SIRT7 inhibitor 97491
CAS No. 1807758-81-1
SIRT7 inhibitor 97491( —— )
Catalog No. M28213 CAS No. 1807758-81-1
SIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 222 | Get Quote |
|
| 10MG | 335 | Get Quote |
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| 25MG | 566 | Get Quote |
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| 50MG | 806 | Get Quote |
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| 100MG | 1098 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameSIRT7 inhibitor 97491
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NoteResearch use only, not for human use.
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Brief DescriptionSIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.
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DescriptionSIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.(In Vitro):SIRT7 inhibitor 97491 decreased SIRT7 activity in a dose-dependent manner. SIRT7 inhibitor 97491 induced expression of p53 and its acetylation by inhibited SIRT7. SIRT7 inhibitor 97491 (1-10 μM) reduces cell growth in MES-SA cells, without causing cytotoxicity in HEK293 cells.(In Vivo):In xenograft mice, SIRT7 inhibitor 97491 (2 mg/kg; i.p) inhibited tumor growth. SIRT7 inhibitor 97491 upregulated apoptotic effects through the caspase related proteins and inhibited cancer growth in vivo.
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In VitroCell Proliferation Assay Cell Line:Human uterine sarcoma MES-SA cells Concentration:1, 5, 10 μM Incubation Time:72 hours Result:Led to more than 50% decrease in cell proliferation at concentrations of 5 and 10 μM. Cell Cytotoxicity Assay Cell Line:Human embryonic kidney cell line HEK293 cells Concentration:1, 5, 10 μM Incubation Time:24 hours Result:HEK293 cells were almost unaffected.
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In VivoAnimal Model:Balb/c nude mice (18-20 g; 6-8 weeks old) with MES-SA cells Dosage:2 mg/kg Administration:Intraperitoneally injected; for 3 weeks, except on weekends. Result:Inhibited cancer growth in vivo.
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Synonyms——
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PathwayChromatin/Epigenetic
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TargetSirtuin
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Recptorβ-Lactamase
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Research Area——
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Indication——
Chemical Information
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CAS Number1807758-81-1
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Formula Weight285.73
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Molecular FormulaC15H12ClN3O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 500 mg/mL (1749.90 mM)
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SMILESNc1cccc(Nc2ncc(-c(cc3)ccc3Cl)o2)c1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Papp-Wallace KM, et al. Strategic Approaches to Overcome Resistance against Gram-Negative Pathogens Using β-Lactamase Inhibitors and β-Lactam Enhancers: Activity of Three Novel Diazabicyclooctanes WCK 5153, Zidebactam (WCK 5107), and WCK 4234. J Med Chem. 2018 May 10;61(9):4067-4086.
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