Open Access Articles- Top Results for Sumatriptan


File:Sumatriptan Structural Formula V.1.svg
Sumatriptan molecule
Systematic (IUPAC) name
Clinical data
Trade names Imitrex, Imigran,Treximet
AHFS/ monograph
Licence data US FDA:link
  • C
tablet, subcutaneous injection, nasal spray
Pharmacokinetic data
Bioavailability 15% (oral)/ 96% (s.c)
Protein binding 14–21%
Metabolism MAO
Half-life 2.5 hours
Excretion 60% urine; 40% feces
103628-46-2 7pxY
PubChem CID 5358
IUPHAR ligand 54
DrugBank DB00669 7pxY
ChemSpider 5165 7pxY
UNII 8R78F6L9VO 7pxY
KEGG D00451 7pxY
ChEBI CHEBI:10650 7pxY
Chemical data
Formula C14H21N3O2S
295.402 g/mol
 14pxY (what is this?)  (verify)

Sumatriptan is a synthetic drug belonging to the triptan class, used for the treatment of migraine headaches. Structurally, it is an analog of the naturally occurring neuro-active alkaloids dimethyltryptamine (DMT), bufotenine, and 5-methoxy-dimethyltryptamine, with an N-methyl sulfonamidomethyl- group at position C-5 on the indole ring.[1]

Sumatriptan is produced and marketed by various drug manufacturers with many different trade names such as Imitrex, Imigran, and Treximet as a combination product with naproxen.

Adverse effects

Large doses of sumatriptan can cause sulfhemoglobinemia, a rare condition in which the blood changes from red to greenish-black, due to the integration of sulfur into the hemoglobin molecule.[2] If sumatriptan is discontinued, the condition reverses within a few weeks.

Serious cardiac events, including some that have been fatal, have occurred following the use of sumatriptan injection or tablets. Events reported have included coronary artery vasospasm, transient myocardial ischemia, myocardial infarction, ventricular tachycardia, and ventricular fibrillation (V-Fib).[citation needed]

The most common side-effects[3] reported by at least 2% of patients in controlled trials of sumatriptan (25, 50, and 100 mg tablets) for migraine are atypical sensations (paresthesias and warm/cold sensations) reported by 4% in the placebo group and 5–6% in the sumatriptan groups, pain and other pressure sensations (including chest pain) reported by 4% in the placebo group and 6–8% in the sumatriptan groups, neurological events (vertigo) reported by less than 1% in the placebo group and less than 1% to 2% in the sumatriptan groups. Malaise/fatigue occurred in less than 1% of the placebo group and 2–3% of the sumatriptan groups. Sleep disturbance occurred in less than 1% in the placebo group to 2% in the sumatriptan group.

Mechanism of action

Sumatriptan is structurally similar to serotonin (5HT), and is a 5-HT (types 5-HT1D and 5-HT1B[4]) agonist. The specific receptor subtypes it activates are present on the cranial arteries and veins. Acting as an agonist at these receptors, sumatriptan reduces the vascular inflammation associated with migraines.

The specific receptor subtype it activates is present in the cranial and basilar arteries. Activation of these receptors causes vasoconstriction of those dilated arteries. Sumatriptan is also shown to decrease the activity of the trigeminal nerve, which, it is presumed, accounts for sumatriptan's efficacy in treating cluster headaches. The injectable form of the drug has been shown to abort a cluster headache within fifteen minutes in 96% of cases.[5]


Sumatriptan is administered in several forms: tablets, subcutaneous injection, and nasal spray. Oral administration (as succinate) suffers from poor bioavailability, partly due to presystemic metabolism—some of it gets broken down in the stomach and bloodstream before it reaches the target arteries. A new rapid-release tablet formulation has the same bioavailability, but the maximum concentration is achieved on average 10–15 minutes earlier. When injected, sumatriptan is faster-acting (usually within 10 minutes), but the effect lasts for a shorter time. Sumatriptan is metabolised primarily by monoamine oxidase A into an indole acetic acid analogue, part of which is further conjugated with glucuronic acid. These metabolites are excreted in the urine and bile. Only about 3% of the active drug may be recovered unchanged.

There is no simple, direct relationship between sumatriptan concentration (pharmacokinetics) per se in the blood and its anti-migraine effect (pharmacodynamics). This paradox has, to some extent, been resolved by comparing the rates of absorption of the various sumatriptan formulations, rather than the absolute amounts of drug that they deliver.[6][7]


Sumatriptan was the first clinically available triptan (in 1991). In the United States, it is available only by medical prescription. However, it can be bought over the counter in the UK[8] and Sweden.[9] Several dosage forms for sumatriptan have been approved, including tablets, solution for injection, and nasal inhalers.

On April 15, 2008, the US FDA approved Treximet, a combination of sumatriptan and naproxen, an NSAID.[10] This combination has shown a benefit over either medicine used separately.[11]

In July 2009, the US FDA approved a single-use jet injector formulation of sumatriptan. The device delivers a subcutaneous injection of 6 mg sumatriptan, without the use of a needle. Autoinjectors with needles have been previously available in Europe and North America for several years.[12]

Phase III studies with a iontophoretic transdermal patch (Zelrix/Zecuity) started in July 2008.[13] This patch uses low voltage controlled by a pre-programmed microchip to deliver a single dose of sumatriptan through the skin within 30 minutes.[14][15] Zecuity was approved by the US FDA in January 2013.[16]


File:Sumatriptan vails 100 5509.jpg
Sumatriptan vials 100 5509

On November 6, 2008, Par Pharmaceutical announced that it would begin shipping generic versions of sumatriptan injection (sumatriptan succinate injection) 4 mg and 6 mg starter kits and 4 mg and 6 mg pre-filled syringe cartridges to the trade immediately. In addition, Par anticipates launching the 6 mg vials early in 2009.[17]

Mylan Laboratories Inc., Ranbaxy Laboratories, Sandoz (a subsidiary of Novartis), Dr. Reddy's Laboratories and other companies have received FDA approval for generic versions of Imitrex tablets in 25-, 50-, and 100-milligram doses since 2009. The drug is available in U.S. and European markets, since Glaxo's patent protections have expired in those jurisdictions. However, sales of a generic delivered via nasal spray are still restricted in the United States.

See also Sumavel DosePro (above).[12]


One-pot procedure

Knoll variation

File:Sumatriptan synthesis Knoll.png
WO 0134561  This is based on the original procedure. The hydrazine is prepared using "one-pot" methodology.
  • Treatment of the appropriately functionalized hydrazine hydrochloride with 4-chlorobutanal dimethyl acetal in ethanol and aqueous HCl gives an intermediate hydrazone.
  • Disodium phosphate was added and the reaction mixture was refluxed. This reaction is known as the Grandberg variation of the Fischer indole synthesis and involves displacement of the chloro group with the ammonia released during the formation of the indole ring.
  • Reaction of the 1° amine with formaldehyde and sodium borohydride in the presence of a buffer completes the synthesis.

Japp-Klingemann reaction

File:Sumatriptan synthesis J-K.png
A group from Hungary has synthesized sumatriptan utilizing a Japp-Klingemann reaction/decarboxylation strategy.[20]

See also


  1. ^ The presence of the sulfonamide group in the molecule does not make sumatriptan a "sulfa drug".
  2. ^ "Patient bleeds dark green blood". BBC News. 8 June 2007. Retrieved 6 March 2010. 
  3. ^ Tablets
  4. ^ Razzaque Z, Heald MA, Pickard JD et al. (1999). "Vasoconstriction in human isolated middle meningeal arteries: determining the contribution of 5-HT1B- and 5-HT1F-receptor activation". Br J Clin Pharmacol 47 (1): 75–82. PMC 2014192. PMID 10073743. doi:10.1046/j.1365-2125.1999.00851.x. 
  5. ^ Treatment of acute cluster headache with sumatriptan. The Sumatriptan Cluster Headache Study Group. N Engl J Med 1991;325:322-6.
  6. ^ Fox, A. W. (2004). "Onset of effect of 5-HT1B/1D agonists: a model with pharmacokinetic validation". Headache 44 (2): 142–147. PMID 14756852. doi:10.1111/j.1526-4610.2004.04030.x.  edit
  7. ^ Freidank-Mueschenborn, E.; Fox, A. (2005). "Resolution of concentration-response differences in onset of effect between subcutaneous and oral sumatriptan". Headache 45 (6): 632–637. PMID 15953294. doi:10.1111/j.1526-4610.2005.05129a.x.  edit
  8. ^ "Press release: First Over The Counter (OTC) migraine pill made available". Medicines and Healthcare Products Regulatory Agency. Archived from the original on 2014-12-05. Retrieved January 28, 2015. 
  9. ^ European Medicines Agency (November 23, 2011). "Assessment Report: Sumatriptan Galpharm 50 mg Tablets" (PDF). European Medicines Agency. p. 20. Retrieved January 28, 2015. 
  10. ^ GSK press release – Treximet (sumatriptan and naproxen sodium) tablets approved by FDA for acute treatment of migraine
  11. ^ Brandes JL, Kudrow D, Stark SR et al. (April 2007). "Sumatriptan-naproxen for acute treatment of migraine: a randomized trial". JAMA 297 (13): 1443–54. PMID 17405970. doi:10.1001/jama.297.13.1443. 
  12. ^ a b Brandes, J.; Cady, R.; Freitag, F.; Smith, T.; Chandler, P.; Fox, A.; Linn, L.; Farr, S. (2009). "Needle-free subcutaneous sumatriptan (Sumavel DosePro): bioequivalence and ease of use.". Headache 49 (10): 1435–1444. PMID 19849720. doi:10.1111/j.1526-4610.2009.01530.x.  edit
  13. ^ Clinical trial number NCT00724815 for "The Efficacy and Tolerability of NP101 Patch in the Treatment of Acute Migraine (NP101-007)" at
  14. ^ SmartRelief -electronically assisted drug delivery (iontophoresis)
  15. ^ Pierce, M; Marbury, T; O'Neill, C; Siegel, S; Du, W; Sebree, T (2009). "Zelrix: a novel transdermal formulation of sumatriptan". Headache 49 (6): 817–25. PMID 19438727. doi:10.1111/j.1526-4610.2009.01437.x. 
  16. ^ Zecuity Approved by the FDA for the Acute Treatment of Migraine
  17. ^ "PAR PHARMACEUTICAL BEGINS SHIPMENT OF SUMATRIPTAN INJECTION". Par Pharmaceutical. 2008-11-06. Retrieved 2008-11-25. [dead link]
  18. ^ Drugs of the Future, 1989,14, 35-39.
  19. ^ Pete, B. L.; Bitter, I. N.; Szántay, Jr., C.; Schön, I. N.; Töke, L. S. (1998). "Synthesis of 5-Substituted Indole Derivatives, I. An Improved Method for the Synthesis of Sumatriptan". Heterocycles 48 (6): 1139. doi:10.3987/COM-97-8087.  edit
  20. ^ Pete, B. L.; Bitter, I. N.; Harsányi, K. L. N.; Tõke, L. S. (2000). "Synthesis of 5-Substituted Indole Derivatives, Part II. Synthesis of Sumatriptan through the Japp-Klingemann Reaction". Heterocycles 53 (3): 665. doi:10.3987/COM-99-8815.  edit