| Identification | Back Directory | [Name]
NOMIFENSINE MALEATE SALT | [CAS]
32795-47-4 | [Synonyms]
hoe984
Alival
merital
meritalam
hostalival
NSC-289114
NOMIFENSINE MALEATE
alival(antidepressant)
(±)-Nomifensine maleat
NOMIFENSINE MALEATE SALT
nomifensinhydrogenmaleate
nomifensinehydrogenmaleate
Nomifensine Maleic Acid Salt
NOMIFENSINE MALEATE SALT USP/EP/BP
2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinolin-2-ium-8-amine
1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolinamine maleate
8-amino-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinolinemaleate
1,2,3,4-tetrahydro-8-amino-2-methyl-4-phenyl-isoquinolinmaleate
2-Methyl-4-phenyl-1,2,3,4-tetrahydroisoquinolin-8-amine maleate
Dopamine Receptor,inhibit,Inhibitor,Nomifensine maleate,Nomifensine
8-ammonio-1,2,3,4-tetrahydro-2-methyl-4-phenylisoquinolinium maleate
1,2,3,4-TETRAHYDRO-2-METHYL-4-PHENYL-8-ISOQUINOLINAMINE MALEATE SALT
1,2,3,4-tetrahydro-2-methyl-4-phenyl-8-isoquinolinamin(z)-2-butenedioate | [EINECS(EC#)]
251-223-7 | [Molecular Formula]
C20H22N2O4 | [MDL Number]
MFCD00069320 | [MOL File]
32795-47-4.mol | [Molecular Weight]
354.4 |
| Chemical Properties | Back Directory | [Melting point ]
199-201° | [storage temp. ]
Refrigerator, Under Inert Atmosphere | [solubility ]
DMSO (Slightly), Methanol (Slightly, Heated) | [form ]
Solid | [color ]
Crystals from EtOH | [Water Solubility ]
Water : 2.2 mg/mL (6.21 mM; Need ultrasonic) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
22-36/37/38 | [Safety Statements ]
26-36 | [RIDADR ]
3249 | [WGK Germany ]
3
| [RTECS ]
NX4912800
| [HazardClass ]
6.1(b) | [PackingGroup ]
III | [Toxicity]
LD50 in mice, rats (mg/kg): 400, 430 orally; 90, 72 i.v.; in mice (mg/kg): 410 s.c. (Hoffman, 1973) |
| Hazard Information | Back Directory | [Chemical Properties]
Pale Yellow Solid | [Originator]
Alival,Hoechst,W. Germany ,1976 | [Uses]
A novel antidepressant distinguished from existing tricyclic and tetracyclic antidepressants by its bicyclic structure. | [Uses]
Antidepressant;Dopamine uptake inhibitor | [Manufacturing Process]
A solution of N-(2-aminobenzyl)-1-phenyl-2-methylaminoethanol-1 was prepared by the reaction of α-bromo-acetophenone and (2nitrobenzyl)methylamine, followed by hydrogenation of the nitro group by means of nickel on diatomaceous earth at room temperature and reduction of the CO group by means of sodium borohydride. The intermediate thus produced was dissolved in 100 ml of methylene chloride and introduced dropwise into 125 ml of sulfuric acid at 10° to 15°C. After a short standing, the reaction mixture was poured onto ice and rendered alkaline by means of a sodium hydroxide solution. By extraction with ether, there was obtained 1,2,3,4-tetrahydro-2-methyl-4-phenyl-8-amino-isoquinoline. The base is reacted with maleic acid to give the maleate; melting point of the maleate 199° to 201°C (from ethanol).
| [Brand name]
Merital (Hoechst-Roussel). | [Therapeutic Function]
Psychostimulant | [Biochem/physiol Actions]
Nomifensine maleate is a selective dopamine uptake inhibitor interacting with the dopamine transporter, at a site different from that of cocaine; antidepressant. Nomifensine serves as an antidepressant and is known to cause frequent hemolytic anemia. The aniline group in this compound results in blood and liver toxicities. | [Safety Profile]
Poison by ingestion,subcutaneous, intravenous, and intraperitoneal routes.Human systemic effects by intravenous route: heart ratechanges, blood pressure elevation. Experimentalreproductive effects. An antidepressant. When heated to decomposition it em | [storage]
Store at +4°C |
|
|