3-(哌啶-1-基)丙基 4-氨基-5-氯-2-甲氧基苯甲酸酯 盐酸盐结构式
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常用名 | 3-(哌啶-1-基)丙基 4-氨基-5-氯-2-甲氧基苯甲酸酯 盐酸盐 | 英文名 | RS 23597-190 |
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| CAS号 | 149719-06-2 | 分子量 | 363.27900 | |
| 密度 | N/A | 沸点 | 486.5ºC at 760 mmHg | |
| 分子式 | C16H24Cl2N2O3 | 熔点 | N/A | |
| MSDS | 中文版 | 闪点 | 248ºC |
用途RS 23597-190(EP-A-501322)是一种高亲和力和选择性5-HT4受体拮抗剂。RS 23597-190抑制5-HT诱发的心动过速。RS 23597-190显著抑制高糖中超氧化物的产生[1][2]。 |
| 中文名 | 3-(1-哌啶)-4-氨基-5-氯-2-甲氧基苯甲酸丙酯盐酸盐 |
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| 英文名 | 3-piperidin-1-ylpropyl 4-amino-5-chloro-2-methoxybenzoate,hydrochloride |
| 英文别名 | 更多 |
| 描述 | RS 23597-190(EP-A-501322)是一种高亲和力和选择性5-HT4受体拮抗剂。RS 23597-190抑制5-HT诱发的心动过速。RS 23597-190显著抑制高糖中超氧化物的产生[1][2]。 |
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| 相关类别 | |
| 靶点实验 |
5-HT4 Receptor |
| 体外研究 | RS 23597-190(10µM;4天)在高葡萄糖 (30mM)条件下显着抑制661瓦细胞中超氧化物的产生[2]。 |
| 体内研究 | RS 23597-190(6.0 mg/kg静脉注射) 抑制微型猪中 5吨诱导的心动过速[1]. 动物模型:双侧迷走神经切除微ig[1]剂量:6.0 mg/kg给药:静脉注射结果:拮抗5-HT诱发的心动过速,半衰期为77(63-99)分钟。 |
| 参考文献 |
| 沸点 | 486.5ºC at 760 mmHg |
|---|---|
| 分子式 | C16H24Cl2N2O3 |
| 分子量 | 363.27900 |
| 闪点 | 248ºC |
| 精确质量 | 362.11600 |
| PSA | 64.79000 |
| LogP | 4.28470 |
| InChIKey | QLZLBYYNMGQIAR-UHFFFAOYSA-N |
| SMILES | COc1cc(N)c(Cl)cc1C(=O)OCCCN1CCCCC1.Cl |
| 蒸汽压 | 1.29E-09mmHg at 25°C |
| 储存条件 | 室温 |
| 危害码 (欧洲) | Xn |
|---|---|
| 海关编码 | 2933399090 |
| 海关编码 | 2933399090 |
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| 中文概述 | 2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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