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Sirt1/2-IN-2

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Catalog No. T79563Cas No. 670267-73-9

Sirt1/2-IN-2 (compound hsa55) is a dual inhibitor, targeting SIRT1 with an IC50 of 1.8 μM and SIRT2 with an IC50 of 2.4 μM. It effectively inhibits p53 deacetylation while enhancing the acetylation of p53 and α-tubulin, promoting apoptosis and exhibiting anti-proliferative effects on human leukemia cell lines [1].

Sirt1/2-IN-2

Sirt1/2-IN-2

😃Good
Catalog No. T79563Cas No. 670267-73-9
Sirt1/2-IN-2 (compound hsa55) is a dual inhibitor, targeting SIRT1 with an IC50 of 1.8 μM and SIRT2 with an IC50 of 2.4 μM. It effectively inhibits p53 deacetylation while enhancing the acetylation of p53 and α-tubulin, promoting apoptosis and exhibiting anti-proliferative effects on human leukemia cell lines [1].
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50 mgInquiry8-10 weeks
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Product Introduction

Bioactivity
Description
Sirt1/2-IN-2 (compound hsa55) is a dual inhibitor, targeting SIRT1 with an IC50 of 1.8 μM and SIRT2 with an IC50 of 2.4 μM. It effectively inhibits p53 deacetylation while enhancing the acetylation of p53 and α-tubulin, promoting apoptosis and exhibiting anti-proliferative effects on human leukemia cell lines [1].
In vitro
Sirt1/2-IN-2 (compound hsa55) induces apoptosis in various tumor cell lines at 5 μM over 48 hours, with IC50 values of 13 μM for MV4-11, 11.5 μM for MOLM-13, 34.4 μM for THP1, and 27.5 μM for Jurkat cells [1]. At 100 μM for 30 minutes, it reduces the thermal stability of SIRT1 and SIRT2 proteins at different temperatures. At 25 μM and 30 μM over 24 hours, the compound increases acetylated p53 and α-tubulin levels in MOLM-13 cells [1].
Chemical Properties
Molecular Weight398.46
FormulaC18H14N4O3S2
Cas No.670267-73-9
Storage & Solubility Information
StorageShipping with blue ice.

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