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SAG

Cat. No. M14928
SAG Structure
Size Price Availability Quantity
1mg USD 55  USD55 In stock
5mg USD 145  USD145 In stock
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Quality Control & Documentation
Biological Activity

SAG is a potent Smoothened (Smo) receptor agonist (EC50=3 nM; Kd=59 nM). SAG activates the Hedgehog signaling pathway and counteracts Cyclopamine inhibition of Smo.

Chemical Information
Molecular Weight 490.06
CAS Number 912545-86-9
Solubility (25°C) DMSO ≥ 38 mg/mL
Storage 2-8°C, protect from light
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Deming Guo, et al. Investigation of sag behaviour for aluminium conductor steel reinforced considering tensile stress distribution

[2] Erdal Sag. ECI Biocommentary: Erdal Sag

[3] Eef van der Worp, et al. Variation in sag values in daily disposable, reusable and toric soft contact lenses

[4] Aiyu Liu, et al. SAG expression associates with COPB2-related signaling and a poorer prognosis in breast cancer

[5] Joshua A Metzl. Naviculocuneiform Sag in the Acquired Flatfoot: What to Do

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MRT-81 

MRT-81 is a potent antagonist of human and rodent smoothened (Smo) receptors, with an IC50 value of 41 nM in the Shh-light2 cells. MRT-81 has potent hedgehog inhibiting activity. MRT-81 can be used for the research of cancer.

Fluticasone

Fluticasone is a corticosteroid and Smo agonist with an IC50 of 99 nM, which activates the Hedgehog signaling pathway and promotes the proliferation of primary neural stem or precursor cells, and can be used in respiratory related studies.

HhAntag 

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PF-5274857 hydrochloride 

PF-5274857 hydrochloride is a potent, selective, orally active and brain-penetrant antagonist of Smo, with an IC50 of 5.8 nM and Ki of 4.6 nM. PF-5274857 hydrochloride has potential for research of tumor types including brain tumors and brain metastasis driven by an activated Hh pathway.

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Keywords: SAG supplier, Smo, inhibitors, activators


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