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PathWhiz ID Pathway Meta Data

PW128113

Pw128113 View Pathway
drug action

Fluspirilene Mechanism of Action Action Pathway

Homo sapiens
Fluspirilene is an antipsychotic agent used in the treatment of schizophrenia. Fluspirilene is a relatively long-acting injectable depot antipsychotic drug used for schizophrenia. Fluspirilene does not differ greatly from other depot antipsychotics (fluphenazine decanoate, fluphenazine enathate, perphenazine onanthat, pipotiazine undecylenate) with respect to treatment efficacy, response or tolerability.

PW144621

Pw144621 View Pathway
drug action

Flutamide Drug Metabolism Action Pathway

Homo sapiens

PW176051

Pw176051 View Pathway
metabolic

Flutamide Predicted Metabolism Pathway new

Homo sapiens
Metabolites of Flutamide are predicted with biotransformer.

PW146017

Pw146017 View Pathway
drug action

Flutemetamol (18F) Drug Metabolism Action Pathway

Homo sapiens

PW127830

Pw127830 View Pathway
drug action

Fluticasone Action Pathway

Homo sapiens
Fluticasone is a corticosteroid used in the treatment of corticosteroid-responsive dermatoses, asthma, and moderate to severe Chronic Obstructive Pulmonary Disease (COPD). Fluticasone is a synthetic glucocorticoid available as 2 esters, Fluticasone furoate, and Fluticasone propionate. It is available as an inhaler, nasal spray, and topical cream. As this molecule is a glucocorticoid, its mechanism of action is that of the glucocorticoid response element (GRE) of influencing COX-2/prostaglandin G/H synthase 2 suppression and lipocortin/annexin induction. By binding to the glucocorticoid receptor, it influences transcription factors AP-1 and NF-kB to block the transcription of COX-2/prostaglandin G/H synthase 2 which reduces the amount of prostanoids being produced from arachidonic acid. Prostanoids such as PGI2 and thromboxane A2 influence the effects of inflammation through vasoconstriction/dilation, pain sensitivity, and platelet aggregation. Fluticasone also affects the promoter of annexin-1, an important inflammatory protein as it affects leukocytes and blocks phospholipase A2 which reduces the amount of arachidonic acid being cleaved from the phospholipid bilayer. Reducing the amount of arachidonic acid formed further decreases the concentrations of prostanoids mentioned calming inflammation.

PW132543

Pw132543 View Pathway
metabolic

Fluticasone Drug Metabolism

Homo sapiens
Fluticasone is a drug that is not metabolized by the human body as determined by current research and biotransformer analysis. Fluticasone passes through the liver and is then excreted from the body mainly through the kidney.

PW146688

Pw146688 View Pathway
drug action

Fluticasone Drug Metabolism Action Pathway

Homo sapiens

PW127836

Pw127836 View Pathway
drug action

Fluticasone furoate Action Pathway

Homo sapiens
Fluticasone furoate is a synthetic trifluorinated corticosteroid that can be used as maintenance treatment for asthma and/or chronic obstructive pulmonary disease (COPD). This drug is also available as a nasal spray to manage the symptoms of allergic rhinitis. Fluticasone furoate has been shown in vitro to exhibit a binding affinity for the human glucocorticoid receptor that is approximately 29.9 times that of dexamethasone and 1.7 times that of fluticasone propionate. As this molecule is a glucocorticoid, its mechanism of action is that of the glucocorticoid response element (GRE) of influencing COX-2/prostaglandin G/H synthase 2 suppression and lipocortin/annexin induction. By binding to the glucocorticoid receptor, it influences transcription factors AP-1 and NF-kB to block the transcription of COX-2/prostaglandin G/H synthase 2 which reduces the amount of prostanoids being produced from arachidonic acid. Prostanoids such as PGI2 and thromboxane A2 influence the effects of inflammation through vasoconstriction/dilation, pain sensitivity, and platelet aggregation. Fluticasone furoate also affects the promoter of annexin-1, an important inflammatory protein as it affects leukocytes and blocks phospholipase A2 which reduces the amount of arachidonic acid being cleaved from the phospholipid bilayer. Reducing the amount of arachidonic acid formed further decreases the concentrations of prostanoids mentioned calming inflammation.

PW145881

Pw145881 View Pathway
drug action

Fluticasone furoate Drug Metabolism Action Pathway

Homo sapiens

PW127837

Pw127837 View Pathway
drug action

Fluticasone propionate Action Pathway

Homo sapiens
Fluticasone propionate is a synthetic glucocorticoid used to treat asthma, as well as inflammatory and pruritic dermatoses. This molecule can also besused as a nasal spray to treat allergic and nonallergic rhinitis. As this molecule is a glucocorticoid, its mechanism of action is that of the glucocorticoid response element (GRE) of influencing COX-2/prostaglandin G/H synthase 2 suppression and lipocortin/annexin induction. By binding to the glucocorticoid receptor, it influences transcription factors AP-1 and NF-kB to block the transcription of COX-2/prostaglandin G/H synthase 2 which reduces the amount of prostanoids being produced from arachidonic acid. Prostanoids such as PGI2 and thromboxane A2 influence the effects of inflammation through vasoconstriction/dilation, pain sensitivity, and platelet aggregation. This drug also affects the promoter of annexin-1, an important inflammatory protein as it affects leukocytes and blocks phospholipase A2 which reduces the amount of arachidonic acid being cleaved from the phospholipid bilayer. Reducing the amount of arachidonic acid formed further decreases the concentrations of prostanoids mentioned calming inflammation. Fluticasone propionate is administered as an inhaler, a nasal spray or as a topical ointment.