Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7288
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dc.contributor.authorHammerschmidt, Stefan Josef-
dc.contributor.authorMüller, Patrick-
dc.contributor.authorSchirmeister, Tanja-
dc.date.accessioned2022-07-04T08:29:48Z-
dc.date.available2022-07-04T08:29:48Z-
dc.date.issued2021-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7302-
dc.description.abstractThe SARS-CoV-encoded papain-like cysteine protease (PLpro) plays crucial roles in viral replication and maturation processes. It is required to cleave the precursor polyproteins into functional proteins. Thus, it is considered to be a promising target for developing specific drugs. For rational optimization of hit compounds, information about the structure-activity relationship (SAR) is fundamental. Herein, we characterize isoindolines as a new class of PLpro inhibitors.en_GB
dc.language.isogerde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleSARS-CoV-PLpro-Inhibitoren als mögliche Breitspektrum-Virostatikade_DE
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-7288-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleBiospektrumde
jgu.journal.volume27de
jgu.pages.start254de
jgu.pages.end256de
jgu.publisher.year2021-
jgu.publisher.nameSpektrumde
jgu.publisher.placeHeidelbergde
jgu.publisher.issn1868-6249de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.1007/s12268-021-1576-6de
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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