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dc.contributor.authorZhong, Cheng
dc.contributor.authorRamek, Alexander
dc.contributor.authorKoehler, Angela Nicole
dc.date.accessioned2020-08-12T11:54:59Z
dc.date.available2020-08-12T11:54:59Z
dc.date.issued2016-07
dc.date.submitted2016-06
dc.identifier.issn1948-5875
dc.identifier.urihttps://hdl.handle.net/1721.1/126533
dc.description.abstractTraditional fragment-based drug discovery (FBDD) relies heavily on structural analysis of the hits bound to their targets. Herein, we present a complementary approach based on diversity-oriented synthesis (DOS). A DOS-based fragment collection was able to produce initial hit compounds against the target GSK3β, allow the systematic synthesis of related fragment analogues to explore fragment-level structure-activity relationship, and finally lead to the synthesis of a more potent compound.en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionof10.1021/ACSMEDCHEMLETT.6B00230en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleDiversity-Oriented Synthesis as a Strategy for Fragment Evolution against GSK3βen_US
dc.typeArticleen_US
dc.identifier.citationWang, Yikai et al. “Diversity-Oriented Synthesis as a Strategy for Fragment Evolution against GSK3β.” ACS medicinal chemistry letters, vol. 7, 2016, pp. 852-856 © 2016 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalACS medicinal chemistry lettersen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-03-11T17:51:16Z
dspace.date.submission2020-03-11T17:51:19Z
mit.journal.volume7en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusComplete


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