Sumatriptan succinate

CAT:
804-HY-B0121-01
Size:
10 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 succinate - image 1

Sumatriptan succinate

  • Description:

    Sumatriptan succinate (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 succinate can be used for migraine headache research[1][2][3][4].
  • Product Name Alternative:

    GR 43175 succinate
  • UNSPSC:

    12352005
  • Hazard Statement:

    H318
  • 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-succinate.html
  • Purity:

    99.89
  • Solubility:

    DMSO : 50 mg/mL (ultrasonic) |H2O : ≥ 100 mg/mL
  • Smiles:

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

    C18H27N3O6S
  • Molecular Weight:

    413.49
  • Precautions:

    H318
  • References & Citations:

    [1]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. |[2]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. |[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:

    4°C (Powder, sealed storage, away from moisture)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • Isoform:

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

    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. |ACS Environ Au. 2025 Aug 8.|Anal Chem. 2025 Jun 3;97 (21) :11099-11109.
  • CAS Number:

    103628-48-4