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View all Voltage-gated Potassium (K<sub>V</sub>) Channels products.CP 339818 hydrochloride is a potent, non-peptide KV1.3 channel antagonist that preferentially binds to the C-type inactivated state of the channel (IC50 ~ 200 nM). Inhibits KV1.4 with an IC50 of ~ 300 nM. Selective over KV1.1, KV1.2, KV1.5, KV1.6, KV3.1-4, and KV4.2.
分子量 | 340.89 |
公式 | C21H24N2.HCl |
储存 | Store at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 478341-55-8 |
PubChem ID | 20761468 |
InChI Key | JIRISCAPZWLWCG-UHFFFAOYSA-N |
Smiles | CCCCC\N=C2C1=CC=CC=C1N(CC3=CC=CC=C3)C=C/2.Cl |
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。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Jager et al (1998) Regulation of mammalian Shaker-related K+ channels: evidence for non-conducting closed and non-conducting inactivated. J.Physiol. 506 291 PMID: 9490854
Nguyen et al (1996) Novel nonpeptide agents potently block the C-type inactivated conformation of Kv1.3 and suppress T cell activation. Mol.Pharmacol. 50 1672 PMID: 8967992
关键词: CP 339818 hydrochloride, CP 339818 hydrochloride supplier, Non-peptide, potent, KV13, channels, blockers, Potassium, KV, voltage-gated, voltage-dependent, K+, CP339818, hydrochloride, Voltage-Gated, Channels, 1399, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 CP 339818 hydrochloride 的部分引用包括:
Meredith et al (2015) Kv1 channels and neural processing in vestibular calyx afferents. J Neurosci 9 85 PMID: 26082693
平均评分: 5 (Based on 1 Review.)
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