3-TYP

CAS No. 120241-79-4

3-TYP ( 3-TYP )

Catalog No. M17877 CAS No. 120241-79-4

3-TYP is a selectiveSIRT3inhibitor.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 47 In Stock
10MG 80 In Stock
25MG 160 In Stock
50MG 248 In Stock
100MG 446 In Stock
500MG 1008 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    3-TYP
  • Note
    Research use only, not for human use.
  • Brief Description
    3-TYP is a selectiveSIRT3inhibitor.
  • Description
    3-TYP is an inhibitor of SIRT3.
  • Synonyms
    3-TYP
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    SIRT1; SIRT2; SIRT3
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    120241-79-4
  • Formula Weight
    146.15
  • Molecular Formula
    C7H6N4
  • Purity
    98%
  • Solubility
    DMSO : 100 mg/mL. 684.23 mM; Ethanol : 16.67 mg/mL 114.06 mM;
  • SMILES
    C1(C2=CN=NN2)=CC=CN=C1
  • Chemical Name
    3-(1H-1,2,3-triazol-4-yl) pyridine

Shipping & Storage Information

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

Reference

1. Pi H, et al. SIRT3-SOD2-mROS-dependent autophagy in cadmium-induced hepatotoxicity and salvage by melatonin. Autophagy. 2015;11(7):1037-51.
molnova catalog
related products
  • Polygalasaponin F

    Polygalasaponin F has anti-neuroinflammatory activity, can inhibit the release of inflammatory cytokines TNF-α and NO induced by lipopolysaccharides (LPS) and reduce the expression of inducible nitric oxide synthases.

  • NSI-189 Phosphate

    NSI-189 Phosphate is a novel neurogenic molecule with pleiotropic properties, including antidepressant, procognitive, synaptoplastic, and neurotrophic activities demonstrated in preclinical studies.?Its antidepressant activity is monoamine-independent.NSI-189 actively stimulated remodeling of the stroke brain.?

  • D-tetrahydropalmatin...

    D-Tetrahydropalmatine is a organic cation transporter 1 (OCT1) inhibitor it can obviously inhibit the uptake of monocrotaline (MCT) in MDCK-hOCT1 cells and isolate rat primary hepatocytes and attenuate the viability reduction and LDH release of the primary cultured rat hepatocytes caused by MCT.