Chemical Structure : Paxilline
CAS No.: 57186-25-1
货号: PC-70220Not For Human Use, Lab Use Only.
Paxilline is a potent blocker of high-conductance Ca2+-activated K+ (BKCa, KCa1.1) channels that binds to the α-subunit of BKCa with Ki of 1.9 nM.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥1980 | In stock | |
5 mg | ¥3980 | In stock | |
10 mg | ¥5980 | In stock | |
25 mg | Get quote |
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Paxilline is a potent blocker of high-conductance Ca2+-activated K+ (BKCa, KCa1.1) channels that binds to the α-subunit of BKCa with Ki of 1.9 nM.
Paxilline also enhances TRAIL-mediated apoptosis of glioma cells via modulation of c-FLIP, survivin and DR5.
分子量 | 435.56 | |
分子式 | C27H33NO4 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
(2R,4bS,6aS,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 |
1. Kang YJ, et al. Exp Mol Med. 2011 Jan 31;43(1):24-34.
2. Sanchez M, et al. Neuropharmacology. 1996;35(7):963-8.
3. Zhou Y, et al. J Gen Physiol. 2014 Nov;144(5):415-40.
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