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Pathways

PathWhiz ID Pathway Meta Data

PW176006

Pw176006 View Pathway
metabolic

Clobazam Predicted Metabolism Pathway new

Homo sapiens
Metabolites of Clobazam are predicted with biotransformer.

PW147056

Pw147056 View Pathway
metabolic

Clobetasol Drug Metabolism Pathway

Homo sapiens

PW127776

Pw127776 View Pathway
drug action

Clobetasol propionate Action Pathway

Homo sapiens
Clobetasol propionate is a corticosteroid derived from prednisolone but with a higher specificity for glucocorticoid receptors than mineralocorticoid receptors. It is used to treat corticosteroid-responsive dermatoses and moderate to severe plaque psoriasis. 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. Clobetasol propionate 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. Lower doses of corticosteroids provide an anti-inflammatory effect, while higher doses are immunosuppressive. Clobetasol propionate is administered as a topical cream, foam, aerosol, shampoo, gel, or ointment.

PW145111

Pw145111 View Pathway
drug action

Clobetasol propionate Drug Metabolism Action Pathway

Homo sapiens

PW176007

Pw176007 View Pathway
metabolic

Clobetasol propionate Predicted Metabolism Pathway new

Homo sapiens
Metabolites of Clobetasol propionate are predicted with biotransformer.

PW127778

Pw127778 View Pathway
drug action

Clobetasone Action Pathway

Homo sapiens
Clobetasone is a corticosteroid synthetically derived from cortisone. In dermatology, topical clobestasone helps to reduce the itchiness and erythema associated with eczema and dermatitis. In ophthalmology, clobetasone butyrate eye drops have been shown to be safe and effective in the treatment of dry eyes in Sjögren's Syndrome. As this drug is a glucocorticoid, its mechanism of action is that of the glucocorticoid response element (GRE) 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. Clobetasone 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.

PW146597

Pw146597 View Pathway
drug action

Clobetasone Drug Metabolism Action Pathway

Homo sapiens

PW063744

Pw063744 View Pathway
drug action

Clocinizine H1-Antihistamine Action

Homo sapiens
Clocinizine is a first-generation diphenylmethylpiperazine H1-antihistamine. H1-antihistamines interfere with the agonist action of histamine at the H1 receptor and are administered to attenuate inflammatory process in order to treat conditions such as allergic rhinitis, allergic conjunctivitis, and urticaria. Reducing the activity of the NF-κB immune response transcription factor through the phospholipase C and the phosphatidylinositol (PIP2) signalling pathways also decreases antigen presentation and the expression of pro-inflammatory cytokines, cell adhesion molecules, and chemotactic factors. Furthermore, lowering calcium ion concentration leads to increased mast cell stability which reduces further histamine release. First-generation antihistamines readily cross the blood-brain barrier and cause sedation and other adverse central nervous system (CNS) effects (e.g. nervousness and insomnia). Second-generation antihistamines are more selective for H1-receptors of the peripheral nervous system (PNS) and do not cross the blood-brain barrier. Consequently, these newer drugs elicit fewer adverse drug reactions.

PW127779

Pw127779 View Pathway
drug action

Clocortolone Action Pathway

Homo sapiens
Clocortolone, brand name Cloderm, is a corticosteroid used as a topical cream to treat inflammatory and pruritic dermatoses of the scalp. Clocortolone is a moderate potency topical corticosteroid that should not be used with occlusive dressings. As this drug is a glucocorticoid, its mechanism of action is that of the glucocorticoid response element (GRE) 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. Clocortolone 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.

PW144943

Pw144943 View Pathway
drug action

Clocortolone Drug Metabolism Action Pathway

Homo sapiens