位置:首页 > 产品库 > ONO-7300243
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
ONO-7300243
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
ONO-7300243图片
CAS NO:638132-34-0
规格:≥98%
包装与价格:
包装价格(元)
5mg询价
10mg询价
25mg询价
50mg询价
100mg询价
250mg询价
500mg询价

理化性质和储存条件
Molecular Weight (MW)461.55
FormulaC28H31NO5
CAS No.638132-34-0
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 92 mg/mL (199.3 mM)
Water: <1 mg/mL
Ethanol: 92 mg/mL (199.3 mM)
SMILES CodeO=C(O)CC1=CC=C(CN(C(C2=CC(OC)=C(C)C(OC)=C2)=O)CCCC3=CC=CC=C3)C=C1
SynonymsONO 7300243, ONO7300243; ONO-7300243
实验参考方法
In Vitro

In vitro activity: ONO-7300243 (also named as ONO 7300243, ONO7300243) is a novel, potent and selective antagonist of LPA1(Lysophosphatidic Acid Receptor) with an IC50 of 160 nM. ONO-7300243 was identified from a high throughout screening and subsequent structural optimizaiton. A


Kinase Assay: ONO-7300243 shows modest in vitro activity (IC50=0.16 μM). ONO-7300243 exhibits almost identical levels of antagonist activity in vitro.


Cell Assay: lthough ONO-7300243 showed only modest in vitro activity (IC50 = 0.16 μM), it showed much stronger effects in vivo (88% inhibition at 10 mg/kg i.d., 62% inhibition at 3 mg/kg i.d.). ONO-7300243 showed good membrane permeability and good metabolic stability against rat liver microsomes.

In VivoONO-7300243 inhibited the LPA-induced IUP(intraurethral pressure) increase in a dose-dependent manner (ID50 = 11.6 mg/kg p.o.) up to 1 h after dosing. Significant effects were observed at 10 and 30 mg/kg (p<0.05 vs vehicle). ONO-7300243 (30 mg/kg, p.o.) led to a significant decrease in the IUP in conscious rats without LPA stimulation compared with the vehicle without affecting the mean blood pressure (MBP). In a a rat pharmacokinetic study, ONO-7300243 showed a rapid clearance (CLtot = 15.9 mL/min/kg at 3 mg/kg i.v.) and a short half-life (0.3 h).
Animal modelRats
Formulation & DosageFormulated in 0.5% methyl cellulose; 3 mg/kg for i.v. or 10 mg/kg for p.o.; i.v. or p.o.
ReferencesACS Med Chem Lett. 2016 Aug 19;7(10):913-918.
 
 
维奥蛋白资源库 - 中文蛋白资源 CopyRight © 2010-2024