Title : Pharmacogenetics of phase I and phase II drug metabolism.

Pub. Date : 2010

PMID : 19835560






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Variant alleles of UGT1A1 are less capable of conjugating and eliminating SN-38, the active form of the topoisomerase inhibitor irinotecan, and defective alleles for NAT2 are responsible for the well-described acetylation polymorphism that leads to impaired clearance of isoniazid and other agents. Isoniazid UDP glucuronosyltransferase family 1 member A1 Homo sapiens