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. Author manuscript; available in PMC: 2023 Aug 2.
Published in final edited form as: Arch Toxicol. 2022 Sep 9;96(12):3219–3231. doi: 10.1007/s00204-022-03369-0

Table 1.

Contribution of CYP isoforms in the formation of metabolites of perhexiline in cDNA-expressed CYP bactosomes

M1 (trans-OH-Phx-1) M2 M3 (trans-OH-Phx-2) M4 M5 (cis-OH-Phx) M6

EV 0 0 0 0 0 0.2
CYP1A2 0 0 0 2.4 0.2 7.8
CYP2C19 19.5 27.5 92.6 62.5 3.1 2.9
CYP2D6 100 100 6.5 100 100 0.6
CYP3A4 91.3 0 100 0 22.9 100
*

To demonstrate the relative contribution of individual CYP enzymes, for each metabolite, the highest abundance level observed was set to 100% and the abundance generated by other CYP enzymes was expressed as percentages accordingly. All six metabolites detected were mono-hydroxylated derivatives of perhexiline based on their exact masses