AZD8848
目录号: PL12305 纯度: ≥98%
CAS No. :866269-28-5
商品编号 规格 价格 会员价 是否有货 数量
PL12305-5mg 5mg ¥5563.64 请登录
PL12305-10mg 10mg ¥9890.91 请登录
PL12305-25mg 25mg ¥20400.00 请登录
PL12305-50mg 50mg ¥31527.27 请登录
PL12305-100mg 100mg ¥46981.82 请登录
PL12305-200mg 200mg 询价 询价
PL12305-500mg 500mg 询价 询价
PL12305-10mM*1mLinDMSO 10mM*1mLinDMSO ¥6120.00 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
AZD8848
英文名称
AZD8848
英文别名
AZD8848;322ZMR6920;methyl 2-(3-(((3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl)(3-morpholinopropyl)amino)methyl)phenyl)acetate;GTPL9256;AZD 8848;DB14868;Q27074812;Benzeneacetic acid, 3-(((3-(6-amino-2-butoxy-7,8-dihydro-8-oxo-9H-purin-9-yl)propyl)(3-(4-morpholinyl)propyl)amino)methyl)-, methyl ester;Methyl (3-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl
Cas No.
866269-28-5
分子式
C29H43N7O5
分子量
569.70
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
AZD8848 是一种选择性的 TLR7 前体药激动剂,用于哮喘和过敏性鼻炎的研究。
生物活性
AZD8848 is a selective toll-like receptor 7 (TLR7) antedrug agonist which is developed for the research of asthma and allergic rhinitis.
性状
Solid
IC50 & Target[1][2]
TLR7
体外研究(In Vitro)
AZD8848 shows good activity against TLR7, with cellular pEC50s of 7.0 and 6.6 for human TLR7 and rat TLR7, respectively.
AZD8848 has an EC50 of 4 nM in the induction of IFNα from human PBMCs and an IC50 of 0.2-1.0 nM for the inhibition of IL-5, irrespective of whether the T cells have been polyclonally stimulated with PHA or via antigen presentation.
AZD8848 is a potent, selective TLR7 agonist antedrug able to inhibit Th2 responses in vitro.
AZD8848 has no activity against human TLR8 or against any of the other human TLRs.
has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
AZD8848 (0.1-1 mg/kg; intratracheal) has a good pharmacokinetics in the Brown Norway rat.
AZD8848 (0.3 mg/kg; Intratracheal) suppresses the ovalbumin (OVA) challenge in the rat allergy model.
has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
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]. Delaney S, et al. Tolerability in man following inhalation dosing of the selective TLR7 agonist, AZD8848. BMJ Open Respir Res. 2016 Feb 23;3(1):e000113.
溶解度数据
In Vitro: DMSO : 25 mg/mL (43.88 mM; ultrasonic and warming and heat to 60°C)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