Alternative NamesShh Signaling Antagonist VI
Observed Molecular Weight520.62
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