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Referencias:

• Savary, S., Teng, P.S., Willocquet, L., Nutter Jr., F.W., Quantification and modeling of crop losses: A review of purposes (2006) Annual Review of Phytopathology, 44, pp. 89-112. , DOI 10.1146/annurev.phyto.44.070505.143342
• Knight, S.C., Anthony, V.M., Brady, A.M., Greenland, A.J., Heaney, S.P., Murray, D.C., Powell, K.A., Youle, D., Rationale and perspectives on the development of fungicides (1997) Annual Review of Phytopathology, 35, pp. 349-372. , DOI 10.1146/annurev.phyto.35.1.349
• Brogden, K.A., Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria (2005) Nat Rev Microbiol, 3, pp. 238-250. , doi:10.1038/nrmicro1098
• Marcos, J.F., Muñoz, A., Pérez-Payá, E., Misra, S., López-García, B., Identification and rational design of novel antimicrobial peptides for plant protection (2008) Annu Rev Phytopathol, 46, pp. 273-330. , doi:10.1146/annurev.phyto.121307.094843
• Straus, S.K., Hancock, R.E.W., Mode of action of the new antibiotic for Gram-positive pathogens daptomycin: Comparison with cationic antimicrobial peptides and lipopeptides (2006) Biochimica et Biophysica Acta - Biomembranes, 1758 (9), pp. 1215-1223. , DOI 10.1016/j.bbamem.2006.02.009, PII S0005273606000435
• Makovitzki, A., Avrahami, D., Shai, Y., Ultrashort antibacterial and antifungal lipopeptides (2006) Proceedings of the National Academy of Sciences of the United States of America, 103 (43), pp. 15997-16002. , DOI 10.1073/pnas.0606129103
• Makovitzki, A., Viterbo, A., Brotman, Y., Chet, I., Shai, Y., Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides (2007) Applied and Environmental Microbiology, 73 (20), pp. 6629-6636. , DOI 10.1128/AEM.01334-07
• Zuckermann, R.N., Martin, E.J., Spellmeyer, D.C., Stauber, G.B., Shoemaker, K.R., Kerr, J.M., Figliozzi, G.M., Moos, W.H., Discovery of nanomolar ligands for 7-transmembrane G-protein-coupled receptors from a diverse N-(substituted)glycine peptoid library (1994) Journal of Medicinal Chemistry, 37 (17), pp. 2678-2685
• Shin, S.B.Y., Yoo, B., Todaro, L.J., Kirshenbaum, K., Cyclic peptoids (2007) Journal of the American Chemical Society, 129 (11), pp. 3218-3225. , DOI 10.1021/ja066960o
• Masip, I., Cortes, N., Abad, M.-J., Guardiola, M., Perez-Paya, E., Ferragut, J., Ferrer-Montiel, A., Messeguer, A., Design and synthesis of an optimized positional scanning library of peptoids: Identification of novel multidrug resistance reversal agents (2005) Bioorganic and Medicinal Chemistry, 13 (6), pp. 1923-1929. , DOI 10.1016/j.bmc.2005.01.024
• Zuckermann, R.N., Kerr, J.M., Kent, S.B.H., Moos, W.H., Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis (1992) J Am Chem Soc, 114, pp. 10646-10647. , doi:10.1021/ja00052a076
• Chongsiriwatana, N.P., Miller, T.M., Wetzler, M., Vakulenko, S., Karlsson, A.J., Palecek, S.P., Mobashery, S., Barron, A.E., Short alkylated peptoid mimics of antimicrobial lipopeptides (2011) Antimicrob Agents Chemother, 55, pp. 417-420. , doi:10.1128/AAC.01080-10
• Dömling, A., Recent developments in isocyanide based multicomponent reactions in applied chemistry (2006) ChemRev, 106, pp. 17-89. , doi:10.1021/cr0505728
• Xu, P., Zhang, T., Wang, W., Zou, X., Zhang, X., Fu, Y., Synthesis of PNA monomers and dimers by ugi four-component reaction (2003) Synthesis, (8), pp. 1171-1176
• Rivera, D.G., Wessjohann, L.A., Supramolecular compounds from multiple ugi multicomponent macrocyclizations: Peptoid-based cryptands, cages, and cryptophanes (2006) Journal of the American Chemical Society, 128 (22), pp. 7122-7123. , DOI 10.1021/ja060720r
• Vercillo, O.E., Andrade, C.K.Z., Wessjohann, L.A., Design and synthesis of cyclic RGD pentapeptoids by consecutive Ugi reactions (2008) Org Lett, 10, pp. 205-208. , doi:10.1021/ol702521g
• Henze, M., Kreye, O., Brauch, S., Nitsche, C., Naumann, K., Wessjohann, L.A., Westermann, B., Photoaffinity-labeled peptoids and depsipeptides by multicomponent reactions (2010) Synthesis, 17, pp. 2997-3003. , doi:10.1055/s-0030-1258182
• Sui, Q., Borchardt, D., Rabenstein, D.L., Kinetics and equilibria of cis/trans isomerization of backbone amide bonds in peptoids (2007) Journal of the American Chemical Society, 129 (39), pp. 12042-12048. , DOI 10.1021/ja0740925
• Heerma, W., Verluis, C., De Koster, C.G., Kruijtzer, J.A.W., Zigrovic, I., Liskamp, R.M.J., Comparing mass spectrometric characteristics of peptides and peptoids (1996) Rapid Commun Mass Spectrom, 10, pp. 459-464. , doi:10.1002/(SICI)1097-0231(19960315)10:4〈459::AID-RCM501〉3.0. CO;2-J
• Roepstorff, P., Fohlman, J., Proposal for a common nomenclature for sequence ions in mass spectra of peptides (1984) Biomed Mass Spectrom, 11, p. 601. , doi:10.1002/bms.1200111109
• Jacob, M.R., Walker, L.A., Natural products and antifungal drug discovery (2005) Methods in Molecular Medicine, 118, pp. 83-110. , Ernst EJ, Rogers PD (eds) antifungal agents: methods and protocols 1st ed. Humana Press Inc, Totowa, NJ
• Hadacek, F., Greger, H., Testing of antifungal natural products: Methodologies, comparability of results and assay choice (2000) Phytochemical Analysis, 11 (3), pp. 137-147. , DOI 10.1002/(SICI)1099-1565(200005/06)11:3<137::AID-PCA514>3.0. CO;2-I
• Makovitzki, A., Viterbo, A., Brotman, Y., Chet, I., Shai, Y., Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides (2007) Applied and Environmental Microbiology, 73 (20), pp. 6629-6636. , DOI 10.1128/AEM.01334-07
• Shai, Y., Mode of action of membrane active antimicrobial peptides (2002) Pept Sci, 66, pp. 236-248. , doi:10.1002/bip.10260

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