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Indobufen

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Indobufen
Clinical data
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
  • 2-(4-(1-Oxoisoindolin-2-yl)phenyl)butanoic acid
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.058.496Edit this at Wikidata
Chemical and physical data
FormulaC18H17NO3
Molar mass295.338 g·mol−1
3D model (JSmol)
  • O=C(O)C(c1ccc(cc1)N3C(=O)c2ccccc2C3)CC
  • InChI=1S/C18H17NO3/c1-2-15(18(21)22)12-7-9-14(10-8-12)19-11-13-5-3-4-6-16(13)17(19)20/h3-10,15H,2,11H2,1H3,(H,21,22) ☒N
  • Key:AYDXAULLCROVIT-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Indobufen is aplatelet aggregation inhibitor.[1] It acts as a reversiblecyclooxygenase inhibitor.[2]

References

[edit]
  1. ^The Merck Index (12th ed.). p. 4991.
  2. ^Eligini S, Violi F, Banfi C, Barbieri SS, Brambilla M, Saliola M, et al. (January 2006)."Indobufen inhibits tissue factor in human monocytes through a thromboxane-mediated mechanism".Cardiovascular Research.69 (1):218–26.doi:10.1016/j.cardiores.2005.07.013.PMID 16154551.
Antiplatelet drugs
Glycoprotein IIb/IIIa inhibitors
ADP receptor/P2Y12inhibitors
Prostaglandin analogue (PGI2)
COX inhibitors
Thromboxane inhibitors
Phosphodiesterase inhibitors
Other
Anticoagulants
Vitamin K antagonists
(inhibitII,VII,IX,X)
Factor Xa inhibitors
(with some II inhibition)
Heparin group/
glycosaminoglycans/
(bindantithrombin)
Direct Xa inhibitors ("xabans")
Direct thrombin (IIa) inhibitors
Other
Thrombolytic drugs/
fibrinolytics
Non-medicinal
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