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Tanja Schirmeister (1963-)

Pharmazeutin

Name	Tanja Schirmeister
Time	1963- (Date of birth and death)
Place	Mainz (Wirkungsort) Deutschland
Gender	weiblich
Academic degree	Prof. Dr.
Profession	Pharmazeutin (characteristic profession) Hochschullehrerin
Variant	T. Schirmeister Schirmeister
Related	Johannes Gutenberg-Universität Mainz
Topic	Personen zu Chemie
Source	Wikipedia: https://de.wikipedia.org/w/index.php?oldid=206335076 (Stand: 28.04.2024)
Record type	Person
GND-Identifier	123234891
Record ID	123234891
Involved in show all Profiling Cysteine Proteases Activities in Neuroinflammatory Cells Peptidyl nitroalkene inhibitors of main protease rationalized by computational and crystallographic investigations as antivirals against SARS-CoV-2 Next Generation of Fluorometric Protease Assays: 7‐Nitrobenz‐2‐oxa‐1,3‐diazol‐4‐yl‐amides (NBD‐Amides) as Class‐Spanning Protease Substrates Subnanomolar Cathepsin S Inhibitors with High Selectivity: Optimizing Covalent Reversible α‐Fluorovinylsulfones and α‐Sulfonates as Potential Immunomodulators in Cancer Inhibitory effects of 190 compounds against SARS‐CoV‐2 M pr o protein: Molecular docking interactions Beyer/Walter_QuickFit Namensreaktionen : 120 Lernkarten zur Organischen Chemie Chemie für Studierende der Medizin und Biowissenschaften Chemie für Studierende der Medizin und Biowissenschaften Development of reduced peptide bond pseudopeptide Michael acceptors for the treatment of Human African Trypanosomiasis BANΔIT: B’‐Factor Analysis for Drug Design and Structural Biology Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2 Front Cover: Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2 (2/2021) Similarities and Differences between Crystal and Enzyme Environmental Effects on the Electron Density of Drug Molecules Structure, interdomain dynamics, and pH-dependent autoactivation of pro-rhodesain, the main lysosomal cysteine protease from African trypanosomes Development of Novel Benzodiazepine‐Based Peptidomimetics as Inhibitors of Rhodesain from Trypanosoma brucei rhodesiense Naphthoquinones as covalent reversible inhibitors of cysteine proteases : studies on inhibition mechanism and kinetics Naphthoquinones as covalent reversible inhibitors of cysteine proteases-studies on inhibition mechanism and kinetics Structure, interdomain dynamics and pH-dependent autoactivation of pro-rhodesain, the main lysosomal cysteine protease from African trypanosomes Synthese und Charakterisierung E/Z-photoisomerisierbarer Inhibitoren zur reversiblen Modulation der Deacetylase-Aktivität von Sirtuinen Biomedizinische Anwendung von Nanodiamant: Untersuchungen zu den Wechselwirkungen mit der biologischen Umgebung und zur gezielten Wirkstofffreisetzung In silico structure-based optimisation of pyrrolidine carboxamides as Mycobacterium tuberculosis enoyl-ACP reductase inhibitors Chemie für Mediziner Chemie für Mediziner Organische Chemie In silico-Design, Synthese und Evaluation von Kinase- und Proteasom-Inhibitoren sowie Fluoreszenzsonden. Organische Chemie Development of Rhodesain Inhibitors with a 3‐Bromoisoxazoline Warhead Synthesis and Molecular Modeling Studies of Derivatives of a Highly Potent Peptidomimetic Vinyl Ester as Falcipain‐2 Inhibitors Die Bedeutung ionischer Bindungsanteile in Schwefeldioxid – Bindungsordnungen aus Röntgenbeugungsdaten † Synthese neuer Cystein-Protease-Inhibitoren sowie deren theoretische und experimentelle Untersuchung hinsichtlich der Struktur-Wirkungs-Beziehung cDNA-Microarray-Analyse von ZNS-Kaliumkanal defizienten Mäusen Expression und Reinigung der SARS-Coronavirus-M pro und deren Co-Kristallisation mit spezifischen Inhibitoren Synthese von Pyridin-, Pyridylessigsäure- und Thiazol-Derivaten als potentielle Inhibitoren der SARS-CoV-Mpro ChemInform Abstract: Synthesis of Novel Peptidomimetics as Inhibitors of Protozoan Cysteine Proteases Falcipain‐2 and Rhodesain. Chemie für Mediziner Enzymatische Hydrolyse E/Z-diastereotoper Diester und E/Z-diastereomerer Monoester

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Katalog der Deutschen Nationalbibliothek

Tanja Schirmeister (1963-)

Profiling Cysteine Proteases Activities in Neuroinflammatory Cells

Peptidyl nitroalkene inhibitors of main protease rationalized by computational and crystallographic investigations as antivirals against SARS-CoV-2

Next Generation of Fluorometric Protease Assays: 7‐Nitrobenz‐2‐oxa‐1,3‐diazol‐4‐yl‐amides (NBD‐Amides) as Class‐Spanning Protease Substrates

Subnanomolar Cathepsin S Inhibitors with High Selectivity: Optimizing Covalent Reversible α‐Fluorovinylsulfones and α‐Sulfonates as Potential Immunomodulators in Cancer

Inhibitory effects of 190 compounds against SARS‐CoV‐2 M pr o protein: Molecular docking interactions

Beyer/Walter_QuickFit Namensreaktionen : 120 Lernkarten zur Organischen Chemie

Chemie für Studierende der Medizin und Biowissenschaften

Chemie für Studierende der Medizin und Biowissenschaften

Development of reduced peptide bond pseudopeptide Michael acceptors for the treatment of Human African Trypanosomiasis

BANΔIT: B’‐Factor Analysis for Drug Design and Structural Biology

Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2

Front Cover: Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2 (2/2021)

Similarities and Differences between Crystal and Enzyme Environmental Effects on the Electron Density of Drug Molecules

Structure, interdomain dynamics, and pH-dependent autoactivation of pro-rhodesain, the main lysosomal cysteine protease from African trypanosomes

Development of Novel Benzodiazepine‐Based Peptidomimetics as Inhibitors of Rhodesain from Trypanosoma brucei rhodesiense

Naphthoquinones as covalent reversible inhibitors of cysteine proteases : studies on inhibition mechanism and kinetics

Naphthoquinones as covalent reversible inhibitors of cysteine proteases-studies on inhibition mechanism and kinetics

Structure, interdomain dynamics and pH-dependent autoactivation of pro-rhodesain, the main lysosomal cysteine protease from African trypanosomes

Synthese und Charakterisierung E/Z-photoisomerisierbarer Inhibitoren zur reversiblen Modulation der Deacetylase-Aktivität von Sirtuinen

Biomedizinische Anwendung von Nanodiamant: Untersuchungen zu den Wechselwirkungen mit der biologischen Umgebung und zur gezielten Wirkstofffreisetzung

In silico structure-based optimisation of pyrrolidine carboxamides as Mycobacterium tuberculosis enoyl-ACP reductase inhibitors

Chemie für Mediziner

Chemie für Mediziner

Organische Chemie

In silico-Design, Synthese und Evaluation von Kinase- und Proteasom-Inhibitoren sowie Fluoreszenzsonden.

Organische Chemie

Development of Rhodesain Inhibitors with a 3‐Bromoisoxazoline Warhead

Synthesis and Molecular Modeling Studies of Derivatives of a Highly Potent Peptidomimetic Vinyl Ester as Falcipain‐2 Inhibitors

Die Bedeutung ionischer Bindungsanteile in Schwefeldioxid – Bindungsordnungen aus Röntgenbeugungsdaten †

Synthese neuer Cystein-Protease-Inhibitoren sowie deren theoretische und experimentelle Untersuchung hinsichtlich der Struktur-Wirkungs-Beziehung

cDNA-Microarray-Analyse von ZNS-Kaliumkanal defizienten Mäusen

Expression und Reinigung der SARS-Coronavirus-M pro und deren Co-Kristallisation mit spezifischen Inhibitoren

Synthese von Pyridin-, Pyridylessigsäure- und Thiazol-Derivaten als potentielle Inhibitoren der SARS-CoV-Mpro

ChemInform Abstract: Synthesis of Novel Peptidomimetics as Inhibitors of Protozoan Cysteine Proteases Falcipain‐2 and Rhodesain.

Chemie für Mediziner

Enzymatische Hydrolyse E/Z-diastereotoper Diester und E/Z-diastereomerer Monoester