Hello Bio/NS 309/HB1049/50mg
商品编号：
HB1049-50mg
品牌：
hellobio
市场价：
¥3315.00
美元价：
2550.00
产品分类：
酸碱缓冲液
联系Q Q：
3392242852
电话号码：
4000-520-616
电子邮箱：
info@ebiomall.com
商品介绍
Product overview
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NameNS 309
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Short descriptionPotent, selective KCa3.1 / KCa2 channel subfamily activator
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Biological descriptionPotent and selective KCa3.1 channel and KCa2 channel subfamily activator (EC50 = 0.3 µM for KCa2.3). Exhibits little or no activity at KCa1.1 channels. Displays >1000 fold higher potency than 1-EBIO.
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Biological actionActivator
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Purity>98%
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Our products in actionSubmit Your Citation Now
Properties
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Chemical name6,7-Dichloro-1H-indole-2,3-dione 3-oxime
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Molecular Weight231.04
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Chemical structure
![NS 309 [18711-16-5]](images/hellobio/201710/hb1049.png "NS 309 [18711-16-5]")
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Molecular FormulaC8H4Cl2N2O2
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CAS Number18711-16-5
Storing and Using Your Product
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Storage instructions+4°C
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Solubility overviewsoluble in DMSO (100mM)
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ImportantThis product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
References for NS 309
Activation of human IK and SK Ca2+ -activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime).
Strøbaek D et al (2004) Biochim Biophys Acta 1665(1-2) : 1-5.PubMedID: 15471565NS309 decreases rat detrusor smooth muscle membrane potential and phasic contractions by activating SK3 channels.
Parajuli SP et al (2013) Br J Pharmacol 168(7) : 1611-25.PubMedID: 23145946Selective positive modulation of the SK3 and SK2 subtypes of small conductance Ca2+-activated K+ channels.
Hougaard C et al (2007) Br J Pharmacol 151(5) : 655-65.PubMedID: 17486140
品牌介绍
Hello Bio是由一群经验丰富的科学家和化学家们创立的充满活力的生物企业，总部位于英国布里斯托尔，在美国普林斯顿设有分公司，主旨在于提供质优价廉的生命科学研究工具，主要产品线为小分子化合物，如激动剂、拮抗剂、抑制剂等，部分产品价格甚至低至其他供应商的50%。热销产品线：酶抑制剂和激动剂ROCK inhibitor Y-27632, PKA inhibitor KT 5720 , adenylyl cyclase activator Forskolin, and novel GRK2/3 inhibitor Cmpd101等。 离子通道调节剂NMDA antagonist D-AP5, sodium channel blocker tetrodotoxin citrate, TRP antagonist capsazepine, and GABAA antagonist SR 95531 等。信号通路工具各种信号通路抑制剂、激动剂表观遗传学研究工具potent HDAC inhibitor Trichostatin A, DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine,BET bromodomain inhibitor (+)-JQ1 and potent,selective GLP / G9a HMTase inhibitor BIX 01294 等受体配体novel selective GRK2/3 inhibitor, NMDA antagonist D-AP5, Group I mGlu agonist (S)-3,5-DHPG, and GABAA antagonist SR 95531.等干细胞调节剂ROCK inhibitor Y-27632, SB 431542 DAPT.
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