suvn-911

CAS No. 2414674-71-6

suvn-911( —— )

Catalog No. M28905 CAS No. 2414674-71-6

suvn-911 is a potent and selective antagonist of neuronal nicotinic acetylcholine α4β2 receptor (Ki = 1.5 nM) with antidepressant activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 260 Get Quote
10MG 430 Get Quote
25MG 710 Get Quote
50MG 972 Get Quote
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Biological Information

  • Product Name
    suvn-911
  • Note
    Research use only, not for human use.
  • Brief Description
    suvn-911 is a potent and selective antagonist of neuronal nicotinic acetylcholine α4β2 receptor (Ki = 1.5 nM) with antidepressant activity.
  • Description
    suvn-911 is a potent and selective antagonist of neuronal nicotinic acetylcholine α4β2 receptor (Ki = 1.5 nM) with antidepressant activity.(In Vitro):suvn-911 shows good selectivity against over 70 receptors which includes GPCRs, ion channels, enzymes, peptides, steroids, second messengers, growth factors, and prostaglandins. suvn-911 displays high selectivity for α4β2 over α3β4 nAChR.(In Vivo):In male Wistar rats, suvn-911 (1.0-10.0 mg/kg; p.o.) showed significant antidepressant-like activity with no signs of tachyphylaxis. suvn-911 (3 mg/kg; p.o.) showed high oral exposures, longer half-lives(T1/2 = 3.34 hr), and adequate brain penetration in Wistar rats. suvn-911 showed metabolic stability and no cardiovascular and gastrointestinal side effects.
  • In Vitro
    SUVN-911 displays high selectivity for α4β2 over α3β4 nAChR.SUVN-911 shows good selectivity against over 70 receptors which includes GPCRs, ion channels, enzymes, peptides, steroids, second messengers, growth factors and prostaglandins.
  • In Vivo
    SUVN-911 is devoid of cardiovascular and gastrointestinal side effects.SUVN-911 (1.0-10.0 mg/kg; p.o.; daily; for 3 days) shows significant antidepressant effects.SUVN-911 shows metabolic stability in rats.SUVN-911 (3 mg/kg; p.o.) has shown high oral exposures, longer half-lives and adequate brain penetration in Wistar rats. Animal Model:Male Wistar rats (180-230 g)Dosage:1 mg/kg, 3 mg/kg, 10.0 mg/kg Administration:Oral administration, daily, for 3 days Result:Showed anti depressant like activity with no signs of tachyphylaxis.Animal Model:Male Wistar rats (225 ± 25 g) Dosage:3 mg/kg (Pharmacokinetic Analysis) Administration:Oral administration Result:AUC=3507 ng*h/mL, T1/2=3.34 hours.
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    AChR
  • Recptor
    5-HT6
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2414674-71-6
  • Formula Weight
    224.69
  • Molecular Formula
    C11H13ClN2O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (478.65 mM)
  • SMILES
    ClC1=CC=C(OC[C@H]2N[C@H](C3)[C@H]3C2)C=N1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Svenningsson P, et al. Biochemical and behavioral evidence for antidepressant-like effects of 5-HT6 receptor stimulation. J Neurosci. 2007 Apr 11;27(15):4201-9.
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