Literatura académica sobre el tema "Cyclotripeptides"
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Artículos de revistas sobre el tema "Cyclotripeptides"
CERRINI, SILVIO, ENRICO GAVUZZO, GINO LUCENTE y FRANCESCO PINNEN. "Ten-membered cyclotripeptides". International Journal of Peptide and Protein Research 31, n.º 5 (12 de enero de 2009): 447–53. http://dx.doi.org/10.1111/j.1399-3011.1988.tb00902.x.
Texto completoCERRINI, S., E. GAVUZZO, G. LUCENTE, F. PINNEN y G. ZANOTTI. "Ten-membered cyclotripeptides". International Journal of Peptide and Protein Research 34, n.º 1 (12 de enero de 2009): 6–13. http://dx.doi.org/10.1111/j.1399-3011.1989.tb01000.x.
Texto completoCERRINI, S., E. GAVUZZO, G. LUCENTE, G. LUISI, F. PINNEN y L. RADICS. "Ten-membered cyclotripeptides". International Journal of Peptide and Protein Research 38, n.º 4 (12 de enero de 2009): 289–97. http://dx.doi.org/10.1111/j.1399-3011.1991.tb01507.x.
Texto completoZanotti, Giancarlo, Francesco Pinnen, Gino Lucente, Silvio Cerrini y Enrico Gavuzzo. "Endoannular interactions in cysteine-containing cyclotripeptides: one-step synthesis and crystal structure of a tetracyclic aza-cyclol". Journal of the Chemical Society, Perkin Transactions 1, n.º 9 (1988): 2647. http://dx.doi.org/10.1039/p19880002647.
Texto completoZhao, Lishuang, Zhiqiang Wang, Hongyue Zhang, Wenting Li, Qunfeng Yue y Yingxue Jin. "Design, Preparation of 3-Hydroxy Isoindolinone Cyclotripeptides, and the In Vitro Antitumor Activities Against Cervical Carcinoma HeLa Cells". Journal of Heterocyclic Chemistry 55, n.º 5 (23 de marzo de 2018): 1205–18. http://dx.doi.org/10.1002/jhet.3154.
Texto completoLu, Xi-Lin, Zhong-Liang Xu, Xiao-Li Yao, Feng-Juan Su, Cheng-Hui Ye, Jing Li, Yong-Cheng Lin et al. "Marine Cyclotripeptide X-13 Promotes Angiogenesis in Zebrafish and Human Endothelial Cells via PI3K/Akt/eNOS Signaling Pathways". Marine Drugs 10, n.º 12 (7 de junio de 2012): 1307–20. http://dx.doi.org/10.3390/md10061307.
Texto completoEbada, Sherif S., Thomas Fischer, Alexandra Hamacher, Feng-Yu Du, Yoen Ok Roth, Matthias U. Kassack, Bin-Gui Wang y Eckhard H. Roth. "Psychrophilin E, a new cyclotripeptide, from co-fermentation of two marine alga-derived fungi of the genus Aspergillus". Natural Product Research 28, n.º 11 (31 de enero de 2014): 776–81. http://dx.doi.org/10.1080/14786419.2014.880911.
Texto completoFernández, Diana Uría, Regine Fuchs, Mathias Schäfer, Herbert Budzikiewicz y Jean-Marie Meyer. "The Pyoverdin of Pseudomonas fluorescens G173, a Novel Structural Type Accompanied by Unexpected Natural Derivatives of the Corresponding Ferribactin". Zeitschrift für Naturforschung C 58, n.º 1-2 (1 de febrero de 2003): 1–10. http://dx.doi.org/10.1515/znc-2003-1-201.
Texto completoHaas, Katharina y Wolfgang Beck. "Halbsandwich-Komplexe von Ruthenium(II), Rhodium(III) und Iridium(III) mit Tripeptidestern aus α-, β- und γ-Aminosäuren als Liganden. — Peptidsynthese und Cyclisierung zu Cyclotripeptiden am Metallzentrum". Zeitschrift für anorganische und allgemeine Chemie 628, n.º 4 (mayo de 2002): 788. http://dx.doi.org/10.1002/1521-3749(200205)628:4<788::aid-zaac788>3.0.co;2-v.
Texto completoPINNEN, F., G. ZANOTTI y G. LUCENTE. "ChemInform Abstract: TEN-MEMBERED CYCLOTRIPEPTIDES: INFLUENCE OF THE RING-FLEXIBILITY ON INTRAMOLECULAR REACTIONS". Chemischer Informationsdienst 16, n.º 13 (2 de abril de 1985). http://dx.doi.org/10.1002/chin.198513309.
Texto completoTesis sobre el tema "Cyclotripeptides"
Han, Guanghui. "Total synthesis of cyclotripeptidic natural products in the aurantiomide series, under oxidative functionnalisation conditions". Electronic Thesis or Diss., Institut polytechnique de Paris, 2024. http://www.theses.fr/2024IPPAX029.
Texto completoThe quinazoline heterocycle, as a pharmacophore, is significant in recent anticancer drug discovery and in natural products containing the piperazino[2,1-b]quinazolin-3,6-dione core. Compounds like anacine and its derivatives, found in marine Sponge-derived Penicillium species, show promising biological activities. However, their synthesis presents numerous challenges. In this study, we devised a three-step strategy, leveraging microwave-assisted condensation of tripeptides, to directly synthesize compounds bearing the piperazino[2,1-b]quinazolin-3,6-dione heterocyclic structure. Additionally, we successfully completed the full synthesis of anacine and polonimide C. Recognizing that aurantiomides A-C and verrucine F are oxidatized variants of anacine and verrucine A at the C-1 position, we employed DDQ to achieve the selective and efficient C-1 oxidation of the piperazino[2,1-b]quinazolin-3,6-dione structure. This approach demonstrated high efficacy across several substrates and allowed the conversion of anacine to aurantiomide C. Furthermore, we observed the spontaneous installation of the alkylidene group via autooxidation during the cyclocondensation process. Additionally, the successful application of nickel-catalyzed aminocarbonylation of a bromoethyl intermediate enabled us to achieve the first total synthesis of aurantiomide C, polonimide A, and verrucine F
Capítulos de libros sobre el tema "Cyclotripeptides"
Rothe, M. y J. Haas. "Cyclization and cyclo-oligomerization of tripeptides: How are cyclotripeptides formed?" En Peptides 1990, 212–13. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3034-9_88.
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