2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐
| 中文名称 | 2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐 |
|---|---|
| 中文同义词 | 2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐;化合物 T13918;R-568 盐酸盐;(R)-3-(2-氯苯基)-N-(1-(3-甲氧基苯基)乙基)丙-1-胺盐酸盐;R-568 盐酸盐,10 MM DMSO 溶液 |
| 英文名称 | 2-Chloro-N-[(1R)-1-(3-methoxyphenyl)ethyl]-benzenepropanaminehydrochloride |
| 英文同义词 | 2-Chloro-N-[(1R)-1-(3-methoxyphenyl)ethyl]-benzenepropanaminehydrochloride;R 568 hydrochloride;Tecalcet (Hydrochloride);R-568;(R)-3-(2-Chlorophenyl)-N-(1-(3-methoxyphenyl)ethyl)propan-1-amine hydrochloride;3-(2-chlorophenyl)-N-[(1R)-1-(3-methoxyphenyl)ethyl]propan-1-amine, hydrochloride;Benzenepropanamine, 2-chloro-N-[(1R)-1-(3-methoxyphenyl)ethyl]-, hydrochloride (1:1);R-568 hydrochloride >=95% (HPLC) |
| CAS号 | 177172-49-5 |
| 分子式 | C18H23Cl2NO |
| 分子量 | 340.28732 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 177172-49-5.mol |
| 结构式 | ![]() |
2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐 性质
| 熔点 | 183.3-184.4 °C |
|---|---|
| 储存条件 | Inert atmosphere,Room Temperature |
| 溶解度 | DMSO:50 mg/mL(146.93 mM;需要超声波) |
| 形态 | 粉末 |
| 颜色 | 白色至米白色 |
| 旋光度 (Optical Rotation) | [α]/D +35 to +40°, c =0.5 in chloroform-d |
| InChI | 1S/C18H22ClNO.ClH/c1-14(16-8-5-10-17(13-16)21-2)20-12-6-9-15-7-3-4-11-18(15)19;/h3-5,7-8,10-11,13-14,20H,6,9,12H2,1-2H3;1H/t14-;/m1./s1 |
| InChIKey | YJXUXANREVNZLH-PFEQFJNWSA-N |
| SMILES | C[C@@H](NCCCC1=C(C=CC=C1)Cl)C2=CC=CC(OC)=C2.Cl |
Tecalcet (NPS 568, 0.1-100 μM) increase [Ca
2+
]i in a concentrationdependent and stereoselective manner.
Tecalcet (NPS 568, 0.1-100 nM) shiftes the concentration-response curve for extracellular Ca
2+
to the left without affecting the maximal response and, thereby, decreases
the EC
50
value for extracellular Ca21 to 0.61±0.04 mM.
Tecalcet (1.5 and 15 mg/kg, orally, twice daily for 4 days) inhibits PT cell proliferation in rats with renal insufficiency.
| Animal Model: | 10-wk-old Male Sprague-Dawley rats weighing 310-350 g. |
| Dosage: | 1.5 and 15 mg/kg. |
| Administration: | Orally twice daily for 4 days. |
| Result: |
Did not significantly change serum 1,25 (OH)
2
D
3
levels. In contrast, serum PTH levels were reduced by in a dose-dependent manner.
Clearly reduced the number of BrdU-positive PT cells by 20% at a low dose (1.5 mg/kg body wt), and by 50% at a high dose (15 mg/kg body wt), indicating an antiproliferative effect on PT cells. Reduced PT cell volume in a dose-dependent manner. |
安全信息
| WGK Germany | WGK 3 |
|---|---|
| 存储类别 | 11 - 可燃固体 |
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026/06/05 | HY-10167A | 2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐 Tecalcet Hydrochloride | 177172-49-5 | 1 mg | 335元 |
| 2026/06/05 | HY-10167A | 2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐 Tecalcet Hydrochloride | 177172-49-5 | 5mg | 938元 |
![2-氯-N-[(1R)-1-(3-甲氧基苯基)乙基]苯丙胺盐酸盐 结构式](CAS/20200331/GIF/177172-49-5.gif)