Quinacrine Dihydrochloride

CAS: 69-05-6

Ref. TR-Q550610

Información del producto

• Nombre: Quinacrine Dihydrochloride
• Sinónimos: Mepacrine Hydrochloride, 1,4-Pentanediamine, N4-(6-chloro-2-methoxy-9-acridinyl)-N1,N1-diethyl-, hydrochloride (1:2), 1,4-Pentanediamine, N4-(6-chloro-2-methoxy-9-acridinyl)-N1,N1-diethyl-, dihydrochloride (9CI), Acridine, 6-chloro-9-[[4-(diethylamino)-1-methylbutyl]amino]-2-methoxy-, dihydrochloride (8CI), 2-Chloro-5-(ω-diethylamino-α-methylbutylamino)-7-methoxyacridine dihydrochloride, 2-Methoxy-6-chloro-9-(4-diethylamino-1-methylbutylamino)acridine dihydrochloride, 3-Chloro-7-methoxy-9-(1-methyl-4-diethylaminobutylamino)acridine dihydrochloride, 3-Chloro-9-(4'-diethylamino-1'-methylbutylamino)-7-methoxyacridine dihydrochloride, 6-Chloro-9-[[4-(diethylamino)-1-methylbutyl]amino]-2-methoxyacridine dihydrochloride, 866RP, Acrichin dihydrochloride, Atabrine hydrochloride, Atebrin, Atebrine, Atebrine hydrochloride, Chemiochin, Chinacrin hydrochloride, Crinodora, Erion, Malaricida, Mecryl, Mepacrine dihydrochloride, Mepacrine hydrochloride, Methoquine, Metochin, Metoquin, Metoquine, NSC 14229, Palacrin, Palusan, Pentilen, Quinacrine hydrochloride, SN 390
• CAS: 69-05-6

Descripción

Stability Hygroscopic
Applications Quinacrine 2HCl is a lipophilic cationic drug with multiple actions that is commonly used as an anti-protozoal agent. It is a non-selective MAO-A/B inhibitor.
References Bockelmann, S., et al.: J. Biol. Chem., 285, 38304 (2010); Wrench, A., et al.: PLoS ONE, 8, e54498 (2013); Kasymov, V., et al.: J. Neuroscience, 33, 435 (2013); Mori, T., et al.: Biol. Pharm. Bull., 35, 2243 (2012)

• Marca: TRC

Propiedades químicas

• Peso molecular: 472.88
• Fórmula: C₂₃H₃₀ClN₃O•2(HCl)
• Color/Forma: Light Yellow to Very Dark Yellow Solid
• InChI: , InChI=1S/C23H30ClN3O.2ClH/c1-5-27(6-2)13-7-8-16(3)25-23-19-11-9-17(24)14-22(19)26-21-12-10-18(28-4)15-20(21)23, 2*1H, /h9-12,14-16H,5-8,13H2,1-4H3,(H,25,26)
• Clave InChI: InChIKey=UDKVBVICMUEIKS-UHFFFAOYSA-N
• SMILES: CCN(CC)CCCC(C)Nc1c2ccc(Cl)cc2nc2ccc(OC)cc12.Cl.Cl