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Involvement of CYP4F2 in the Metabolism of a Novel Monophosphate Ester Prodrug of Gemcitabine and Its Interaction Potential In Vitro.


ABSTRACT: Compound-3 is an oral monophosphate prodrug of gemcitabine. Previous data showed that Compound-3 was more potent than gemcitabine and it was orally active in a tumor xenograft model. In the present study, the metabolism of Compound-3 was investigated in several well-known in vitro matrices. While relatively stable in human and rat plasma, Compound-3 demonstrated noticeable metabolism in liver and intestinal microsomes in the presence of NADPH and human hepatocytes. Compound-3 could also be hydrolyzed by alkaline phosphatase, leading to gemcitabine formation. Metabolite identification using accurate mass- and information-based scan techniques revealed that Compound-3 was subjected to sequential metabolism, forming alcohol, aldehyde and carboxylic acid metabolites, respectively. Results from reaction phenotyping studies indicated that cytochrome P450 4F2 (CYP4F2) was a key CYP isozyme involved in Compound-3 metabolism. Interaction assays suggested that CYP4F2 activity could be inhibited by Compound-3 or an antiparasitic prodrug pafuramidine. Because CYP4F2 is a key CYP isozyme involved in the metabolism of eicosanoids and therapeutic drugs, clinical relevance of drug-drug interactions mediated via CYP4F2 inhibition warrants further investigation.

SUBMITTER: Wang Y 

PROVIDER: S-EPMC6100113 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Involvement of CYP4F2 in the Metabolism of a Novel Monophosphate Ester Prodrug of Gemcitabine and Its Interaction Potential In Vitro.

Wang Yedong Y   Li Yuan Y   Lu Jia J   Qi Huixin H   Cheng Isabel I   Zhang Hongjian H  

Molecules (Basel, Switzerland) 20180516 5


Compound-<b>3</b> is an oral monophosphate prodrug of gemcitabine. Previous data showed that Compound-<b>3</b> was more potent than gemcitabine and it was orally active in a tumor xenograft model. In the present study, the metabolism of Compound-<b>3</b> was investigated in several well-known in vitro matrices. While relatively stable in human and rat plasma, Compound-<b>3</b> demonstrated noticeable metabolism in liver and intestinal microsomes in the presence of NADPH and human hepatocytes. Co  ...[more]

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