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Sumatriptan succinate is a 5-HT1 serotonin receptor agonist. Sumatriptan reduces the vascular inflammation associated with migraine. Sumatriptan displays the highest affinity for 5-HT1D (Ki = 17 nM) and 5-HT1B (Ki = 27 nM) binding sites and is slightly less potent at 5-HT1A binding sites (Ki = 100 nM). Sumatriptan at a clinically relevant dose (100 mg/kg, s.c.) leads to a significant reduction of the mechanical allodynia-like behaviour on both the injured and the contralateral sides (peak-effects 6.3 g and 4.4 g, respectively) in a rat model of trigeminal neuropathic pain. Sumatriptan results in oral bioavailabilities of 37, 58 and 23% in rat, dog and rabbit, respectively. sumatriptan is cleared rapidly by metabolic and renal clearance with a half-life of 1-2 hour.
Cephalalgia. 2025 Feb 17;45(2):3331024251317446.
Chronification of migraine sensitizes to CGRP in male and female mice
Sumatriptan succinate purchased from AbMole
Cephalalgia. 2021 Sep 12;3331024211039813.
A prolactin-dependent sexually dimorphic mechanism of migraine chronification
Sumatriptan succinate purchased from AbMole
Cephalalgia. 2020 Aug;40(9):903-912.
Evaluation of LY573144 (lasmiditan) in a preclinical model of medication overuse headache
Sumatriptan succinate purchased from AbMole
Cephalalgia. 2020 Aug;40(9):892-902.
Ubrogepant does not induce latent sensitization in a preclinical model of medication overuse headache
Sumatriptan succinate purchased from AbMole
eNeuro. 2018 July 5;5(4):ENEURO.0116-18.
Loss of Blood-Brain Barrier Integrity in a KCl-Induced Model of Episodic Headache Enhances CNS Drug Delivery
Sumatriptan succinate purchased from AbMole
Cephalalgia. 2017 Jul;37(8):780-794.
Kappa opioid receptor antagonists: A possible new class of therapeutics for migraine prevention
Sumatriptan succinate purchased from AbMole
Cephalalgia. 2016 May 19.
Prevention of stress- or nitric oxide donor-induced medication overuse headache by a calcitonin gene-related peptide antibody in rodents.
Sumatriptan succinate purchased from AbMole
| Cell Experiment | |
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| Cell lines | |
| Preparation method | |
| Concentrations | |
| Incubation time | |
| Animal Experiment | |
|---|---|
| Animal models | Adult male Sprague–Dawley rats model |
| Formulation | sterile 0.9% saline solution |
| Dosages | 0.6 mg/kg/day for 7 days |
| Administration | subcutaneously injection |
| Molecular Weight | 413.49 |
| Formula | C14H21N3O2S.C4H6O4 |
| CAS Number | 103628-48-4 |
| Solubility (25°C) | DMSO 50 mg/mL Water 90 mg/mL |
| Storage | -20°C, dry, sealed |
| Related 5-HT Receptor Products |
|---|
| Buspirone
Buspirone is an orally active 5-HT1A receptor agonist, and a dopamine D2 autoreceptorsant antagonist. |
| Clomipramine Hydrochloride
Clomipramine HCl is a hydrochloride salt of clomipramine which is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively. |
| Quetiapine Sulfone
Quetiapine Sulfone is a 5-HT receptor agonist with a pEC50 value of 4.77 for human 5-HT1A. Quetiapine hemifumarate is a dopamine receptor antagonist with a pIC50 value of 6.33 for human D2. |
| Quetiapine sulfoxide
Quetiapine sulfoxide is a 5-HT receptor agonist with a pEC50 value of 4.77 for human 5-HT1A. Quetiapine hemifumarate is a dopamine receptor antagonist with a pIC50 value of 6.33 for human D2. |
| Iloperidone
Iloperidone, a serotonin (5-HT2) receptor inhibitor, is used to study schizophrenia. |
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