Smoothened Agonist (SAG) HCl
Names
[ CAS No. ]:
2095432-58-7
[ Name ]:
Smoothened Agonist (SAG) HCl
Biological Activity
[Description]:
SAG (hydrochloride) is a potent Smo receptor agonist, and activates the Hedgehog signaling pathway, with a Kd of 59 nM.
[Related Catalog]:
[Target]
Kd: 59 nM (Smo)[1].
[In Vitro]
SAG (hydrochloride) acts downstream of Ptch1 in the Hh pathway and counteracts cyclopamine inhibition of Smo. SAG induces firefly luciferase expression in Shh-LIGHT2 cells with an EC50 of 3 nM and then inhibits expression at higher concentrations. In Smo-expressing Cos-1 cells, SAG yields an apparent dissociation constant (KD) of 59 nM for the SAG/Smo complex[1]. SAG and purmorphamine verride the inhibitory effect of robotnikinin since Smo functions downstream of Shh/Ptc1[2].
[In Vivo]
In CD-1 mice, SAG (1.0 mM) or NELL-1 (600 μg/ml) alone results in increased bone formation at 4 and 8 weeks, but significantly greater bone formation with both components combined (SAG + NELL-1). The combination of the two compounds exhibits a significant increase in new bone formation, accompanied by increased defect vascularization[3]. SAG (15, 17, or 20 mg/kg, i.p.) induces pre-axial polydactyly prevalently. The highest SAG dose is effective in ca. 80% of the embryos and increased Gli1 and Gli2 mRNA expression in the limb bud, with Gli1 mRNA being the most upregulated[4].
[References]
[Related Small Molecules]
SAG.HCI
|
Purmorphamine
|
LDE225 (NVP-LDE225,Erismodegib)
|
PF-04449913
|
Jervine
|
LY2940680
|
BMS-833923
|
LEQ506
|
MK-4101
|
MRT-83
|
PF-5274857
|
Saridegib
Chemical & Physical Properties
[ Molecular Formula ]:
C28H29Cl2N3OS
[ Molecular Weight ]:
526.52
[ Storage condition ]:
2-8℃
Related Compounds
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