000 01760 a2200469 4500
005 20250518015630.0
264 0 _c20200123
008 202001s 0 0 eng d
022 _a1521-009X
024 7 _a10.1124/dmd.118.084665
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aItkonen, Matti K
245 0 0 _aClopidogrel and Gemfibrozil Strongly Inhibit the CYP2C8-Dependent Formation of 3-Hydroxydesloratadine and Increase Desloratadine Exposure In Humans.
_h[electronic resource]
260 _bDrug metabolism and disposition: the biological fate of chemicals
_c04 2019
300 _a377-385 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aArea Under Curve
650 0 4 _aAryl Hydrocarbon Hydroxylases
_xmetabolism
650 0 4 _aBiotransformation
_xphysiology
650 0 4 _aClopidogrel
_xpharmacology
650 0 4 _aCross-Over Studies
650 0 4 _aCytochrome P-450 CYP2C8
_xmetabolism
650 0 4 _aCytochrome P-450 CYP2C8 Inhibitors
_xpoisoning
650 0 4 _aDrug Interactions
_xphysiology
650 0 4 _aFemale
650 0 4 _aGemfibrozil
_xpharmacology
650 0 4 _aGenotype
650 0 4 _aGlucuronides
_xpharmacology
650 0 4 _aHumans
650 0 4 _aHypolipidemic Agents
_xpoisoning
650 0 4 _aLoratadine
_xanalogs & derivatives
650 0 4 _aMale
650 0 4 _aYoung Adult
700 1 _aTornio, Aleksi
700 1 _aNeuvonen, Mikko
700 1 _aNeuvonen, Pertti J
700 1 _aNiemi, Mikko
700 1 _aBackman, Janne T
773 0 _tDrug metabolism and disposition: the biological fate of chemicals
_gvol. 47
_gno. 4
_gp. 377-385
856 4 0 _uhttps://doi.org/10.1124/dmd.118.084665
_zAvailable from publisher's website
999 _c29242086
_d29242086