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

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Showing 6011 - 6020 of 167129 results

Status:
Investigational
Source:
NCT03168737: Phase 1 Interventional Active, not recruiting Malignant Breast Neoplasm
(2017)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Fluorine-18 is a fluorine radioisotope used in positron emission tomography (PET). It is used commonly for tumor, cardiac, and brain imaging, as well as to detect infections.
Status:
Investigational
Source:
Radiother Oncol. Mar 2004;70(3):295-9.: Phase 3 Human clinical trial Completed N/A
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Targets:


Misonidazole is a nitroimidazole with radiosensitizing and antineoplastic properties. Exhibiting high electron affinity, misonidazole induces the formation of free radicals and depletes radioprotective thiols, thereby sensitizing hypoxic cells to the cytotoxic effects of ionizing radiation. This single-strand breaks in DNA induced by this agent result in the inhibition of DNA synthesis. The drug also possesses a substantial cytotoxic effect, independent of radiation, which is selectively expressed in hypoxic cells. Misonidazole may be cytotoxic to the normal hypoxic tissues in the human body, making this became a major concern in the clinical application of the drug. Misonidazole leads to strand breaks in cellular DNA and those cells which fail to survive also fail to repair these strand breaks. Misonidazole depletes intracellular glutathione and is more toxic in glutathione depleted cells.
Status:
Investigational
Source:
USAN:Acetyltannic Acid
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Acetyltannic acid is an astringent (intestinal) for foals, calves, dogs. It is used for treatment of diarrhoea.
Status:
Investigational
Source:
INN:nemazoline
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Nemazoline (A-57219) is a nasal decongestant. It has alpha 1-agonist/alpha 2-antagonist activity and was more effective and long-acting than oxymetazoline on canine nasal mucosa, in-vitro and in-vivo. Upon intranasal administration to dogs, the compound was devoid of systemic effects up to a concentration 1000 times that needed for local decongestant effect (1.65 micrograms, atomized from a 1 microgram mL-1 solution) suggesting limited mucosal absorption. After nasal administration to rats for 15 days at a concentration 1000 times greater than that required for nasal decongestion, no mucosal tissue toxicity or systemic effects were seen.
Status:
Investigational
Source:
INN:napitane [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Napitane [A 75200, ABT 200] is a norepinephrine uptake inhibitor and α2 adrenoceptor antagonist. It was undergoing clinical trials with Abbott in the USA as a treatment for depression. However it was discontinued later. Napitane is a potent alpha 2-adrenoceptor antagonist (Ki = 1.2 nM) with modest norepinephrine uptake-blocking activity (IC50 = 841 nM).
Status:
Investigational
Source:
INN:ciclopramine
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Ciclopramine is a tetracyclic antidepressant patented by the pharmaceutical company “Chemische Fabrik Promonta G.m.b.H.” for central nervous system disorders treatment.
Status:
Investigational
Source:
NCT00983060: Phase 2 Interventional Completed Chronic Hepatitis C Genotype-1 Relapse
(2009)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

9-(N-methyl-L-isoleucine)-cyclosporin A (NIM-811, SDZ 811) is a cyclosporin A analog that is completely devoid of immunosuppressive capacity but exhibits potent and selective anti-human immunodeficiency virus type 1 (HIV-1) activity. NIM-811 interferes at two stages of the viral replication cycle: (i) translocation of the preintegration complex to the nucleus and (ii) production of infectious virus particles. NIM-811 induces a concentration-dependent reduction of HCV RNA in the replicon cells with an IC50 of 0.66 uM at 48 h. NIM-811 blocks the mitochondrial permeability transition induced by calcium and inorganic phosphate. NIM-811 blocks cell killing and prevents in situ mitochondrial inner membrane permeabilization and depolarization during tumor necrosis factor-α–induced apoptosis to cultured rat hepatocytes.Novartis discontinued development of SDZ 811 as an oral therapy for hepatitis C and HIV-1 infections.
Status:
Investigational
Source:
INN:ioglunide
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Ioglunide is an iodobenzene derivative patented by Laboratoires Andre Guerbet as an oil-based X-ray contrast medium. Iophendylate was commonly used in conventional myelography from the 1940s to the late 1980s before the utilization of computed tomography (CT), magnetic resonance imaging (MRI) and water-soluble contrast agents. Ioglunide, which was never shown to be safe, was initially introduced for use in small amounts for locating spinal tumors. It next appeared on the world scene for high volume, routine use, in diagnosing disc herniations.
Status:
Investigational
Source:
INN:iofratol
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Iofratol, is a dimeric, hexaiodinated radiographic contrast agent that was being developed by Bracco as a potential X-ray contrast medium for angiography and myelography.
Status:
Investigational
Source:
INN:mebolazine
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Mebolazine is an androgenic anabolic steroid.

Showing 6011 - 6020 of 167129 results