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Robert Epple
Observed names:
Epple, R.,
Epple, Robert,
R. EPPLE,
R. Epple
Observed institutions:
Scripps Research Institute,
Genomics Institute of the Novartis Research Foundation,
ETH Zurich,
Laboratory of Organic Chemistry,
Novartis Foundation
ORCID:
0000-0001-7157-806X
Observed ORCID:
0000-0001-7157-806X
OpenAlex ID:
A5020078905
Overcoming EGFR(T790M) and EGFR(C797S) resistance with mutant-selective allosteric inhibitors
2016
·
Yong Jia
, Cai-Hong Yun
, et al.
·
Nature
·
926
Osmium-Catalyzed Dihydroxylation of Olefins in Acidic Media: Old Process, New Tricks
2002
·
Philippe Dupau
, Robert Epple
, et al.
·
Advanced Synthesis & Catalysis
·
248
EGF816 Exerts Anticancer Effects in Non–Small Cell Lung Cancer by Irreversibly and Selectively Targeting Primary and Acquired Activating Mutations in the EGF Receptor
2016
·
Yong Jia
, Jose Juarez
, et al.
·
Cancer Research
·
121
PDF
A New Approach to Osmium-Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins
2002
·
Malin A. Andersson
, Robert Epple
, et al.
·
Angewandte Chemie International Edition
·
119
Discovery of (R,E)-N-(7-Chloro-1-(1-[4-(dimethylamino)but-2-enoyl]azepan-3-yl)-1H-benzo[d]imidazol-2-yl)-2-methylisonicotinamide (EGF816), a Novel, Potent, and WT Sparing Covalent Inhibitor of Oncogenic (L858R, ex19del) and Resistant (T790M) EGFR Mutants for the Treatment of EGFR Mutant Non-Small-Cell Lung Cancers
2016
·
Gérald Lelais
, Robert Epple
, et al.
·
Journal of Medicinal Chemistry
·
95
Investigation of Flavin-Containing DNA-Repair Model Compounds
1997
·
Robert Epple
, Ernst-Udo Wallenborn
, et al.
·
Journal of the American Chemical Society
·
72
Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: Heterocyclic P3
2006
·
David C. Tully
, Hong Liu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
57
Repair of UV Light Induced DNA Lesions: A Comparative Study with Model Compounds
1998
·
Thomas Carell
, Robert Epple
·
European Journal of Organic Chemistry
·
53
Novel Bisaryl Substituted Thiazoles and Oxazoles as Highly Potent and Selective Peroxisome Proliferator-Activated Receptor δ Agonists
2009
·
Robert Epple
, Christopher Cow
, et al.
·
Journal of Medicinal Chemistry
·
48
Synthesis of Flavin‐Containing Model Compounds for DNA Photolyase Mediated DNA Repair
1996
·
Thomas Carell
, Robert Epple
, et al.
·
Angewandte Chemie International Edition in English
·
46
A Comparative Repair Study of Thymine- and Uracil-Photodimers with Model Compounds and a Photolyase Repair Enzyme
2000
·
Jens Butenandt
, Robert Epple
, et al.
·
Chemistry - A European Journal
·
40
1,3,5-Trisubstituted aryls as highly selective PPARδ agonists
2006
·
Robert Epple
, Mihai Azimioara
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
39
Solid-Phase Synthesis of Nucleoside Analogues
2003
·
Robert Epple
, Romas Kudirka
, et al.
·
Journal of Combinatorial Chemistry
·
36
Synthesis and SAR of arylaminoethyl amides as noncovalent inhibitors of cathepsin S: P3 cyclic ethers
2006
·
David C. Tully
, Hong Liu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
32
A New Approach to Osmium-Catalyzed Asymmetric Dihydroxylation and Aminohydroxylation of Olefins
2002
·
Malin A. Andersson
, Robert Epple
, et al.
·
Angewandte Chemie
·
30
3,4,5-Trisubstituted isoxazoles as novel PPARδ agonists. Part 2
2006
·
Robert Epple
, Mihai Azimioara
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
29
Discovery of the First Potent, Selective, and Orally Bioavailable Signal Peptide Peptidase-Like 2a (SPPL2a) Inhibitor Displaying Pronounced Immunomodulatory Effects In Vivo
2018
·
Juraj Velcicky
, Ursula Bodendorf
, et al.
·
Journal of Medicinal Chemistry
·
28
Flavin- and Deazaflavin-Containing Model Compounds Mimic the Energy Transfer Step in Type-II DNA-Photolyases
1998
·
Robert Epple
, Thomas Carell
·
Angewandte Chemie International Edition
·
28
Efficacy and Tolerability of Pyrazolo[1,5-a]pyrimidine RET Kinase Inhibitors for the Treatment of Lung Adenocarcinoma
2020
·
Casey J. N. Mathison
, Donatella Chianelli
, et al.
·
ACS Medicinal Chemistry Letters
·
26
3,4,5-Trisubstituted isoxazoles as novel PPARδ agonists: Part 1
2006
·
Robert Epple
, Ross Russo
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
24
Efficient Light-Dependent DNA Repair Requires a Large Cofactor Separation
1999
·
Robert Epple
, Thomas Carell
·
Journal of the American Chemical Society
·
22
Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1
2005
·
Hong Liu
, David C. Tully
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
19
Synthesis and structure of (carboxymethyl)‐functionalized cyclobuta‐fused uracil dimers
1997
·
Thomas Carell
, Robert Epple
, et al.
·
Helvetica Chimica Acta
·
18
新規PPARδ作動薬としての3,4,5‐三置換イソオキサゾール:1部
2006
·
Robert Epple
, Russo Ross
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin S
2007
·
Arnab K. Chatterjee
, Hong Liu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
16
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Works count:
61
Citation count:
2,279
H-index:
21
I10-index:
30
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