UCL 2077

Discontinued Product

2661 has been discontinued.

View all Calcium-Activated Potassium (K<sub>Ca</sub>) Channels products.
说明: Slow afterhyperpolarization (sAHP) channel blocker; sub-type selective Kv channel effects
化学名: N-Trityl-3-pyridinemethanamine
纯度: ≥99% (HPLC)
说明书
引用文献 (2)
评论 (1)

生物活性 for UCL 2077

UCL 2077 is a slow afterhyperpolarization (sAHP) channel blocker; reduces sAHP in hippocampal slice preparations. Displays no effect on Ca2+ currents or the time course of sAHP/sIAHP. Exhibits potent inhibition of KCNQ1 and KCNQ2, but differential effects at other KCNQs. Rescues memory retrieval in dopamine β-hydroxylase knockout mice.

技术数据 for UCL 2077

分子量 350.46
公式 C25H22N2
储存 Store at RT
纯度 ≥99% (HPLC)
CAS Number 918311-87-2
PubChem ID 24868317
InChI Key PQFNWDHABGBCHB-UHFFFAOYSA-N
Smiles C(NC(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C1=CN=CC=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。

Tocris products are intended for laboratory research use only, unless stated otherwise.

关键词: UCL 2077, UCL 2077 supplier, Slow, hyperpolarization, sAHP, channels, blockers, Potassium, KCa, Channels, ca2+-activated, ca2+-dependent, K+, UCL2077, Ca2+-Activated, Voltage-Gated, 2661, Tocris Bioscience

2 篇 UCL 2077 的引用文献

引用文献是使用了 Tocris 产品的出版物。 UCL 2077 的部分引用包括:

Zhang et al (2013) The slow afterhyperpolarization: a target of β1-adrenergic signaling in hippocampus-dependent memory retrieval. J Neurosci 33 5006 PMID: 23486971

Paz et al (2018) Inhibition of striatal cholinergic interneuron activity by the Kv7 opener retigabine and the nonsteroidal anti-inflammatory drug diclofenac. Neuropharmacology 137 309 PMID: 29758221


UCL 2077 的评论

平均评分: 5 (Based on 1 Review.)

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UCL 2077 in BK channel study.
By Anonymous on 12/03/2018
分析类型: In Vitro
种属: Human

UCL 2077 has been used in our lab for assessing its blocking capacity in BK channels. the results were reliable and reproducible. Great product and will purchase again.

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