Record Information
Version1.0
Creation Date2019-07-14 16:35:35 UTC
Last Updated2019-10-01 21:41:00 UTC
CypComp IDCC01898
Compound Information
NameBPR0L075
Structure ImageUzjvbxkfbqndtq uhfffaoysa n
InChIKeyUZJVBXKFBQNDTQ-UHFFFAOYSA-N
PubChem ID10359957
CypCompound Information
SetCypBoM Training Set
Bonds of Metabolism (BoMs)
CYP1A2CYP2A6CYP2B6CYP2C8CYP2C9CYP2C19CYP2D6CYP2E1CYP3A4
  • <5,H;Hydroxylation;R1>
  • <3,H;Hydroxylation;R2>
  • <8,7;Cleavage;R3>
  • <8,H;Oxidation;R3>
  • Not Available
  • Not Available
  • Not Available
  • <5,H;Hydroxylation;R1>
  • <3,H;Hydroxylation;R2>
  • <8,7;Cleavage;R3>
  • <8,H;Oxidation;R3>
  • <21,20;Cleavage;R4>
  • <21,H;Oxidation;R4>
  • <23,22;Cleavage;R5>
  • <23,H;Oxidation;R5>
  • <25,24;Cleavage;R6>
  • <25,H;Oxidation;R6>
  • <5,H;Hydroxylation;R1>
  • <3,H;Hydroxylation;R2>
  • <8,7;Cleavage;R3>
  • <8,H;Oxidation;R3>
  • <21,20;Cleavage;R4>
  • <21,H;Oxidation;R4>
  • <23,22;Cleavage;R5>
  • <23,H;Oxidation;R5>
  • <25,24;Cleavage;R6>
  • <25,H;Oxidation;R6>
  • <5,H;Hydroxylation;R1>
  • <3,H;Hydroxylation;R2>
  • <8,7;Cleavage;R3>
  • <8,H;Oxidation;R3>
  • <23,22;Cleavage;R4>
  • <23,H;Oxidation;R4>
  • <5,H;Hydroxylation;R1>
  • <3,H;Hydroxylation;R2>
  • <8,7;Cleavage;R3>
  • <8,H;Oxidation;R3>
  • <21,20;Cleavage;R4>
  • <21,H;Oxidation;R4>
  • <23,22;Cleavage;R5>
  • <23,H;Oxidation;R5>
  • <25,24;Cleavage;R6>
  • <25,H;Oxidation;R6>
  • <5,H;Hydroxylation;R1>
  • <3,H;Hydroxylation;R2>
  • <8,7;Cleavage;R3>
  • <8,H;Oxidation;R3>
  • <21,20;Cleavage;R4>
  • <21,H;Oxidation;R4>
  • <23,22;Cleavage;R5>
  • <23,H;Oxidation;R5>
  • <25,24;Cleavage;R6>
  • <25,H;Oxidation;R6>
References
  1. Yao HT, Wu YS, Chang YW, Hsieh HP, Chen WC, Lan SJ, Chen CT, Chao YS, Chang L, Sun HY, Yeh TK: Biotransformation of 6-methoxy-3-(3',4',5'-trimethoxy-benzoyl)-1H-indole (BPR0L075), a novel antimicrotubule agent, by mouse, rat, dog, and human liver microsomes. Drug Metab Dispos. 2007 Jul;35(7):1042-9. doi: 10.1124/dmd.106.014597. Epub 2007 Apr 2. [PubMed:17403915 ]
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