SIRT2-IN-9

Modify Date: 2024-10-04 12:29:54

SIRT2-IN-9 Structure
SIRT2-IN-9 structure
Common Name SIRT2-IN-9
CAS Number 522650-91-5 Molecular Weight 438.57
Density N/A Boiling Point N/A
Molecular Formula C21H22N6OS2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of SIRT2-IN-9


SIRT2-IN-9 (compound 12) is a selective inhibitor of SRIT2 with an IC50 value of 1.3 μM. SIRT2-IN-9 inhibits proliferative activity of MCF-7 breast cancer cells. SIRT2-IN-9 can be used for the research of cancer[1].

 Names

Name SIRT2-IN-9

 SIRT2-IN-9 Biological Activity

Description SIRT2-IN-9 (compound 12) is a selective inhibitor of SRIT2 with an IC50 value of 1.3 μM. SIRT2-IN-9 inhibits proliferative activity of MCF-7 breast cancer cells. SIRT2-IN-9 can be used for the research of cancer[1].
Related Catalog
Target

SIRT2:1.3 μM (IC50)

SIRT1:>300 μM (IC50)

SIRT3:>300 μM (IC50)

In Vitro SIRT2-IN-9 (1-100 μM; 15 min) dose-dependently inhibits SRIT2 with an IC50 value of 1.3 μM, and inhibits SRIT1 and SRIT3 with IC50s >300 μM[1]. SIRT2-IN-9 (0-50 μM; 72 h) affects cell viability of MCF-7 cells[1]. SIRT2-IN-9 (0-50 μM; 6 h) affects acetylation of α-tubulin protein[1]. Cell Proliferation Assay[1] Cell Line: MCF-7 breast cancer cell line Concentration: 0-50 μM Incubation Time: 72 hours Result: Dose-dependently inhibited cell proliferation of MCF-7 breast cancer cells. Western Blot Analysis[1] Cell Line: MCF-7 breast cancer cell line Concentration: 6.25, 12.5, 25 and 50 μM Incubation Time: 6 hours Result: Dose-dependently increased acetylation of α-tubulin protein.
References

[1]. Yang SY, Li LL. The purposes of 5H- [1,2,4] triazine [5,6-b] indole derivatives of 3 substitutions. CN108309982A. 2017.

 Chemical & Physical Properties

Molecular Formula C21H22N6OS2
Molecular Weight 438.57
Storage condition -20°C
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