Prof. Dr. Rainer Riedl

Leitungsfunktion

• Leitung Center for Drug Discovery and Pharmaceutical Product Development + Head of Organic and Medicinal Chemistry

Tätigkeit an der ZHAW als

Professor of Organic and Medicinal Chemistry

www.zhaw.ch/icbt/organic-and-medicinal-chemistry/

Arbeits- und Forschungsschwerpunkte, Spezialkenntnisse

Drug discovery
Rational drug design
Development of structure activity relationships
Generation of lead structures
Development of clinical candidates
Structure based drug design
Organic chemistry
Natural products
Solid phase synthesis
Microwave assisted synthesis
Microreactors
Protein-protein interactions
Cheminformatics
Computational chemistry
Combinatorial chemistry
Catalyst development
SixSigma process optimization

Aus- und Fortbildung

May 2011 - November 2012
CAS University Didactic
PH Zurich, Switzerland

March 2004 - March 2005
Hagener Management Studies, Department of Business Administration and Economics,
University of Hagen, Germany

August 1995 - December 1998
Ph.D. studies, Department of Organic Chemistry, University of
Heidelberg, Germany and Department of Organic Chemistry,
University of Cologne, Germany, under the supervision of Prof. Dr. A.
Berkessel “Combinatorial de novo synthesis of artificial
phosphodiesterases”, summa cum laude

July 1995
German Chemistry Diploma, Department of Organic Chemistry,
University of Heidelberg, Germany, under the supervision of Prof. Dr.
A. Berkessel “En route to the combinatorial syntheses of artificial
phosphodiesterases”, summa cum laude

October 1990 - October 1994
Undergraduate and graduate studies of chemistry at the
University of Heidelberg, Germany

Fellowships and awards:

September 2013 Swiss Chemical Society FH award winner project in the category "Molecules for the Life Sciences": Tackling antibiotic resistance by transcription regulator inhibitory compounds.

November 2006 Eli Lilly Protease Platform Library Design Award

February 2006 Eli Lilly Recognition Grant

November 2000 Liebig habilitation fellowship of the Fonds der Chemischen Industrie

February 1999 Feodor-Lynen postdoctoral fellowship of the Alexander von Humboldt Stiftung

May 1998 Kurt-Alder-award for Ph.D. thesis (combinatorial catalyst development), Department of Organic Chemistry, University of Cologne, Germany

February 1996 Ph.D. fellowship of the Stiftung Stipendien-Fonds des Verbands der Chemischen Industrie, Germany

December 1995 Dr. Sophie-Bernthsen-award, Department of Organic Chemistry, University of Heidelberg, Germany

August 1995 Fellowship of the Graduiertenkolleg “Selectivity in organic and organometallic synthesis and catalysis”, Departments of Organic and Inorganic Chemistry, University of Heidelberg, Germany

December 1993 Procter & Gamble award, Department of Organic Chemistry, University of Heidelberg, Germany

October 1990 Fellowship of the Studienstiftung des deutschen Volkes (German National Scholarship Foundation)

July 1990 Book award of the Fonds der Chemischen Industrie, Germany

July 1990 Bronze medal for the Federal Republic of Germany at the International Olympiad of Chemistry (IChO) 1990, Paris, France

Beruflicher Werdegang

since February 2009 Head of Organic Chemistry and Medicinal Chemistry at ZHAW

August 2007 - January 2009
Senior Research Scientist, Eli Lilly Corporate Center,
Indianapolis, USA, Discovery Chemistry Research and Technology

October 2005 - July 2007
Senior Research Scientist, Eli Lilly Research Lab Hamburg,
Discovery Chemistry Research and Technology

October 2005 - July 2007
SixSigma Green Belt at Eli Lilly Research Lab Hamburg, Discovery
Chemistry Research and Technology

April 2002 – September 2005
Research Scientist, lab leader, Eli Lilly Research Lab Hamburg,
Discovery Chemistry Research and Technology

November 2000 - December 2001
Habilitand at the Laboratory of Organic Chemistry, ETH Zurich, Switzerland

February 1999 - September 2000
Postdoctoral scientist with Prof. Dr. Peter Schultz, University of
California, Berkeley, USA and at The Scripps Research Institute,
La Jolla, USA

Mitglied in Netzwerken

• Alexander von Humboldt Foundation
• Swiss Chemical Society
• Studienstiftung des Deutschen Volkes
• Biotechnet Switzerland
• Schweizerische Akademie der Technischen Wissenschaften

• Induktion der Wirkstoffbildung bei Actinomyceten / Stellv. ProjektleiterIn / Projekt laufend
• Morbillivirus cell entry machinery: mechanisms, structures and antiviral drug discovery / Co-ProjektleiterIn / Projekt laufend
• Identifizierung und Charakterisierung von Wirkstoffen aus Actinomyceten aus der Schweiz gegen pathogene Bakterien / ProjektleiterIn / Projekt abgeschlossen
• Novel Antimicrobials for Life-Threatening Infections / ProjektleiterIn / Projekt abgeschlossen
• Virus cell entry machinery: antiviral drug discovery / ProjektleiterIn / Projekt abgeschlossen
• Dynamic combinatorial chemistry in drug discovery / ProjektleiterIn / Projekt abgeschlossen
• New antileishmanial and antitrypanosomal drugs / ProjektleiterIn / Projekt abgeschlossen
• New drugs for the treatment of protozoal infections derived from natural products / ProjektleiterIn / Projekt abgeschlossen
• Kinetische Struktur-Aktivitäts-Beziehungen und röntgenkristallographische Bestimmung des Bindungsmodus von niedermolekularen Wirkstoffmolekülen / ProjektleiterIn / Projekt abgeschlossen
• Development of high temperature resistant, synergistic biocidal products for protection of PVC against microbial infestation for commercial product applications / ProjektleiterIn / Projekt abgeschlossen
• HIT to LEAD to Preclinical Candidate development of a Transcription Repressor Inhibitory Compound (TRIC) that increases antibiotic susceptibility of multidrug resistant staphylococci / ProjektleiterIn / Projekt abgeschlossen
• Prevention of undesired interactions between biocides and additives in synthetic materials to improve efficacy and to reduce the necessary amount of biocides / ProjektleiterIn / Projekt abgeschlossen
• Development of a software to analyse chemical and biological data: CyBy2 / ProjektleiterIn / Projekt abgeschlossen
• HIT to LEAD to Candidate development of a Transcription Repressor Inhibitory Compound (TRIC), which switches off bacterial resistance to a broad band antibiotic / ProjektleiterIn / Projekt abgeschlossen
• Isolation, Identifikation und medizinalchemische Optimierung von biogenen Wirkstoffen / ProjektleiterIn / Projekt abgeschlossen
• Identification of novel targets and drug candidates against multi-drug resistant bacteria / ProjektleiterIn / Projekt abgeschlossen

Beiträge in wissenschaftlicher Zeitschrift, peer-reviewed

• Fischer, Thomas; Riedl, Rainer,

  2017.

  Cover picture : targeted fluoro positioning for the discovery of a potent and highly selective matrix metalloproteinase inhibitor (ChemistryOpen 2/2017).

  ChemistryOpen.

  6(2),

  S. 165.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1689

• Fischer, Thomas; Riedl, Rainer,

  2017.

  Cover profile : targeted fluoro positioning for the discovery of a potent and highly selective matrix metalloproteinase inhibitor.

  ChemistryOpen.

  6(2),

  S. 167.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1688

• Fischer, Thomas; Riedl, Rainer,

  2017.

  Development of a non-hydroxamate dual matrix metalloproteinase (MMP)-7/-13 inhibitor.

  Molecules.

  22(9).

  Verfügbar unter: https://doi.org/10.21256/zhaw-1692

• Abu Eid, Sameer; Adams, Michael; Scherer, Thomas; Torres-Gómez, Héctor Manuel; Hackl, Martina Theresa; Kaplanian, Mairam; Riedl, Rainer; Luger, Anton; Fürnsinn, Clemens,

  2017.

  Emodin : a compound with putative antidiabetic potential, deteriorates glucose tolerance in rodents.

  European Journal of Pharmacology.

  798,

  S. 77-84.

  Verfügbar unter: https://doi.org/10.1016/j.ejphar.2017.01.022

• Chellat, Mathieu F.; Riedl, Rainer,

  2017.

  Pseudouridimycin : das erste Nukleosid-Analogon, das bakterielle RNA-Polymerase selektiv inhibiert.

  Angewandte Chemie.

  129(43),

  S. 13364-13366.

  Verfügbar unter: https://doi.org/10.1002/ange.201708133

• Chellat, Mathieu F.; Riedl, Rainer,

  2017.

  Pseudouridimycin : the first nucleoside analogue that selectively inhibits bacterial RNA polymerase.

  Angewandte Chemie: International Edition.

  56(43),

  S. 13184-13186.

  Verfügbar unter: https://doi.org/10.1002/anie.201708133

• Fischer, Thomas; Riedl, Rainer,

  2017.

  Targeted fluoro positioning for the discovery of a potent and highly selective matrix metalloproteinase inhibitor.

  ChemistryOpen.

  6(2),

  S. 192-195.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1690

• Senn, Nicole; Ott, Michael; Lanz, Jan; Riedl, Rainer,

  2017.

  Targeted polypharmacology : discovery of a highly potent non-hydroxamate dual matrix metalloproteinase (MMP)-10/-13 inhibitor.

  Journal of Medicinal Chemistry.

  60(23),

  S. 9585-9598.

  Verfügbar unter: https://doi.org/10.1021/acs.jmedchem.7b01001

• Chellat, Mathieu F.; Raguž, Luka; Riedl, Rainer,

  2016.

  Antibiotikaresistenzen gezielt überwinden.

  Angewandte Chemie.

  128(23),

  S. 6710-6738.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1681

• Fischer, Thomas; Riedl, Rainer,

  2016.

  Molecular recognition of the catalytic zinc(II) ion in MMP-13 : structure-based evolution of an allosteric inhibitor to dual binding mode inhibitors with improved lipophilic ligand efficiencies.

  International Journal of Molecular Sciences.

  17(3/314).

  Verfügbar unter: https://doi.org/10.21256/zhaw-1683

• Chellat, Mathieu F.; Raguž, Luka; Riedl, Rainer,

  2016.

  Targeting antibiotic resistance.

  Angewandte Chemie: International Edition.

  55(23),

  S. 6600-6626.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1682

• Todorova, Milka; Trendafilova, Antoaneta; Danova, Kalina; Simmons, Luke; Wolfram, Evelyn; Meier, Beat; Riedl, Rainer; Evstatieva, Luba,

  2015.

  Highly oxygenated sesquiterpenes in Artemisia alba Turra.

  Phytochemistry.

  110,

  S. 140-149.

  Verfügbar unter: https://doi.org/10.1016/j.phytochem.2014.12.008

• Lanz, Jan; Riedl, Rainer,

  2015.

  Merging allosteric and active site binding motifs : de novo generation of target selectivity and potency via natural-product-derived fragments.

  ChemMedChem.

  10(3),

  S. 451-454.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1687

• Fischer, Thomas; Riedl, Rainer,

  2013.

  Strategic targeting of multiple water-mediated interactions : a concise and rational structure-based design approach to potent and selective MMP-13 inhibitors.

  ChemMedChem.

  8(9),

  S. 1457-1461.

  Verfügbar unter: https://doi.org/10.21256/zhaw-1686

• Höck, Stefan; Riedl, Rainer,

  2012.

  chemf : a purely functional chemistry toolkit.

  Journal of Cheminformatics.

  4(38).

  Verfügbar unter: https://doi.org/10.21256/zhaw-1684

• Höck, Stefan; Riedl, Rainer,

  2012.

  CyBy2 : a structure-based data management tool for chemical and biological data.

  Chimia.

  66(3),

  S. 132-134.

  Verfügbar unter: https://doi.org/10.2533/chimia.2012.132a

• Höck, Stefan; Marti, Roger; Riedl, Rainer; Simeunovic, Marina,

  2010.

  Thermal cleavage of the Fmoc protection group.

  Chimia.

  64(3),

  S. 200-202.

  Verfügbar unter: https://doi.org/10.2533/chimia.2010.200

• Heuser, Stefan; Barrett, David G.; Berg, Martina; Bonnier, Benjamin; Kahl, Astrid; Luz De La Puente, Maria; Oram, Niall; Riedl, Rainer; Roettig, Ulrike; Gil, Gema Sanz; Seger, Erich; Steggles, David J.; Wanner, Jutta; Weichert, Andreas G.,

  2006.

  Synthesis of novel cyclopropylic sulfones and sulfonamides acting as glucokinase activators.

  Tetrahedron Letters.

  47(16),

  S. 2675-2678.

  Verfügbar unter: https://doi.org/10.1016/j.tetlet.2006.02.110

• Supekova, Lubica; Pezacki, John Paul; Su, Andrew I.; Loweth, Colin J.; Riedl, Rainer; Geierstanger, Bernhard; Schultz, Peter G.; Wemmer, David E.,

  2002.

  Genomic effects of polyamide/DNA interactions on mRNA expression.

  Chemistry & Biology.

  9(7),

  S. 821-827.

  Verfügbar unter: https://doi.org/10.1016/S1074-5521(02)00174-6

• Berkessel, Albrecht; Riedl, Rainer,

  2000.

  Combinatorial de novo synthesis of catalysts : how much of a hit-structure is needed for activity?.

  Journal of Combinatorial Chemistry.

  2(3),

  S. 215-219.

  Verfügbar unter: https://doi.org/10.1021/cc990073i

• Riedl, Rainer; Tappe, Robert; Berkessel, Albrecht,

  1998.

  Probing the scope of the asymmetric dihydroxylation of polymer-bound olefins : monitoring by HRMAS NMR allows for reaction control and on-bead measurement of enantiomeric excess.

  Journal of the American Chemical Society.

  120(35),

  S. 8994-9000.

  Verfügbar unter: https://doi.org/10.1021/ja980183d

• Berkessel, Albrecht; Riedl, Rainer,

  1997.

  Fluorescence reporters for phosphodiesterase activity.

  Angewandte Chemie: International Edition.

  36(13-14),

  S. 1481-1483.

  Verfügbar unter: https://doi.org/10.1002/anie.199714811

• Berkessel, Albrecht; Riedl, Rainer,

  1997.

  Fluoreszenz-Reporter für Phosphodiesterase-Aktivität.

  Angewandte Chemie.

  109(13-14),

  S. 1518-1520.

  Verfügbar unter: https://doi.org/10.1002/ange.19971091313

Bücher und Monographien, peer-reviewed

• Riedl, Rainer,

  1998.

  Kombinatorische de novo Synthese von künstlichen Phosphorsäurediesterasen : Inaugural-Dissertation zur Erlangung des Doktorgrades der Mathematisch-Naturwissenschaftlichen Fakultät der Universität zu Köln.

  Köln:

  Universität zu Köln.

  Verfügbar unter: http://kups.ub.uni-koeln.de/573/

Weitere Publikationen

• Riedl, Rainer,

  2014.

  Fighting the resistance.

  Horizon 2020 Projects.

  2014(4),

  S. 130.

• Riedl, Rainer,

  2014.

  Nicht nur Metalloproteasen im Visier.

  Chemie Plus.

  2014(4),

  S. 30-31.

• Riedl, Rainer,

  2013.

  Bridging the disciplines : cancer diagnostics & treatment.

  Pan European Networks: Science & Technology.

  7,

  S. 240-241.

• Riedl, Rainer; Höck, Stefan,

  2013.

  CyBy² : clevere Handhabung strukturbasierter Datensätze.

  Transfer.

  2013(1),

  S. 3.

  Verfügbar unter: https://www.zhaw.ch/storage/lsfm/forschung/transfer/2013-1-icbc.pdf

• Riedl, Rainer,

  2013.

  Drug discovery through a chemist’s eyes.

  International Innovation - EuroFocus.

  18,

  S. 103.

• Riedl, Rainer,

  2013.

  Organic chemistry : the heart and soul of drug discovery.

  International Innovation - EuroFocus.

  18,

  S. 104-105.

• Fischer, Thomas; Riedl, Rainer,

  2012.

  Design, synthesis and biological testing of novel MMP-inhibitors [Poster].

  In:

  SCS Fall Meeting 2012, Swiss Chemical Society (SCS), ETH Zurich, Zurich, Switzerland, 13 September 2012.

• Riedl, Rainer; Höck, Stefan,

  2012.

  Enhancing CyBy2 : visualization of structure activity relationships of large datasets [Poster].

  In:

  SCS Fall Meeting 2012, Swiss Chemical Society (SCS), ETH Zurich, Zurich, Switzerland, 13 September 2012.

• Riedl, Rainer; Fischer, Thomas,

  2012.

  Structure based design and synthesis of novel MMP inhibitors [Poster].

  In:

  19th EuroQSAR: Knowledge Enabled Ligand Design, Vienna, Austria, 26–30 August 2012.

• Riedl, Rainer; Brand, Michael,

  2012.

  Synthese und medizinalchemische Optimierung von Tetrazyklinanaloga.

  À Jour: SVC - Chemie, Life Sciences & Biotechnologie.

  2012(1),

  S. 10-11.

• Riedl, Rainer; Fischer, Thomas; Züger, Patrik; Brand, Michael,

  2011.

  Structure based design and synthesis of novel MMP inhibitors [Poster].

  In:

  SCS Fall meeting 2011 : Swiss Chemical Society (SCS), Lausanne, 9. September 2011.

• Riedl, Rainer; Brand, Michael; Sephton, Mark,

  2011.

  Synthesis of tetracycline analogues [Poster].

  In:

  SCS Fall meeting 2011 : Swiss Chemical Society (SCS), Lausanne, 9. September 2011.

• Riedl, Rainer; Höck, Stefan,

  2011.

  CyBy2 : a modular rich client for the chemical and biological information management [Poster].

  In:

  SCS Fall meeting 2011: Swiss Chemical Society (SCS), École polytechnique fédérale de Lausanne (EPFL), Lausanne, Switzerland, 9 September 2011.

• Riedl, Rainer; Fischer, Thomas,

  2010.

  Fragment based scaffold hopping in drug discovery [Poster].

  In:

  SCS Fall Meeting 2010, Swiss Chemical Society SCS, ETH Zurich, Zurich, Switzerland, 16 September 2010.

• Riedl, Rainer; Höck, Stefan; Kunz, Laura,

  2010.

  Profiling H-bond properties of fragments [Poster].

  In:

  SCS Fall Meeting 2010, Swiss Chemical Society (SCS), Zürich, 16. September 2010.

Mündliche Konferenzbeiträge und Abstracts

• Riedl, Rainer,

  2013.

  Tackling antibiotic resistance.

  In:

  ILMAC 2013, 19. Internationale Fachmesse für Laboratoriums- und Verfahrenstechnik, Messtechnik und Automatik in der Chemie (ILMAC), Basel, Schweiz, 24.-27. September 2013.

• Riedl, Rainer,

  2011.

  Drug discovery in the academic setting.

  In:

  3. Wädenswiler Chemietag: Medizinalchemie - Fokus Wirkstoffentwicklung, ZHAW, Wädenswil, 16. Juni 2011.

• Riedl, Rainer,

  2010.

  Structure activity relationship within a gene switching system.

  In:

  Synthetic Biotechnology, Symposium : Schweizerische Akademie der Technischen Wissenschaften (SATW), Basel, 18.-19. November 2010.

• Riedl, Rainer,

  2010.

  Structure based drug design.

  In:

  Biotech in Medicine : Olten Meeting, Olten, 24. November 2010.

Patente und Patentanmeldungen

• Agnello, Stefano; Adams, Michael; Kaiser, Marcel; Mäser, Pascal; Urban, Alexander; Raguz, Luka; Riedl, Rainer,

  2018.

  Antiprotozoal compounds.

  Patentnummer EP3345917 A1

  (2018-07-11)

  .

  Verfügbar unter: https://register.epo.org/espacenet/regviewer?AP=17150353&CY=EP&LG=en&DB=REG

• Weichert, Andreas Gerhard; Barrett, David Gene; Heuser, Stefan; Riedl, Rainer; Tebbe, Mark Joseph; Zaliani, Andrea,

  2011.

  Substituted arylcyclopropylacetamides as glucokinase activators.

  Patentnummer EP1585739 B1

  (2011-04-20)

  .

  Verfügbar unter: https://register.epo.org/application?number=EP03815189

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