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

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Showing 6121 - 6130 of 167129 results

Status:
Investigational
Source:
NCT01702467: Phase 1 Interventional Completed Alzheimer's Disease
(2012)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

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

Class (Stereo):
CHEMICAL (ACHIRAL)

Indimilast is dioxodihydropyridopyrimidine derivative patented by global pharmaceutical company AstraZeneca as phosphodiesterase IV inhibitor. Indimilast modulates lung inflammation and causes bronchodilation by increasing intracellular cyclic adenosine 3', 5'-monophosphate in airway smooth muscle and inflammatory cells. Indimilast is potentially useful in chronic obstructive pulmonary disease but its activity was never evaluated in clinical trials.
Status:
Investigational
Source:
INN:iprocrolol
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

IPROCROLOL is a beta-adrenoceptor antagonist with antiarrhythmic properties.
Status:
Investigational
Source:
INN:iozomic acid
Source URL:

Class (Stereo):
CHEMICAL (MIXED)

Iozomic Acid is triiodobenzoic acid derivative patented by Pharmacia Aktiebolag as X-ray contrast agent for Coronary Angiography.
HU-308 ([(1R,2R,5R)-2-[2,6-dimethoxy-4-(2-methyloctan-2-yl)phenyl]-7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl]methanol) is a potent, selective agonist for the CB2 receptor. The synthesis and characterization took place in the laboratory of Prof. Mechoulam at the Hebrew University of Jerusalem in the late 1990s. It has analgesic effects, promotes proliferation of neural stem cells,[3] and protects both liver and blood vessel tissues against oxidative stress via inhibition of TNF-α. In vivo, HU-308 has hypotensive, analgesic, and anti-inflammatory activities in mice that can be reversed by the CB2 receptor antagonist SR 144528 but not the CB1 receptor antagonist rimonabant. Pretreatment of mice with HU-308 decreases the I/R-induced tissue damage, inflammatory cell infiltration, tissue, and serum TNF-α, MIP-1, and MIP-2 levels, tissue lipid peroxidation, and apoptosis. HU-308 increases proliferation of HT29 colon cancer cells and growth of tumors in an HT29 mouse xenograft model. The physiological and toxicological properties of this compound have not been evaluated in humans.
Status:
Investigational
Source:
Int J Dermatol. Jan 2007;46(1):89-93.: Not Applicable Human clinical trial Completed Acne Vulgaris
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
INN:fursalan
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Fursalan was studied as a disinfectant. Information about the current use of this compound is not available.
Status:
Investigational
Source:
INN:recainam
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Recainam is an investigational Class I anti-arrhythmic agent that has been studied for its potential in treatment of heart rhythm disorders. No severe adverse events of intravenous recainam adminstration were reported in a study in patients with frequent ventricular premature complexes (extra heart beats) and nonsustained ventricular tachycardia (abnormally fast heartbeat).
Status:
Investigational
Source:
NCT02342249: Phase 2 Interventional Completed Influenza A
(2014)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)


JNJ-872 is an inhibitor of influenza virus replication that offers a potential for the treatment of pandemic and seasonal influenza.
Status:
Investigational
Source:
INN:odalprofen
Source URL:

Class (Stereo):
CHEMICAL (MIXED)

Odalprofen was used as an analgesic. Information about the current use of this compound is not available.

Showing 6121 - 6130 of 167129 results