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Search results for phenyl root_names_stdName in Standardized Name (approximate match)
Status:
Investigational
Source:
NCT00667394: Phase 2 Interventional Completed Glioblastoma
(2008)
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Millennium Pharmaceuticals Inc's tandutinib (MLN-518), a piperazinyl derivative of quinazoline, is an orally active inhibitor of FLT3 kinase and family members PDGFR beta and c-Kit. Tandutinib inhibited FLT3 phosphorylation, downstream signaling and malignant growth in vitro and in animal models. The drug exhibited limited activity as a single agent in phase I and II clinical trials in patients with AML and myelodysplastic syndrome, but displayed promising antileukemic activity (90% complete remissions) in a phase I/II trial in patients with newly diagnosed AML when administered in combination with cytarabine and daunorubicin. Phase II clinical trials for tandutinib in patients with Glioblastoma have being discontinued. The use of tandutinib to treat AML has been granted fast-track status by the U.S. Food and Drug Administration. Phase II trials were underway., but later withwrawn.
Status:
Investigational
Source:
NCT00300963: Phase 2 Interventional Completed Schizophrenia
(2004)
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Talnetant (SB-223412) is a selective, orally active neurokinin 3 receptor antagonist and is under development for the potential treatment of several disorders, including irritable bowel syndrome, schizophrenia, chronic obstructive pulmonary disease, cough, overactive bladder and urinary incontinence. The most common adverse effects were headache, fatigue, and nausea.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Tarazepide is a cholecystokinin-A receptor (CCK-A) receptor antagonist that was studied as an antispasmodic agent. However, information about the current use of this drug is not available.
Status:
Investigational
Source:
INN:deutolperisone [INN]
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Deutolperisone is the muscle relaxant.
Status:
Investigational
Source:
Acta Trop. Apr 1997;65(1):23-31.: Not Applicable Veterinary clinical trial Completed Trypanosomiasis, African/blood/prevention & control
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Conditions:
Ethidium is a DNA intercalating agent first discovered as and used as a veterenary trypanocide. A bromide salt is commonly used as a fluorescent tag in molecular biology. The fluorescene of ethidium bromide increased 21 fold upon binding to double-stranded RNA, 25 fold upon binding double stranded DNA. Because of the binding to DNA, ethidium bromide is a powerful inhibitor of DNA polymerase.
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Imazodan, a phosphodiesterase III inhibitor was developed by Parke-Davis to treat heart failure and ischemic heart disorders. However, the study of this drug was discontinued.
Status:
Investigational
Source:
INN:methaphenilene [INN]
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Methaphenilene, an antihistaminic agent, was studied as a peroxisome proliferator. Information about the current use of this compound is not available.
Status:
Class (Stereo):
CHEMICAL (ACHIRAL)
ISOMETAMIDIUM (as a chloride salt) is widely used in tropical countries as an antiprotozoal agent to control animal trypanosomiasis. It is used principally in cattle but also in sheep, goats, buffalos, donkeys, horses, camels and dogs.
Status:
Class (Stereo):
CHEMICAL (ACHIRAL)
Class (Stereo):
CHEMICAL (ACHIRAL)
Bromoxanide shows high activity against 6-week-old worms of F. hepatica and the nematode Hae- monchus contortus at very low doses.