SNAP-94847

CAS No. 487051-12-7

SNAP-94847( —— )

Catalog No. M20136 CAS No. 487051-12-7

SNAP-94847 is a selective and competitive MCH1 receptor (MCH1-R) antagonist (Ki: 2.2 nM). It has anxiolytic and antidepressant activity and reduces food intake in mice.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 96 In Stock
10MG 146 In Stock
25MG 308 In Stock
50MG 453 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SNAP-94847
  • Note
    Research use only, not for human use.
  • Brief Description
    SNAP-94847 is a selective and competitive MCH1 receptor (MCH1-R) antagonist (Ki: 2.2 nM). It has anxiolytic and antidepressant activity and reduces food intake in mice.
  • Description
    SNAP-94847 is a selective and competitive MCH1 receptor (MCH1-R) antagonist (Ki: 2.2 nM). It has anxiolytic and antidepressant activity and reduces food intake in mice.
  • In Vitro
    ——
  • In Vivo
    SNAP 94847 (oral gavage; 20?mg/kg; 14 days) shows an exaggerated locomotor response to acute quinpirole [treatment:?F(2,19)=11.31,?treatment?×?time:?F(34,323)?=?4.061], the effect of SNAP 94847 on quinpirole-evoked ambulations over the entire observation period is significant compared to the untreated animals.SNAP 94847 (oral administration; 20?mg/kg; 21 days) in drink water, produces a significant increase in ambulation relative to untreated animals [treatment:?F(3,28)?=?8.971; treatment?×?time:?F(51,476)=11.50]. shows a marked increase in locomotion is apparent after 40?min in the SNAP 94847-treated group,this effect is significant over 180?min.SNAP 94847 (oral administration; 10?mg/kg), has a good bioavailability (59%), low plasma and blood clearances of 4.2 L/hr/kg and 3.3 L/hr/kg, respectively, and the half-life was shown to be 5.2 h in rats in a PK study. Animal Model:Rat Dosage:20?mg/kg Administration:Oral administration; 20?mg/kg; 14 days Result:Exhibited a exaggerated locomotor response to acute quinpirole.Animal Model:Rat (PK study)Dosage:10 mg/kg Administration:oral gavage; 10 mg/kg Result:Exhibited good physicochemical properties in rats.
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    MCHR
  • Recptor
    MCH1-R
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    487051-12-7
  • Formula Weight
    478.57
  • Molecular Formula
    C29H32F2N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 20 mg/mL (41.79 mM)
  • SMILES
    Cl.CC(C)C(=O)Nc1ccc(C)c(c1)C1CCN(Cc2ccc(Oc3ccc(F)c(F)c3)cc2)CC1
  • Chemical Name
    N-(3-{1-[4-(34-Difluorophenoxy)benzyl]-4-piperidinyl}-4-methylphenyl)-2-methylpropanamide

Shipping & Storage Information

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

Reference

1.Chen CA et al. Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists part 2: A hybrid strategy combining key fragments of HTS hits. J Med Chem. 2007 Aug 9;50(16):3883-90.
molnova catalog
related products
  • TC-MCH 7c

    TC-MCH 7c is an oral, selectable and blood-brain barrier penetrating MCH1R antagonist with IC50 performance of 5.6 nM against hMCH1R, and TC-MCH 7c is a phenylpyridone derivative with MCH1R Ki of 3.4 nM against human. In mice, MCH1R Ki was 3.0 nM.

  • GW-803430

    GW-803430 (GW-3430) is an orally active and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist used in the study of obesity.

  • AZD-1979

    A potent, selective melanin concentrating hormone receptor 1 (MCH-R1) antagonist with binding Ki of 12.2 nM.