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Bemesetron

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Bemesetron
Clinical data
ATC code
  • none
Identifiers
  • [(1S,5R)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3,5-dichlorobenzoate
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.164.757Edit this at Wikidata
Chemical and physical data
FormulaC15H17Cl2NO2
Molar mass314.21 g·mol−1
3D model (JSmol)
  • CN3[C@@H]1CC[C@H]3C[C@H](C1)OC(=O)c2cc(Cl)cc(Cl)c2
  • InChI=1S/C15H17Cl2NO2/c1-18-12-2-3-13(18)8-14(7-12)20-15(19)9-4-10(16)6-11(17)5-9/h4-6,12-14H,2-3,7-8H2,1H3/t12-,13+,14+ checkY
  • Key:MNJNPLVXBISNSX-WDNDVIMCSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Bemesetron (MDL-72222) is adrug which acts as anantagonist at the5HT3receptor.[1] It hasantiemetic effects comparable tometoclopramide,[2] however it is not used clinically, instead its main application is in scientific research studying the involvement of the 5HT3 receptor in the actions of drugs of abuse.[3][4][5][6]

See also

[edit]

References

[edit]
  1. ^Shearman GT, Tolcsvai L (1987). "Effect of the selective 5-HT3 receptor antagonists ICS 205-930 and MDL 72222 on 5-HTP-induced head shaking and behavioral symptoms induced by 5-methoxy-N,N,dimethyltryptamine in rats: comparison with some other 5-HT receptor antagonists".Psychopharmacology.92 (4):520–3.doi:10.1007/bf00176488.PMID 3114804.S2CID 25814825.
  2. ^Homesley HD, Hahne WF, McLees B, et al. (April 1993). "Randomized comparison of the antiemetic efficacy of a serotonin type 3 receptor antagonist (MDL 72,222) with a high-dose metoclopramide regimen".Am. J. Clin. Oncol.16 (2):175–9.doi:10.1097/00000421-199304000-00020.PMID 8452114.S2CID 11733418.
  3. ^McKinzie DL, McBride WJ, Murphy JM, Lumeng L, Li TK (October 2000). "Effects of MDL 72222, a serotonin3 antagonist, on operant responding for ethanol by alcohol-preferring P rats".Alcohol. Clin. Exp. Res.24 (10):1500–4.doi:10.1111/j.1530-0277.2000.tb04567.x.PMID 11045857.
  4. ^Kankaanpää A, Meririnne E, Seppälä T (February 2002). "5-HT3 receptor antagonist MDL 72222 attenuates cocaine- and mazindol-, but not methylphenidate-induced neurochemical and behavioral effects in the rat".Psychopharmacology.159 (4):341–50.doi:10.1007/s00213-001-0939-4.PMID 11823886.S2CID 21614467.
  5. ^Kos T, Popik P, Pietraszek M, et al. (May 2006). "Effect of 5-HT3 receptor antagonist MDL 72222 on behaviors induced by ketamine in rats and mice".Eur Neuropsychopharmacol.16 (4):297–310.doi:10.1016/j.euroneuro.2005.10.001.PMID 16288851.S2CID 43575963.
  6. ^Yoo JH, Nam YS, Lee SY, Jang CG (January 2008). "Dopamine neurotransmission is involved in the attenuating effects of 5-HT3 receptor antagonist MDL 72222 on acute methamphetamine-induced locomotor hyperactivity in mice".Synapse.62 (1):8–13.doi:10.1002/syn.20461.PMID 17948891.S2CID 20699645.
Drugs used in treatment ofdrug dependence (N07B)
Nicotine dependence
Alcohol dependence
Opioid dependence
Benzodiazepine dependence
5-HT3 serotonin ion
channel antagonists
5-HT serotonin G-protein
receptor antagonists
CB1agonists
(cannabinoids)
D2/D3 antagonists
H1 antagonists
(antihistamines)
mAChantagonists
(anticholinergics)
NK1 antagonists
Others
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Receptor
(ligands)
GlyRTooltip Glycine receptor
NMDARTooltip N-Methyl-D-aspartate receptor
Transporter
(blockers)
GlyT1Tooltip Glycine transporter 1
GlyT2Tooltip Glycine transporter 2
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