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SAG hydrochloride (912545-86-9(free base))

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Catalog No. T4211Cas No. 2095432-58-7
Alias Smoothened Agonist HCl

SAG hydrochloride (912545-86-9(free base)) (Smoothened Agonist HCl) acts as an SMO agonist.

SAG hydrochloride (912545-86-9(free base))

SAG hydrochloride (912545-86-9(free base))

🥰Excellent
Purity: 99.19%
Catalog No. T4211Alias Smoothened Agonist HClCas No. 2095432-58-7
SAG hydrochloride (912545-86-9(free base)) (Smoothened Agonist HCl) acts as an SMO agonist.
Pack SizePriceAvailabilityQuantity
1 mg$47In Stock
5 mg$97In Stock
10 mg$155In Stock
25 mg$289In Stock
50 mg$396In Stock
100 mg$593In Stock
1 mL x 10 mM (in DMSO)$113In Stock
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Purity:99.19%
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Product Introduction

Bioactivity
Description
SAG hydrochloride (912545-86-9(free base)) (Smoothened Agonist HCl) acts as an SMO agonist.
In vitro
SAG regulates Smo activity by binding directly to the Smo heptahelical bundle. [1] SAG induces Smo-dependent signaling through Gli in a GRK2-dependent way. [2] SAG also (1 nM) induces proliferation of neuronal and glial precursors without affecting the differentiation pattern of newly produced cells.
In vivo
In the adult rat hippocampus, the intracerebroventricular administration of SAG (2.5 nM) significantly increases the number of newly generated cells and extends survival of hippocampal cells. [3] In mice, SAG (20 μg/g, i.p.) effectively prevents GC-induced neonatal cerebellar developmental abnormalities.
Animal Research
Animal Models: RatFormulation: DMSODosages: 2.5 nMAdministration: Intracerebroventricular administration(Only for Reference)
AliasSmoothened Agonist HCl
Chemical Properties
Molecular Weight526.52
FormulaC28H29Cl2N3OS
Cas No.2095432-58-7
SmilesCl.CN[C@H]1CC[C@@H](CC1)N(Cc1cccc(c1)-c1ccncc1)C(=O)c1sc2ccccc2c1Cl
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: 38 mg/mL (72.2 mM)
DMSO: 66 mg/mL (125.4 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM1.8993 mL9.4963 mL18.9926 mL94.9632 mL
5 mM0.3799 mL1.8993 mL3.7985 mL18.9926 mL
10 mM0.1899 mL0.9496 mL1.8993 mL9.4963 mL
20 mM0.0950 mL0.4748 mL0.9496 mL4.7482 mL
50 mM0.0380 mL0.1899 mL0.3799 mL1.8993 mL
DMSO
1mg5mg10mg50mg
100 mM0.0190 mL0.0950 mL0.1899 mL0.9496 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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