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Carina Lemke

Biochemikerin

Name	Carina Lemke
Time	2018- (Wirkungsdaten)
Place	Deutschland
Academic degree	M.Sc.
Profession	Biochemikerin (characteristic profession)
Related	Pharmazeutisches Institut (Bonn)
Further information	Doktorandin Rheinische Friedrich-Wilhelms-Universität Bonn seit Okt. 2017
Source	Internet: https://de.linkedin.com/in/carina-lemke-bonn (stand 01/2020)
Record type	Person
GND-Identifier	1202348831
Record ID	1202348831
Involved in show all Targeting the Main Protease of SARS-CoV-2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors Two Tags in One Probe: Combining Fluorescence‐ and Biotin‐based Detection of the Trypanosomal Cysteine Protease Rhodesain Andrographolide Derivatives Target the KEAP1/NRF2 Axis and Possess Potent Anti‐SARS‐CoV‐2 Activity Front Cover: Andrographolide Derivatives Target the KEAP1/NRF2 Axis and Possess Potent Anti‐SARS‐CoV‐2 Activity (ChemMedChem 5/2022) Die Hauptprotease von SARS‐CoV‐2 als Zielstruktur: Von der Etablierung eines Hochdurchsatz‐Screenings zum Design maßgeschneiderter Inhibitoren Targeting the Main Protease of SARS‐CoV‐2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors Design, Synthesis and Biological Evaluation of Highly Potent Simplified Archazolids Chromenones as Multineurotargeting Inhibitors of Human Enzymes

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Katalog der Deutschen Nationalbibliothek

Carina Lemke

Targeting the Main Protease of SARS-CoV-2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors

Two Tags in One Probe: Combining Fluorescence‐ and Biotin‐based Detection of the Trypanosomal Cysteine Protease Rhodesain

Andrographolide Derivatives Target the KEAP1/NRF2 Axis and Possess Potent Anti‐SARS‐CoV‐2 Activity

Front Cover: Andrographolide Derivatives Target the KEAP1/NRF2 Axis and Possess Potent Anti‐SARS‐CoV‐2 Activity (ChemMedChem 5/2022)

Die Hauptprotease von SARS‐CoV‐2 als Zielstruktur: Von der Etablierung eines Hochdurchsatz‐Screenings zum Design maßgeschneiderter Inhibitoren

Targeting the Main Protease of SARS‐CoV‐2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors

Design, Synthesis and Biological Evaluation of Highly Potent Simplified Archazolids

Chromenones as Multineurotargeting Inhibitors of Human Enzymes