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

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Showing 6471 - 6480 of 13501 results

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

Class (Stereo):
CHEMICAL (MIXED)

Conditions:

Tisocromide exerts antihypoxic and antidepressant action. The details regarding mechanism of action and use are not available.
Status:
Investigational
Source:
INN:tivirapine
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Tivirapine, also known as R-86183, is a HIV-1 specific reverse transcriptase inhibitor. It inhibits the replication of HIV-1, but not HIV-2, in a variety of CD4+ T-cell lines and peripheral blood lymphocytes. Whereas an HIV-1 strain containing the Leu-100-->Ile mutation in the RT gene is about 400-fold less susceptible, R86183 still inhibits the replication of an HIV-1 strain containing the Tyr-181-->Cys RT mutation by 50% at a concentration of 130 nM. Tivirapine had been in phase I clinical trial for the treatment of HIV-1 infection. However, this development was discontinued.
Status:
Investigational
Source:
NCT00739739: Phase 2 Interventional Completed Interstitial Cystitis
(2008)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
NCT00570752: Phase 2 Interventional Completed Vascular Diseases
(2008)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



BMS-582949 acts as a dual action kinase inhibitor. It inhibits both p38 mitogen-activated protein kinase (p38 MAPK) activity and activation of p38. As a blocking agent for activation of p38 kinase BMS-582949 appeared to be well suited to resist such cellular responses that would drive p38 activation more strongly. BMS-582949 is in Phase II clinical trials for the treatment of rheumatoid arthritis, psoriasis, and atherosclerosis.
Status:
Investigational
Source:
NCT00169559: Phase 2 Interventional Completed Dyslipidaemias
(2003)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Conditions:

GW 590735 is a selective and potent agonist of peroxisome proliferator-activated receptor alpha (PPARα), a ligand-activated transcription factor that plays a key role in lipid homeostasis. Activation of PPARα results in increased clearance of triglyceride (TG) rich very low-density lipoprotein. GW 590735 was in phase II clinical trial for the treatment of dyslipidemia, but that study was discontinued.
Status:
Investigational
Source:
INN:epiroprim
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Epiroprim (Ro 11-8958) is a dihydrofolate reductase inhibitor. Epiroprim displayed activity against a broad range of bacteria including mycobacteria, staphylococci, enterococci, pneumococci, and streptococci as well as against Toxoplasma gondii. Epiroprim development has been discontinued.
Status:
Investigational
Source:
INN:sulfaclorazole
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Sulfaclorazole is a benzenesulfonamide derivative patented by Farbwerke Hoechst A.-G. as an antibacterial agent that active against Streptococcus pyogenes.
Status:
Investigational
Source:
INN:besunide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Besunide was studied as a diuretic agent.
Status:
Investigational
Source:
INN:besulpamide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Besulpamide has been developed as a diuretic agent.
Status:
Investigational
Source:
INN:etiracetam [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Etiracetam is a nootropic agent. (-)-(S) enantiomer of etiracetam levetiracetam (Keppra®) is used for the treatment of epilepsy.

Showing 6471 - 6480 of 13501 results