Clinical data | |
---|---|
Pronunciation | /taɪˈzænɪdiːn/ tye-ZAN-i-deen |
Trade names | Zanaflex, Sirdalud, and others |
Other names | 4-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl)-8-thia-7,9-diazabicyclo[4.3.0]nona-2,4,6,9-tetraen-5-amine |
AHFS/Drugs.com | Monograph |
MedlinePlus | a601121 |
License data |
|
Routes of administration | By mouth |
Drug class | α2-adrenergic receptor agonist |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Bioavailability | ~40%[1] |
Protein binding | ~30% |
Metabolism | Liver (CYP1A2, 95%) |
Elimination half-life | 2.54 hours (tizanidine), 20–40 hours (inactive metabolites)[1] |
Excretion | Urine (60%), feces (20%) |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.125.400 |
Chemical and physical data | |
Formula | C9H8ClN5S |
Molar mass | 253.71 g·mol−1 |
3D model (JSmol) | |
| |
| |
(verify) |
Tizanidine, sold under the brand name Zanaflex among others, is an alpha-2 (α2) adrenergic receptor agonist,[2] similar to clonidine, that is used to treat muscle spasticity due to spinal cord injury, multiple sclerosis, and spastic cerebral palsy.[3] Effectiveness appears similar to baclofen or diazepam.[4] It is taken by mouth.[5]
Common side effects of tizanidine include dry mouth, sleepiness, weakness, and dizziness.[5] Serious side effects may include low blood pressure, liver problems, psychosis, and QT prolongation.[5] It is unclear if use in pregnancy and breastfeeding is safe.[6] It is an α2-adrenergic agonist, but how it works is not entirely clear.[5]
Tizanidine was approved for medical use in the United States in 1996.[5] It is available as a generic medication.[3] In 2022, it was the 94th most commonly prescribed medication in the United States, with more than 6 million prescriptions.[7][8]
Zanaflex PI
was invoked but never defined (see the help page).Katzung
was invoked but never defined (see the help page).