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

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Showing 1871 - 1880 of 36617 results

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

Class (Stereo):
CHEMICAL (ACHIRAL)

Clodanolene is a skeletal muscle contraction antagonist, closely related to dantrolene sodium. The drug has no measurable direct effect on the peripheral or central nervous systems. In a mouse of muscle spasticity (Straub-tail mouse), clodanolene induced skeletal muscle relaxation more effectively than neuromuscular blocking agents, local anesthetics, or centrally-acting muscle relaxants. Indirect evidence indicates clodanolene acts on caffeine-sensitive calcium stores in the muscle cells.
Status:
Investigational
Source:
INN:fenestrel
Source URL:

Class (Stereo):
CHEMICAL (MIXED)

Fenestrel (ORF-3858) is a nonsteroidal antizygotic compound. It antagonizes progesterone. Fenestrel is a post-coital contraceptive.
Status:
Investigational
Source:
INN:trimoprostil
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Trimoprostil is a synthetic prostaglandin E2 derivative and prostanoid receptor agonist, with potential gastric secretion inhibitor and antiulcerogenic activity. It has been shown to reduce hydrogen ion secretion, to enhance gastric bicarbonate secretion and to reduce aspirin-induced gastric mucosal injury. In contrast to many E prostaglandins, it does not lower the tone of the lower oesophageal sphincter. Trimoprostil was well tolerated and more effective than placebo in the treatment of mild to moderate symptomatic reflux oesophagitis. It may be protective to human squamous oesophageal mucosa. Trimoprostil was not as effective as cimetidine in the treatment of duodenal ulcer.
Status:
Investigational
Source:
INN:terbucromil
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

It is known that the terbucromil possessed uricosuric effects in man. However, information about the current development and use of this compound is not available.
Status:
Investigational
Source:
INN:dazmegrel
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



Dazmegrel [UK 38485] is a thromboxane synthetase inhibitor which was undergoing development in the treatment of thrombosis, ischaemic heart disease, arrhythmias and asthma. Pfizer were conducting phase II studies in Denmark and the UK, phase I studies in Germany and Italy, and preclinical studies in France. Later this research was discontinued.
Status:
Investigational
Source:
NCT01344148: Not Applicable Interventional Unknown status AIDS
(2009)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
NCT00801268: Not Applicable Interventional Terminated Polycystic Kidney
(2008)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



Emodin is a naturally occurring anthraquinone present in the roots of numerous plants and lichens and an active ingredient of various Chinese herbs. Emodin possesses various biological properties and serves as an anti-bacterial and anti-inflammatory agent. Emodin was studied as a potential anti-cancer agent: e.g., it was shown, that compound inhibits the invasion and migration of colon cancer cells in vitro and in vivo by blocking EMT, which is related with the inhibition of Wnt/β-catenin signaling pathway. Besides, emodin effectively ameliorates asthmatic airway inflammation and alternatively activated macrophages (AAMs) polarization, and thus can be a potential agent for the treatment of asthma. It is known that the Inhibition of AAMs is an alternative therapeutic strategy for treating asthma. Some experiments have revealed that emodin can be a beneficial dietary supplement in prolonging lifespan.
Status:
Investigational
Source:
NCT02977234: Phase 1/Phase 2 Interventional Unknown status Hydrosalpinx
(2016)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
INN:risocaine
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Conditions:

There is no information in the scientific papers related to the biological properties of risocaine (also known as n-propyl 4-aminobenzoate). However, exists mention, that it is used as a local anesthetic.
Status:
Investigational
Source:
INN:parbendazole
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Parbendazole is a potent inhibitor of microtubule assembly that was studied as an anthelmintic agent. Information about the current use of this drug is not available.

Showing 1871 - 1880 of 36617 results