U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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Showing 31 - 40 of 186 results

Status:
Investigational
Source:
INN:bifepramide [INN]
Source URL:

Class (Stereo):
CHEMICAL (UNKNOWN)

Bifepramide, (+)- belong to the class of parasympatholytic agents that reduce the activity of the parasympathetic nervous system.
Status:
Investigational
Source:
INN:isomolpan [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

ISOMOLPAN is a selective D3/D2 receptor agonist.
Status:
Investigational
Source:
INN:ibazocine
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Ibazocine is an analgesic that has never been marketed.
Status:
Investigational
Source:
INN:solypertine [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Solypertine (WIN-18413-2) is an antiadrenergic drug. Solypertine selectively blocked the conditioned avoidance response in rats. Solypertine potentiated hexobarbitone sleeping time, caused hypothermia and afforded protection from amphetamine toxicity inaggregated mice.
Status:
Investigational
Source:
INN:carbenzide
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Carbenzide is hydrazine derivative with the high antidepressant activity and low toxicity patented by pharmaceutical company Warner-Lambert Pharmaceutical Co. Carbenzide acts via monoamine oxidase (MAO) inhibition and increase the level of brain serotonin.
Status:
Investigational
Source:
INN:eproxindine [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Eproxindine (KC 3791) is an antiarrythmic. It is able to inactivate voltage-dependent sodium channels. Eproxindine also proved to be capable of blocking open potassium channels at outwardly directed potassium currents
Status:
Investigational
Source:
INN:lodaxaprine [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Lodaxaprine is a chemically original compound which possesses the pharmacological properties of a potent, p.o. active anticonvulsant. In mice, lodaxaprine antagonized electroconvulsive shock and chemically induced seizures with an overall potency comparable to that of carbamazepine. In naturally photosensitive Senegalese Papio-papio baboons lodaxaprine antagonized myoclonus and cortical paroxysmal discharges. In this model lodaxaprine was approximately one-fourth as potent as phenobarbital, twice as potent as carbamazepine and 6 times more potent than sodium valproate. Lodaxaprine had been in phase II clinical trial for the treatment of epilepsy. However, this development was discontinued.
Status:
Investigational
Source:
INN:mobenzoxamine [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Mobenzoxamine is gastro-intestinal function modulator, that enhanced gastric emptying. In preclinical models clathrate compound of mobenzoxamine with beta-cyclodextrin showed a clear amelioration of the delayed gastric emptying induced by Barium chloride. On isolated guinea pig ileum, Mobenzoxamine inhibited contractions induced by various agonists equally to or more potently than trimebutine or papaverine.
Status:
Investigational
Source:
INN:methiomeprazine [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Status:
Investigational
Source:
INN:exepanol [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Exepanol (KC 2450), a benzoxepine derivative, is a gastrokinetic. It facilitated the peristaltic reflex. Exepanol enhances resting pressure of the lower esophageal sphincter.