Afizagabar (Synonyms: S44819; Egis-13529)
目录号: PL02424 纯度: ≥98%
CAS No. :1398496-82-6
商品编号 规格 价格 会员价 是否有货 数量
PL02424-5mg 5mg ¥8036.00 请登录
PL02424-10mg 10mg ¥13661.00 请登录
PL02424-25mg 25mg ¥28930.00 请登录
PL02424-50mg 50mg ¥48218.00 请登录
PL02424-100mg 100mg ¥73934.00 请登录
PL02424-200mg 200mg 询价 询价
PL02424-500mg 500mg 询价 询价
PL02424-10mM*1mLinDMSO 10mM*1mLinDMSO ¥8840.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
Afizagabar
英文名称
Afizagabar
英文别名
Afizagabar;ZD6M94A8IH;s44819;2H-[1,3]oxazolo[4,5-h][2,3]benzodiazepin-2-one;5-(4-fluoro-1-benzothiophen-2-yl)-8-methyl-1,9-dihydro-;Afizagabar [INN];BDBM126719;US8778932, 21;2H-Oxazolo(4,5-H)(2,3)benzodiazepin-2-one, 5-(4-fluorobenzo(b)thien-2-yl)-1,9-dihydro-8-methyl-;5-(4-Fluoro-1-benzothiophen-2-yl)-8-methyl-1,9-dihydro- 2H-(1,3)oxazolo(4,5-H)(2,3)benzodiazepin-2-one;5-(4-Fluorobenzo[b]thiophen-2-yl)-8-methyl-1,9-dihydro-2H-ox
Cas No.
1398496-82-6
分子式
C19H12FN3O2S
分子量
365.38
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Afizagabar (S44819) 是一种首创的,有竞争性的,选择性的 α5-GABAAR 拮抗剂,对α5β2γ2 的IC50 值 585 nM,对 α5β3γ2 的 Ki 为 66 nM。Afizagabar 增强海马突触可塑性并显示促认知功效。
生物活性
Afizagabar (S44819) is a first-in-class, competitive, and selective antagonist at the GABA-binding site of the α5-GABAAR, with an IC 50 of 585 nM for α5β2γ2 and a K i of 66 nM for α5β3γ2. Afizagabar enhances hippocampal synaptic plasticity and exhibits pro-cognitive efficacy.
性状
Solid
体外研究(In Vitro)
Afizagabar (S44819) is a competitive α5-GABAAR antagonist (Kb=221 nM). Afizagabar selectively inhibits extrasynaptic α5-GABAARs of mouse CA1 pyramidal neurons. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Afizagabar (1 and 3 mg/kg; i.p.) significantly diminishes the marked increase in total errors induced by Scopolamine. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Sprague Dawl
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Etherington LA, et al. Selective inhibition of extra-synaptic α5-GABAA receptors by S44819, a new therapeutic agent. Neuropharmacology. 2017;125:353-364.
溶解度数据
In Vitro: DMSO : 6.25 mg/mL (17.11 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2