Zolmitriptan
Zolmitriptan is a selective serotonin receptor agonist. (In Vitro) :Zolmitriptan (311C90) exhibits higher affinity to 5-HT than sumatriptan (pKA=6.63±0.04 and 6.16±0.03, respectively) . 311C90 displays high affinity at human recombinant 5-HT1D and 5-HT1B receptors in transfected CHO-K1 cell membranes (pIC50 values=9.16±0.12 and 8.32±0.09, respectively) . (In Vivo) :Zolmitriptan (311C90; 3-30 μg/kg, i.v.) causes a dose-dependent inhibition of [125I]-albumin extravasation within the ipsilateral dura mater. Zolmitriptan also produces dose-dependent falls in cranial vascular conductance (32.3% at 30 μg/kg) . Zolmitriptan is an anti-migraine agent with action at 5-HT1B/D receptors. Zolmitriptan is an effective and behaviorally specific anti-aggressive agent in situations that engender moderate and alcohol-heightened levels of aggression. Zolmitriptan (1-30 mg/kg, i.p.) exerts behaviorally specific anti-aggressive effects in mice."
Product Specifications
CAS Number
139264-17-8
Product Name Alternative
BW 311C90 | Zomig
Field of Research
Pharmacology & Drug Discovery
Purity
>98% (HPLC)
Solubility
Ethanol: 58 mg/mL (201.83 mM) ; DMSO: 58 mg/mL (201.83 mM)
Smiles
O=C1OC[C@H] (CC2=CC3=C (NC=C3CCN (C) C) C=C2) N1
Molecular Formula
C16H21N3O2
Molecular Weight
287.36
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
(4S) -4-[[3-[2- (dimethylamino) ethyl]-1H-indol-5-yl]methyl]-1,3-oxazolidin-2-one
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