SRT 1720

CAS No. 925434-55-5

SRT 1720 ( SRT-1720;SRT1720 )

Catalog No. M16631 CAS No. 925434-55-5

A potent, selective SIRT1 activator with EC1.5 of 0.16 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 30 In Stock
5MG 48 In Stock
10MG 76 In Stock
25MG 151 In Stock
50MG 290 In Stock
100MG 412 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SRT 1720
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective SIRT1 activator with EC1.5 of 0.16 uM.
  • Description
    A potent, selective SIRT1 activator with EC1.5 of 0.16 uM; displays good selectivity for activation of SIRT1 versus SIRT2 (EC1.5=37 uM) and SIRT3 (EC1.5>300 uM); 1,000-fold more potent than resveratrol; improve insulin sensitivity, lower plasma glucose, and increase mitochondrial capacity in obese mice model.
  • Synonyms
    SRT-1720;SRT1720
  • Pathway
    Chromatin/Epigenetic
  • Target
    Sirtuin
  • Recptor
    SIRT1;SIRT2
  • Research Area
    Metabolic Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    925434-55-5
  • Formula Weight
    469.56
  • Molecular Formula
    C25H23N7OS
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    C1CN(CCN1)CC2=CSC3=NC(=CN23)C4=CC=CC=C4NC(=O)C5=NC6=CC=CC=C6N=C5
  • Chemical Name
    2-Quinoxalinecarboxamide, N-[2-[3-(1-piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl]phenyl]-

Shipping & Storage Information

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

Reference

1. Milne JC, et al. Nature. 2007 Nov 29;450(7170):712-6.
2. Pacholec M, et al. J Biol Chem. 2010 Mar 12;285(11):8340-51.
3. Funk JA, et al. J Pharmacol Exp Ther. 2010 May;333(2):593-601.
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