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Wikipedia

Guanoxabenz

Guanoxabenz is a metabolite of guanabenz.[1]

Guanoxabenz
Names
IUPAC name
2-{[(2,6-dichlorophenyl)methylidene]amino}-1-hydroxyguanidine
Identifiers
  • 24047-25-4 Y
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL461343 Y
ChemSpider
  • 7842543 Y
KEGG
  • D04398 Y
MeSH Guanoxabenz
  • 9567831
UNII
  • P9HIK5V7WK Y
  • InChI=1S/C8H8Cl2N4O/c9-6-2-1-3-7(10)5(6)4-12-13-8(11)14-15/h1-4,15H,(H3,11,13,14)/b12-4+ Y
    Key: QKIQJNNDIWGVEH-UUILKARUSA-N Y
  • InChI=1/C8H8Cl2N4O/c9-6-2-1-3-7(10)5(6)4-12-13-8(11)14-15/h1-4,15H,(H3,11,13,14)/b12-4+
    Key: QKIQJNNDIWGVEH-UUILKARUBE
  • Clc1cccc(Cl)c1\C=N\N=C(/N)NO
Properties
C8H8Cl2N4O
Molar mass 247.08 g/mol
Pharmacology
C02CC07 (WHO)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

References Edit

  1. ^ Clement, B.; Demesmaeker, M. (1997). "Formation of guanoxabenz from guanabenz in human liver. A new metabolic marker for CYP1A2". Drug Metabolism and Disposition. 25 (11): 1266–1271. PMID 9351903.


guanoxabenz, metabolite, guanabenz, namesiupac, name, dichlorophenyl, methylidene, amino, hydroxyguanidineidentifierscas, number, 24047, model, jsmol, interactive, imagechembl, chembl461343, ychemspider, 7842543, ykegg, d04398, ymesh, pubchem, 9567831unii, p9h. Guanoxabenz is a metabolite of guanabenz 1 Guanoxabenz NamesIUPAC name 2 2 6 dichlorophenyl methylidene amino 1 hydroxyguanidineIdentifiersCAS Number 24047 25 4 Y3D model JSmol Interactive imageChEMBL ChEMBL461343 YChemSpider 7842543 YKEGG D04398 YMeSH GuanoxabenzPubChem CID 9567831UNII P9HIK5V7WK YInChI InChI 1S C8H8Cl2N4O c9 6 2 1 3 7 10 5 6 4 12 13 8 11 14 15 h1 4 15H H3 11 13 14 b12 4 YKey QKIQJNNDIWGVEH UUILKARUSA N YInChI 1 C8H8Cl2N4O c9 6 2 1 3 7 10 5 6 4 12 13 8 11 14 15 h1 4 15H H3 11 13 14 b12 4 Key QKIQJNNDIWGVEH UUILKARUBESMILES Clc1cccc Cl c1 C N N C N NOPropertiesChemical formula C8H8Cl2N4OMolar mass 247 08 g molPharmacologyATC code C02CC07 WHO Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox referencesReferences Edit Clement B Demesmaeker M 1997 Formation of guanoxabenz from guanabenz in human liver A new metabolic marker for CYP1A2 Drug Metabolism and Disposition 25 11 1266 1271 PMID 9351903 nbsp This antihypertensive related article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Guanoxabenz amp oldid 1052781848, wikipedia, wiki, book, books, library,

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