Trisubstituted Pyridinylimidazoles as Potent Inhibitors of the Clinically Resistant L858R/T790M/C797S EGFR Mutant: Targeting of Both Hydrophobic Regions and the Phosphate Binding Site

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dc.contributor.author Juchum, Michael
dc.contributor.author Laufer, Stefan
dc.contributor.author Günther, Marcel
dc.contributor.author Döring, Eva
dc.date.accessioned 2017-09-21T14:40:30Z
dc.date.available 2017-09-21T14:40:30Z
dc.date.issued 2017
dc.identifier.issn 1520-4804
dc.identifier.uri http://hdl.handle.net/10900/77932
dc.language.iso en de_DE
dc.publisher Amer Chemical Soc de_DE
dc.relation.uri http://dx.doi.org/10.1021/acs.jmedchem.7b00316 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 540 de_DE
dc.title Trisubstituted Pyridinylimidazoles as Potent Inhibitors of the Clinically Resistant L858R/T790M/C797S EGFR Mutant: Targeting of Both Hydrophobic Regions and the Phosphate Binding Site de_DE
dc.type Artikel de_DE
utue.quellen.id 20170815222223_00193
utue.publikation.seiten 5613-5637 de_DE
utue.personen.roh Gunther, Marcel
utue.personen.roh Lategahn, Jonas
utue.personen.roh Juchum, Michael
utue.personen.roh Doring, Eva
utue.personen.roh Keul, Marina
utue.personen.roh Engel, Julian
utue.personen.roh Tumbrink, Hannah L.
utue.personen.roh Rauh, Daniel
utue.personen.roh Laufer, Stefan
dcterms.isPartOf.ZSTitelID Journal of Medicinal Chemistry de_DE
dcterms.isPartOf.ZS-Issue 13 de_DE
dcterms.isPartOf.ZS-Volume 60 de_DE
utue.fakultaet 07 Mathematisch-Naturwissenschaftliche Fakultät de_DE


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