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

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Showing 361 - 370 of 3145 results

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

Class (Stereo):
CHEMICAL (ACHIRAL)

Valdipromide is an antidepressant.
Status:
Investigational
Source:
INN:clorindanic acid [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Clorindanic acid is a choleretic indanol derivative. Sterling Drug Inc. patented the compound in the 1960s. The compound is claimed to cause an increase in the rate of bile flow when administered to dogs. In rats, clorindanic acid was shown to have mild analgesic activity and hyperthermic effect.
Status:
Investigational
Source:
Tokai J Exp Clin Med. May 1990;15(2-3):123-7.: Not Applicable Human clinical trial Completed Liver Cirrhosis, Alcoholic/physiopathology
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
NCT00000806: Phase 1 Interventional Completed HIV Infections
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Telinavir (previously known as SC-52151) was developed as an anti-HIV aspartyl protease inhibitor for the treatment of HIV Infections. Telinavir participated in Phase I/II clinical study. In spite of the drug was well tolerated no antiviral activity was produced and further development of the drug was discontinued.
Status:
Investigational
Source:
INN:levomequitazine [INN]
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Levomequitazine is the L-enantiomer of mequitazine. The antihistaminergic activity mainly resides in the S-enantiomer, L-mequitazine, whereas the anticholinergic activity mainly resides in the D-enantiomer. It was shown, that L-enantiomer of mequitazine is less potent antagonist of human M3 muscarinic acetylcholine receptors than D-enantiomer. In vitro binding studies have shown that the affinity of L-mequitazine for H1 receptors is approximately ten times higher and to muscarinic receptors ten times lower, compared to d-mequitazine. Memory impairment was observed after administration of L-mequitazine 10 mg alone on delayed recall. This could be due to indirect effects of H1 receptor blockade. L-mequitazine 10 mg produced mild driving impairment, whereas L-mequitazine 2.5 and 5.0 mg show no effects on driving. Levomequitazine had been in phase III clinical trials by Pierre Fabre for the treatment of perennial allergic rhinitis and seasonal allergic rhinitis.
Status:
Investigational
Source:
INN:clofenamic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Clofenamic acid is a derivative of anthranilic acid, discovered by Parke-Davis. It possesses anti-inflammatory activity in the carrageenan-induced rat foot edema test.
Status:
Investigational
Source:
INN:clinolamide [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Clinolamide (cyclohexylamine of linoleic acid) is a drug developed by a Japanese company Sumitomo Chemical Co. Ltd. Clinolamide has been found to lower serum and liver cholesterol levels and to reduce the severity of atherosclerosis in cholesterol-fed rabbits.
Status:
Investigational
Source:
INN:tizoprolic acid [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Tizoprolic acid is an anti-lipolytic drug, a blood ketone lowering agent.
Status:
Investigational
Source:
INN:nixylic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Nixylic acid, an anilinonicotinic acid derivative, is an anti-inflammatory agent.
Status:
Investigational
Source:
INN:xanoxic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Xanoxic acid was developed as a bronchodilator that has never been marketed. Information about the current use of this agent is not available.