Xylochemical Synthesis and Biological Evaluation of the Orchidaceous Natural Products Isoarundinin I, Bleochrin F, Blestanol K, and Pleionol
- Publikationstyp:
- Zeitschriftenaufsatz
- Metadaten:
-
- Autoren
- Leander Geske
- Joris Baier
- Joelle C Boulos
- Thomas Efferth
- Till Opatz
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000901968200001&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.1021/acs.jnatprod.2c00830
- eISSN
- 1520-6025
- Externe Identifier
- Clarivate Analytics Document Solution ID: 7F6PY
- PubMed Identifier: 36538372
- ISSN
- 0163-3864
- Zeitschrift
- JOURNAL OF NATURAL PRODUCTS
- Datum der Veröffentlichung
- 2022
- Status
- Published
- Titel
- Xylochemical Synthesis and Biological Evaluation of the Orchidaceous Natural Products Isoarundinin I, Bleochrin F, Blestanol K, and Pleionol
- Sub types
- Article
- Early Access
Datenquelle: Web of Science (Lite)
- Andere Metadatenquellen:
-
- Autoren
- Leander Geske
- Joris Baier
- Joelle C Boulos
- Thomas Efferth
- Till Opatz
- DOI
- 10.1021/acs.jnatprod.2c00830
- eISSN
- 1520-6025
- ISSN
- 0163-3864
- Ausgabe der Veröffentlichung
- 1
- Zeitschrift
- Journal of Natural Products
- Sprache
- en
- Online publication date
- 2022
- Paginierung
- 131 - 137
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Herausgeber
- American Chemical Society (ACS)
- Herausgeber URL
- http://dx.doi.org/10.1021/acs.jnatprod.2c00830
- Datum der Datenerfassung
- 2023
- Titel
- Xylochemical Synthesis and Biological Evaluation of the Orchidaceous Natural Products Isoarundinin I, Bleochrin F, Blestanol K, and Pleionol
- Ausgabe der Zeitschrift
- 86
Datenquelle: Crossref
- Abstract
- The first total syntheses of the orchid-derived natural products isoarundinin I (<b>1</b>), (±)-bleochrin F ((±)-<b>2</b>), (±)-blestanol K ((±)-<b>3</b>), and (±)-pleionol ((±)-<b>4</b>) from renewable starting materials are reported, along with the evaluation of their biological activities. The total syntheses were based on regioselective aromatic bromination reactions in combination with a key acid-promoted regioselective intramolecular cyclization. The biological results suggest that isoarundinin I (<b>1</b>), (±)-blestanol K ((±)-<b>3</b>), and (±)-pleionol ((±)-<b>4</b>) have the potential to inhibit the growth of both sensitive and multidrug-resistant cancer cells.
- Addresses
- Department of Chemistry, Organic Chemistry Section, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany.
- Autoren
- Leander Geske
- Joris Baier
- Joelle C Boulos
- Thomas Efferth
- Till Opatz
- DOI
- 10.1021/acs.jnatprod.2c00830
- eISSN
- 1520-6025
- Externe Identifier
- PubMed Identifier: 36538372
- Funding acknowledgements
- Rhineland Palatinate Center for Natural Products Research:
- German Federal Ministry of Education and Research: 01DG17013
- Open access
- false
- ISSN
- 0163-3864
- Ausgabe der Veröffentlichung
- 1
- Zeitschrift
- Journal of natural products
- Schlüsselwörter
- Biological Products
- Drug Resistance, Multiple
- Cyclization
- Drug Resistance, Neoplasm
- Stereoisomerism
- Halogenation
- Sprache
- eng
- Medium
- Print-Electronic
- Online publication date
- 2022
- Paginierung
- 131 - 137
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Datum der Datenerfassung
- 2022
- Titel
- Xylochemical Synthesis and Biological Evaluation of the Orchidaceous Natural Products Isoarundinin I, Bleochrin F, Blestanol K, and Pleionol.
- Sub types
- Research Support, Non-U.S. Gov't
- Journal Article
- Ausgabe der Zeitschrift
- 86
Datenquelle: Europe PubMed Central
- Abstract
- The first total syntheses of the orchid-derived natural products isoarundinin I (1), (±)-bleochrin F ((±)-2), (±)-blestanol K ((±)-3), and (±)-pleionol ((±)-4) from renewable starting materials are reported, along with the evaluation of their biological activities. The total syntheses were based on regioselective aromatic bromination reactions in combination with a key acid-promoted regioselective intramolecular cyclization. The biological results suggest that isoarundinin I (1), (±)-blestanol K ((±)-3), and (±)-pleionol ((±)-4) have the potential to inhibit the growth of both sensitive and multidrug-resistant cancer cells.
- Autoren
- Leander Geske
- Joris Baier
- Joelle C Boulos
- Thomas Efferth
- Till Opatz
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/36538372
- DOI
- 10.1021/acs.jnatprod.2c00830
- eISSN
- 1520-6025
- Ausgabe der Veröffentlichung
- 1
- Zeitschrift
- J Nat Prod
- Schlüsselwörter
- Biological Products
- Drug Resistance, Multiple
- Drug Resistance, Neoplasm
- Cyclization
- Halogenation
- Stereoisomerism
- Sprache
- eng
- Country
- United States
- Paginierung
- 131 - 137
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2023
- Titel
- Xylochemical Synthesis and Biological Evaluation of the Orchidaceous Natural Products Isoarundinin I, Bleochrin F, Blestanol K, and Pleionol.
- Sub types
- Journal Article
- Research Support, Non-U.S. Gov't
- Ausgabe der Zeitschrift
- 86
Datenquelle: PubMed
- Beziehungen:
- Eigentum von