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Paxilline

蕈青霉素
Catalog No.
B6920
高电导Ca2+激活的K+(BKCa,KCa1.1)通道阻断剂
组合的产品项目
规格价格库存 数量
5mg
¥ 2,329.00
Ship with 10-15 days
10mg
¥ 3,737.00
Ship with 10-15 days

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背景

Paxilline is an indole diterpene from fungi which potently and reversibly inhibits large conductance Ca2+-activated K+ (BKCa, KCa1.1) channels[1,2]. It also enhances the binding of charybdotoxin, a peptidyl neurotoxin, to BKCa channels. Paxilline also inhibits the sarco/endoplasmic reticulum Ca2+ ATPase (IC50 = 5 - 50 μM)[3].

References:

[1]. Sanchez M, McManus O B. Paxilline inhibition of the alpha-subunit of the high-conductance calcium-activated potassium channel. Neuropharmacology, 1996,  35(7): 963-968.

[2]. Li G, Cheung D W. Effects of paxilline on K+ channels in rat mesenteric arterial cells. European Journal of Pharmacology , 1999, 372: 103-107.

[3]. Knaus H G, McManus O B, Lee S H, et al. Tremorgenic indole alkaloids potently inhibit smooth muscle high-conductance calcium-activated potassium channels. Biochemistry, 1994, 33(19): 5819-5828.

化学属性

Physical AppearanceA crystalline solid
StorageDesiccate at -20°C
M.Wt435.56
Cas No.57186-25-1
FormulaC27H33NO4
SolubilitySoluble in DMSO
Chemical Name(2R,4bS,6aR,12bS,12cR,14aS)-4b-hydroxy-2-(2-hydroxypropan-2-yl)-12b,12c-dimethyl-5,6,6a,7,12,12b,12c,13,14,14a-decahydro-2H-chromeno[5',6':6,7]indeno[1,2-b]indol-3(4bH)-one
SDFDownload SDF
Canonical SMILESO[C@]1(C2=C3)[C@@](CC[C@@H]2O[C@H](C(C)(C)O)C3=O)(C)[C@](C(NC4=CC=CC=C54)=C5C6)(C)[C@@H]6CC1
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化学结构

Paxilline