research use only

3-TYP Sirtuin inhibitor

Cat.No.S8628

3-TYP (3-(1H-1,2,3-triazol-4-yl) pyridine) is a selective SIRT3 inhibitor which is selective for Sirt3 over Sirt1 and Sirt2. The IC50 values for SITR1, SIRT2, SIRT3 are 88 nM, 92 nM, 16 nM respectively.
3-TYP Sirtuin inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 146.15

Jump to

Quality Control

Batch: Purity: 99.98%
99.98

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
HeLa Cytotoxicity assay 1 to 6 hrs Cytotoxicity against human HeLa cells assessed as cell death after 1 to 6 hrs, IC50=4.7μM 22835719
SK-MEL-28 Function assay 100 uM 24 hrs Reduction in ATP level in human SK-MEL-28 cells at 100 uM maintained in Locke's solution after 24 hrs by luciferase-based assay in absence of GF and glucose 22835719
SK-MEL-28 Function assay 100 uM 24 hrs Increase in superoxide level in human SK-MEL-28 cells maintained in medium containing GF and glucose at 100 uM after 24 hrs by DHE-based fluorescence ssay 22835719
SK-MEL-28 Function assay 100 uM 24 hrs Increase in superoxide level in human SK-MEL-28 cells at 100 uM maintained in Locke's solution after 24 hrs by DHE-based fluorescence assay in absence of GF and glucose 22835719
Click to View More Cell Line Experimental Data

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (684.22 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 29 mg/mL

Water : 1.25 mg/mL

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg
g
μL

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO
%
% Tween 80
% ddH2O
% DMSO
+
%

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 addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 146.15 Formula

C7H6N4

Storage (From the date of receipt)
CAS No. 120241-79-4 Download SDF Storage of Stock Solutions

Synonyms 3-(1H-1,2,3-triazol-4-yl) pyridine Smiles C1=CC(=CN=C1)C2=NNN=C2

Mechanism of Action

Targets/IC50/Ki
SIRT3
(cell-free)
16 nM
SIRT1
(cell-free)
88 nM
SIRT2
(cell-free)
92 nM
In vitro
Melatonin-induced increases in deacetylated-SOD2 expression and SOD2 activity are significantly attenuated by 3-TYP in HepG2 cells exposed to Cd (cadmium).
References

Tech Support

Handling Instructions

Tel: +1-832-582-8158 Ext:3

If you have any other enquiries, please leave a message.

Signaling Pathway Map