Title : Enantioselectivity in the cytochrome P450-dependent conversion of tegafur to 5-fluorouracil in human liver microsomes.

Pub. Date : 2013 Oct

PMID : 25505563






5 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Enantioselectivity in the cytochrome P450-dependent conversion of tegafur to 5-fluorouracil in human liver microsomes. Tegafur cytochrome P450 family 4 subfamily F member 3 Homo sapiens
2 Tegafur (FT) is a prodrug of 5-fluorouracil (5-FU) used in cancer chemotherapy, and the bioactivation of FT to 5-FU is mainly catalyzed by cytochrome P450 (CYP) in hepatic microsomes. Tegafur cytochrome P450 family 4 subfamily F member 3 Homo sapiens
3 Tegafur (FT) is a prodrug of 5-fluorouracil (5-FU) used in cancer chemotherapy, and the bioactivation of FT to 5-FU is mainly catalyzed by cytochrome P450 (CYP) in hepatic microsomes. Tegafur cytochrome P450 family 4 subfamily F member 3 Homo sapiens
4 Tegafur (FT) is a prodrug of 5-fluorouracil (5-FU) used in cancer chemotherapy, and the bioactivation of FT to 5-FU is mainly catalyzed by cytochrome P450 (CYP) in hepatic microsomes. Tegafur cytochrome P450 family 4 subfamily F member 3 Homo sapiens
5 Tegafur (FT) is a prodrug of 5-fluorouracil (5-FU) used in cancer chemotherapy, and the bioactivation of FT to 5-FU is mainly catalyzed by cytochrome P450 (CYP) in hepatic microsomes. Tegafur cytochrome P450 family 4 subfamily F member 3 Homo sapiens