Similar to Delucemine
Cyclic compounds (2)
Sigma Aldrich (6)
TCI Chemicals (2)
AK Scientific (1)
Corontin · Difril · Segontin
Prenylamine (Segontin) is a calcium channel blocker of the amphetamine chemical class which was used as a vasodilator in the treatment of angina pectoris; it was introduced in the 1960s by German manufacturer Albert-Roussel pharma gmbh which was acquired by Hoechst AG in 1974 and which in turn became part of Sanofi Aventis in 2005. It was withdrawn from market worldwide in 1988 because it caused QT prolongation and Torsades de pointes which in turn caused sudden death. The cardiac side effects were not detected during clinical development, but only emerged after the drug was widely used.
Sensit · Fendilin · Senzit
Fendiline is a calcium channel blocker. It is nonselective.
Fendiline hydrochloride (13636-18-5)
Sensit · Fendiline · Fendilin
Pragman · N,N-dimethyl-3-phenyl-3-(p-tolyl)propylamine · tolpropamine hydrochloride
Tolpropamine is an antihistamine and anticholinergic used as an antipruritic.
3,3-Diphenylpropylamine is a form of diphenylpropylamine.
Fenpiprane is a drug used for functional gastrointestinal disorders.
Emepronium Bromide (3614-30-0)
Emepronium · Cetiprin
Emepronium (as emepronium bromide) is an anticholinergic drug used in urology as an antispasmodic. It can cause ulceration of esophagus, so it should be taken in orthostatic position with sufficient amounts of liquids.
Trimethyldiphenylpropylamine (N,N,1-Trimethyl-3,3-diphenylpropylamine) is a drug used for functional gastrointestinal disorders. It's tradename is Recipavrin. See also: Emepronium
Diisopromine or disoprominum, usually as the hydrochloride salt, is a synthetic spasmolytic which neutralizes spastic conditions of the biliary tract and of the sphincter of Oddi. It was discovered at Janssen Pharmaceutica in 1955. It is sold in South Africa under the brand name Agofell syrup as a mixture with sorbitol, and elsewhere as Megabyl.
HCl of prozapine · hexadiphene · maleate of prozapine
Delucemine (NPS-1506) is a drug which acts as an NMDA antagonist and a serotonin reuptake inhibitor, and has neuroprotective effects. It was originally investigated for the treatment of stroke and in 2004 was studied as a potential antidepressant.