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Dr.
Edgar Specker studierte Chemie an der Universität Münster. Nach seiner Diplomarbeit bei der Bayer AG erhielt er seinen Doktortitel im Jahr 2004 in der Arbeitsgruppe von Prof. Klebe an der Universität in Marburg. Seine PostDoc Zeit verbrachte er in der Arbeitsgruppe von Prof. Bradley an den Universitäten Southampton und Edinburgh. Ende 2005 arbeitete er als Medizinalchemiker in der Biotech Firma Zedira GmbH, wo er Inhibitoren von Transglutaminasen zur Behandlung von Zöliakie synthetisierte. Im Jahr 2007 wechselte er zur Pharmafirma Jerini AG und kollaborierte dort in einem Drug Discovery Projekt mit der Firma Alcon. Für das Compound Management am FMP ist er seit 2010 zunächst als Teil der Screening Unit und anschließend als Mitarbeiter in der Arbeitsgruppe Medizinische Chemie tätig. Seit 2020 ist er Leiter der eigenständigen Technologieplattform Compound Management am FMP. Er hat über die letzten drei Jahre das Compound Management von EU-OPENSCREEN ERIC mit aufgebaut. Zudem ist er Mitgründer der Start-up Firma Trypto Therapeutics GmbH.
Novel Tryptophan Hydroxylase Inhibitor TPT-001 Reverses PAH, Vascular Remodeling, and Proliferative-Proinflammatory Gene Expression
JACC: Basic to Translational Science 2024
online lesenTPT‐004, a Next‐Generation Inhibitor of Tryptophan Hydroxylase, Ameliorates Pulmonary Arterial Hypertension in Rats
Journal of the American Heart Association 2024
online lesenDesign, Quality and Validation of the EU-OPENSCREEN Fragment Library Poised to a High-Throughput Screening Collection
RSC Medicinal Chemistry 2024
online lesenIdentification of drug-like molecules targeting the ATPase activity of dynamin-like EHD4
PLOS ONE 2024
online lesenStructure-Based Design of Xanthine-Imidazopyridines and -Imidazothiazoles as Highly Potent and In Vivo Efficacious Tryptophan Hydroxylase Inhibitors
Journal of Medicinal Chemistry 2023
online lesenSmall Molecules Targeting Human UDP‐GlcNAc 2‐Epimerase
ChemBioChem 2023
online lesenSmall molecule inhibiting microglial nitric oxide release could become a potential treatment for neuroinflammation
PLOS ONE 2023
online lesenDiscovery of tetrazolo-pyridazine-based small molecules as inhibitors of MACC1-driven cancer metastasis
Biomedicine & Pharmacotherapy 2023
online lesenStructural Basis for Highly Selective Class II Alpha Phosphoinositide-3-Kinase Inhibition
Journal of Medicinal Chemistry 2023
online lesenStructure-Based Design of Xanthine-Benzimidazole Derivatives as Novel and Potent Tryptophan Hydroxylase Inhibitors
Journal of Medicinal Chemistry 2022
online lesenProbing Factor Xa Protein–Ligand Interactions: Accurate Free Energy Calculations and Experimental Validations of Two Series of High-Affinity Ligands
Journal of Medicinal Chemistry 2022
online lesenTopical inflammasome inhibition with disulfiram prevents irritant contact dermatitis
Clinical and Translational Allergy 2021
online lesenEnhanced Properties of a Benzimidazole Benzylpyrazole Lysine Demethylase Inhibitor: Mechanism-of-Action, Binding Site Analysis, and Activity in Cellular Models of Prostate Cancer
Journal of Medicinal Chemistry 2021
online lesenSmall-Molecule Lysophosphatidic Acid Receptor 5 (LPAR5) Antagonists: Versatile Pharmacological Tools to Regulate Inflammatory Signaling in BV-2 Microglia Cells
Frontiers in Cellular Neuroscience 2019
online lesenEU-OPENSCREEN: A Novel Collaborative Approach to Facilitate Chemical Biology
SLAS Discovery 2019
online lesenA New Highly Thyrotropin Receptor-Selective Small-Molecule Antagonist with Potential for the Treatment of Graves' Orbitopathy
Thyroid 2019
online lesenUse of a sequential high throughput screening assay to identify novel inhibitors of the eukaryotic SRP-Sec61 targeting/translocation pathway
PLOS ONE 2018
online lesenCellFy: A Cell-Based Fragment Screen against C-Type Lectins
ACS Chemical Biology 2018
online lesenIdentification of a Novel Benzimidazole Pyrazolone Scaffold That Inhibits KDM4 Lysine Demethylases and Reduces Proliferation of Prostate Cancer Cells
SLAS Discovery 2017
online lesenStatin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1
PLOS Biology 2017
online lesenSmall-molecule inhibition of STOML3 oligomerization reverses pathological mechanical hypersensitivity
Nature Neuroscience 2017
online lesenPharmacological restoration and therapeutic targeting of the B-cell phenotype in classical Hodgkin lymphoma
Blood 2017
online lesenA Small-Molecule Antagonist of the β-Catenin/TCF4 Interaction Blocks the Self-Renewal of Cancer Stem Cells and Suppresses Tumorigenesis
Cancer Research 2016
online lesenTemperature dependence of cross-effect dynamic nuclear polarization in rotating solids: advantages of elevated temperatures
Physical Chemistry Chemical Physics 2016
online lesenDesign of a General‐Purpose European Compound Screening Library for EU‐OPENSCREEN
ChemMedChem 2014
online lesenTractable synthesis of multipurpose screening compounds with under-represented molecular features for an open access screening platform
Molecular Diversity 2014
online lesenNeurotoxin II Bound to Acetylcholine Receptors in Native Membranes Studied by Dynamic Nuclear Polarization NMR
Journal of the American Chemical Society 2011
online lesenAspartic Acid Proteases as Therapeutic Targets. Edited by Arun K. Ghosh.
ChemMedChem 2011
online lesenZwei neue privilegierte Bausteine und ein unerwarteter Bindungsmodus für HIV‐Protease‐Inhibitoren †
Angewandte Chemie 2005
online lesenAn Old Target Revisited: Two New Privileged Skeletons and an Unexpected Binding Mode For HIV‐Protease Inhibitors †
Angewandte Chemie 2005
online lesenHydroxyethylene sulfones as a new scaffold to address aspartic proteases
Journal of medicinal chemistry 2005
online lesenDde-protected PNA monomers, orthogonal to Fmoc, for the synthesis of PNA–peptide conjugates
Tetrahedron 2005
online lesenDas Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP) gehört zum Forschungsverbund Berlin e.V. (FVB), einem Zusammenschluss von sieben natur-, lebens- und umweltwissenschaftlichen Instituten in Berlin. Die Einrichtungen sind Mitglieder der Leibniz-Gemeinschaft.
Leibniz-Forschungsinstitut für Molekulare Pharmakologie im Forschungsverbund Berlin e.V. (FMP)
Campus Berlin-Buch
Robert-Roessle-Str. 10
13125 Berlin, Deutschland