Anna K. H. Hirsch

Affiliations: 
University of Groningen, Groningen, Netherlands 
Area:
drug design
Website:
http://www.rug.nl/scheikunde/onderzoek/scholen/stratingh/groepen/hirsch/object521614416?lang=nl
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"Anna Hirsch"
Bio:

http://dx.doi.org/10.3929/ethz-a-005664687

Mean distance: 7.51
 
SNBCP

Parents

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Timothy F. Jamison research assistant MIT
Steven Victor Ley research assistant Cambridge
François N. Diederich grad student 2008 ETH Zürich
 (A Novel Approach towards Antimalarials: Design and Synthesis of Inhibitors of the Kinase IspE)
Jean-Marie Lehn post-doc 2010 Université Louis Pasteur, Strasbourg
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Publications

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Liu Y, Bos IST, Oenema TA, et al. (2018) Delivery System for Budesonide Based on Lipid-DNA. European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V
Liu Y, Stuart MCA, Buhler E, et al. (2018) Dynamic Proteoids Generated From Dipeptide-Based Monomers. Macromolecular Rapid Communications. e1800099
Liu Y, de Vries JW, Liu Q, et al. (2017) Lipid-DNAs as Solubilizers of mTHPC. Chemistry (Weinheim An Der Bergstrasse, Germany)
Liu Y, Stuart M, Witte M, et al. (2017) Saccharide-Containing Dynamic Proteoids. Chemistry (Weinheim An Der Bergstrasse, Germany)
Liu Y, Lehn JM, Hirsch AK. (2017) Molecular Biodynamers: Dynamic Covalent Analogues of Biopolymers. Accounts of Chemical Research
Morales Angeles D, Liu Y, Hartman AM, et al. (2017) Pentapeptide-rich peptidoglycan at the Bacillus subtilis cell-division site. Molecular Microbiology
Dockerty P, Edens JG, Tol MB, et al. (2017) Bicyclic enol cyclocarbamates inhibit penicillin-binding proteins. Organic & Biomolecular Chemistry
Mondal M, Unver MY, Pal A, et al. (2016) Fragment-Based Drug Design Facilitated by Protein-Templated Click Chemistry: Fragment Linking and -Optimization of Inhibitors of the Aspartic Protease Endothiapepsin. Chemistry (Weinheim An Der Bergstrasse, Germany)
Monjas L, Hirsch AK. (2015) Harnessing dynamic combinatorial chemistry in the search for new ligands for protein targets. Future Medicinal Chemistry
Masini T, Lacy B, Monjas L, et al. (2015) Validation of a homology model of Mycobacterium tuberculosis DXS: rationalization of observed activities of thiamine derivatives as potent inhibitors of two orthologues of DXS. Organic & Biomolecular Chemistry
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