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Status:
Possibly Marketed Outside US
Source:
NCT00357019: Phase 4 Interventional Completed Keratoconjunctivitis, Vernal
(2001)
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
ISOSPAGLUMIC ACID is used as an antiallergic agent.
Status:
Possibly Marketed Outside US
Class (Stereo):
CHEMICAL (RACEMIC)
Targets:
Conditions:
Oxyfedrine, an amino ketone derivative and partial agonist at beta receptors, has been shown to have potent antianginal properties and to increase coronary blood flow in normal and ischemic myocardial regions.
Status:
Possibly Marketed Outside US
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Class (Stereo):
CHEMICAL (RACEMIC)
Trimethyldiphenylpropylamine (Recipavrin) is a methadon analog with antispasmodic properties. It exerts both musculotropic (antibarium) and anticholinergic action, relieves smooth muscle spasms, e.g. dysmenorrhea and pains associated with gallstones. It was marketed in Sweden in the 1960s as a spasmolytic drug under tradename Recipavrin.
Status:
Possibly Marketed Outside US
Source:
Amidefrine mesylate
Source URL:
Class (Stereo):
CHEMICAL (UNKNOWN)
Status:
Possibly Marketed Outside US
Source:
Amidefrine mesylate
Source URL:
Class (Stereo):
CHEMICAL (UNKNOWN)
Status:
Possibly Marketed Outside US
Source:
Ambenoxan by ZYF Pharm Chemical
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Ambenoxan is a muscle relaxant. Ambenoxan exerts its effects via an action on brain and/or spinal mechanisms. Ambenoxan has been shown to produce skeletal muscle flaccidity without loss of the righting reflex when administered orally or parenterally to rats, rabbits, dogs and monkeys. The drug is approximately twice as toxic orally as it is subcutaneously, which suggests that the compound is effectively absorbed by the oral route. Ambenoxan may be of value in the treatment of spastic disorders resulting from upper motor neurone damage in the brain or spinal cord, disseminated sclerosis, spastic diplegia and spastic hemiplegia.
Status:
Possibly Marketed Outside US
Source:
Althiazide by Solchem
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Altizide, a thiazide diuretic, and aldosterone antagonist, in combination with spironolactone was marketed under brand name Aldactazine to treat patients with mild to moderate hypertension. In addition, Aldactazine was investigated for the treatment of congestive cardiac insufficiency.
Status:
Possibly Marketed Outside US
Source:
Althiazide by Solchem
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Altizide, a thiazide diuretic, and aldosterone antagonist, in combination with spironolactone was marketed under brand name Aldactazine to treat patients with mild to moderate hypertension. In addition, Aldactazine was investigated for the treatment of congestive cardiac insufficiency.
Status:
Possibly Marketed Outside US
Source:
NCT01956409: Phase 4 Interventional Unknown status Breast Cancer Diagnosis
(2012)
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Fluorocholine-F18 is a tracer for positron emission tomography that can be used in oncology for the evaluation of metastatic prostate cancer, hepatocellular carcinoma, and recurrent brain tumor. After crossing the cell membrane by a carrier-mediated mechanism, Fluorocholine-F18 is converted to cytidinediphosphatecholine and incorporated into phosphatidylcholine which is a component of the cell membrane. This process has been found to be upregulated in malignant cells, providing a mechanism for the enhanced accumulation of radiolabelled choline by neoplasms.
