Radafaxine hydrochloride

小分子

盐酸雷达法辛

1-[2-[Bis-(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine dihydrochloride | (+)-(2s,3s)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride salt | (2S,3S)-2-(3-Chlorophenyl)-3,5,5-trimethyl-2-morpholinol | HY-17590 | UNII-SYD411HZ3S

Radafaxine hydrochloride

R646904-5mg

5mg

≥99%

2-8°C储存,干燥

冰袋运输

Radafaxine hydrochloride (GW-353162A) is a DAT (dopamine transporter) and NET(norepinephrine transporter) transporters inhibitor, and nAChR family modulator. Radafaxine hydrochloride (GW-353162A) is a potent metabolite of bupropion and selective for inhibiting the reuptake of norepinephrine over dopamine . In Vitro The relatively low potency of Radafaxine hydrochloride (GW-353162A) in blocking DAT and its slow blockade suggests that it is unlikely to have reinforcing effects. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid

盐酸瑞达法辛 (GW-353162A) 是一种 DAT（多巴胺转运体）和 NET（去甲肾上腺素转运体）转运体抑制剂和 nAChR 家族调节剂。盐酸雷达法辛 (GW-353162A) 是安非他酮的强效代谢物，对抑制多巴胺转运体和去甲肾上腺素转运体具有选择性。

106083-71-0

C13H19Cl2NO2

292.2 g/mol

9838996

C[C@H]1[C@@](OCC(N1)(C)C)(C2=CC(=CC=C2)Cl)O.Cl

(2S,3S)-2-(3-chlorophenyl)-3,5,5-trimethylmorpholin-2-ol;hydrochloride

1S/C13H18ClNO2.ClH/c1-9-13(16,17-8-12(2,3)15-9)10-5-4-6-11(14)7-10;/h4-7,9,15-16H,8H2,1-3H3;1H/t9-,13+;/m0./s1

ORXTVTDGPVINDN-BTJVGWIPSA-N

CC1C(OCC(N1)(C)C)(C2=CC(=CC=C2)Cl)O.Cl

9838996

H2O : 33.33 mg/mL (114.07 mM; Need ultrasonic) DMSO : 25 mg/mL (85.56 mM; Need ultrasonic)

3

3

1

291.079 Da

291.079 Da

41.500 Ų

18

0

285.000

0

2

NONHforallmodesoftransport