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Références Bibliographiques Références bibliographiques Abad, M.J., Bedoya, L.M., Bermejo, P., 2013. Essential oils from the Asteraceae family active against multidrug-resistant bacteria, in : Rai, M.K., Kon, K.V. (Eds.), Fighting multidrug resistance with herbal extracts, essential oils and their components, First edition, Elsevier, Oxford, pp. 204-221 Adams, D.W., Errington, J., 2009. Bacterial cell division: assembly, maintenance and Alkawash, M.A., Soothill, J.S., Schiller, N.L., 2006. Alginate lyase enhances antibiotic killing of mucoid Pseudomonas aeruginosa in biofilms. Acta Pathol Microbiol Immunol Scand 114 (2) 131-138. Adis, R., Profile, D., 2010. Fidaxomicin. Drugs RD 10 (1), 37-45 Ahn, K-S., Hahm, M.S., Park, E., Lee, H-K., Kim, I-H., 1998. Corosolic acid isolated from the fruit of Cratoegus pinnatifida var. psilosa is a protein kinase C inhibitor as well as a cytotoxic agent. Planta Medica 64, 468-470 Aladedunye, F.A., Okorie, D.A., Ighodaro, O.M., 2008. Anti- inflammatory and antioxidant activities and constituents of Platostoma africanum P. Beauv. Nat. Prod. Res. 22 (12), 1067–1073. Al-Jaber, H.I., Abrouni, K.K., Al-Qudah, M.A., Abu Zarga, M.H., 2012. New terpenes from Salvia palaestina Benth. and Salvia syriaca L. growing wild in Jordan. J Asian Nat Prod Res. 14(7), 618-625. Alhede, M., Jakobsen, T.H., Givskov, M., 2011. Novel and future treatment strategies, in : Bjarnsholt, T., Moser, C., Jensen, P.O., Høiby, N. (Eds.), Biofilm Infections, Springer, New York, pp. 231-250 Allahverdiyev, A.M., Bagirova, M., Yaman, S., Koc, R.C., Abamor, E.S., Ates, S.C. Baydar, S.Y., Elcicek, S., Oztel, O.N., 2013. Development of New Antiherpetic Drugs Based on Plant Compounds, in : Rai, M.K., Kon, K.V. (Eds.), Fighting multidrug resistance with herbal extracts, essential oils and their components, First edition, Elsevier, Oxford, pp. 225-259 Almeida, L.S., Murata, R.M., Yatsuda, R., Dos Santos, M.H., Nagem, T.J., Alencar, S.M., Koo, H., Rosalen, P.L., 2008. Antimicrobial activity of Rheedia brasiliensis and 7- epiclusianone against Streptococcus mutans. Phytomedicine, 15, 886-891 Alqahtani, A., Hamid, K., Kam, A., Wong, K.H., Abdelhak, Z., Razmovski-Naumovski, V., Chan, K., Li, K.M., Groundwater, P.W., Li, G.Q., 2013. The pentacyclic triterpenoids in herbal medicines and their pharmacological activities in diabetes and diabetic complications. Curr. Med. Chem. 20, 908−931. Al-Oqail, M.M., Hassan, W.H., Khan, S.I., Khan, I.A., 2013. Solanopubamine, a rare steroidal alkaloid from Solanum schimperianum: Synthesis of some new alkyl and acyl derivatives, their anticancer and antimicrobial evaluation. J. Saudi Chem. Soc. 17, 67-76. Ambrosio, S.R., Furtado, N.A.J.C., De Oliveira, D.C.R., Da Costa, F.B., Martins, C.H.G., De Carvalho, T.C., Porto, T.S., Veneziani, R.C.S., 2008. Antimicrobial activity of kaurane diterpenes against oral pathogens. Z. Naturforsch. C 63, 326-330. Amiguet, V.T., Petit, P., Ta, C.A., Nunez, R., Sanchez-Vindas, P., Alvarez, L.P., Smith, M.L., Arnason, J.T., Durst, T., 2006. Phytochemistry and antifungal properties of the newly discovered tree Pleodendron costaricense. J. Nat. Prod. 69, 1005-1009. Anand, T.P., Bhat, A.W., Shouche, Y.S., Roy, U., Siddharth, J., Siddhartha, Sarma, S.P., 2006. Antimicrobial activity of marine bacteria associated with sponges from the waters off the coast of South East India. Microbiol Res 161, 252-262 Andries, K., Verhasselt, P., Guillemont, J., Gohlmann, H.W.H., Neefs, J-M., Winkler, H., Van Gestel, J., Timmerman, P., Min Zhu, Lee, E., Williams, P., De Chaffoy, D., Huitric, E., Hoffner, S., Cambau, E., Truffot-Pernot, C., Lounis, N., Jarlier, V., 2005. A Diarylquinoline Drug Active on the ATP Synthase of Mycobacterium tuberculosis. Science 307, 223-227 Ankli, A., Heilmann, J., Heinrich, M., Sticher, O., 2000. Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri. Phytochemistry 54, 531-537. Ankri, S., Mirelman, D., 1999. Antimicrobial properties of allicin from garlic. Microbes. Infect. 2, 1999, 125-129 Apfel, C.M., Locher, H., Evers, S., Takacs, B., Hubschwerlen, C., Pirson, 2001. Peptide Deformylase as an Antibacterial Drug Target: Target Validation and Resistance Development. Antimicrob Agents Chemother 45 (4), 1058-1064 APG IV, 2016. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Bot J Linn Soc 181, 1–20 Appelbaum, P.C., 2006. MRSA-the tip of the iceberg. Clin. Microbiol. Infect. 12, 3-10. Aqil, M., 1995. Flavonoidic glycosides from Eupatorium africanum. Ultra Sci Phys Sci 7(1), 1-6. Arthur, H.R., Rosalind, Chan, P.K., Loo, S.N., Tam, S.W., Tung, S., 1966. New alkaloids from Hong Kong plants. Phytochemistry 5(3), 379-83. Arbeit, R.D., Maki, D, Tally, F.P., Campanaro, E., Eisenstein, B.I., 2004. The safety and efficacy of daptomycin for the treatment of complicated skin and skin-structure infections. Clin Infect Dis 38, 1673-1681 Asif, M., Kaur, A., 2015. Mini review on diarylquinolone compound Bedaquiline and some other quinolone derivatives and their antitubercular activity. Res. J. Pharm.Toxicol. 1, 6-11 Atkinson, S., Chang, C.-Y., Sockett, R.E., Cámara, M., Williams, P., 2006. Quorum sensing in Yersinia enterocolitica controls swimming and swarming motility. J. Bacteriol. 188, 1451-1461 Aubart, K., Zalacain, M., 2006. Peptide deformylase inhibitors, in : King, F.D., Lawton, G. (Eds.), Progress in Medicinal Chemistry, First Edition, Vol. 44, Elsevier, UK, pp. 109- 143 Awanchiri, S.S., Trinh-Van-Dufat, H., Shirri, J.C., Dongfack, M.D.J., Nguenang, G.M., Boutefnouchet, S., Fomum, Z.T., Seguin, E., Verite, P., Tillequin, F., Wandji, J., 2009. Triterpenoids with antimicrobial activity from Drypetes inaequalis. Phytochemistry, 70, 419-522. Awad, A.B., Downie, A.C., Fink, C.S., Inhibition of growth and stimulation of apoptosis by β-sitosterol treatment of MDA-MB-231 human breast cancer cells in culture, Int. Mol. Med. 5 (2000) 541–545. Bai, K.K., Yu, Z., Chen, F.L., Li, F., Li, W.Y., Guo, Y.H., 2012. Synthesis and evaluation of ursolic acid derivatives as potent cytotoxic agents. Bioorg. Med. Chem. Lett. 7, 2488– 2493. Bailey, L., Gylfe, A., Sundin, C. et al. 2007. Small molecule inhibitors of type III secretion in Yersinia block the Chlamydia pneumoniae infection cycle. FEBS Lett 581, 587-595 Banno, N., Akihisa, T., Tokuda, H., Yasukawa, K., Higashihara, H., Ukiya, M., Watanabe, K., Kimura, Y., Hasegawa, J., Nishino, H., 2004. Triterpene acids from the leaves of Perilla frutescens and their anti-inflammatory and antitumor-promoting effects. Biosci. Biotechnol. Biochem. 68 (1), 85–90 Bak, J., Begovic, T., Bjarnsholt, T. & Nielsen, A., 2011. A UVC device for intra-luminal disinfection of catheters: in vitro tests on soft polymer tubes contaminated with Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli and Candida albicans. Photochem. Photobiol. 87, 1123-1128 Baldé, A.M., Pieters, L.A., Gergely, A., Kolodziej, H., Claeys, M., Vlietinck, A.J., 1991a. A- Type Proanthocyanidins from stem-bark of Pavetta-Owariensis. Phytochemistry 30 (1), 337-342 Baldé, A.M., Claeys, M., Pieters, L., Wray, V., Vlietinck, A., 1991b. Ferulic acid esters from stem bark of Pavetta owariensis. Phytochemistry 30b (3), 1024-1026 Baldé, A.M., Pieters, L.A., Wray, V., Kolodziej, H., Vanden Berghe, D.A., Claeys, M., Vlietinck, A.J., 1991c. Dimeric and trimeric proanthocyanidins possessing a doubly linked structure from Pavetta owariensis. Phytochemistry 30 (12), 4129-4135 Baldé, A.M., Pieters, L.A., Claeys, M., Traoré, M.S., Baldé, M.A., Diallo, M.S.T., Baldé E.S., Diané S., Vlietinck A. J., 2015. Quinic acid esters from Pavetta owariensis var. owariensis (Rubiaceae). J Plant Sci 3, 20-23 Baldé, A.M., de Bruyne, T, Pieters, L., Kolodziej, H., Vanden Berghe, D., Claeys, M., Vlietinck, A., 1995a. Oligomeric proanthocyanidins possessing a doubly linked structure from Pavetta owariensis. Phytochemistry 38 (3), 719-723 Baldé, A.M., de Bruyne, T, Pieters, L., Kolodziej, H., Vanden Berghe, D., Claeys, M., Vlietinck, A., 1995b. Tetrameric proanthocyanidins containing a double interflavanoid (A-type) linkage from Pavetta owariensis. Phytochemistry 40 (3), 933-938 Baltz, R.H, 2009. 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