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Pathways

PathWhiz ID Pathway Meta Data

PW000325

Pw000325 View Pathway
drug action

Chlorothiazide Action Pathway

Homo sapiens
Chlorothiazide (also known as Diuril) is an organic compound that used for diuretic. It can inhibit the solute carrier family 12 member 3 (also known as sodium-chloride symporter) in the nephron to prevent water reabsorption. Solute carrier family 12 member 3 is also used for sodium reabsorption that count for 5% of total amount. Solute carrier family 12 member 3 transports chloride and sodium from lumen to epithelial cell, and sodium/potassium ATPases facilitate the export of sodium to basolateral interstitium to provide sodium gradient that will increase the osmolarity in interstitium, which lead to establishment of osmotic gradient for water reabsorption.

PW132394

Pw132394 View Pathway
metabolic

Chlorothiazide Drug Metabolism

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

PW144983

Pw144983 View Pathway
drug action

Chlorothiazide Drug Metabolism Action Pathway

Homo sapiens

PW145329

Pw145329 View Pathway
drug action

Chloroxine Drug Metabolism Action Pathway

Homo sapiens

PW146245

Pw146245 View Pathway
drug action

Chloroxylenol Drug Metabolism Action Pathway

Homo sapiens

PW057579

Pw057579 View Pathway
drug action

Chlorphenamine H1-Antihistamine Action

Homo sapiens
Chlorphenamine (chlorpheniramine) is a first-generation alkylamine 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.

PW146872

Pw146872 View Pathway
drug action

Chlorphenesin carbamate Drug Metabolism Action Pathway

Homo sapiens

PW176427

Pw176427 View Pathway
metabolic

Chlorphenesin carbamate Predicted Metabolism Pathway

Homo sapiens
Metabolites of Template3MB4 are predicted with biotransformer.

PW144961

Pw144961 View Pathway
drug action

Chlorphenesin Drug Metabolism Action Pathway

Homo sapiens

PW176455

Pw176455 View Pathway
metabolic

Chlorphenesin Predicted Metabolism Pathway

Homo sapiens
Metabolites of Chlorphenesin are predicted with biotransformer.