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Batanopride

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Batanopride
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 4-amino-5-chloro-N-(2-diethylaminoethyl)-2-(3-oxobutan-2-yloxy)benzamide
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC17H26ClN3O3
Molar mass355.86 g·mol−1
3D model (JSmol)
  • Clc1cc(c(OC(C(=O)C)C)cc1N)C(=O)NCCN(CC)CC
  • InChI=1S/C17H26ClN3O3/c1-5-21(6-2)8-7-20-17(23)13-9-14(18)15(19)10-16(13)24-12(4)11(3)22/h9-10,12H,5-8,19H2,1-4H3,(H,20,23) checkY
  • Key:ZYOJXUNLLOBURP-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Batanopride (BMY-25,801) is anantiemeticdrug of thebenzamide class which acts as aselective5-HT3 receptorantagonist.[1] It was trialled to reduce nausea during cancer chemotherapy, but was never approved for medical use due to dose-limiting side effects includinghypotension andlong QT syndrome.[2]

References

[edit]
  1. ^Gylys JA, Wright RN, Nicolosi WD, Buyniski JP, Crenshaw RR (March 1988). "BMY-25801, an antiemetic agent free of D2-dopamine receptor antagonist properties".The Journal of Pharmacology and Experimental Therapeutics.244 (3):830–7.PMID 2978041.
  2. ^Fleming GF, Vokes EE, McEvilly JM, Janisch L, Francher D, Smaldone L (1991). "Double-blind, randomized crossover study of metoclopramide and batanopride for prevention of cisplatin-induced emesis".Cancer Chemotherapy and Pharmacology.28 (3):226–7.doi:10.1007/bf00685516.PMID 1855280.S2CID 22520773.
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
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