A192621

A192621

中文名称A192621
中文同义词化合物 T14068;化合物 A-192621
英文名称A192621
英文同义词(2R,3R,4S)-4-(1,3-BENZODIOXOL-5-YL)-1-[2-[(2,6-DIETHYLPHENYL)AMINO]-2-OXOETHYL]-2-(4-PROPOXYPHENYL)PYRROLIDINE-3-CARBOXYLIC ACID;A192621;A192621,CID 5310991;3-Pyrrolidinecarboxylic acid, 4-(1,3-benzodioxol-5-yl)-1-[2-[(2,6-diethylphenyl)amino]-2-oxoethyl]-2-(4-propoxyphenyl)-, (2R,3R,4S)-;A192621 >=98 (HPLC)
CAS号195529-54-5
分子式C33H38N2O6
分子量558.66
EINECS号
相关类别制剂-拮抗剂
Mol文件195529-54-5.mol
结构式A192621 结构式

A192621 性质

沸点738.3±60.0 °C(Predicted)
密度1.233±0.06 g/cm3(Predicted)
储存条件-20°C
形态粉末
酸度系数(pKa)3.52±0.60(Predicted)
颜色白色至米色

A192621 用途与合成方法

A-192621 是一种有效的非肽,口服活性,选择性内皮素 B (ETB) 受体拮抗剂,IC50 为 4.5 nM,Ki 为 8.8 nM。A-192621 的选择性比 ETA 高 636 倍 (IC50 为 4280 nM,Ki 为 5600 nM)。A-192621 促进 PASMC 细胞凋亡,并引起动脉血压升高和血浆 ET-1 水平升高。

ET B

4.5 nM (IC 50 )

ET B

8.8 nM (Ki)

ET A

4280 nM (IC 50 )

ET A

5600 nM (Ki)

A-192621 (1-100 μM; 48 hours; PASMCs) treatment markedly reduces the cell viability of PASMCs in a dose-dependent manner.
A-192621 (1-100 μM; 48 hours; PASMCs) treatment significantly increases the caspase-3/7 activity and cleaved caspase-3 expression in PASMCs. A-192621 induces apoptosis in a dose-dependent manner and increases the cells' susceptibility to apoptosis by Doxorubicin treatment.

Cell Viability Assay

Cell Line: Pulmonary arterial smooth muscle cells (PASMCs) with Doxorubicin
Concentration: 1 μM, 10 μM, 50 μM, 100 μM
Incubation Time: 72 hours
Result: The viability of PASMCs was significantly decreased in a dose-dependent manner.

Western Blot Analysis

Cell Line: Pulmonary arterial smooth muscle cells (PASMCs) with Doxorubicin
Concentration: 1 μM, 10 μM, 100 μM
Incubation Time: 72 hours
Result: The caspase-3/7 activity in PASMCs was significantly increased in a dose-dependent manner.

A-192621 (30-100 mg/kg; oral administration; daily; for 3 days; male Sprague-Dawley rats) treatment inhibits both dilatory and pressor responses induced by S6c mediated by ET B with an ED 50 value of 30 mg/kg, and failed to inhibit the ET-1-induced pressor response mediated by ET A . A-192621 alone causes elevation of arterial blood pressure and an elevation in the plasma ET-1 level in the conscious normotensive rat.

Animal Model: Male Sprague-Dawley rats (250-350 g)
Dosage: 30 mg/kg 100 mg/kg
Administration: Oral administration; daily; for 3 days
Result: Inhibited both dilatory and pressor responses induced by S6c mediated by ET B with an ED 50 value of 30 mg/kg.

安全信息

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/11/08HY-120295A192621
A-192621
1 mg1850元
2024/11/08HY-120295A192621
A-192621
195529-54-55mg4680元

A192621 上下游产品信息

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