Granisetron

Granisetron
Systematic (IUPAC) name
1-methyl-N-((1R,3r,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl)-1H-indazole-3-carboxamide
Clinical data
Trade names Kytril
AHFS/Drugs.com monograph
MedlinePlus a601211
Pregnancy cat. B1 (Au),
Legal status S4 (Au), POM (UK), ℞-only (U.S.)
Routes Oral, intravenous, transdermal
Pharmacokinetic data
Bioavailability 60%
Protein binding 65%
Metabolism Hepatic Brandy's
Half-life 3–14 hours
Excretion Renal 11–12%, faecal 38%
Identifiers
CAS number 109889-09-0 Y
ATC code A04AA02
PubChem CID 3510
DrugBank DB00889
ChemSpider 10482033 Y
UNII WZG3J2MCOL Y
KEGG D04370 Y
ChEMBL CHEMBL519643 N
Chemical data
Formula C18H24N4O 
Mol. mass 312.41 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Granisetron is a serotonin 5-HT3 receptor antagonist used as an antiemetic to treat nausea and vomiting following chemotherapy. Its main effect is to reduce the activity of the vagus nerve, which is a nerve that activates the vomiting center in the medulla oblongata. It does not have much effect on vomiting due to motion sickness. This drug does not have any effect on dopamine receptors or muscarinic receptors.

Granisetron was developed by chemists working at the British drug company Beecham around 1988 and is available as a generic. It is produced by Roche Laboratories under the trade name Kytril. The drug was approved in the United Kingdom in 1991 and in United States in 1994 by the FDA.

A granisetron transdermal patch with the trade name Sancuso was approved by the US FDA on September 12, 2008.[1] Sancuso is manufactured by ProStrakan, Inc., a pharmaceutical company headquartered in Bedminster, NJ, with global headquarters in Scotland.

Granisetron breaks down slowly, staying in the body for a long time. One dose usually lasts 4 to 9 hours and is usually administered once or twice daily. This drug is removed from the body by the liver and kidneys.

Contents

Indications

Adverse effects

Granisetron is a well-tolerated drug with few side effects. Headache, dizziness, and constipation are the most commonly reported side effects associated with its use. There have been no significant drug interactions reported with this drug's use. It is broken down by the liver's cytochrome P450 system and it has little effect on the metabolism of other drugs broken down by this system.

External links

See also

References