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Lerisetron

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Lerisetron
Clinical data
Other namesF-0930-RS
ATC code
  • None
Identifiers
  • 1-Benzyl-2-piperazin-1-yl-1H-benzimidazole
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H20N4
Molar mass292.386 g·mol−1
  • InChI=1S/C18H20N4/c1-2-6-15(7-3-1)14-22-17-9-5-4-8-16(17)20-18(22)21-12-10-19-11-13-21/h1-9,19H,10-14H2 checkY
  • Key:PWWDCRQZITYKDV-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Lerisetron (code nameF-0930-RS) is a drug which acts as anantagonist at the5-HT3receptor.[1] It is a potentantiemetic[2][3] and was inclinical trials for the treatment of nausea associated with cancerchemotherapy.[4]

See also

[edit]

References

[edit]
  1. ^Orjales A, Mosquera R, Labeaga L, Rodes R (February 1997). "New 2-piperazinylbenzimidazole derivatives as 5-HT3 antagonists. Synthesis and pharmacological evaluation".Journal of Medicinal Chemistry.40 (4):586–93.doi:10.1021/jm960442e.PMID 9046349.
  2. ^Gomez-de-Segura IA, Grande AG, De Miguel E (1998)."Antiemetic effects of Lerisetron in radiation-induced emesis in the dog".Acta Oncologica.37 (7–8):759–63.doi:10.1080/028418698430160.PMID 10050999.
  3. ^Cooper M, Sologuren A, Valiente R, Smith J (2002). "Effects of lerisetron, a new 5-HT3 receptor antagonist, on ipecacuanha-induced emesis in healthy volunteers".Arzneimittel-Forschung.52 (9):689–94.doi:10.1055/s-0031-1299952.PMID 12404884.S2CID 24423582.
  4. ^Huckle R (July 2003). "Lerisetron. FAES".Current Opinion in Investigational Drugs.4 (7):874–7.PMID 14619411.
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
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