Selisistat (SEN0014196; EX 527)
This product is for research use only, not for human use. We do not sell to patients.
For small sizes, please check our retail website as below: www.invivochem.com
Size | Price | Stock |
---|---|---|
500mg | $510 | In Stock |
1g | $780 | In Stock |
5g | $1170 | In Stock |
Cat #: V0429 CAS #: 49843-98-3 Purity ≥ 98%
Description: Selisistat (formerly SEN-0014196; EX-527) is a novel, highly potent and selective inhibitor of SIRT1 (Sirtuin1, a NAD-dependent and class III histone deacetylase enzyme) with important biological activity.
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- Physicochemical and Storage Information
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- Related Biological Data
- Stock Solution Preparation
- Quality Control Documentation
Molecular Weight (MW) | 248.71 |
---|---|
Molecular Formula | C13H13ClN2O |
CAS No. | 49843-98-3 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 50 mg/mL (201.0 mM)r |
Water: <1 mg/mLr | |
Ethanol: 18 mg/mL (72.4 mM) | |
Solubility In Vivo | 1% DMSO+30% polyethylene glycol+1% Tween 80: 14mg/mL |
SMILES Code | O=C(C1C(NC2=C3C=C(Cl)C=C2)=C3CCC1)N |
Synonyms | Selisistat; EX 527; SEN 0014196; EX527; SEN-0014196; SEN0014196; EX-527 |
Protocol | In Vitro | Selisistat (1-10 μM) inhibits the deacetylation activity of both human SirT1 and Drosophila Sir2 in transfected cells. |
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In Vivo | Selisistat (5 and 20 mg/kg, PO, daily; transgenic R6/2 mice beginning at 4.5 weeksof age to death) is protective in the R6/2 mouse model of Huntington’s disease (HD). |
These protocols are for reference only. InvivoChem does not
independently validate these methods.
Solvent volume to be added | Mass (the weight of a compound) | |||
---|---|---|---|---|
Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 4.0207 mL | 20.1037 mL | 40.2075 mL | 80.4149 mL |
5mM | 0.8041 mL | 4.0207 mL | 8.0415 mL | 16.0830 mL |
10mM | 0.4021 mL | 2.0104 mL | 4.0207 mL | 8.0415 mL |
20mM | 0.2010 mL | 1.0052 mL | 2.0104 mL | 4.0207 mL |
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start)
×
Volume(start)
=
Concentration(final)
×
Volume(final)
This equation is commonly abbreviated as: C1 V1 = C2 V2
Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg
Average weight of animals g
Dosing volume per animal µL
Number of animals
Step Two: Enter the in vivo formulation
%DMSO
+
%
+
%Tween 80
+
%ddH2O
Calculation Results:
Working concentration:
mg/ml;
Method for preparing DMSO master liquid:
mg
drug pre-dissolved in
µL
DMSO(Master liquid concentration
mg/mL)
,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:
Take
µL
DMSO master liquid, next add
µL
PEG300, mix and clarify, next add
µL
Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
Note:
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.