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SIRT7 inhibitor 97491

SKU: orb1303559

Description

The small molecule inhibitor 97491 selectively targets SIRT7 (IC50 = 325 nM), functioning as a specific HDAC inhibitor. It induces apoptosis via caspase activation and is a valuable research tool for studying SIRT7's role in cancer biology and cellular processes in vitro.

Research Area

Cell Biology, Epigenetics & Chromatin, Epigenetics & Chromatin; Pharmacology & Drug Discovery, Molecular Biology

Images & Validation

Key Properties

CAS Number1807758-81-1
MW285.73
Purity99.79% (May vary between batches)
FormulaC15H12ClN3O
SMILESNc1cccc(Nc2ncc(o2)-c2ccc(Cl)cc2)c1
TargetSirtuin
SolubilityDMSO:250 mg/mL (874.95 mM);10% DMSO+90% Corn Oil:5 mg/mL (17.5 mM)

Bioactivity

Target IC50
SIRT7:325 nM
In Vivo
The SIRT7 inhibitor 97491 (2 mg/kg; intraperitoneally injected; for 3 weeks, except on weekends) effectively suppresses tumor growth in xenograft mice. Utilizing Balb/c nude mice (18-20 g; 6-8 weeks old) implanted with MES-SA cells, the dosage administered was 2 mg/kg via intraperitoneal injection over a three-week period, excluding weekends. The outcome was a significant inhibition of cancer growth in vivo.
In Vitro
SIRT7 inhibitor 97491 (1-10 μM) effectively reduces the proliferation of human uterine sarcoma MES-SA cells by over 50% at 5 and 10 μM after 72 hours, without cytotoxic effects on HEK293 human embryonic kidney cells after 24 hours of exposure, indicating selective action.

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

deacetylase, Inhibitor, p53 K373/382, inhibit, Apoptosis, Sirtuin, SIRT7, SIRT7 inhibitor 97491, SIRT-7 inhibitor 97491, tumor
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Quality Guarantee

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Key Properties

No computed properties available.

Protocol Information

Available Sizes

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1 mg
$ 140.00
5 mg
$ 290.00
1 ml x 10 mM (in DMSO)
$ 320.00
10 mg
$ 420.00
25 mg
$ 670.00
50 mg
$ 940.00
100 mg
$ 1,260.00
DispatchUsually dispatched within 5-10 working days
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