RS 8359

CAS No. 105365-76-2

RS 8359( —— )

Catalog No. M26814 CAS No. 105365-76-2

RS 8359 is a reversible inhibitor of monoamine oxidase A (MAO-A) with a selectivity ratio of about 2200 for the A:B enzyme types.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 533 Get Quote
10MG 767 Get Quote
25MG 1161 Get Quote
50MG 1557 Get Quote
100MG 2115 Get Quote
500MG 4221 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    RS 8359
  • Note
    Research use only, not for human use.
  • Brief Description
    RS 8359 is a reversible inhibitor of monoamine oxidase A (MAO-A) with a selectivity ratio of about 2200 for the A:B enzyme types.
  • Description
    RS 8359 is a reversible inhibitor of monoamine oxidase A (MAO-A) with a selectivity ratio of about 2200 for the A:B enzyme types. RS 8359 has antidepressant activity.(In Vivo):RS 8359 shows relatively little effect upon blood pressure when administered together with tyramine, thus effectively eliminating the 'cheese' effect which has contributed to the limited clinical use of the classical monoamine oxidase inhibitors. RS 8359 shows little affinity for the common central nervous system receptors and little anticholinergic effect.
  • In Vitro
    ——
  • In Vivo
    RS 8359 shows relatively little effect upon blood pressure when administered together with tyramine. RS-8359 shows little affinity for the common central nervous system receptors and little anticholinergic effect.
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    MAO
  • Recptor
    Wnt| β-catenin
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    105365-76-2
  • Formula Weight
    252.277
  • Molecular Formula
    C14H12N4O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (198.20 mM)
  • SMILES
    OC1CCc2c1ncnc2Nc1ccc(cc1)C#N
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.1. Waaler J, et al. Novel synthetic antagonists of canonical Wnt signaling inhibit colorectal cancer cell growth. Cancer Res. 2011;71(1):197-205.
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