
SNAP-94847
CAS No. 487051-12-7
SNAP-94847 ( —— )
产品货号. M20136 CAS No. 487051-12-7
SNAP-94847 是一种选择性竞争性 MCH1 受体 (MCH1-R) 拮抗剂 (Ki: 2.2 nM)。它具有抗焦虑和抗抑郁活性,并能减少小鼠的食物摄入量。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥867 | 有现货 |
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10MG | ¥1312 | 有现货 |
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25MG | ¥2770 | 有现货 |
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50MG | ¥4074 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称SNAP-94847
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SNAP-94847 是一种选择性竞争性 MCH1 受体 (MCH1-R) 拮抗剂 (Ki: 2.2 nM)。它具有抗焦虑和抗抑郁活性,并能减少小鼠的食物摄入量。
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产品描述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.
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体外实验——
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体内实验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.
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同义词——
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通路GPCR/G Protein
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靶点MCHR
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受体MCH1-R
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研究领域——
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适应症——
化学信息
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CAS Number487051-12-7
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分子量478.57
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分子式C29H32F2N2O2
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纯度>98% (HPLC)
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溶解度DMSO: 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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化学全称N-(3-{1-[4-(34-Difluorophenoxy)benzyl]-4-piperidinyl}-4-methylphenyl)-2-methylpropanamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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.
产品手册




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SNAP-94847
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