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

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Showing 1291 - 1300 of 149123 results

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

Class (Stereo):
CHEMICAL (ACHIRAL)

Etolotifen is an antiasthmatic agent.
Status:
Investigational
Source:
INN:broxaldine
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Broxaldine, also known as brobenzoxaldine, is a dibromo derivative of quinaldine. It was used in combination with other halogenated hydroxyquinoline compound broxyquinoline (INTESTOPAN) for the treatment of intestinal amoebiasis and childhood diarrhea. In a specific ratio of 5/1, they were shown to act synergistically against several pathogens.
Status:
Investigational
Source:
INN:gamcemetinib [INN]
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

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

Class (Stereo):
CHEMICAL (ABSOLUTE)

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

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
NCT02913443: Phase 1 Interventional Completed Small Cell Lung Cancer
(2016)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
INN:glicaramide
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Glicaramide is a compound with anti-diabetic (hypoglycemic) activity. It is a second-generation sulfonylurea with a structure similar to glibenclamide, but with 2-methoxy-5-chlorobenzyl replaced by a cyclic acyl group. Peroxisome proliferator-activated receptor gamma (PPARgamma) agonistic activity of glicaramide has been observed as well. Glicaramide has been suggested to have more pronounced extra-pancreatic effects than glibenclamide or tolbutamide.
Status:
Investigational
Source:
INN:ciclotizolam
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Ciclotizolam is triazolothienodiazepines derivative useful as anticonvulsants, muscle relaxants, anxiolytics, anti-tension agents, and appetite stimulators for mammals.
Status:
Investigational
Source:
INN:meluadrine
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)



Meluadrine (Hoku 81) is a beta-adrenergic receptor agonist with tocolytic activity. Meluadrine binds to and activates beta-2 adrenergic receptors of myometrial smooth muscle in the uterus, thereby activates adenyl cyclase, an enzyme that catalyzes the conversion of adenosine triphosphate (ATP) to cyclic-3',5'-adenosine monophosphate (cAMP). Increased cAMP levels leads to a reduction in intracellular calcium concentration, thereby causes smooth muscle relaxation and decreases the intensity of uterine contractions. Meluadrine is a bronchodilator, and one of the metabolites of tulobuterol. Meluadrine was approximately 8 times more potent than tulobuterol, approximately twice as potent as salbutamol, and approximately as potent as isoprenaline in relaxing effect on the isolated tracheal smooth muscle preparation of guinea pigs.
Status:
Investigational
Source:
NCT02489344: Phase 2 Interventional Completed Fabry Disease
(2015)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)



Ibiglustat (GZ/SAR402671 or Genz-682452) is a small molecule inhibitor of glucosylceramide synthase. Ibiglustat has been demonstrated to effectively lower glycosphingolipid synthesis. Genzyme, a Sanofi Company is developing Ibiglustat for the treatment of Parkinson's Disease, Gaucher Disease, and Fabry Disease.

Showing 1291 - 1300 of 149123 results