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287206-61-5

中文名稱 MA-2029
英文名稱 MA 2029
CAS 287206-61-5
分子式 C31H45FN4O4
分子量 556.71
MOL 文件 287206-61-5.mol
更新日期 2023/03/20 15:41:21
287206-61-5 結(jié)構(gòu)式 287206-61-5 結(jié)構(gòu)式

基本信息

中文別名
化合物 T15946
英文別名
MA 2029
4-Fluoro-N-methyl-L-phenylalanyl-N-methyl-L-valyl-3-(1,1-dimethylethyl)-N-ethyl-L-tyrosinamide

物理化學(xué)性質(zhì)

沸點(diǎn)765.1±60.0 °C(Predicted)
密度1.128±0.06 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度Soluble to 20 mM in 1eq. HCl and to 100 mM in DMSO
酸度系數(shù)(pKa)11.24±0.20(Predicted)
形態(tài)粉末
顏色White to off-white
MA-2029價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2024/11/08HY-107642MA-2029
MA-2029
287206-61-51mg1600元
2024/11/08HY-107642MA-2029
MA-2029
287206-61-55mg5000元
2023/03/20HY-107642MA-2029
MA-2029
287206-61-510mg9800元

常見問題列表

生物活性
MA-2029 是一種選擇性、口服活性和競爭性的胃動素受體 (motilin receptor) 拮抗劑 (IC50=4.9 nM)。MA-2029 對胃動素受體的選擇性高于其他受體和離子通道。MA-2029 可用于與胃腸動力紊亂相關(guān)的胃腸道疾病。
靶點(diǎn)

IC50: 4.9 nM (motilin receptor)

體外研究

MA-2029 (1 to 30 nM) competitively inhibits motilin-induced contractions in isolated rabbit duodenal longitudinal muscle strips, with a pA 2 value 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 [ 125 I]motilin to motilin receptors in a homogenate of rabbit colon smooth muscle tissue and membranes of HEK 293 cells expressing human motilin receptors. The pK i of MA-2029 is 8.58±0.04 in the rabbit colon homogenate and 8.39 in the HEK 293 cells.

體內(nèi)研究

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.
MA-2029 (10 mg/kg; p.o.) treatment shows that the t 1/2 is 2 hours.
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.

Animal Model: Male Japanese-white rabbits (about 2-3 kg)
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)
Dosage: 10 mg/kg
Administration: Oral administration (Pharmacokinetic Analysis)
Result: The t 1/2 is 2 hours.
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