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About This Item
化学式:
(C2H5)4N(Br)
CAS番号:
分子量:
210.16
Beilstein:
3563430
MDL番号:
UNSPSCコード:
12352107
PubChem Substance ID:
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危険有害性情報
注意書き
危険有害性の分類
Aquatic Chronic 3
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
361.4 °F - closed cup
引火点(℃)
183 °C - closed cup
適用法令
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Jan Code
30-0770-2-25G-J:
30-0770-5-500G-J:
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Min Shen et al.
Vascular pharmacology, 58(1-2), 64-70 (2012-07-24)
Evidence has indicated that resveratrol (Res) produces vasorelaxation and may decrease the coronary heart disease mortality. However, several pathways involved in the mechanism of vasorelaxation are still unclear. This study was designed, therefore, to test the probable ion channels or
Sébastien Dilly et al.
Biochemical pharmacology, 85(4), 560-569 (2012-12-29)
Valine residues in the pore region of SK2 (V366) and SK3 (V520) were replaced by either an alanine or a phenylalanine to evaluate the impact on the interactions with the allosteric blocker apamin. Unlike TEA which showed high sensitivity to
Gonzalo Budelli et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(41), 16657-16662 (2013-09-27)
High-conductance Ca(2+)- and voltage-activated K(+) (Slo1 or BK) channels (KCNMA1) play key roles in many physiological processes. The structure of the Slo1 channel has two functional domains, a core consisting of four voltage sensors controlling an ion-conducting pore, and a
Guillermo J Pérez et al.
American journal of physiology. Cell physiology, 304(3), C280-C286 (2012-12-01)
We studied principal neurons from canine intracardiac (IC) ganglia to determine whether large-conductance calcium-activated potassium (BK) channels play a role in their excitability. We performed whole cell recordings in voltage- and current-clamp modes to measure ion currents and changes in
Vivek Garg et al.
The Journal of general physiology, 140(3), 307-324 (2012-08-30)
Ether-à-go-go (EAG) and EAG-related gene (ERG) K(+) channels are close homologues but differ markedly in their gating properties. ERG1 channels are characterized by rapid and extensive C-type inactivation, whereas mammalian EAG1 channels were previously considered noninactivating. Here, we show that
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