Andraxan is a toluidine derivative and a nonsteroidal antiandrogen that is structurally related to bicalutamide and nilutamide. Andraxan and its more potent active metabolite 2-hydroxyAndraxan competitively block dihydrotestosterone binding at androgen receptors, forming inactive complexes which cannot translocate into the cell nucleus. Formation of inactive receptors inhibits androgen-dependent DNA and protein synthesis, resulting in tumor cell growth arrest or transient tumor regression.
Other names for this medication:
Flutamide,
Andraxan,
Drogenil,
Etaconil,
Flutamida,
Flutan,
Ftda,
Fugerel,
Odyne,
Prostamide,
Prostandril,
Tafenil,
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Lansol,
Xanaes,
Pantecta,
Tamsin,
Griseofulvin,
Larona,
Solans,
Refluyet,
Omeran,
Aldactone,
Kenazol,
Synergin,
Roxithromycine,
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Colpofilin,
Fulviderm,
Aluron,
Lucen,
Rexan,
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Amoklavin,
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Winpen,
Gantrisin,
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The objective of the work is isolation of toxic peptides from Amanita phalloides--amatoxins (alfa-, beta-, gamma-amanitin) and phallotoxins (phalloidin, phallacidin, phallisin, phallisacin) by liquid chromatography on Sephadex LH-20 according to Yocum modification. In the 16 rats of Group II, after the section of the sural and peroneal branches a terminoterminal suture between their proximal stumps was made. As hyperosmolar diabetic non-ketotic coma results medicine acyclovir side effects in severe fluid depletion, electrolyte disturbance, profound hyperglycaemia and an altered mental state, the guiding principles of therapy include aggressive rehydration, insulin therapy, correction of electrolyte abnormalities and treatment of any underlying illnesses.
Myelinated nerve fibers in the parathyroid gland of the dog: a light and electron-microscopic study. Patients older tetraciclina acne antes e depois da than 80 years have increased mortality risk after esophagectomy, independent of comorbidity. Male Wistar rats were subjected to acute endotoxemia (Escherichia coli lipopolysaccharide (LPS) 6 mg kg(-1) intravenously (i.v.) for 6 h) and treated with vehicle (saline, 1 ml kg(-1) i.v.) or DL-propargylglycine (PAG, 10-100 mg kg(-1) i.v.), an inhibitor of the H2S-synthesizing enzyme cystathionine-gamma-lyase (CSE). Tear function in relation to the World Health Organization classification of cicatrization in trachoma.
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Cdk10, a Cdc2-related kinase, associates with the Ets2 transcription factor and modulates its transactivation activity. A 21mer peptide imitating this domain has been synthesized together with two mutants, one with ketilept drug store a S184 substituted by K and the other with the S184 deleted. The effects of heat-shock on nuclear matrix-associated DNA-replication complexes. The in vivo antibacterial activity of SC-004, a pivaloyloxymethyl ester of SC-002, was 1.2-8 times more protective against systemic infections due to Streptococcus pneumoniae, Escherichia coli and Klebsiella pneumoniae than that of CFDN.
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Do total and high density lipoprotein cholesterol and triglycerides act independently in dental antibiotics augmentin the prediction of ischemic heart disease? However, many aspects of antidepressant action are not understood.
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O2 and CO2 diffusivities for porous barriers and bactropin information now O2 and CO2 permeability coefficients for nonporous membranes were determined. When tested on guinea-pig ileum, compounds exhibited H1-antagonistic activity, (pA2 values) in the range of 8.6 to 9.7. In fetuses with polyhydramnios, no abnormal renal artery flow velocity waveforms were found.