000 01544 a2200421 4500
005 20250514234812.0
264 0 _c20051220
008 200512s 0 0 eng d
022 _a0960-894X
024 7 _a10.1016/j.bmcl.2005.06.056
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVrudhula, Vivekananda M
245 0 0 _aAnalogs of a potent maxi-K potassium channel opener with an improved inhibitory profile toward cytochrome P450 isozymes.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry letters
_cOct 2005
300 _a4286-90 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAnimals
650 0 4 _aAryl Hydrocarbon Hydroxylases
_xantagonists & inhibitors
650 0 4 _aBinding Sites
650 0 4 _aCytochrome P-450 CYP2C9
650 0 4 _aCytochrome P-450 Enzyme Inhibitors
650 0 4 _aHumans
650 0 4 _aInhibitory Concentration 50
650 0 4 _aIsoenzymes
_xantagonists & inhibitors
650 0 4 _aOocytes
650 0 4 _aQuinolones
_xchemical synthesis
650 0 4 _aStructure-Activity Relationship
650 0 4 _aXenopus laevis
700 1 _aDasgupta, Bireshwar
700 1 _aBoissard, Christopher G
700 1 _aGribkoff, Valentin K
700 1 _aSantone, Kenneth S
700 1 _aDalterio, Richard A
700 1 _aLodge, Nicholas J
700 1 _aStarrett, John E
773 0 _tBioorganic & medicinal chemistry letters
_gvol. 15
_gno. 19
_gp. 4286-90
856 4 0 _uhttps://doi.org/10.1016/j.bmcl.2005.06.056
_zAvailable from publisher's website
999 _c15712794
_d15712794