SIRT6-IN-6
Based on 1 Customer Validation
SIRT6-IN-6 (compound 6d) is a potent and selective SIRT6 inhibitor with an IC50 of 4.93 μM and a Ki of ~10 μM. SIRT6-IN-6 shows selectivity against other members of the HDAC family (SIRT1-3 and HDAC1-11). SIRT6-IN-6 significantly increases the level of glucose transporter GLUT-1, thereby reducing blood glucose in a mouse model of type 2 diabetes. SIRT6-IN-6 can be used for type 2 diabetes research.
For research use only. We do not sell to patients.
- Purity: 98.59%
- CAS No.: 23491-48-7
- Formula: C11H16N4O2
- Molecular Weight:236.28
-
Storage:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Biological Activity
|
SIRT6 4.93 μM (IC50) |
SIRT1 >200 μM (IC50) |
SIRT2 >200 μM (IC50) |
SIRT3 >200 μM (IC50) |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| SK-HEP1 | IC50 |
4.26 μM
Compound: 5a
|
Cytotoxicity against human SK-HEP1 cells incubated for 72 hrs by CCK8 assay
Cytotoxicity against human SK-HEP1 cells incubated for 72 hrs by CCK8 assay
|
[PMID: 39323022] |
Chemical Information
-
CAS No. 23491-48-7
-
Appearance Solid
-
Molecular Weight 236.28
-
Formula C11H16N4O2
-
Color Light yellow to yellow
-
SMILES
O=N(=O)C1=CC=C(C=C1N)N2CCN(C)CC2
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Purity & Documentation
-
Data Sheet (268 KB)
-
SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
-
Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)