Misplaced Pages

Terbutaline

Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by 88.209.212.200 (talk) at 01:14, 25 December 2011 (Side effects: Change "Maternal" to "Adult" to better reflect usage in asthma treatment (as opposed to usage in delaying labor).). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 01:14, 25 December 2011 by 88.209.212.200 (talk) (Side effects: Change "Maternal" to "Adult" to better reflect usage in asthma treatment (as opposed to usage in delaying labor).)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff) Pharmaceutical compound
Terbutaline
Clinical data
AHFS/Drugs.comMonograph
MedlinePlusa682144
Pregnancy
category
  • B
Routes of
administration
SQ, Oral, Inhaled
ATC code
Legal status
Legal status
  • UK: POM (Prescription only)
Pharmacokinetic data
MetabolismGI tract (oral), liver; CYP450: unknown
Elimination half-life3-4h
Excretionurine 90% (60% unchanged), bile/faeces
Identifiers
IUPAC name
  • (RS)-5-benzene-1,3-diol
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.041.244 Edit this at Wikidata
Chemical and physical data
FormulaC12H19NO3
Molar mass225.284 g/mol g·mol
3D model (JSmol)
SMILES
  • Oc1cc(cc(O)c1)C(O)CNC(C)(C)C
InChI
  • InChI=1S/C12H19NO3/c1-12(2,3)13-7-11(16)8-4-9(14)6-10(15)5-8/h4-6,11,13-16H,7H2,1-3H3
  • Key:XWTYSIMOBUGWOL-UHFFFAOYSA-N
  (what is this?)  (verify)

Terbutaline (trade names Brethine, Bricanyl, Brethaire, or Terbulin) is a β2-adrenergic receptor agonist.

Terbutaline is currently on the World Anti-Doping Agency's list of prohibited drugs for Olympic athletes, except when administered by inhalation and a Therapeutic Use Exemption (TUE) has been obtained in advance.

Terbutaline is currently used to delay preterm labor for 48 hours to allow for fetal lung maturity through steroid injections. It should not be used to prevent preterm labor or delay labor past 48-72 hours. In February 2011, the Food and Drug Administration has ordered to put a boxed warning on the drug's label. Pregnant women should not be given injections of the drug terbutaline for the prevention of preterm labor or for long-term (beyond 48-72 hours) management of preterm labor, and should not be given oral terbutaline for any type of prevention or treatment of preterm labor "due to of the potential for serious internal heart problems and death."

The American College of Obstetricians and Gynecologists also discourages the use of terbutaline for preventing preterm labor.

Uses

Terbutaline is used as a fast-acting bronchodilator (often used as a short-term asthma treatment) and as a tocolytic to delay premature labor. The inhaled form of terbutaline starts working within 15 minutes and can last up to 6 hours.

Terbutaline as a treatment for premature labor is an off-label use not approved by the FDA. It is a pregnancy category 'B' medication and is routinely prescribed to stop contractions. After successful intravenous tocolysis, little evidence exists that oral terbutaline is effective. However, following uterine inversion in the third stage of pregnancy, Terbutaline (or either Halothane or magnesium sulfate) can be utilized to relax the uterus if necessary prior to uterine replacement.

Structure activity relationships

The tertiary butyl group in terbutaline makes it more selective for β2-receptors. Since there is no hydroxy group on the 4 position of the benzene ring - the molecule is less susceptible to metabolism by COMT enzyme.

Side effects

Chemistry

It is synthesized by brominating 3,5-dibenzyloxyacetophenone into the appropriate 3,5-dibenzyloxybromoacetophenone, which is reacted with N-benzyl-N-tert-butylamine, giving the aminoketone. Reduction of this product by hydrogen over a palladium catalyst leads to terbutaline.

References

  1. "Most Popular E-mail Newsletter". USA Today.
  2. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm243840.htm
  3. http://www.magmutual.com/pr_marketing/terbutaline.html
  4. Mohamed Ismail NA, Ibrahim M, Mohd Naim N, Mahdy ZA, Jamil MA, Mohd Razi ZR (2008). "Nifedipine versus terbutaline for tocolysis in external cephalic version". Int J Gynaecol Obstet. 102 (3): 263–6. doi:10.1016/j.ijgo.2008.04.010. PMID 18554601. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  5. Goldenberg, RL (2002). "High-Risk Pregnancy Series: An Expert's View". Obstetrics & Gynecology. 100 (5): 1020–1037. {{cite journal}}: Text "part 1" ignored (help)
  6. Medicinal Chemistry of Adrenergics and Cholinergics
  7. Shen, Howard (2008). Illustrated Pharmacology Memory Cards: PharMnemonics. Minireview. p. 7. ISBN 1-59541-101-1.
  8. Draco Lunts Farmcetiska Actiebolag, GB 1199630  (1967)
  9. Draco Lunts Farmcetiska Actiebolag, BE 704932  (1968)
  10. A. L. Swensson, I. K. Weterlin, U.S. patent 3,937,838 (1976)
Adrenergic receptor modulators
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
Tocolytics/labor repressants (G02CA)
β2 adrenoreceptor agonists
Oxytocin antagonists
NSAIDs
Calcium channel blockers
Myosin inhibitors
Drugs for obstructive airway diseases: asthma/COPD (R03)
Adrenergics, inhalants
Short-acting β2 agonists
Long-acting β2 agonists
Ultra-long-acting β2 agonists
Other
Glucocorticoids
Anticholinergics/
muscarinic antagonist
Mast cell stabilizers
Xanthines
Eicosanoid inhibition
Leukotriene antagonists
Arachidonate 5-lipoxygenase inhibitors
Thromboxane receptor antagonists
Non-xanthine PDE4 inhibitors
Others/unknown
Combination products
Categories:
Terbutaline Add topic