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

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Showing 961 - 970 of 15581 results

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

Class (Stereo):
CHEMICAL (RACEMIC)

Setazindol is an anorectic.
Status:
Investigational
Source:
INN:hexapradol
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Hexapradol was developed as a psychoanaleptic but was never marketed. Information about the current use of this drug is not available.
Status:
Investigational
Source:
INN:cliropamine
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Cliropamine (D 16427) is a positive inotropic compound.
Status:
Investigational
Source:
NCT00300963: Phase 2 Interventional Completed Schizophrenia
(2004)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)



Talnetant (SB-223412) is a selective, orally active neurokinin 3 receptor antagonist and is under development for the potential treatment of several disorders, including irritable bowel syndrome, schizophrenia, chronic obstructive pulmonary disease, cough, overactive bladder and urinary incontinence. The most common adverse effects were headache, fatigue, and nausea.
Status:
Investigational
Source:
INN:methaphenilene [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Methaphenilene, an antihistaminic agent, was studied as a peroxisome proliferator. Information about the current use of this compound is not available.
Status:
Investigational
Source:
INN:nantradol
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Levonantradol is a synthetic cannabinoid analogue of delta (9)-tetrahydrocannabinol (delta(9)-THC) administered intramuscularly. It has antiemetic and anti-analgesic properties. Although its precise mechanism of action is unknown, levonantradol appears to bind and activate the cannabinoid receptors CB1 and/or CB2. Antiemetic effect of levonantradol significantly superior to chlorpromazine. However, its adverse central effects limit its utility. The main adverse events are drowsiness and dizziness. Levonantradol, administered intramuscularly to the patients suffering from postoperative pain, manifested significant analgesic efficacy. Analgesia persisted for more than 6 h with the 2.5 and 3 mg doses of levonantradol. Drowsiness was frequent but few other psychoactive effects were reported.
Status:
Investigational
Source:
INN:atocalcitol
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)


Conditions:

Atocalcitol is a vitamin D analogue. A hallmark of vitamin D3 analogues in psoriasis amelioration is the ability to inhibit the proliferation of keratinocytes. Atocalcitol had been in phase II clinical trials for the treatment of psoriasis. However, this research has been discontinued.
Status:
Investigational
Source:
INN:brotianide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

BROTIANIDE is salicylanilide derivative used to treat fascioliasis in sheep. A dose of 7 mg/kg of brotianide shows 91-99% activity against 7-14 weeks old flukes; however, its activity against 6 weeks old flukes is weak (50-90%). It also possesses 85-90% activity against paramphistomes in sheep and cattle. The maximum tolerated dose of brotianide is 27 mg/kg in sheep.
Status:
Investigational
Source:
INN:bromoxanide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Bromoxanide shows high activity against 6-week-old worms of F. hepatica and the nematode Hae- monchus contortus at very low doses.
Status:
Investigational
Source:
INN:clazuril [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Clazuril is benzene-acetonitrile derivative, developed by Janssen Pharmaceutica as an anticoccidial agent for the treatment of pigeons. The anticoccidial effect is due to a cidal effect on the endogenous stages of the Eimeria species.