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  Structural analogs of tylophora alkaloids may not be functional analogs

Gao, W., Chen, A.-P.-C., Leung, C.-H., Gullen, E. A., Fürstner, A., Shi, Q., et al. (2008). Structural analogs of tylophora alkaloids may not be functional analogs. Bioorganic & Medicinal Chemistry Letters, 18(1), 704-709. doi:10.1016/j.bmcl.2007.11.054.

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 Urheber:
Gao, Wenli1, Autor
Chen, Annie Pei-Chun1, Autor
Leung, Chung-Hang1, Autor
Gullen, Elizabeth A.1, Autor
Fürstner, Alois2, Autor           
Shi, Qian3, Autor
Wei, Linyi3, Autor
Lee, Kuo-Hsiung3, Autor
Cheng, Yung-Chi1, Autor
Affiliations:
1Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06510, USA, ou_persistent22              
2Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              
3Natural Products Research Laboratories, School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, USA, ou_persistent22              

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Schlagwörter: tylophora alkaloids; structure-activity relationship; protein; DNA; and RNA synthesis
 Zusammenfassung: Phenanthroindolizidine-based tylophora alkaloids have been reported to have potential antitumor, anti-immuno and, anti-inflammatory activity. The structure–activity relationships of a series of tylophora alkaloids were studied to guide future drug design. Our results indicate that although these compounds are structural analogs, their potency of cytotoxicity, selectivity against NF-κB signaling pathway, and their inhibitory effects against protein and nucleic acid synthesis are different. Because they do not have an identical spectrum of targets, the studied compounds are structural, but may not be functional analogs.

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Sprache(n): eng - English
 Datum: 2007-11-132007-09-292007-11-152007-11-212008-01-15
 Publikationsstatus: Erschienen
 Seiten: 6
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1016/j.bmcl.2007.11.054
 Art des Abschluß: -

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Titel: Bioorganic & Medicinal Chemistry Letters
  Andere : Bioorg. Med. Chem. Lett.
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: Oxford : Pergamon
Seiten: - Band / Heft: 18 (1) Artikelnummer: - Start- / Endseite: 704 - 709 Identifikator: ISSN: 0960-894X
CoNE: https://pure.mpg.de/cone/journals/resource/954925579103