000 01314 a2200349 4500
005 20250515195744.0
264 0 _c20100427
008 201004s 0 0 eng d
022 _a1464-3391
024 7 _a10.1016/j.bmc.2009.10.055
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDietrich, Justin
245 0 0 _aApplication of a novel [3+2] cycloaddition reaction to prepare substituted imidazoles and their use in the design of potent DFG-out allosteric B-Raf inhibitors.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry
_cJan 2010
300 _a292-304 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aCyclization
650 0 4 _aHumans
650 0 4 _aImidazoles
_xchemical synthesis
650 0 4 _aMice
650 0 4 _aModels, Molecular
650 0 4 _aProtein Binding
650 0 4 _aProtein Kinase Inhibitors
_xchemistry
650 0 4 _aProto-Oncogene Proteins B-raf
_xantagonists & inhibitors
700 1 _aGokhale, Vijay
700 1 _aWang, Xiadong
700 1 _aHurley, Laurence H
700 1 _aFlynn, Gary A
773 0 _tBioorganic & medicinal chemistry
_gvol. 18
_gno. 1
_gp. 292-304
856 4 0 _uhttps://doi.org/10.1016/j.bmc.2009.10.055
_zAvailable from publisher's website
999 _c19345149
_d19345149