PathWhiz ID | Pathway | Meta Data |
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PW176006View Pathway |
Clobazam Predicted Metabolism Pathway newHomo sapiens
Metabolites of Clobazam are predicted with biotransformer.
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Creator: Omolola Created On: November 29, 2023 at 13:10 Last Updated: November 29, 2023 at 13:10 |
PW147056View Pathway |
Clobetasol Drug Metabolism PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 10, 2023 at 13:45 Last Updated: October 10, 2023 at 13:45 |
PW127776View Pathway |
drug action
Clobetasol propionate Action PathwayHomo 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.
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Creator: Daphnee Created On: June 01, 2023 at 13:47 Last Updated: June 01, 2023 at 13:47 |
PW145111View Pathway |
drug action
Clobetasol propionate Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 15:06 Last Updated: October 07, 2023 at 15:06 |
PW176007View Pathway |
Clobetasol propionate Predicted Metabolism Pathway newHomo sapiens
Metabolites of Clobetasol propionate are predicted with biotransformer.
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Creator: Omolola Created On: November 29, 2023 at 13:11 Last Updated: November 29, 2023 at 13:11 |
PW127778View Pathway |
drug action
Clobetasone Action PathwayHomo 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.
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Creator: Daphnee Created On: June 01, 2023 at 14:46 Last Updated: June 01, 2023 at 14:46 |
PW146597View Pathway |
drug action
Clobetasone Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 18:36 Last Updated: October 07, 2023 at 18:36 |
PW063744View Pathway |
drug action
Clocinizine H1-Antihistamine ActionHomo 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.
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Creator: Carin Li Created On: September 24, 2017 at 17:40 Last Updated: September 24, 2017 at 17:40 |
PW127779View Pathway |
drug action
Clocortolone Action PathwayHomo 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.
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Creator: Daphnee Created On: June 01, 2023 at 15:46 Last Updated: June 01, 2023 at 15:46 |
PW144943View Pathway |
drug action
Clocortolone Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 14:45 Last Updated: October 07, 2023 at 14:45 |