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

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Showing 501 - 510 of 1728 results

Status:
Investigational
Source:
INN:carbantel
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Carbantel is imidoylurea derivative patented by pharmaceutical company Sterling Drug Inc. As anthelmintic agent.
Status:
Investigational
Source:
Acta Trop. Apr 1997;65(1):23-31.: Not Applicable Veterinary clinical trial Completed Trypanosomiasis, African/blood/prevention & control
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Targets:


Ethidium is a DNA intercalating agent first discovered as and used as a veterenary trypanocide. A bromide salt is commonly used as a fluorescent tag in molecular biology. The fluorescene of ethidium bromide increased 21 fold upon binding to double-stranded RNA, 25 fold upon binding double stranded DNA. Because of the binding to DNA, ethidium bromide is a powerful inhibitor of DNA polymerase.
Status:
Investigational
Source:
INN:fludazonium chloride
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

FLUDAZONIUM is a topical antiinfective agent.
Status:
Investigational
Source:
INN:laurcetium bromide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

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:salazosulfamide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Salazosulfamide was studied for the treatment of ankylosing spondylitis. It was found that salazosulfamide efficacy is associated with N-acetyltransferase 1 polymorphisms and in particularly, NAT1 AA/GG genotype at 263 locus. However, future studies should be conducted to investigate these issues.
Status:
Investigational
Source:
INN:zinoconazole
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Zinoconazole, an imidazole derivative that was used as an antifungal agent. Information about the current use of this compound is not available.
Status:
Investigational
Source:
INN:ontianil [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
INN:amifloxacin
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Amifloxacin [WIN 49375] is a fluoroquinolone antibacterial with a broad range of activity against aerobic Gram-negative and some aerobic Gram-positive organisms. Amifloxacin is a DNA gyrase inhibitor. The 50% inhibiory concentration for supercoiling activity of E.coli KL16 DNA gyrase of amifloxacin (MIC, 0.10 ug/ml) was 2.47 ug/ml. Amifloxacin was in trials for the treatment of gram-negative infections, septic shock and urinary tract infections. However, development of amifloxacin has been discontinued.