T-448 free base

CAS No. 1597426-52-2

T-448 free base ( T448;T 448 )

Catalog No. M12283 CAS No. 1597426-52-2

T-448 free base (T448) is a specific inhibitor of LSD1 enzyme activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 1053 Get Quote
50MG 2142 Get Quote
100MG 2790 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    T-448 free base
  • Note
    Research use only, not for human use.
  • Brief Description
    T-448 free base (T448) is a specific inhibitor of LSD1 enzyme activity.
  • Description
    T-448 free base (T448) is a specific inhibitor of LSD1 enzyme activity, enhances H3K4 methylation in primary cultured rat neurons but has little impact on LSD1-GFI1B complex in human TF-1a erythroblasts; increases brain H3K4 methylation and partially restored learning function in mice with NMDA receptor hypofunction, shows unique therapeutic approaches for central nervous system disorders associated with epigenetic dysregulation.
  • Synonyms
    T448;T 448
  • Pathway
    Chromatin/Epigenetic
  • Target
    Histone Demethylase
  • Recptor
    Histone Demethylase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1597426-52-2
  • Formula Weight
    328.43
  • Molecular Formula
    C17H20N4OS
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC1=NN=C(S1)NC(=O)C2=CC=CC(=C2)C3CC3NC4CCC4
  • Chemical Name
    3-((1S,2R)-2-(cyclobutylamino)cyclopropyl)-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide

Shipping & Storage Information

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

Reference

1. Matsuda S, et al. Neuropsychopharmacology. 2018 Dec 22. doi: 10.1038/s41386-018-0300-9.
molnova catalog
related products
  • SD-70

    A small molecule tumor translocation inhibitor that inhibits the prostate cancer cell transcriptional program.

  • Bizine

    Bizine is a phenelzine analog that inhibits LSD1 with Ki of 59 nM.

  • KDM5-C70

    KDM5-C70 is the cell-permeable derivative of KDM5-C49, potent, selective and cell permeable KDM5 inhibitor with IC50 of 0.3, 0.3 and 0.58 uM for KDM5A, B and C, respectively.