(Z)-4-[3-[2-(Trifluoromethyl)-9H-Thioxanthen-9-Ylidene]Propyl]Piperazine-1-Ethanol

CAS : 53772-82-0

Ref. 3D-FT100846

Informations sur le produit

• Nom: (Z)-4-[3-[2-(Trifluoromethyl)-9H-Thioxanthen-9-Ylidene]Propyl]Piperazine-1-Ethanol
• Synonymes: (Z)-4-(3-(2-(Trifluoromethyl)-9H-thioxanthen-9-ylidene)propyl)-1-piperazineethanol, 1-Piperazineethanol, 4-(3-(2-(trifluoromethyl)-9H-thioxanthen-9-ylidene)propyl)-, (Z)-, 1-Piperazineethanol, 4-[(3Z)-3-[2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]-, 4-[(3Z)-3-[2-(Trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]-1-piperazineethanol, 9H-Thioxanthene, 1-piperazineethanol deriv., Penthixol, Z-Flupentixol, Zuflupentixol, alpha-Flupenthixol, cis-(Z)-Flupenthixol, cis-(Z)-Flupentixol, cis-Flupenthixol, cis-Flupentixol, α-Flupenthixol

Description

The model system is a useful tool for the study of dopamine receptors. It has been shown to be an effective inhibitor of 5-HT2 receptors and locomotor activity in vitro. The model system has also been used to demonstrate that low doses of flupenthixol and flupentixol act as p-gp substrates in vitro, which may be due to their ability to inhibit dopamine uptake. This model system has also been used to develop an analytical method for measuring dopamine levels in human serum.
Designed by:

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 434.52 g/mol
• Formule: C₂₃H₂₅F₃N₂OS
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C23H25F3N2OS/c24-23(25,26)17-7-8-22-20(16-17)18(19-4-1-2-6-21(19)30-22)5-3-9-27-10-12-28(13-11-27)14-15-29/h1-2,4-8,16,29H,3,9-15H2/b18-5-
• Code InChI: InChIKey=NJMYODHXAKYRHW-DVZOWYKESA-N
• SMILES: OCCN1CCN(CC/C=C2/c3ccccc3Sc3ccc(C(F)(F)F)cc32)CC1