盐酸曲普利啶结构式
|
常用名 | 盐酸曲普利啶 | 英文名 | Triprolidine hydrochloride |
|---|---|---|---|---|
| CAS号 | 6138-79-0 | 分子量 | 314.85200 | |
| 密度 | N/A | 沸点 | 462ºC at 760 mmHg | |
| 分子式 | C19H25ClN2O | 熔点 | 115-120ºC | |
| MSDS | 中文版 美版 | 闪点 | 233.2ºC | |
| 符号 |
GHS07 |
信号词 | Warning |
盐酸曲普利啶用途盐酸曲普利啶是一种口服活性、细胞渗透性和第一代组胺H1拮抗剂[1]。盐酸曲普利啶是一种抗组胺药,可用于过敏性鼻炎、哮喘和荨麻疹[2]。 |
| 中文名 | 盐酸曲普利啶 |
|---|---|
| 英文名 | triprolidine hydrochloride monohydrate |
| 英文别名 | 更多 |
| 描述 | 盐酸曲普利啶是一种口服活性、细胞渗透性和第一代组胺H1拮抗剂[1]。盐酸曲普利啶是一种抗组胺药,可用于过敏性鼻炎、哮喘和荨麻疹[2]。 |
|---|---|
| 相关类别 | |
| 靶点 |
H1 Receptor |
| 体内研究 | 曲普利啶(间隔内注射;0.5μl中0.5μM;破伤风后30、60和180 min)对基线fEPSPs没有显著影响,但是,与盐水注射(60 min时为208%)相比,步行时诱导的长时程增强(LTP)较小(60 min时为基线值的173%)[2]。动物模型:成年雄性Long-Evans TMN(tuberomamillary nucleus,TMN)损伤大鼠[2]剂量:0.5μl给药0.5μm:间隔内灌注;破伤风后30、60、180min结果:LTP的步行相关增强减弱。 |
| 参考文献 |
| 沸点 | 462ºC at 760 mmHg |
|---|---|
| 熔点 | 115-120ºC |
| 分子式 | C19H25ClN2O |
| 分子量 | 314.85200 |
| 闪点 | 233.2ºC |
| 精确质量 | 314.15500 |
| PSA | 16.13000 |
| LogP | 4.65740 |
| InChIKey | WYUYEJNGHIOFOC-NWBUNABESA-N |
| SMILES | Cc1ccc(C(=CCN2CCCC2)c2ccccn2)cc1.Cl |
| 外观性状 | 白色结晶粉末 |
| 储存条件 | 2-8°C |
| 稳定性 | Stable, but discolours in light. Incompatible with strong oxidizing agents. |
| 水溶解性 | >=10 g/100 mL at 20 ºC |
| 符号 |
GHS07 |
|---|---|
| 信号词 | Warning |
| 危害声明 | H302-H315-H319-H335 |
| 警示性声明 | P301 + P312 + P330-P305 + P351 + P338 |
| 个人防护装备 | dust mask type N95 (US);Eyeshields;Gloves |
| 危害码 (欧洲) | Xn:Harmful; |
| 风险声明 (欧洲) | R22;R36/37/38 |
| 安全声明 (欧洲) | S26-S36 |
| 危险品运输编码 | NONH for all modes of transport |
| WGK德国 | 3 |
| RTECS号 | UT7658000 |
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| MFCD00150574 |
| Triprolidine hydrochloride |