Sirt1/2-IN-2

SKU:BHB21902076
Overview
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Sirt1/2-IN-2 (CAS 670267-73-9) is an inhibitor supplied as a solid. Relevant to Cell Cycle/DNA Damage and Apoptosis research. Molecular formula C18H14N4O3S2, molecular weight 398.46 g/mol.
Purity 90%
CAS Number 670267-73-9
Molecular Weight 398.46 g/mol
Form Solid
Storage Powder -20°C; in solvent -80°C
Options selector
Catalog no. Size
HY-155727-5MG 5 mg
HY-155727-10MG 10 mg
HY-155727-25MG 25 mg
HY-155727-50MG 50 mg
HY-155727-100MG 100 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
  • Lead time: shown per option in the variant selector.
  • Storage: Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
CAS no. 670267-73-9
Applications
  • Functional Assay (In Vitro)
Molecular weight 398.46
Molecular formula C18H14N4O3S2
Purity 90%
SMILES O=S(NC1=CC(SC2=NN=CN2)=C(C3=C1C=CC=C3)O)(C4=CC=CC=C4)=O
Form Solid
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-155727
Main SKU BHB21902076
Inhibitors

Compound Overview

Sirt1/2-IN-2 is a dual inhibitor of SIRT1 and SIRT2, with IC50 values of 1.8 μM and 2.4 μM, respectively. It completely blocks p53 deacetylation and increases p53 and α-tubulin acetylation, inducing apoptosis and showing anti-proliferative activity against human leukemia cell lines[1]. It is supplied as a white to off-white solid (C18H14N4O3S2, MW 398.46) at 90% purity.

Physical & Chemical Properties

CAS Number 670267-73-9
Molecular Formula C18H14N4O3S2
Molecular Weight 398.46 g/mol
Purity 90%
Appearance Solid
Color White to off-white
SMILES O=S(NC1=CC(SC2=NN=CN2)=C(C3=C1C=CC=C3)O)(C4=CC=CC=C4)=O
Signaling Pathway Cell Cycle/DNA Damage; Apoptosis; Epigenetics
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.

Biological Activity

IC50 & Target

IC50: 1.8 μM (SIRT1), 2.4 μM (SIRT2), 65 μM (SIRT3)[1]

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Cai H, et al. Discovery of Novel SIRT1/2 Inhibitors with Effective Cytotoxicity against Human Leukemia Cells. J Chem Inf Model. 2023 Aug 14;63(15):4780-4790.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

Sirt1/2-IN-2 (compound hsa55) (5 μM; 48 h) induces apoptosis in several tumor cell types, with IC50 values of 13 μM (MV4-11), 11.5 μM (MOLM-13), 34.4 μM (THP1), and 27.5 μM (Jurkat)[1]. At 100 μM (30 min), Sirt1/2-IN-2 lowers the thermal stability of both SIRT1 and SIRT2 proteins across a range of temperatures, and at 25 μM and 30 μM (24 h) it raises the level of acetylated p53 and α-tubulin in MOLM-13 cells[1].

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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