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Search results for nonoxynol root_codes_url in Code URL (approximate match)
Class (Stereo):
CHEMICAL (RACEMIC)
Draquinolol is a cardioselective beta-adrenoceptor antagonist with a long duration of action in vivo. The long duration of action of draquinolol in vivo is due to the formation of a tight complex with beta 1-adrenoceptors. Draquinolol reduced an exercise tachycardia.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Orestrate was developed as an estrogenic steroid that has never been marketed.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Estrapronicate is a synthetic estrogen exerting anabolic properties.
Status:
Investigational
Source:
INN:quinezamide [INN]
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Quinezamide is a pyrazolo[1,5-c]quinazoline derivative patented by E. Gy. T. Gyogyszervegyeszeti Gyar, Hung as antiulcerogenic compound.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Tamethicillin is a basic ester pro-drug of methicillin (MET) which is converted in the body by non-specific esterases to MET. Tamethicillin was used as an antibacterial agent in the veterinary as a useful alternative for the treatment of mastitis in livestock, especially in mastitis due to beta-lactamase-producing Staphylococcus.
Class (Stereo):
CHEMICAL (ACHIRAL)
Glicondamide is a derivative of sulphonamides (antibacterial sulfa drugs). It acts by increasing the release of insulin from pancreatic beta cells, resulting in lower blood glucose levels.
Class (Stereo):
CHEMICAL (RACEMIC)
Brefonalol also known as BDF 8186, a beta-adrenergic blocking agent with vasodilating properties. This drug was being developed for the treatment of hypertension, arrhythmias and angina pectoris. However, these studies were discontinued.
Class (Stereo):
CHEMICAL (RACEMIC)
ISOXAPROLOL is a potent beta-adrenoceptor antagonist with antihypertensive properties. It was effective in lowering blood pressure in acute trials on spontaneously hypertensive rats at a dosage of 15 mg/kg.
Class (Stereo):
CHEMICAL (RACEMIC)
Fadolmidine (MPV 2426) is an alpha2-adrenoceptor agonist. Fadolmidine displayed high affinity and full agonist efficacy at all three human alpha2-adrenoceptor subtypes (A, B and C). Various preclinical models of pain have been employed and have demonstrated fadolmidine potential as an analgesic, including its potential for use in neuropathies and post-operative pain. A Phase II clinical trial successfully demonstrated that intrathecal fadolmidine, in combination with bupivacaine, produced analgesic effects compared to bupivacaine alone in bunionectomy patients.
Class (Stereo):
CHEMICAL (RACEMIC)