Cat. No. 1955
Chemical Name: 6-[2-[4-[Bis(4-fluorophenyl)methyle
Biological ActivityPotent and long-acting 5-HT2 receptor antagonist (Ki = 0.39 nM). Anxiolytic in vivo.
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Certificate of Analysis / Product Datasheet / Safety Datasheet
Watanabe et al (1992) Syntheses and 5-HT2 antagonist activity of bicyclic 1,2,4-triazol-3(2H)-one and 1,3,5-triazine-2,4(3H)-dione derivatives. J.Med.Chem. 35 189. PMID: 1732528.
Janssen (1985) Pharmacology of potent and selective S2-serotonergic antagonists. J.Cardiovasc.Pharmacol. 7 S2. PMID: 2412048.
Leysen et al (1985) Receptor-binding properties in vitro and in vivo of ritanserin. Mol.Pharmacol. 27 600. PMID: 2860558.
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Citations are publications that use Tocris products. Selected citations for Ritanserin include:
Bracha et al (2013) The expression and role of serotonin receptor 5HTR2A in canine osteoblasts and an osteosarcoma cell line. Physiol Behav 9 251. PMID: 24330646.
Jahchan et al (2013) A drug repositioning approach identifies tricyclic antidepressants as inhibitors of small cell lung cancer and other neuroendocrine tumors. Cancer Discov 3 1364. PMID: 24078773.
Mondal et al (2013) Mechanism of ghrelin-induced gastric contractions in Suncus murinus (house musk shrew): involvement of intrinsic primary afferent neurons. PLoS One 8 e60365. PMID: 23565235.
Do you know of a great paper that uses Ritanserin from Tocris? If so please let us know.
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Keywords: Ritanserin, supplier, Potent, 5-HT2, antagonists, Non-Selective, Serotonin, Receptors, Tocris Bioscience, Non-selective 5-HT2 Antagonist products
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April 10 - 13, 2017