Granisetron hydrochloride
Chemical Name: 1-Methyl-N-[(3-endo)-9-methyl-9-azabicyclo[3.3.1]non-3-yl]-1H-indazole-3-carboxamide hydrochloride
Purity: ≥99%
Biological Activity
Granisetron hydrochloride is a 5-HT3 receptor antagonist that possesses potent antiemetic activity.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Modulation of proteoglycan receptor PTP? enhances MMP-2 activity to promote recovery from multiple sclerosis
F Luo, AP Tran, L Xin, C Sanapala, BT Lang, J Silver, Y Yang
Nat Commun, 2018;9(1):4126. -
Selective and functional 5-hydroxytryptamine3 receptor antagonism by BRL 43694 (granisetron).
Sanger and Nelson
Eur.J.Pharmacol., 1989;159:113 -
Granisetron. A review of its pharmacological properties and therapeutic use as an antiemetic.
Plosker and Goa
Drugs, 1991;42:805 -
Anti-emetic effect of ondans. and granis. after exposure to mixed neutron and gamma irradiation.
Martin et al.
Rad.Res., 1998;149:631
Product Datasheets
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Citations for Granisetron hydrochloride
The citations listed below are publications that use Tocris products. Selected citations for Granisetron hydrochloride include:
4 Citations: Showing 1 - 4
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Development of Plate Reader and On-Line Microfluidic Screening to Identify Ligands of the 5-Hydroxytryptamine Binding Protein in Venoms.
Authors: Otvos Et al.
Neuropharmacology 2015;7:2336
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Pronociceptive and Antinociceptive Effects of Bupren. in the Spinal Cord Dorsal Horn Cover a Dose Range of Four Orders of Magnitude.
Authors: Gerhold Et al.
J Neurosci 2015;35:9580
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Unique ionotropic receptors for D-aspartate are a target for serotonin-induced synaptic plasticity in Aplysia californica.
Authors: Carlson and Fieber
Comp Biochem Physiol C Toxicol Pharmacol 2012;155:151
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Polysynaptic excitatory postsynaptic potentials that trigger spasms after spinal cord injury in rats are inhibited by 5-HT1B and 5-HT1F receptors.
Authors: Murray Et al.
J Neurophysiol 2011;106:925
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