Show simple item record

dc.contributor.authorTajabadi, Fatemeh Mazraati
dc.contributor.authorPouwer, Rebecca H
dc.contributor.authorLiu, Miaomiao
dc.contributor.authorDashti, Yousef
dc.contributor.authorCampitelli, Marc R
dc.contributor.authorMurtaza, Mariyam
dc.contributor.authorMellick, George D
dc.contributor.authorWood, Stephen A
dc.contributor.authorJenkins, Ian D
dc.contributor.authorQuinn, Ronald J
dc.date.accessioned2019-07-04T12:42:13Z
dc.date.available2019-07-04T12:42:13Z
dc.date.issued2018
dc.identifier.issn0022-2623
dc.identifier.doi10.1021/acs.jmedchem.8b00194
dc.identifier.urihttp://hdl.handle.net/10072/382484
dc.description.abstractA chemoinformatic method was developed to extract nonflat scaffolds embedded in natural products within the Dictionary of Natural Products (DNP). The cedrane scaffold was then chosen as an example of a nonflat scaffold that directs substituents in three-dimensional (3D) space. A cedrane scaffold that has three orthogonal handles to allow generation of 1D, 2D, and 3D libraries was synthesized on a large scale. These libraries would cover more than 50% of the natural diversity of natural products with an embedded cedrane scaffold. Synthesis of three focused natural product-like libraries based on the 3D cedrane scaffold was achieved. A phenotypic assay was used to test the biological profile of synthesized compounds against normal and Parkinson’s patient-derived cells. The cytological profiles of the synthesized analogues based on the cedrane scaffold revealed that this 3D scaffold, prevalidated by nature, can interact with biological systems as it displayed various effects against normal and Parkinson’s patient-derived cell lines.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.publisher.placeColumbus, Ohio
dc.relation.ispartofpagefrom6609
dc.relation.ispartofpageto6628
dc.relation.ispartofissue15
dc.relation.ispartofjournalJournal of Medicinal Chemistry
dc.relation.ispartofvolume61
dc.subject.fieldofresearchMedicinal and biomolecular chemistry
dc.subject.fieldofresearchMedicinal and biomolecular chemistry not elsewhere classified
dc.subject.fieldofresearchOrganic chemistry
dc.subject.fieldofresearchPharmacology and pharmaceutical sciences
dc.subject.fieldofresearchcode3404
dc.subject.fieldofresearchcode340499
dc.subject.fieldofresearchcode3405
dc.subject.fieldofresearchcode3214
dc.titleDesign and Synthesis of Natural Product Inspired Libraries Based on the Three-Dimensional (3D) Cedrane Scaffold: Toward the Exploration of 3D Biological Space
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
dc.description.versionAccepted Manuscript (AM)
gro.facultyGriffith Sciences, Griffith Institute for Drug Discovery
gro.rights.copyrightThis document is the Postprint: Accepted Manuscript version of a Published Work that appeared in final form in Journal of Medicinal Chemistry, copyright 2018 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see 10.1021/acs.jmedchem.8b00194
gro.hasfulltextFull Text
gro.griffith.authorJenkins, Ian D.
gro.griffith.authorQuinn, Ronald J.
gro.griffith.authorMellick, George
gro.griffith.authorLiu, Miaomiao
gro.griffith.authorMurtaza, Mariyam


Files in this item

This item appears in the following Collection(s)

  • Journal articles
    Contains articles published by Griffith authors in scholarly journals.

Show simple item record