2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate

2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate

中文名称2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate
中文同义词化合物CLP-290;(Z)-5-氟-2-((4-氧代-2-(四氢哒嗪-1(2H)-基)噻唑-5(4H)-亚基)甲基)苯基吡咯烷-1-羧酸酯;吡咯烷-1-甲酸[(Z)-5-氟-2-[[4-氧代-2-[四氢哒嗪-1(2H)-基]噻唑-5(4H)-亚基]甲基]苯基]酯;CLP-290,K + / CL-共转运蛋白2(KCC2)激活剂
英文名称2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate
英文同义词2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate;CLP-290;(Z)-5-Fluoro-2-((4-oxo-2-(tetrahydropyridazin-1(2H)-yl)thiazol-5(4H)-ylidene)methyl)phenyl pyrrolidine-1-carboxylate;[5-Fluoro-2-[(Z)-(2-hexahydropyridazin-1-yl-4-oxo-thiazol-5-ylidene)methyl]phenyl] pyrrolidine;CLP 290;CLP290;2-([(5Z)-2-(1,2-DIAZINAN-1-YL)-4-OXO-4,5-DIHYDRO-1,3-THIAZOL-5-YLIDENE]METHYL)-5-FLUOROPHENYL PYRROL;1-Pyrrolidinecarboxylic acid, 5-fluoro-2-[(Z)-[4-oxo-2-(tetrahydro-1(2H)-pyridazinyl)-5(4H)-thiazolylidene]methyl]phenyl ester;5-Fluoro-2-(Z)-(2-hexahydropyridazin-1-yl-4-oxo-thiazol-5-ylidene)methylphenyl pyrrolidine-1-carboxylate
CAS号1181083-81-7
分子式C19H21FN4O3S
分子量404.46
EINECS号604-604-1
相关类别
Mol文件1181083-81-7.mol
结构式2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate 结构式

2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate 性质

沸点553.7±60.0 °C(Predicted)
密度1.47±0.1 g/cm3(Predicted)
储存条件2-8°C(protect from light)
溶解度DMSO:23.74(最大浓度 mg/mL);58.7(最大浓度 mM)
DMSO:PBS (pH 7.2) (1:6):1.0(最大浓度 mg/mL);2.47(最大浓度. mM)
DMF:1.0(最大浓度 mg/mL);2.47(最大浓度 mM)
乙醇:2.02(最大浓度 mg/mL);4.99(最大浓度 mM)
形态结晶固体
酸度系数(pKa)1.29±0.20(Predicted)

2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate 用途与合成方法

CLP290 是一种神经特异性 K+-Cl− 共转运体 KCC2 的口服激活剂,具有研究多种神经和精神疾病的潜力。CLP290 能显著降低 STZ 大鼠的血液中 AVP 和血糖水平。

KCC2

CLP290 (oral gavage; 100 mg/kg; twice a day; 7 day) enhances KCC2 activity and restores Cl - transport in superficial dorsal horn (SDH) neurons of morphine-treated rats, and prevents morphine-induced hyperalgesia (MIH) in rat.

Animal Model: Adult male rats (300 g, >postnatal day 60)
Dosage: 100 mg/kg
Administration: Oral gavage; 100 mg/kg; twice a day; 7day
Result: Rescued established MIH and prevented its development by restoring Cl - transport or preventing its deficiency in the SDH.

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
2024/01/25HY-103023CLP2901 mg377元
2024/01/25HY-1030232{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate
CLP290
1181083-81-710mM * 1mLin DMSO740元

2{[(5Z)2(1,2diazinan1yl)4oxo4,5dihydro1,3thiazol5ylidene]Methyl}5fluorophenyl pyrrolidine1carboxylate 上下游产品信息

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