000 01734 a2200433 4500
005 20250511191137.0
264 0 _c19921015
008 199210s 0 0 eng d
022 _a0049-8254
024 7 _a10.3109/00498259209046651
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKumagai, Y
245 0 0 _aAromatic hydroxylation of methylenedioxybenzene (MDB) and methylenedioxymethamphetamine (MDMA) by rabbit liver microsomes.
_h[electronic resource]
260 _bXenobiotica; the fate of foreign compounds in biological systems
_cApr 1992
300 _a395-403 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
650 0 4 _a3,4-Methylenedioxyamphetamine
_xanalogs & derivatives
650 0 4 _aAnimals
650 0 4 _aBenzodioxoles
650 0 4 _aCarbon Monoxide
_xpharmacology
650 0 4 _aChromatography, High Pressure Liquid
650 0 4 _aCytochrome P-450 Enzyme Inhibitors
650 0 4 _aCytochrome P-450 Enzyme System
_xmetabolism
650 0 4 _aDioxoles
_xmetabolism
650 0 4 _aHydroxylation
650 0 4 _aMale
650 0 4 _aMass Spectrometry
650 0 4 _aMicrosomes, Liver
_xdrug effects
650 0 4 _aMixed Function Oxygenases
_xantagonists & inhibitors
650 0 4 _aModels, Biological
650 0 4 _aNADP
_xmetabolism
650 0 4 _aPhenols
_xmetabolism
650 0 4 _aPotentiometry
650 0 4 _aRabbits
700 1 _aSchmitz, D A
700 1 _aCho, A K
773 0 _tXenobiotica; the fate of foreign compounds in biological systems
_gvol. 22
_gno. 4
_gp. 395-403
856 4 0 _uhttps://doi.org/10.3109/00498259209046651
_zAvailable from publisher's website
999 _c1530342
_d1530342