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

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Showing 231 - 240 of 3069 results

Status:
Investigational
Source:
INN:lamtidine
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

LAMTIDINE is an irreversible and specific gastric histamine H2-receptor antagonist.
Status:
Investigational
Source:
INN:becliconazole
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Becliconazole (or 1-CBCMI) is an antimycotic agent. Information about the nowadays application of this drug is not available
Status:
Investigational
Source:
INN:metiprenaline
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Metiprenaline was developed as a bronchodilator. Information about the current use of this compound is not available.
Status:
Investigational
Source:
INN:tiplasinin [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Conditions:

Tiplasinin (PAI-039) is an orally efficacious and selective plasminogen activator inhibitor-1 (PAI-1) inhibitor. Tiplasinin bound specifically to the active conformation of PAI-1 and exhibited reversible inactivation of PAI-1 in vitro. Tiplaxtinin exhibited in vivo oral efficacy in two different models of acute arterial thrombosis. The remarkable preclinical safety and metabolic stability profiles of tiplaxtinin led to advancing the compound to Phase-I clinical trial for Thrombosis, which was later discontinued.
Status:
Investigational
Source:
INN:cliropamine
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Cliropamine (D 16427) is a positive inotropic compound.
Status:
Investigational
Source:
INN:sufugolix [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



Sufugolix (TAK-013 or 5-(N-benzyl-N-methylaminomethyl)-1-(2,6-difluorobenzyl)-6-[4-(3-methoxyureido)phenyl]-3-phenylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione) is a highly potent and orally active non-peptide antagonist of luteinizing hormone-releasing hormone (LHRH) receptor. Sufugolix by oral administration suppresses a pituitary-ovarian axis continuously and reversibly in cynomolgus monkeys. Takeda studied Sufugolix in the trials for the treatment of endometriosis and uterine leiomyoma however development was discontinued.
Status:
Investigational
Source:
INN:trizoxime [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Trizoxime is an antidepressant.
Status:
Investigational
Source:
JAN:L-ISOPRENALINE HYDROCHLORIDE [JAN]
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)


Levisoprenaline (l-isoproterenol) is beta1- and beta2-adrenoreceptor agonist. In Japan, continuous inhalation of levisoprenaline is a recommended treatment for pediatric patients with acute severe exacerbation. Compared with salbutamol, l-isoproterenol reduced modified pulmonary index score more rapidly. But in most countries do not recommend continuous inhalation of l-isoproterenol to treat pediatric patients with acute severe exacerbation of asthma due to worsening asthma control. Levisoprenaline was used to cause experimental chronic heart failure in rats.
Status:
Investigational
Source:
NCT00004428: Phase 1 Interventional Completed Cystic Fibrosis
(1997)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



8-Cyclopentyl-1,3-dipropylxanthine (DPCPX) is a selective high-affinity antagonist radioligand for A1 adenosine receptors. DPCPX is a useful tool with which to explore the potential of activation of adenosine A1 receptors as an important mechanism in physiological and pathophysiological processes.
Status:
Investigational
Source:
NCT00106808: Phase 3 Interventional Completed Type 2 Diabetes Mellitus
(2005)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



Muraglitazar previously known as BMS-298585 has been identified as a non-thiazolidinedione dual agonist of peroxisome proliferator-activated receptor alpha/gamma. Muraglitazar is currently in clinical trial phase III development for the treatment of type 2 diabetes and dyslipidemia.