
你好Bio/Saclofen/HB0963/10mg
市场价:
¥2574.00
美元价:
1980.00
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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NameSaclofen
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Short descriptionSelective, competitive GABAB receptor antagonist
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Biological descriptionSelective and competitive GABAB receptor antagonist. Inhibits baclofen binding (IC50 = 7.8 µM).
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Biological actionAntagonist
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Purity>99%
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Properties
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Chemical name(RS)-3-Amino-2-(4-chlorophenyl)propylsulfonic acid
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Molecular Weight249.72
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Chemical structure
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Molecular FormulaC9H12ClNO3S
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CAS Number125464-42-8
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PubChem identifier122150
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SMILESC1=CC(=CC=C1C(CN)CS(=O)(=O)O)Cl
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InChiInChI=1S/C9H12ClNO3S/c10-9-3-1-7(2-4-9)8(5-11)6-15(12,13)14/h1-4,8H,5-6,11H2,(H,12,13,14)
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InChiKeyJYLNVJYYQQXNEK-UHFFFAOYSA-N
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MDL numberMFCD00216817
Storing and Using Your Product
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Storage instructionsRoom temperature
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Solubility overviewSoluble in water (10mM)
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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 Saclofen
Proposed antagonists at GABAB receptors that inhibit adenylyl cyclase in cerebellar granule cell cultures of rat.
Holopainen I et al (1992) Eur J Pharmacol 227(2) : 225-8.PubMedID: 1330652Inhibition of baclofen binding to rat cerebellar membranes by phaclofen, saclofen, 3-aminopropylphosphonic acid and related GABAB receptor antagonists.
Drew CA et al (1990) Neurosci Lett 113(1) : 107-10.PubMedID: 2164173Antagonism at GABAB receptors by saclofen and related sulphonic analogues of baclofen and GABA.
Kerr DI et al (1989) Neurosci Lett 107(1-3) : 239-44.PubMedID: 2559370
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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