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188116-07-6

中文名称 伊匹妥英
英文名称 1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one
CAS 188116-07-6
分子式 C13H14ClN3O2
分子量 279.72
MOL 文件 188116-07-6.mol
更新日期 2024/05/27 17:16:38
188116-07-6 结构式 188116-07-6 结构式

基本信息

中文别名
伊匹妥英
1-(4-氯苯基)-1,5-二氢-4-(4-吗啉基)-2H-咪唑-2-酮
英文别名
CS-1057
ELB-138
Imepitoin
AWD 131-13
AWD 131-138, >=98%
IMEPITOIN
AWD131-138
AWD 131-138(Imepitoin)
3-(4-chlorophenyl)-5-morpholin-4-yl-4H-imidazol-2-one
1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one
1-(4-CHLOROPHENYL)-4-MORPHOLINO-1H-IMIDAZOL-2(5H)-ONE

物理化学性质

熔点264℃ (ethanol )
沸点421.8±55.0 °C(Predicted)
密度1.42±0.1 g/cm3(Predicted)
储存条件Sealed in dry,2-8°C
酸度系数(pKa)4.39±0.20(Predicted)

安全数据

危险性符号(GHS)
GHS08
警示词警告
危险性描述H361d
伊匹妥英价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-14953伊匹妥英
Imepitoin
188116-07-65mg800元
2024/04/30HY-14953伊匹妥英
Imepitoin
188116-07-610mM * 1mLin DMSO880元
2024/04/30HY-14953伊匹妥英
Imepitoin
188116-07-610mg1200元

常见问题列表

生物活性
Imepitoin (AWD 131-138) 是低亲和力的部分苯二氮(benzodiazepine)受体激动剂,有抗痉挛和抗焦虑作用。
靶点

GABA receptor

体外研究

AWD 131-138 dose-dependently stimulated GABA currents(Recombinant gamma-aminobutyric acid A (GABA(A)) receptors of the subunit compositions alpha1beta2gamma2, alpha1beta3gamma2, alpha2beta2gamma2, alpha3beta2gamma2 and alpha5beta2gamma2). At 10 microM AWD 131-138, this allosteric stimulation amounted in average to about 12-21% of the maximal stimulation achieved using diazepam. The threshold of stimulation was about 0.3-1.0 microM [1].

体内研究

AWD 131-138 did not produce midazolam-like responding or alter response rates at cumulative doses up to 18.0 mg/kg i.m. (plasma levels over 2100 ng/ml). When AWD 131-138 (10-100 microg/kg/injection) was studied by substitution, responding declined to vehicle substitution levels within three sessions. At the dose of 100 microg/kg i.v. AWD 131-138, sufficient drug was self-administered during the first session (about 3.5 mg/kg) to produce plasma levels above 1000 ng/ml, yet responding over the next two sessions dropped to vehicle levels [2]. Prolonged oral administration with twice-daily dosing of ELB 138 with either 5 or 40 mg/kg over a 5-week period was not associated with loss of anticonvulsant efficacy in the PTZ dog model [3].

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