SIRT1-IN-2

Modify Date: 2024-01-05 21:59:42

SIRT1-IN-2 structure	Common Name	SIRT1-IN-2
	CAS Number	2470969-89-0	Molecular Weight	250.72
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₃H₁₅ClN₂O	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of SIRT1-IN-2

SIRT1-IN-2 (compound 3h) is a potent and selective SIRT1 (silent information regulator 1) inhibitor, with an IC50 of 1.6 μM[1].

Name	SIRT1-IN-2

Description	SIRT1-IN-2 (compound 3h) is a potent and selective SIRT1 (silent information regulator 1) inhibitor, with an IC50 of 1.6 μM[1].
Related Catalog	Signaling Pathways >> Epigenetics >> Sirtuin Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> Sirtuin
Target	SIRT1:1.6 μM (IC50) SIRT2:39 μM (IC50)
In Vitro	SIRT1-IN-2 (compound 3h) (0-100 μM, 48 h) inhibits the proliferation of Human cancer cell lines including K562, HCT-116, HepG2, A549, and MCF-7, and shows significantly less cytotoxic on 293T cells and HUVEC[1]. Cell Cytotoxicity Assay Cell Line: Human cancer cell lines (K562, HCT-116, H460, HepG2, A549, HT-29, MCF-7) and normal cell lines (293T, HUVEC). [1] Concentration: 0, 0.01，0.1，1，10，100 μM Incubation Time: 48 h Result: Inhibited the proliferation of Human cancer cell lines including K562, HCT-116, HepG2, A549, and MCF-7, with IC50 values of 51, 37, 40, 48, and 48 μM, respectively. And showed significantly less cytotoxic on 293T cells and HUVEC, with IC50 values of > 100 and 45 μM, respectively.
References	[1]. Laaroussi H, Ding Y, Teng Y, et al. Synthesis of indole inhibitors of silent information regulator 1 (SIRT1), and their evaluation as cytotoxic agents. Eur J Med Chem. 2020;202:112561.

Molecular Formula	C₁₃H₁₅ClN₂O
Molecular Weight	250.72

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