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Submit ReviewCJ 033466 is a potent and selective 5-HT4 partial agonist (EC50= 0.927 nM). Displays > 1000-fold selectivity for 5-HT4 over other 5-HT and D2 receptors. Exhibits gastroprokinetic effects in vivo following oral administration. Weakly blocks hERG (IC50 = 2.6 μM).
分子量 | 377.91 |
公式 | C19H28ClN5O |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 519148-48-2 |
PubChem ID | 10429706 |
InChI Key | ISKHMDNIWXPUGR-UHFFFAOYSA-N |
Smiles | ClC2=C(N)N1C(C(C(NCC3CCN(CC(C)C)CC3)=O)=C2)=NC(C)=C1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
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参考文献是支持产品生物活性的出版物。
Toga et al (2007) The 5-HT4 agonists cisapride, mosapride, and CJ-033466, a novel potent compound, exhibit different human ether-a-go-go-related gene (hERG)-blocking activities. J.Pharmacol.Sci. 105 207 PMID: 17928736
Mikami et al (2008) 5-Amino-6-chloro-N-[(1-isobutylpiperidin-4-yl)methyl]-2-methylimidazo[1,2-α]pyridine-8-carboxamide (CJ-033,466), a novel and selective 5-hydroxytryptamine4 receptor partial agonist: pharmacological profile in vitro and gastroproki J.Pharmacol.Exp.Ther. 325 190 PMID: 18198343
关键词: CJ 033466, CJ 033466 supplier, Selective, 5-HT4, partial, agonists, Serotonin, Receptors, 5-Hydroxytryptamine, CJ033466, 3089, Tocris Bioscience
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