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

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Showing 281 - 290 of 15581 results

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

Class (Stereo):
CHEMICAL (RACEMIC)

Sulfonterol is a benzenemethanol derivative patented by Smith Kline and French Laboratories as a bronchodilator. Sulfonterol acts as a β-adrenergic partial agonist.
Status:
Investigational
Source:
NCT01053962: Phase 2 Interventional Completed Chronic Idiopathic Constipation
(2010)
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Pirnabine is the synthetic dibenzopyran drug. It was developed as anti-glaucoma drug.
Status:
Investigational
Source:
INN:pararosaniline embonate [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Pararosaniline pamoate (CI 403-A) was developed as an orally active drug for the treatment of Schistosoma japonicum infection. The clinical trial has shown that capsules were safe and effective; in addition, this drug was well tolerated with a minimum of side effects, which were mostly mild and transient and did not require interruption of treatment. Besides, pararosaniline pamoate was an inhibitor of E.histolytica Hsp90 (EhHsp90) with promising activity against the parasite Pararosaniline pamoate, that causes amebiasis worldwide. Information about the current use of this drug is not available.
Status:
Investigational
Source:
INN:furcloprofen
Source URL:

Class (Stereo):
CHEMICAL (UNKNOWN)

Furcloprofen was developed as an analgesic agent with anti-inflammatory properties. Information about the current use of this compound is not available.
Status:
Investigational
Source:
INN:desglugastrin [INN]
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Desglugastrin is a gastric acid secretion stimulator. It dose dependently stimulated gastric acid secretion in anaesthetized rats. In view of the trophic action of gastrointestinal hormones on the exocrine pancreas, the effects of desglugastrin on the growth of hamster pancreatic well differentiated adenocarcinoma were investigated in vitro. Desglugastrin exhibited the greatest effect on thymidine incorporation into these cells after a lag period of 96 h. Doses of desglugastrin caused a significant and dose-dependent increase in thymidine incorporation.
Status:
Investigational
Source:
INN:enpiroline [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Enpiroline (WR 180,409) is an antimalarial compound. It demonstrates activity against Plasmodium falciparum both in vitro and in non-immune infected subjects. Additionally, it exerts antischistosomal activity.
Status:
Investigational
Source:
INN:indorenate [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Indorenate (TR3369, INDO) is a serotonin-like compound with high affinity for 5- HT1A receptors and a lower affinity for 5-HT1C and 5-HT1B receptors. Indorenate possesses antihypertensive and anxiolytic activity in animal behaviour tests. Similar to other serotonin receptor agonists, Indorenate also has anorectic activity; this effect was blocked by the administration of the 5-HT2A/2C receptor antagonists cinanserin, cyproheptadine, metergoline and methysergide. A unpublished clinical trial confirmed its antihypertensive activity in men.
Status:
Investigational
Source:
INN:flutroline [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Flutroline, an antipsychotic drug that was studied to treat patients with schizophrenia. Clinical trials have shown that the drug was a safe, effective, and 20 mg and above offered the best potential for optimal clinical effectiveness. However, information about the further development of this drug is not available.
Status:
Investigational
Source:
INN:lotucaine
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Lotucaine is a local anesthetic.
Status:
Investigational
Source:
INN:tigestol
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Tigestol is an Estrene derivative patented by Organon Laboratories Ltd. as an anabolic, androgenic, and progestative agent.