Gvanoksabenz
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| Nazivi | |
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| IUPAC naziv 2[(2,6-dihlorofenil)metiliden]amino1-hidroksiguanidin | |
| Identifikacija | |
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3D model (Jmol) |
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| ChemSpider |
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| KEGG[1] |
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| MeSH | Guanoxabenz |
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SMILES
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| Svojstva | |
| C8H8Cl2N4O | |
| Molarna masa | 247,08 g/mol |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
 Y verifikuj (šta je  Y Н ?) | |
| Reference infokutije | |
Gvanoksabenz je metabolit gvanabenza.[4]
Reference
- ^ Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- ^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
- ^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
- ^ Clement, B.; Demesmaeker, M. (1997). „Formation of guanoxabenz from guanabenz in human liver. A new metabolic marker for CYP1A2”. Drug metabolism and disposition: the biological fate of chemicals. 25 (11): 1266—1271. PMID 9351903.
Spoljašnje veze
Portal Hemija
- п
- р
- у
Adrenergici
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