Anna Hirsch
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German-Luxembourg chemist and professor of medicinal chemistry
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Anna Hirschchemistry Degrees
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Chemistry
Why Is Anna Hirsch Influential?
(Suggest an Edit or Addition)According to Wikipedia, Anna Katharina Herta Hirsch is a German-Luxembourg chemist and professor of medicinal chemistry at Saarland University. Since 2017, she has headed the Department of Drug Design and Optimization at the Helmholtz Institute for Pharmaceutical Research Saarland .
Anna Hirsch's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Phosphate recognition in structural biology. (2007) (233)
- Towards the sustainable discovery and development of new antibiotics (2021) (198)
- Dynamic combinatorial chemistry: a tool to facilitate the identification of inhibitors for protein targets. (2015) (125)
- Concepts and Core Principles of Fragment-Based Drug Design (2019) (68)
- Structure-based design of inhibitors of the aspartic protease endothiapepsin by exploiting dynamic combinatorial chemistry. (2014) (63)
- Development of inhibitors of the 2C-methyl-D-erythritol 4-phosphate (MEP) pathway enzymes as potential anti-infective agents. (2014) (55)
- “Guanigma”: The Revised Structure of Biogenic Anhydrous Guanine (2015) (53)
- From Wood to Tetrahydro-2-benzazepines in Three Waste-Free Steps: Modular Synthesis of Biologically Active Lignin-Derived Scaffolds (2019) (50)
- Plant cystoliths: a complex functional biocomposite of four distinct silica and amorphous calcium carbonate phases. (2012) (50)
- Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment‐Based Drug Design Facilitated by Dynamic Combinatorial Chemistry (2016) (49)
- Biodynamers: self-organization-driven formation of doubly dynamic proteoids. (2012) (47)
- Molecular Biodynamers: Dynamic Covalent Analogues of Biopolymers (2017) (45)
- Druggability of the enzymes of the non-mevalonate-pathway. (2013) (40)
- Inhibitors of the kinase IspE: structure-activity relationships and co-crystal structure analysis. (2008) (38)
- Exploiting specific interactions toward next-generation polymeric drug transporters. (2013) (37)
- Nonphosphate Inhibitors of IspE Protein, a Kinase in the Non‐Mevalonate Pathway for Isoprenoid Biosynthesis and a Potential Target for Antimalarial Therapy (2007) (36)
- Infrared Absorption Spectrum of Brushite from First Principles (2014) (35)
- Optically functional isoxanthopterin crystals in the mirrored eyes of decapod crustaceans (2018) (32)
- Bioconjugates to specifically render inhibitors water-soluble (2010) (32)
- Molekulare Erkennung von Phosphaten in der Strukturbiologie (2007) (31)
- Total synthesis, stereochemical elucidation and biological evaluation of Ac2SGL; a 1,3-methyl branched sulfoglycolipid from Mycobacterium tuberculosis (2013) (31)
- Biologically Controlled Morphology and Twinning in Guanine Crystals. (2017) (30)
- The isoprenoid-precursor dependence of Plasmodium spp. (2012) (29)
- Double conjugate addition of dithiols to propargylic carbonyl systems to generate protected 1,3-dicarbonyl compounds. (2006) (28)
- Tracheal brush cells release acetylcholine in response to bitter tastants for paracrine and autocrine signaling (2020) (26)
- Fighting malaria: structure-guided discovery of nonpeptidomimetic plasmepsin inhibitors. (2015) (25)
- Pentapeptide‐rich peptidoglycan at the Bacillus subtilis cell‐division site (2017) (25)
- A natural-product switch for a dynamic protein interface. (2014) (25)
- Glucansucrase (mutant) enzymes from Lactobacillus reuteri 180 efficiently transglucosylate Stevia component rebaudioside A, resulting in a superior taste (2018) (24)
- Spray-drying of inhalable, multifunctional formulations for the treatment of biofilms formed in cystic fibrosis. (2019) (23)
- Synthesis and Characterization of Cytidine Derivatives that Inhibit the Kinase IspE of the Non‐Mevalonate Pathway for Isoprenoid Biosynthesis (2008) (23)
- Mastering the Gram-Negative Bacterial Barrier - Chemical Approaches to Increase Bacterial Bioavailability of Antibiotics. (2021) (23)
- Strukturbasiertes Design von Hemmstoffen der Aspartylprotease Endothiapepsin mittels dynamischer kombinatorischer Chemie (2014) (22)
- Anhydrous β-guanine crystals in a marine dinoflagellate: Structure and suggested function. (2019) (22)
- Molecular insight into specific 14-3-3 modulators: Inhibitors and stabilisers of protein-protein interactions of 14-3-3. (2017) (21)
- Flotillin-mediated membrane fluidity controls peptidoglycan synthesis and MreB movement (2020) (20)
- N-Aryl-3-mercaptosuccinimides as Antivirulence Agents Targeting Pseudomonas aeruginosa Elastase and Clostridium Collagenases (2020) (20)
- Validation of a homology model of Mycobacterium tuberculosis DXS: rationalization of observed activities of thiamine derivatives as potent inhibitors of two orthologues of DXS. (2015) (19)
- Compounds Interfering with Embryonic Lethal Abnormal Vision (ELAV) Protein-RNA Complexes: An Avenue for Discovering New Drugs. (2017) (19)
- A New PqsR Inverse Agonist Potentiates Tobramycin Efficacy to Eradicate Pseudomonas aeruginosa Biofilms (2021) (18)
- Structure‐Based Design of Potent Small‐Molecule Binders to the S‐Component of the ECF Transporter for Thiamine (2015) (17)
- Energy‐Coupling Factor Transporters as Novel Antimicrobial Targets (2018) (17)
- Novel Compounds Targeting the RNA-Binding Protein HuR. Structure-Based Design, Synthesis, and Interaction Studies. (2019) (16)
- Total Synthesis of (−)‐Doliculide, Structure–Activity Relationship Studies and Its Binding to F‐Actin (2012) (16)
- Fine-tuning Nanocarriers Specifically toward Cargo: A Competitive Study on Solubilizing Related Photosensitizers for Photodynamic Therapy. (2017) (16)
- Biogenic Scatterers, Mirrors, Multilayer Reflectors and Photonic Crystals. Futuristic Ancient Technologies (2018) (16)
- Low-Dimensional Metal–Organic Coordination Structures on Graphene (2019) (16)
- Protein‐Templated Dynamic Combinatorial Chemistry: Brief Overview and Experimental Protocol (2019) (16)
- Citraconate inhibits ACOD1 (IRG1) catalysis, reduces interferon responses and oxidative stress, and modulates inflammation and cell metabolism (2022) (16)
- Membrane fluidity controls peptidoglycan synthesis and MreB movement (2019) (15)
- Fragment growing exploiting dynamic combinatorial chemistry of inhibitors of the aspartic protease endothiapepsin (2015) (15)
- Fragmentverknüpfung und ‐optimierung von Hemmstoffen der Aspartylprotease Endothiapepsin: Fragmentbasiertes Wirkstoffdesign beschleunigt durch dynamische kombinatorische Chemie (2016) (14)
- De novo fragment-based design of inhibitors of DXS guided by spin-diffusion-based NMR spectroscopy (2014) (14)
- Discovery of Small-Molecule Stabilizers of 14-3-3 Protein-Protein Interactions via Dynamic Combinatorial Chemistry. (2020) (13)
- The Non-Mevalonate Pathway to Isoprenoid Biosynthesis: A Potential Source of New Drug Targets (2008) (13)
- Novel 15-Lipoxygenase-1 Inhibitor Protects Macrophages from Lipopolysaccharide-Induced Cytotoxicity (2019) (12)
- Guanine and 7,8-dihydroxanthopterin reflecting crystals in the zander fish eye: crystal locations, compositions, and structures. (2019) (12)
- Structure-Based Optimization of Inhibitors of the Aspartic Protease Endothiapepsin (2015) (12)
- Combinatorial screening for specific drug solubilizers with switchable release profiles. (2015) (12)
- Druggability Assessment of Targets Used in Kinetic Target-Guided Synthesis. (2018) (12)
- A combinatorial approach for the discovery of drug-like inhibitors of 15-lipoxygenase-1. (2019) (11)
- Proteoid Dynamers with Tunable Properties (2016) (11)
- Protein‐Templated Hit Identification through an Ugi Four‐Component Reaction** (2020) (10)
- Substrate‐Inspired Fragment Merging and Growing Affords Efficacious LasB Inhibitors (2021) (10)
- Fragment‐Based Drug Design Facilitated by Protein‐Templated Click Chemistry: Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin (2016) (10)
- Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism (2019) (10)
- Terahertz spectroscopy of 2,4,6-trinitrotoluene molecular solids from first principles (2018) (10)
- 7-Hydroxycoumarins Are Affinity-Based Fluorescent Probes for Competitive Binding Studies of Macrophage Migration Inhibitory Factor (2020) (9)
- Insight into the complete substrate-binding pocket of ThiT by chemical and genetic mutations. (2017) (9)
- Designed Spiroketal Protein Modulation (2017) (8)
- Identification of N,N-arylalkyl-picolinamide derivatives targeting the RNA-binding protein HuR, by combining biophysical fragment-screening and molecular hybridization. (2021) (8)
- Semisynthesis and biological evaluation of amidochelocardin derivatives as broad-spectrum antibiotics. (2019) (8)
- Structure and Morphology of Light-Reflecting Synthetic and Biogenic Polymorphs of Isoxanthopterin: A Comparison (2019) (8)
- A rapid synthesis of low-nanomolar divalent LecA inhibitors in four linear steps from d-galactose pentaacetate. (2020) (8)
- Exploration of ligand binding modes towards the identification of compounds targeting HuR: a combined STD-NMR and Molecular Modelling approach (2018) (8)
- Validating the 1,2-Difluoro (BITE) Motif as a Hybrid Bioisostere of CF3 and Et using Matrix Metalloproteases as Structural Probes. (2020) (7)
- Unveiling Adatoms in On-Surface Reactions: Combining Scanning Probe Microscopy with van’t Hoff Plots (2021) (7)
- Analytical Methods in Protein-Templated Dynamic Combinatorial Chemistry (2017) (7)
- Dynamic Combinatorial Chemistry to Identify Binders of ThiT, an S‐Component of the Energy‐Coupling Factor Transporter for Thiamine (2017) (7)
- Micro-rheological properties of lung homogenates correlate with infection severity in a mouse model of Pseudomonas aeruginosa lung infection (2020) (7)
- Design and Synthesis of Bioisosteres of Acylhydrazones as Stable Inhibitors of the Aspartic Protease Endothiapepsin (2018) (6)
- Design and synthesis of thiamine analogues to study their binding to the ECF transporter for thiamine in bacteria (2016) (6)
- Theoretical and structural analysis of long C-C bonds in the adducts of polycyanoethylene and anthracene derivatives and their connection to the reversibility of Diels-Alder reactions. (2014) (6)
- Imidazole- and Benzimidazole-Based Inhibitors of the Kinase IspE: Targeting the Substrate-Binding Site and the Triphosphate-Binding Loop of the ATP Site (2013) (6)
- Phage Display on the Anti‐infective Target 1‐Deoxy‐d‐xylulose‐5‐phosphate Synthase Leads to an Acceptor–Substrate Competitive Peptidic Inhibitor (2017) (6)
- Harnessing dynamic combinatorial chemistry in the search for new ligands for protein targets. (2015) (6)
- Ideas in Chemistry and Molecular Sciences: Where Chemistry Meets Life (2010) (6)
- DXS as a target for structure-based drug design. (2017) (6)
- Exploring the Ribose Sub-Pocket of the Substrate-Binding Site in Escherichia coli IspE: Structure-Based Design, Synthesis, and Biological Evaluation of Cytosines and Cytosine Analogues (2012) (6)
- Hit-optimization using target-directed dynamic combinatorial chemistry: development of inhibitors of the anti-infective target 1-deoxy-d-xylulose-5-phosphate synthase† (2020) (6)
- Structure-Based Design of α-Substituted Mercaptoacetamides as Inhibitors of the Virulence Factor LasB from Pseudomonas aeruginosa (2022) (5)
- A hydrogel-based in vitro assay for the fast prediction of antibiotic accumulation in Gram-negative bacteria (2020) (5)
- Assessment of the rules related to gaining activity against Gram-negative bacteria. (2021) (5)
- Phosphonate as Stable Zinc-binding Group for Inhibitors of Clostridial Collagenase H (ColH) as Pathoblocker Agents. (2021) (5)
- Vibrational properties of isotopically enriched materials: the case of calcite (2018) (5)
- Bicyclic enol cyclocarbamates inhibit penicillin-binding proteins. (2017) (5)
- Donepezil–melatonin hybrids as butyrylcholinesterase inhibitors: Improving binding affinity through varying mode of linking fragments (2018) (5)
- Delivery system for budesonide based on lipid‐DNA (2018) (5)
- Crystalline Sponge Affinity Screening: A Fast Tool for Soaking Condition Optimization without the Need of X-ray Diffraction Analysis. (2021) (5)
- Evaluation of Bacterial RNA Polymerase Inhibitors in a Staphylococcus aureus-based Wound-Infection Model in SKH1 Mice. (2020) (5)
- Fighting antibiotic resistance—strategies and (pre)clinical developments to find new antibacterials (2022) (4)
- Identification of a 1-deoxy-D-xylulose-5-phosphate synthase (DXS) mutant with improved crystallographic properties. (2021) (4)
- Surface state tunable energy and mass renormalization from homothetic quantum dot arrays. (2019) (4)
- Bacteriomimetic Liposomes Improve Antibiotic Activity of a Novel Energy-Coupling Factor Transporter Inhibitor (2021) (4)
- Enhancing glycan stability via site-selective fluorination: modulating substrate orientation by molecular design (2020) (4)
- Furoates and thenoates inhibit pyruvate dehydrogenase kinase 2 allosterically by binding to its pyruvate regulatory site (2016) (4)
- An Efficient Way to Screen Inhibitors of Energy-Coupling Factor (ECF) Transporters in a Bacterial Uptake Assay (2022) (4)
- BOPC1 Enantiomers Preparation and HuR Interaction Study. From Molecular Modeling to a Curious DEEP-STD NMR Application. (2020) (4)
- Rational Adaptation of L3MBTL1 Inhibitors to Create Small‐Molecule Cbx7 Antagonists (2019) (3)
- Comparing the Self‐Assembly of Sexiphenyl‐Dicarbonitrile on Graphite and Graphene on Cu(111) (2019) (3)
- First crystal structures of 1-deoxy-d-xylulose 5-phosphate synthase (DXPS) from Mycobacterium tuberculosis indicate a distinct mechanism of intermediate stabilization (2022) (3)
- Targeting the energy-coupling factor (ECF) transporters: identification of new tool compounds (2021) (3)
- N-Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from Pseudomonas aeruginosa (2021) (3)
- Saccharide‐Containing Dynamic Proteoids (2017) (3)
- Phosphonate as a Stable Zinc‐Binding Group for “Pathoblocker” Inhibitors of Clostridial Collagenase H (ColH) (2021) (3)
- pH-Dependent morphology and optical properties of lysine-derived molecular biodynamers (2020) (3)
- Targeting the IspD Enzyme in the MEP Pathway: Identification of a Novel Fragment Class (2021) (3)
- Structure-Guided Optimization of Small-Molecule Folate Uptake Inhibitors Targeting the Energy-Coupling Factor Transporters (2021) (3)
- Wohlergehen – mehr als nur Gesundheit? (2021) (3)
- N-Aryl Mercaptopropionamides as Broad-Spectrum Inhibitors of Metallo-β-Lactamases. (2022) (3)
- Discovery of the First Selective Nanomolar Inhibitors of ERAP2 by Kinetic Target‐Guided Synthesis (2022) (3)
- Design, synthesis, and biological evaluation of novel benzimidazole derivatives as sphingosine kinase 1 inhibitor (2021) (3)
- "Clicking" fragment leads to novel dual-binding cholinesterase inhibitors. (2021) (3)
- Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism (2019) (2)
- Dynamic Proteoids Generated From Dipeptide-Based Monomers. (2018) (2)
- Lipid‐DNAs as Solubilizers of mTHPC (2017) (2)
- Potential Dental Biofilm Inhibitors: Dynamic Combinatorial Chemistry Affords Sugar‐Based Molecules that Target Bacterial Glucosyltransferase (2020) (2)
- Replacement of an Indole Scaffold Targeting Human 15‐Lipoxygenase‐1 Using Combinatorial Chemistry (2019) (2)
- Metal-ion-induced shape switching: Stereoselective formation of a dinuclear Hg(II) double helicate from a hydrazonobis(acylhydrazone) ligand (2012) (2)
- Polymorphism, Structure, and Nucleation of Cholesterol·H2O at Aqueous Interfaces and in Pathological Media: Revisited from a Computational Perspective (2021) (2)
- Expanding the Myxochelin Natural Product Family by Nicotinic Acid Containing Congeners (2021) (2)
- Dynamic Combinatorial Chemistry Affords Sugar-Based Molecules Targeting Bacterial Glucosyltranseferase as Potential Dental Biofilm Inhibitors. (2020) (2)
- Reversible immobilization of a protein to a gold surface through multiple host-guest interactions. (2019) (2)
- Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections (2022) (2)
- Baicalin lipid nanocapsules for treatment of glioma: characterization, mechanistic cytotoxicity, and pharmacokinetic evaluation (2022) (2)
- Design, Synthesis, Antimicrobial Activity, and Molecular Docking of Some New Diclofenac Derivatives (2022) (1)
- Redesigning of the cap conformation and symmetry of the diphenylethyne core to yield highly potent pan-genotypic NS5A inhibitors with high potency and high resistance barrier (2021) (1)
- François Diederich – In Memoriam ** (2020) (1)
- A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE (2008) (1)
- Frontispiece: Protein‐Templated Hit Identification through an Ugi Four‐Component Reaction (2020) (1)
- Metabolic Profiling of S-praziquantel: Structure Elucidation Using the Crystalline Sponge Method in Combination with Mass Spectrometry and Nuclear Magnetic Resonance (2022) (1)
- Optimized Inhibitors of MDM2 via an Attempted Protein‐Templated Reductive Amination (2019) (1)
- Insights into the biosynthesis of icumazole unveiling a distinctive family of crotonyl-CoA carboxylase/reductase (2022) (1)
- Synthesis and Biological Evaluation of Novel 2-Substituted Analogues of (–)-Pentenomycin I (2020) (1)
- THz Spectroscopy of 2,4,6-trinitrotoluene Molecular Solids from First Principles (2018) (1)
- Rapid Discovery of Aspartyl Protease Inhibitors Using an Anchoring Approach (2020) (1)
- Biogenic twinned crystals exhibiting unique morphological symmetry (2017) (1)
- Author response: Flotillin-mediated membrane fluidity controls peptidoglycan synthesis and MreB movement (2020) (1)
- Ecological engineering of small urban water bodies (2020) (1)
- Identification of RAD51–BRCA2 Inhibitors Using N-Acylhydrazone-Based Dynamic Combinatorial Chemistry (2022) (1)
- Discovery of novel drug-like antitubercular hits targeting the MEP pathway enzyme DXPS by strategic application of ligand-based virtual screening (2022) (1)
- Respiratory Syncytial Virus Two-Step Infection Screen Reveals Inhibitors of Early and Late Life Cycle Stages (2022) (1)
- Isoxanthopterin: An Optically Functional Biogenic Crystal in the Eyes of Decapod Crustaceans (2017) (1)
- Not Every Hit-Identification Technique Works on 1-Deoxy-d-Xylulose 5-Phosphate Synthase (DXPS): Making the Most of a Virtual Screening Campaign. (2023) (1)
- An efficient way to screen inhibitors of energy-coupling factor (ECF) transporters in bacteria uptake assay (2021) (1)
- MEDI 404-Non-phosphate inhibitors of IspE, a kinase in the non-mevalonate pathway for isoprenoid biosynthesis and a potential target for antimalarial therapy (2007) (1)
- Structure-based drug design exploiting dynamic combinatorial chemistry to identify novel inhibitors for the aspartic protease endothiapepsin (2013) (1)
- Design and Synthesis of Novel Bis-Imidazolyl Phenyl Butadiyne Derivatives as HCV NS5A Inhibitors (2022) (1)
- Endothiapepsin with Ligand VSK-B24 (2018) (0)
- Front Cover: Phosphonate as a Stable Zinc‐Binding Group for “Pathoblocker” Inhibitors of Clostridial Collagenase H (ColH) (ChemMedChem 8/2021) (2021) (0)
- Targeting Extracellular Bacterial Proteases for the Development of Novel Antivirulence Agents (2022) (0)
- Exploration of ligand binding modes towards the identification of compounds targeting HuR: a combined STD-NMR and Molecular Modelling approach (2018) (0)
- Targeting Extracellular Bacterial Proteases for the Development of Novel Antivirulence Agents (2022) (0)
- Screening for specific interactions (2013) (0)
- Glucansucrase (mutant) enzymes from Lactobacillus reuteri 180 efficiently transglucosylate Stevia component rebaudioside A, resulting in a superior taste (2018) (0)
- Genotoxic and mutational potential of monocyclic terpenoids (carvacrol, carvone and thymol) in Drosophila melanogaster (2023) (0)
- Screening for specific interactions: Precisely tailored drug transporters for small molecule solubilization and release (2013) (0)
- Organic Quantum dot arrays: Tunable energy and mass renormalization by homothetic porous networks (2019) (0)
- Towards Translation of PqsR Inverse Agonists: From In Vitro Efficacy Optimization to In Vivo Proof‐of‐Principle (Adv. Sci. 5/2023) (2023) (0)
- Tunable energy and mass renormalization from homothetic Quantum dot arrays (2019) (0)
- Electronic Supplementary Information: Surface state tunable energy and mass renormalization from homothetic Quantum dot arrays (2019) (0)
- Alkylphenols as natural prototypes for molecular modifications : SAR study for antiparasitic activity (0)
- University of Groningen Comparing the Self-Assembly of Sexiphenyl-Dicarbonitrile on Graphite and Graphene on Cu(111) Schmidt, (2019) (0)
- Micelles Lipid-DNAs as Solubilizers of m THPC (2018) (0)
- Structural analysis of 1-deoxy-D-xylulose 5-phosphate synthase from Pseudomonas aeruginosa and Klebsiella pneumoniae reveals conformational changes upon cofactor binding (2022) (0)
- t-based design of inhibitors of DXS guided by spin-di ff usion-based NMR spectroscopy † (2014) (0)
- University of Groningen Lipid-DNAs as Solubilizers of mTHPC (2018) (0)
- Studying thiamine binding to ThiT using chemical and biochemical mutations (2016) (0)
- Discovery of Antibacterial Agents Inhibiting the Energy-Coupling Factor (ECF) Transporters by Structure-Based Virtual Screening (2020) (0)
- Novel roles for the TRPM5 ion channel in regulating airway mucociliary clearance (2018) (0)
- Structural studies by cryo-electron microscopy : Achievements , Prospects , and Challenges (2018) (0)
- Proteoid biodynamers for safe mRNA transfection via pH-responsive nanorods enabling endosomal escape. (2022) (0)
- Trendbericht Biochemie 2017: Proteinvermittelte dynamische kombinatorische Chemie (2018) (0)
- Supramolekulare Chemie … und darüber hinaus (2015) (0)
- Towards the sustainable discovery and development of new antibiotics. (2021) (0)
- Towards the Modulation of RNA-Binding Proteins: New Compounds Targeting Protein HuR (2019) (0)
- Selective small-molecule inhibitors of glucansucrases as chemical probes and potential toothpaste additives (2014) (0)
- Supramolecular chemistry … and beyond. (2015) (0)
- Staphylococcus aureus in a wound–infection model (2020) (0)
- Identification of inhibitors of the anti-infective target DXS using ligand-based virtual screening (2018) (0)
- Calculating the Structure of Isoxanthopterin Crystals, Efficient Reflectors in the Crustacean Eyes (2018) (0)
- Pseudomonas aeruginosa Biofilm: A New PqsR Inverse Agonist Potentiates Tobramycin Efficacy to Eradicate Pseudomonas aeruginosa Biofilms (Adv. Sci. 12/2021) (2021) (0)
- Phosphate Recognition in Structural Biology (2007) (0)
- Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity (2021) (0)
- The Structures and Binding Modes of Small-Molecule Inhibitors of Pseudomonas aeruginosa Elastase LasB (2022) (0)
- Design of a multi-component reaction scaffold with inhibitory activity on aspartic proteases (2019) (0)
- Cover Feature: Potential Dental Biofilm Inhibitors: Dynamic Combinatorial Chemistry Affords Sugar‐Based Molecules that Target Bacterial Glucosyltransferase (ChemMedChem 1/2021) (2020) (0)
- Structure-Based Design on the Way to New Anti-Infectives (2010) (0)
- Towards Translation of PqsR Inverse Agonists: From In Vitro Efficacy Optimization to In Vivo Proof‐of‐Principle (2023) (0)
- CCDC 632407: Experimental Crystal Structure Determination (2008) (0)
- Identification of Inhibitors of the Anti-Infective Target DXS Using Dynamic Combinatorial Chemistry (2019) (0)
- Discovery and Characterization of Synthesized and FDA-Approved Inhibitors of Clostridial and Bacillary Collagenases (2022) (0)
- Introduction to the themed collection on fragment-based drug discovery. (2022) (0)
- Structure of Mycobacterium tuberculosis 1-Deoxy-D-Xylulose 5-Phosphate Synthase in Complex with Butylacetylphosphonate (2023) (0)
- Protein-Templated Hit Identification via an Ugi Four-Component Reaction (2020) (0)
- A doubly hermaphroditic chiral crown ether (2014) (0)
- Screening of Natural Products and Small Molecules Uncovers Novel Coronavirus 1a/1b Frameshifting Inhibitors with Antiviral Properties (2022) (0)
- Small-molecule modulators of thiamine transport in pathogenic bacteria (2015) (0)
- Synthesis, biological evaluation, and molecular docking studies of aldotetronic acid-based LpxC inhibitors. (2022) (0)
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