
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)






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5MG | 96 | In Stock |
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10MG | 146 | In Stock |
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25MG | 308 | In Stock |
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50MG | 453 | In Stock |
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Biological Information
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Product NameSNAP-94847
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NoteResearch use only, not for human use.
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Brief DescriptionSNAP-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.
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DescriptionSNAP-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.
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In Vitro——
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In VivoSNAP 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.
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Synonyms——
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PathwayGPCR/G Protein
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TargetMCHR
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RecptorMCH1-R
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Research Area——
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Indication——
Chemical Information
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CAS Number487051-12-7
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Formula Weight478.57
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Molecular FormulaC29H32F2N2O2
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Purity>98% (HPLC)
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SolubilityDMSO: 20 mg/mL (41.79 mM)
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SMILESCl.CC(C)C(=O)Nc1ccc(C)c(c1)C1CCN(Cc2ccc(Oc3ccc(F)c(F)c3)cc2)CC1
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Chemical NameN-(3-{1-[4-(34-Difluorophenoxy)benzyl]-4-piperidinyl}-4-methylphenyl)-2-methylpropanamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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



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