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Record Information
Version1.0
Creation Date2019-07-14 16:37:56 UTC
Last Updated2019-10-01 21:41:53 UTC
CypComp IDCC02328
Compound Information
NameFuran
Structure ImageYlqbmqcuizjeeh uhfffaoysa n
InChIKeyYLQBMQCUIZJEEH-UHFFFAOYSA-N
PubChem ID8029
CypCompound Information
SetCypBoM Training Set
Bonds of Metabolism (BoMs)
CYP1A2CYP2A6CYP2B6CYP2C8CYP2C9CYP2C19CYP2D6CYP2E1CYP3A4
  • Not Available
  • Not Available
  • Not Available
  • Not Available
  • Not Available
  • Not Available
  • Not Available
  • <1,2;Oxidation;R1>
  • <1,5;Reduction;R1>
  • <2,3;Reduction;R1>
  • <3,4;Cleavage;R1>
  • <3,H;Oxidation;R1>
  • <5,4;Oxidation;R1>
  • <1,2;Oxidation;R2>
  • <1,5;Reduction;R2>
  • <2,3;Reduction;R2>
  • <5,4;Cleavage;R2>
  • <5,H;Oxidation;R2>
  • <3,4;Oxidation;R2>
  • Not Available
References
  1. Kedderis GL, Carfagna MA, Held SD, Batra R, Murphy JE, Gargas ML: Kinetic analysis of furan biotransformation by F-344 rats in vivo and in vitro. Toxicol Appl Pharmacol. 1993 Dec;123(2):274-82. doi: 10.1006/taap.1993.1246. [PubMed:8248934 ]
  2. Lu D, Peterson LA: Identification of furan metabolites derived from cysteine-cis-2-butene-1,4-dial-lysine cross-links. Chem Res Toxicol. 2010 Jan;23(1):142-51. doi: 10.1021/tx9003215. [PubMed:20043645 ]
Download FileCC02328.sdf