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17篇 您的检索式：作者名="RaeppelS"

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		题名	作者	年代	出处	被引量
	1	DiScovery of N- (2-aminophenyl) -4- E (4-pyridin-3-ylpyrimidin-2- ylamino) methyl:benzamide (MGCD0103), an orally active histone deacetylase inhibitor 显示文摘	Zhou N Moradei O Raeppel S	2008	JMed Chem2008，51，14：	1
	2	Simultaneous analysis of pesticides from different chemical classes by using a derivatisation step and gas chromatography-mass spectrometry 显示文摘	RAEPPEL C NIEF M FABRITIUS M	2011	J Chromatogr A2011，1218，44：	1
	3	Discovery of a novel and potent series of thieno pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases 显示文摘	CLARIDGE S RAEPPEL F GRANGER M C	2008	Bioorg IVied Chem Lett2008，18，9：	1
	4	Discovery of N-(2-aminophenyl)-4-benzamide (MGCD0103), an orally active histone deacetylase inhibitor 显示文摘	Zhou N Moradei O Raeppel S	2008	J Med Chem2008，51，14：	1
	5	Analytical method for assessing potential dermal exposure to pesticides of a nonagricultural occupationally exposed population显示文摘	Delhomme O Raeppel C Briand O		0，，03：	1
	6	Identification of a novel series of potent RON receptor tyrosine kinase inhibitors 显示文摘	Raeppel S Gaudette F Mannion M	2010	Bioorg Med Chem Lett2010，20，9：	1
	7	Designandsynthesisof4--N-(2-aminophenyl)-benzamidesandtheiranaloguesasanovelclassofhistonedeacetylaseinhibitors显示文摘	PaquinL RaeppelS LeitS etal	2008	BioorgMedChemLett2008，18，3：	1
	8	N-( 3-Fluoro-4-( 2-arylthieno pyridin-7- yloxy ) phenyl ) -2-oxo-3-phenylimidazolidine-1 -carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors 显示文摘	RAEPPEL S CLARIDGE S SAAVEDRA O	2009	Bioorg Med Chem Lett2009，19，5：	1
	9	N-(4-(6,7-Disubstituted-quinolin-4-yloxy ) -3-fluorophenyl ) -2-oxo-3- phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors 显示文摘	MANNION M RAEPPEL S	2009	Bioorg Med Chem Lett2009，19，23：	1
	10	Analytical method for assessing potential dermal exposure to pesticides of a nonagricultural occupationally exposed population显示文摘	Delhomme O Raeppel C Briand O		0，，03：	1
	11	Discoveryof N-{ 2-aminophenyl) (4-pyridin-3-ylpyrimidin-2-ylamino) methyl] benzamide ( MGCD0103 ),anorally active histone deacetylase inhibitor 显示文摘	ZHOU N MORADEI O RAEPPEL S	2008	J MedChem2008，51，14：	1
	12	Design and synthesis of 4- -N- ( 2-aminophenyl ) -benzamides and their analogues as a novel class of histonedeacetylase inhibitors 显示文摘	PAQUIN I RAEPPEL S LEIT S	2008	Bioorg Med Chem Lett2008，18，3：	1
	13	Discovery of A^-( 2-aminophenyl) -4- benzamide ( MGCD0103 ),an orally active histone deacetylase inhibitor 显示文摘	ZHOU N MORADEI O RAEPPEL S	2008	JMed Chem2008，51，14：	1
	14	Design and synthesis of 4--N-(2-aminophenyl)-benzamides and their analogues as a novel class of histone deacetylase inhibitors显示文摘	Paquin I Raeppel S Leit S	2008	Bioorg Med Chem Lett2008，18，3：	1
	15	Discovery of N-(2-aminophenyl)-4-benzamide (MGCD0103),an orally active histone deacetylase inhibitor显示文摘	Zhou N Moradei O Raeppel S	2008	J Med Chem2008，51，14：	1
	16	Identification of potent and selective VEGFR receptor tyrosine kinase inhibitors having new amide isostere headgroups 显示文摘	Gaudette F Raeppel S Nguyen H	2010	Bioorg Med Chem Lett2010，20，3：	1
	17	N-(3-fluoro4-(2-arylthieno pyridin-7-yloxy) phenyl) -2-oxo-3-phenylimid- azolidine-l-carboxamides:a novel series of dual c-met/VEGFR2 receptor tyrosine kinase inhibitors 显示文摘	Raeppel S Claridge S Saavedra O	2009	Bioorg Med Chem Lett2009，19，5：	1

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