您好,欢迎来到化工原料网! [登录] [免费注册]
化工原料网
位置:首页 > 产品库 > MA-2029
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:
 
MA-2029
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。
MA-2029图片
CAS NO:287206-61-5
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
MA-2029 是一种选择性、口服活性和竞争性的胃动素受体 (motilin receptor) 拮抗剂 (IC50=4.9 nM)。MA-2029 对胃动素受体的选择性高于其他受体和离子通道。MA-2029 可用于与胃肠动力紊乱相关的胃肠道疾病。
生物活性

MA-2029 is a selective, orally active, and competitivemotilin receptorantagonist (IC50=4.9 nM). MA-2029 is selective for themotilin receptorover various other receptors and ion channels. MA-2029 may be useful for gastrointestinal disorders associated with disturbed gastrointestinal motility[1].

IC50& Target

IC50: 4.9 nM (motilin receptor)[1]

体外研究
(In Vitro)

MA-2029 (1 to 30 nM) competitively inhibits motilin-induced contractions in isolated rabbit duodenal longitudinal muscle strips, with a pA2value of 9.17±0.01. Contractile responses to acetylcholine and substance P are unaffected even at 1 μM of MA-2029. MA-2029 concentration-dependently inhibits the binding of [125I]motilin to motilin receptors in a homogenate of rabbit colon smooth muscle tissue and membranes of HEK 293 cells expressing human motilin receptors. The pKiof MA-2029 is 8.58±0.04 in the rabbit colon homogenate and 8.39 in the HEK 293 cells[1].

体内研究
(In Vivo)

MA-2029 (0.3-3 mg/kg; p.o.) dose-dependently inhibits the number of abdominal muscle contractions induced under the same conditions and causes significant inhibition at 3 mg/kg[1].
MA-2029 (10 mg/kg; p.o.) treatment shows that the t1/2is 2 hours[1].
The inhibition is significant at 30 min after administration of 3 mg/kg or more and at 4 h after administration of 10 mg/kg or more (MA-2029), so administration of 10 mg/kg or more causes inhibitory effects from 30 min or less to at least 4 h after administration[1].

Animal Model:Male Japanese-white rabbits (about 2-3 kg)[1]
Dosage:0.3, 1, 3 mg/kg
Administration:Oral administration
Result:Dose-dependently inhibited the number of abdominal muscle contractions induced under the same conditions. Caused significant inhibition at 3 mg/kg.
Animal Model:Male Japanese-white rabbits (about 2-3 kg)[1]
Dosage:10 mg/kg
Administration:Oral administration (Pharmacokinetic Analysis)
Result:The t1/2is 2 hours.
分子量

556.71

性状

Solid

Formula

C31H45FN4O4

CAS 号

287206-61-5

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month