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

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Showing 5911 - 5920 of 149123 results

Status:
Investigational
Source:
INN:lanproston
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

LANPROSTON is an analog of prostaglandin F2 alpha. It is used as veterinary medicament.
KW-2449, a multikinase inhibitor of FLT3, ABL, ABL-T315I, and Aurora kinase, is under investigation to treat leukaemia patients. KW-2449 is a multikinase inhibitor of FLT3, ABL, ABL-T315I, and Aurora kinase with IC50 values of 6.6nM, 14nM, 4nM and 48nM, respectively. KW-2449 has potent growth inhibitory activity against various types of leukaemia by several mechanisms of action. Kyowa Hakko Kirin Pharma Inc. (a US subsidiary of Kyowa Hakko Kirin Co) was developing KW-2449 for the treatment of acute lymphoblastic leukaemia; acute myeloid leukaemia; chronic myeloid leukaemia; myelodysplastic syndromes, but later these studies were discontinued.
Status:
Investigational
Source:
INN:lanepitant
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

LANEPITANT is a selective nonpeptide antagonist for the neurokinin-1 receptor. It inhibits neurogenic dural inflammation. LANEPITANT was under development as a potential analgesic drug for the treatment of migraine, arthritis and diabetic neuropathy. However, it failed to show sufficient efficacy to support further development.
Status:
Investigational
Source:
INN:doliracetam
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Doliracetam possesses activity on the central nervous system. It has cognition enhancing properties and might be useful in the treatment of Alzheimer’s disease and epilepsy
Status:
Investigational
Source:
INN:domoprednate
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Domoprednate is a corticosteroid, a glucocorticoid, with anti-inflammatory and anti-allergic properties. Domoprednate is inferior to betamethasone valerate in the same category of dermatoses and equally well tolerated. It can be characterized as a medium-active corticosteroid. Domoprednate can be used topically in the treatment of skin disorders, such as eczema, psoriasis and atopic dermatitis.
Status:
Investigational
Source:
NCT00446134: Phase 2 Interventional Completed Chronic Hepatitis C
(2007)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Taribavirin, an oral prodrug of ribavirin that was developed as nucleoside antimetabolite, which interferes with duplication of viral genetic material. Taribavirin was studied in phase III clinical trial for the treatment of chronic hepatitis C patients. However, this drug not yet approved for pharmaceutical use.
Status:
Investigational
Source:
INN:hexadiline
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Hexadiline was used as an internal standard in liquid chromatography-mass spectrometry.
Status:
Investigational
Source:
INN:dazadrol [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Dazadrol is an antidepressant compound, developed by Schering Corp in the late 1960s. Dazadrol blocks uptake of noradrenaline and inhibits both basal and induced gastric acid secretion in the rat.
Status:
Investigational
Source:
INN:naphthonone [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Naphthonone is an antitussive agent.
Status:
Investigational
Source:
NCT00243230: Phase 2 Interventional Completed HIV Infections
(2005)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)



Vicriviroc or SCH 417690 is a potent and selective antagonist of the CCR5 receptor. vicriviroc binds specifically to the CCR5 receptor and prevents infection of target cells by CCR5-tropic HIV-1 isolates. In antiviral assays, vicriviroc showed potent, broad-spectrum activity against genetically diverse and drug-resistant HIV-1 isolates and was consistently more active than SCH-C in inhibiting viral replication. This compound demonstrated synergistic anti-HIV activity in combination with drugs from all other classes of approved antiretrovirals. Competition binding assays revealed that vicriviroc binds with higher affinity to CCR5 than SCH-C. Functional assays, including inhibition of calcium flux, guanosine 5'-[35S]triphosphate exchange, and chemotaxis, confirmed that vicriviroc acts as a receptor antagonist by inhibiting signaling of CCR5 by chemokines. Finally, vicriviroc demonstrated diminished affinity for the human ether a-go-go related gene transcript ion channel compared to SCH-C, suggesting a reduced potential for cardiac effects. Vicriviroc represented a promising new candidate for the treatment of HIV-1 infection. Vicriviroc for HIV treatment was previously in Phase III studies but has since been discontinued.

Showing 5911 - 5920 of 149123 results