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

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Showing 2281 - 2290 of 42705 results

Status:
Investigational
Source:
NCT00257621: Phase 2 Interventional Completed Infection, Human Immunodeficiency Virus I
(2004)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Brecanavir (previously known as VX-385), a HIV aspartyl protease inhibitor was developed for the treatment of HIV. The inhibition of HIV viral proteinase enzyme prevents cleavage of the gag-pol polyprotein, resulting in noninfectious, immature viral particles. Brecanavir reached Phase II development. However, GlaxoSmithKline announced to discontinue development brecanavir. Because of the inability to develop a viable oral dosage formulation capable of delivering the desired brecanavir levels in patients with multi-drug resistant HIV.
Status:
Investigational
Source:
INN:naxaprostene
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Naxaprostene (CG 4305) is a prostacyclin analogue, which causes concentration dependent inhibition of thrombocyte function. Naxaprostene is more selective for IP receptors and tends towards partial agonism. Naxaprostene prevented thrombotic arterial occlusion in rabbits.
Status:
Investigational
Source:
INN:deprostil
Source URL:

Class (Stereo):
CHEMICAL (UNKNOWN)

Deprostil is prostaglandin E analog. The drug exhibits a prolonged inhibition of basal gastric acid secretion. Deprostil is the orally active anti-ulcer agent. It is a racemate with four possible optical isomers. Like deprostil the (nat)- and (epi)-isomers appear to be potentially useful therapeutic agents for the treatment of hypergastrlc acid secretion and peptic ulcers.
Status:
Investigational
Source:
INN:dicirenone
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Dicirenone is an aldosterone antagonist. It is used as a hypotensive agent. Dicirenone inhibited the effects of aldosterone on urinary K(+):Na(+) ratios and the binding of [(3)H]aldosterone to renal cytoplasmic and nuclear receptors. Dicirenone blocked the action of aldosterone on Na-K ATPase. Cytoplasmic binding of [(3)H]aldosterone and dicirenone was similar in magnitude and involved the same set of sites. It had no effect on adrenal steroidogenesis.
Status:
Investigational
Source:
INN:iotranic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Iotranic Acid is triiodobenzoic acid derivative with potential application as new cholangiographic contrast media for liver imaging
Status:
Investigational
Source:
INN:ioxotrizoic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Ioxotrizoic acid is acylated 3,5-diaminopolyhalobenzoic acid derivative patented by Sterling Drug Inc. as X-ray contrast agent for liver and spleen.
Status:
Investigational
Source:
INN:feloprentan
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Feloprentan is an endothelin receptor antagonist.
Status:
Investigational
Source:
INN:butilfenin
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Butilfenin is N-substituted iminodiacetic acid derivative that was studied as tridentate ligand to form a technetium-99m complex.
Status:
Investigational
Source:
INN:metaterol
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Metaterol is a beta-adrenoceptor agonist. It exerts sympathomimetic and broncholytic properties.
Status:
Investigational
Source:
INN:metheptazine [INN]
Source URL:

Class (Stereo):
CHEMICAL (MIXED)

Metheptazine was studied as an analgesic agent.

Showing 2281 - 2290 of 42705 results