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박철민

Park, Cheol-Min
Synthetic and Medicinal Chemistry Lab.
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dc.citation.endPage 7506 -
dc.citation.number 24 -
dc.citation.startPage 7503 -
dc.citation.title BIOORGANIC & MEDICINAL CHEMISTRY LETTERS -
dc.citation.volume 20 -
dc.contributor.author Bruncko, Milan -
dc.contributor.author Tahir, Stephen K. -
dc.contributor.author Song, Xiaohong -
dc.contributor.author Chen, Jun -
dc.contributor.author Ding, Hong -
dc.contributor.author Huth, Jeffrey R. -
dc.contributor.author Jin, Sha -
dc.contributor.author Judge, Russell A. -
dc.contributor.author Madar, David J. -
dc.contributor.author Park, Chang H. -
dc.contributor.author Park, Cheol-Min -
dc.contributor.author Petros, Andrew M. -
dc.contributor.author Tse, Christin -
dc.contributor.author Rosenberg, Saul H. -
dc.contributor.author Elmore, Steven W. -
dc.date.accessioned 2023-12-22T06:38:49Z -
dc.date.available 2023-12-22T06:38:49Z -
dc.date.created 2014-11-10 -
dc.date.issued 2010-12 -
dc.description.abstract We describe the development of a novel series of N-aryl-benzimidazolone HSP90 inhibitors (9) targeting the N-terminal ATP-ase site. SAR development was influenced by structure-based design based around X-ray structures of ligand bound HSP90 complexes. Lead compounds exhibited high binding affinities, ATP-ase inhibition and cellular client protein degradation. -
dc.identifier.bibliographicCitation BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.20, no.24, pp.7503 - 7506 -
dc.identifier.doi 10.1016/j.bmcl.2010.10.010 -
dc.identifier.issn 0960-894X -
dc.identifier.scopusid 2-s2.0-78449271034 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8540 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78449271034 -
dc.identifier.wosid 000284332900070 -
dc.language 영어 -
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD -
dc.title N-Aryl-benzimidazolones as novel small molecule HSP90 inhibitors -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

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