MDL-800

CAS No. 2275619-53-7

MDL-800 ( MDL800 )

Catalog No. M13621 CAS No. 2275619-53-7

MDL-800 (MDL800) is a first-in-class, selective, cellular active SIRT6 allosteric activator.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 108 Get Quote
10MG 160 Get Quote
25MG 271 Get Quote
50MG 406 Get Quote
100MG 597 Get Quote
500MG 1251 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    MDL-800
  • Note
    Research use only, not for human use.
  • Brief Description
    MDL-800 (MDL800) is a first-in-class, selective, cellular active SIRT6 allosteric activator.
  • Description
    MDL-800 (MDL800) is a first-in-class, selective, cellular active SIRT6 allosteric activator, increases SIRT6 deacetylation activity with EC50 of 10.3 uM in RHKK-ac-AMC and FDL assays; dramatically enhanced SIRT6 deacetylation activity by more than 22-fold, displays no activity toward SIRT1, SIRT3, SIRT4, and HDAC1-11 at 50-100 uM, as well as >10-fold selectivity toward SIRT2, SIRT5, and SIRT7; activates SIRT6 through a surface allosteric site induces H3K9ac and H3K56ac deacetylation and represses proliferation of HCC cells (IC50=23.3 uM); inhibits xenograft tumor growth of HCC cells in immunocompromised mice by activating the deacetylase activity of SIRT6.
  • Synonyms
    MDL800
  • Pathway
    Chromatin/Epigenetic
  • Target
    Sirtuin
  • Recptor
    Sirtuin
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2275619-53-7
  • Formula Weight
    626.29
  • Molecular Formula
    C21H16BrCl2FN2O6S2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(OC)C1=CC(NS(=O)(C2=CC(Cl)=CC(Cl)=C2)=O)=CC=C1S(=O)(NC3=CC(Br)=C(F)C=C3C)=O
  • Chemical Name
    methyl 2-(N-(5-bromo-4-fluoro-2-methylphenyl)sulfamoyl)-5-((3,5-dichlorophenyl)sulfonamido)benzoate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Huang Z, et al. Nat Chem Biol. 2018 Oct 29. doi: 10.1038/s41589-018-0150-0.
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