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

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Showing 6621 - 6630 of 167129 results

Status:
Investigational
Source:
INN:adekalant
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Adekalant (H 345/52) is a new antiarrhythmic compound with low proarrhythmic activity. H 345/52 concentration-dependently blocked HERG-carried currents with an IC50 of 230 nM. H 345/52 preferentially bound to the open channel with unusually rapid kinetics and was trapped by channel closure. Voltage-independent behavior of H 345/52 was observed during both square-pulse and action potential clamp protocols. It is proposed that block of IKr is the principal mechanism by which H 345/52 delays repolarization in human myocardium. H 345/52 blocks I(Kr) with high potency and I(Ca) with somewhat lower potency and was found to delay ventricular repolarisation without substantially increasing temporal or spatial dispersion and without inducing early after-depolarisations or TdP.
Status:
Investigational
Source:
USAN:Acebrochol
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Acebrochol is a neuroactive steroid that may act as a sedative and hypnotic, through the mechanism of altering ligand-gated ion channels and cell surface receptors.
Status:
Investigational
Source:
INN:difemetorex
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Difemetorex is a stimulant drug of the piperidine class. It was used as an appetite suppressant, anorectic agent. Difemetorex has intolerable side effects such as insomnia, which limited its clinical use.
Status:
Investigational
Source:
INN:dietifen [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Targets:

Dietifen is an anesthetic, vasodilator and antifungal agent. The main pharmacological feature of the drug is its ability to cause expansion of the coronary vessels. It also has a moderate spasmolytic activity (reduces spasms of the muscles of the intestine and other internal organs) and somewhat inhibits the conduction of nervous excitement through the vegetative nodes. Significant changes in blood pressure and pulse rate does not cause, does not possess hormonal (estrogenic) activity. It is indicated for the treatment of chronic coronary insufficiency, angina pectoris, severe forms of coronary sclerosis and pre-infarction conditions (simultaneously with anticoagulants).
Status:
Investigational
Source:
INN:parcetasal
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Status:
Investigational
Source:
INN:iosumetic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Iosumetic Acid is a triiodoaminoisophthalic acid derivative patented by Schering A.-G. as contrast medium for direct and indirect lymphography.
Status:
Investigational
Source:
INN:iotrizoic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Iotrizoic Acid is acylated amino acid derivative patented by Swiss pharmaceutical company Cilag-Chemie A.-G. as x-ray contrasting agent
Status:
Investigational
Source:
NCT00533377: Phase 2 Interventional Completed Tibial Fractures
(2008)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Evatanepag (CP-533,536) is a prostaglandin E2 EP2 receptor agonist. It stimulates new bone formation on trabecular, endocortical, and periosteal surfaces and enhances fracture healing. Evatanepag was under development with Pfizer as a bone formation stimulant for therapeutic use in the healing of fractures.
Status:
Investigational
Source:
INN:inproquone [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Inproquone is a benzoquinone derivative used as a cytostatic and alkylating agent for cancer treatment
Status:
Investigational
Source:
INN:iobutoic acid
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Iobutoic Acid is a Triiodo-hydroxybenzamide derivative patented by Laboratoires Andre Guerbet as x-ray contrast media in cholecystography and as a choleretic agent.

Showing 6621 - 6630 of 167129 results