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Restrict the search for
beta carotene
to a specific field?
Status:
Investigational
Source:
INN:benethamine penicillin [INN]
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Benethamine penicillin is a medium-long-acting insoluble penicillin salt. After a single injection, this salt acts and bacteriostatic level of penicillin is maintained in the blood for three to six days.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Lexacalcitol (KH1060) is over 100 times more active than 1alpha,25-dihydroxyvitamin D3 and is of potential interest in the treatment of psoriasis and other diseases characterized by accelerated cell growth and T lymphocyte activation, which was studied in the clinical trial. KH1060 also prevents type I diabetes in the preclinical investigation without significant effects on calcium or bone metabolism. In addition also was shown that neuroblastoma (NB) cell lines were more susceptible to growth inhibition by KH1060, suggesting its possible use in NB to potentiate the action of retinoids, which are in clinical use for this disease. The underlying biochemical reasons for the increased biological activity of KH1060 are unknown, but it can include 1) metabolic considerations in addition to explanations based upon 2) enhanced stability of KH1060-liganded transcriptional complexes.
Status:
Investigational
Source:
INN:dalbraminol [INN]
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Dalbraminol is a beta-adrenergic blocker, developed by Boehringer Mannheim.
Status:
Investigational
Source:
NCT00555919: Phase 2 Interventional Completed Metastatic Breast Cancer
(2008)
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Lonaprisan is an orally bioavailable pentafluoroethyl derivative of a mifepristone-related steroid with antiprogestagenic activity. Lonaprisan is a pure, highly receptor-selective progesterone receptor (PR) antagonist (both PR isoforms PR-A and PR-B); binding of this agent to PRs inhibits PR activation and the associated proliferative effects. Lonaprisan showed limited efficacy as second-line endocrine therapy in postmenopausal women with PR-positive metastatic breast cancer. Lonaprisan had been in phase II clinical trials by Bayer for the treatment of breast cancer and dysmenorrhea. However, this research has been discontinued.
Status:
Investigational
Source:
NCT00040989: Phase 2 Interventional Withdrawn Stage IV Renal Cell Cancer
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Afeletecan (Bay 38-3441) is a camptothecin glycoconjugate which stabilizes the active lactone form of camptothecin and allows selective uptake into tumor cells. Afeletecan is a topoisomerase inhibitor. Afeletecan was in phase I clinical trials with Bayer for the treatment of cancer; however, development appears to have been discontinued.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
Ciladopa, is a troponylpiperazine derivative and dopamine agonist that has been shown to influence dopaminergic mechanisms in animals. Preclinical pharmacological studies have suggested that it has antiparkinsonian activity similar to that of bromocriptine but without many of the troublesome side effects. Unfortunately in some clinical trials no significant differences was found among the treatment groups and placebo.
Status:
Investigational
Source:
INN:pyrrolifene [INN]
Source URL:
Class (Stereo):
CHEMICAL (UNKNOWN)
Pyrroliphene is a dialkylaminodiphenylbutanol ester with antitussive and analgesic activities. In clinical trials the major side effect of Pyrroliphene was sedation, and the other side effect liabilities were similar to those of morphine.
Class (Stereo):
CHEMICAL (RACEMIC)
Trigevolol is a beta-adrenergic blocking agent. It was developed as an antiarrhythmic and antihypertensive drug.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Enadoline (CI-977) is a potent and selective agonist at the kappa-opioid receptor. Enadoline is a potent antinociceptive agent. Clinical use of enadoline was associated with dose-limiting neuropsychiatric adverse events. Enadoline may yet find some application against ischaemic stroke and severe head injury, presumably in comatose patients.
Status:
Investigational
Source:
INN:cefdaloxime [INN]
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Cefdaloxime is a third-generation cephalosporin antibiotic patented by pharmaceutical company Roussel-UCLAF. Cefdaloxime activity was the poorest among the different oral cephalosporins.
