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Etalocib is a leukotriene B4 antagonist drug.
Etizolam is a thienodiazepine drug which is a benzodiazepine analog. The etizolam molecule differs from most other benzodiazepines in that the benzene ring has been replaced by a thiophene ring. It possesses amnesic, anxiolytic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties.
Etolorex is a anorectic of the amphetamine class. It was never marketed.
Febantel is a starting material to produce a broad spectrum benzimidazole anthelmintics and their derivatives such as fenbendazole and oxfendazole used in humans, sheep, cattle, and horses via the removal of a methoxyacetyl group and cyclisation process. Febantel is also used as an anthelmintic itself against gastrointestinal parasites in animals.
Fenbufen is a non-steroidal anti-inflammatory drug used primarily to treat inflammation in osteoarthritis, ankylosing spondylitis, and tendinitis. It can also be used to relieve backaches, sprains, and fractures. Fenbufen is effective when given twice daily and there is some evidence that once daily dosage is adequate in known responders to the drug.
Fentanyl is a potent synthetic narcotic analgesic with a rapid onset and short duration of action.Intravenous fentanyl is extensively used for anesthesia and analgesia, most often in operating rooms and intensive care units. It is often administered in combination with a benzodiazepine, such as midazolam, to produce procedural sedation for endoscopy, cardiac catheterization, oral surgery, etc. Additionally, fentanyl is often used in cancer therapy and other chronic pain management due to its effectiveness in relieving pain. It has also been found to be useful to improve the actions of local anesthetic during root canal treatment.
Fipexide is a psychoactive drug of the piperazine chemical class which was developed in Italy in 1983. It was used as a nootropic drug, mainly for the treatment of senile dementia, but is no longer in common use due to the occurrence of rare adverse drug reactions including fever and hepatitis. Chemically, it is an amide union of parachlorophenoxyacetate and methylenedioxybenzylpiperazine, and notably, has been shown to metabolize to the latter, which plays a significant role in its effects.
Flunixin is a non-steroidal anti-inflammatory drug (NSAID), analgesic, and antipyretic used in horses, cattle and pigs. It is often formulated as the meglumine salt.
Fluorine is the most electronegative and reactive of all elements. Natural fluorine is monoisotopic, consisting of fluorine-19. It has found uses in studies of protein structures and conformational changes. Elemental fluorine is occasionally used as a fluorinating agent in industrial processes. The largest use for elemental fluorine is preparing uranium hexafluoride, used in the production of nuclear fuels. Other than those, elemental fluorine is used for the production of tetrafluoromethane, plasma etching in semiconductor manufacturing, flat panel display production, and microelectromechanical systems fabrication. Inorganic fluorides and organofluorine compounds, a fraction of which are prepared from elemental fluorine, find use in a variety of materials and chemicals, including important pharmaceuticals, agrochemicals, lubricants, and textiles. Hydrofluoric acid and certain fluoride-containing salts are useful etchants for glass. In the electrolysis of the metal and its purification, it acts to lower the melting point of aluminium oxide and acts like a powerful flux for glass. Perfluorooctanoic acid and tetrafluoroethylene are directly used in water resistant coatings and in the production of low friction plastics such as Teflon, or PTFE. Other fluorine-based compounds are used in the production of haloalkanes such as chlorofluorocarbons, which are used extensively in air conditioning and in refrigeration. They have been banned for these applications because they contribute to ozone destruction.
GDC-0941 is an orally bioavailable, and is a potent small-molecule thieno[3,2-d]pyrimidine inhibitor of the class I phosphatidylinositol 3 kinase (PI3K) isoforms p100alpha and p100delta with potential antineoplastic activity.
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