NS9283

CAS No. 913830-15-6

NS9283( NS 9283 | NS-9283 )

Catalog No. M27906 CAS No. 913830-15-6

NS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 87 Get Quote
10MG 132 Get Quote
25MG 282 Get Quote
50MG 444 Get Quote
100MG 651 Get Quote
500MG 1368 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    NS9283
  • Note
    Research use only, not for human use.
  • Brief Description
    NS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.
  • Description
    NS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.(In Vitro):NS9283 increased the potency of varenicline to activate and desensitize α4β2 nAChRs in vitro without affecting other known targets of varenicline.(In Vivo):In male and female C57BL/6J mice, NS9283 (10 mg/kg) reduced ethanol intake in a two-bottle choice, intermittent drinking procedure without affecting saccharin intake, ethanol-induced incoordination or ethanol-induced loss of the righting reflex. Subthreshold doses of NS9283 (2.5 mg/kg) plus varenicline (0.1 mg/kg) synergistically reduced ethanol intake in both sexes. Finally, despite having no aversive valence of its own, NS9283 enhanced ethanol-conditioned place aversion.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    NS 9283 | NS-9283
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    AChR
  • Recptor
    lignostilbene-α,β-dioxygenase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    913830-15-6
  • Formula Weight
    248.245
  • Molecular Formula
    C14H8N4O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 16.67 mg/mL (67.15 mM)
  • SMILES
    N#Cc1cccc(c1)-c1nc(no1)-c1cccnc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Cai S, et al. Synthesis, structure-activity relationships and preliminary mechanism study of N-benzylideneaniline derivatives as potential TLR2 inhibitors. Bioorg Med Chem. 2018 May 1;26(8):2041-2050.
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