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Smo inhibitor SAG

Chemical Structure : Smo inhibitor SAG

CAS No.: 912545-86-9

Smo inhibitor SAG (SAG)

Catalog No.: PC-43256Not For Human Use, Lab Use Only.

SAG is a small molecule Hedgehog (Hh) pathway agonist with EC50 of 3 nM, specifically binds to the Smoothened (Smo) heptahelical bundle (Kd=59 nM).

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

SAG is a small molecule Hedgehog (Hh) pathway agonist with EC50 of 3 nM, specifically binds to the Smoothened (Smo) heptahelical bundle (Kd=59 nM).
SAG effectively activates Shh target gene transcription through the Smoothened (Smo) protein, acts downstream of Ptch1 in the Hh pathway and counteracts cyclopamine inhibition of Smo.
SAG increases Cldn5 expression, decreases endoneurial capillary permeability, and restores thermal algesia to diabetic mice.
SAG inhibits melanin synthesis in melanocytes and pigmentation in a human skin model.

Physicochemical Properties

M.Wt 490.0594
Formula C28H28ClN3OS
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 38 mg/mL

Chemical Name/SMILES

Benzo[b]thiophene-2-carboxamide, 3-chloro-N-[trans-4-(methylamino)cyclohexyl]-N-[[3-(4-pyridinyl)phenyl]methyl]-

References

1. Chen JK, et al. Proc Natl Acad Sci U S A. 2002 Oct 29;99(22):14071-6.

2. Choi H, et al. PLoS One. 2016 Dec 12;11(12):e0168025.

3. Stanton BZ, et al. Nat Chem Biol. 2009 Mar;5(3):154-6.

4. Chapouly C, et al. Cardiovasc Res. 2016 Feb 1;109(2):217-27.

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