Sumatriptan

CAT:
804-HY-B0121B-01
Size:
25 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Sumatriptan - image 1

Sumatriptan

  • Description :

    Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan can be used for migraine headache research[1][2][3][4].
  • Product Name Alternative :

    GR 43175 free base
  • UNSPSC :

    12352005
  • Hazard Statement :

    H361, H412
  • Target :

    5-HT Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein; Neuronal Signaling
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Neurological Disease
  • Assay Protocol :

    https://www.medchemexpress.com/sumatriptan.html
  • Purity :

    99.96
  • Solubility :

    DMSO : 50 mg/mL (ultrasonic)
  • Smiles :

    O=S(CC1=CC2=C(NC=C2CCN(C)C)C=C1)(NC)=O
  • Molecular Formula :

    C14H21N3O2S
  • Molecular Weight :

    295.41
  • Precautions :

    H361, H412
  • References & Citations :

    [1]K L Dechant, et al. Sumatriptan. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in the acute treatment of migraine and cluster headache. Drugs. 1992 May;43 (5) :776-98.|[2]S J Peroutka, et al. Sumatriptan (GR 43175) interacts selectively with 5-HT1B and 5-HT1D binding sites. Eur J Pharmacol. 1989 Apr 12;163 (1) :133-6. |[3]Razzaque Z, et al. Vasoconstriction in human isolated middle meningeal arteries: determining the contribution of 5-HT1B- and 5-HT1F-receptor activation. Br J Clin Pharmacol. 1999 Jan;47 (1) :75-82.|[4]Bates EA, et al. Sumatriptan alleviates nitroglycerin-induced mechanical and thermal allodynia in mice. Cephalalgia. 2010 Feb;30 (2) :170-8.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • Isoform :

    5-HT1 Receptor; mLAG-3
  • Citation 01 :

    ACS Environ Au. 2025 Aug 8.|Anal Chem. 2025 Jun 3;97 (21) :11099-11109.|Cell Rep Methods. 2023 Oct 23;3 (10) :100599.|J Headache Pain. 2024 Oct 30;25 (1) :187.|Mol Pharmacol. 2023 Nov;104 (5) :230-238.|Personalized Medicine Universe. 2019 May.
  • CAS Number :

    [103628-46-2]

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