Nizubaglustat

CAS No. 1633666-49-5

Nizubaglustat( —— )

Catalog No. M36337 CAS No. 1633666-49-5

Nizubaglustat (AZ3102) is an orally available, selective and brain-permeable dual inhibitor of ceramide glucosyltransferase and non-lysosomal glucosylceramide amidase (NLGase) for the study of neurological diseases.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 695 Get Quote
5MG 1007 Get Quote
10MG 1349 Get Quote
25MG 1950 Get Quote
50MG 2558 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Nizubaglustat
  • Note
    Research use only, not for human use.
  • Brief Description
    Nizubaglustat (AZ3102) is an orally available, selective and brain-permeable dual inhibitor of ceramide glucosyltransferase and non-lysosomal glucosylceramide amidase (NLGase) for the study of neurological diseases.
  • Description
    Nizubaglustat is an inhibitor of Ceramide Glucosyltransferase or Glucosylceramide Synthase (GCS). Nizubaglustat also inhibits GBA2, involving in neuropathological lysosomal storage disorders.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Transferase
  • Recptor
    Transferase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1633666-49-5
  • Formula Weight
    433.51
  • Molecular Formula
    C24H32FNO5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    FC1=C(C=CC(COCCCCCN2[C@@H](CO)[C@@H](O)[C@H](O)[C@@H](O)C2)=C1)C3=CC=CC=C3
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Ghisaidoobe AT, et al. Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors. J Med Chem. 2014 Nov 13;57(21):9096-104.?
molnova catalog
related products
  • DGAT1-IN-1

    DGAT1-IN-1 is a potent inhibitor of diacylglycerol O- acyltransferase type 1(DGAT1, IC50 of < 10 nM).

  • Entacapone acid

    Entacapone is a selective and reversible inhibitor of catechol-O-methyltransferase(COMT).

  • SB 271046 hydrochlor...

    SB 271046 hydrochloride is selective, orally active 5-HT6 antagonist.