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● Al-Rehaily A.J., Ahmad M.S., Muhammad I., Al-Thukair A.A., Perzanowski H. P., 2003. Furoquinoline alkaloids from Teclea nobilis. Phytochemistry, 64, 1405-1411.

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BIBLIOGRAFIA

● Aladesanmi A. J., 1988. The stem constituents of Dysoxylum lenticellare.

Tetrahedrin, 44, 3749-3756.

● Al-Rehaily A.J., Ahmad M.S., Muhammad I., Al-Thukair A.A., Perzanowski H. P., 2003. Furoquinoline alkaloids from Teclea nobilis. Phytochemistry, 64, 1405-1411.

● Almeida A. P., Miranda M. M. F. S., Simoni I. C., Wigg M. D., LagrotaM. H. C., Costa S. S., 1998. Flavonol Monoglycosides Isolated from the Antiviral Fractions of Persea americana (Lauraceae) Leaf Infusion. Phytotherapy Research, 12, 562–567.

● Amaro-Luis JM, Massanet GM, Pando E, Rodriguez-Luis F, Zubia E., 1990. New coumarins from Pilocarpus goudotianus. Planta Medica, 56, 304-306.

● Bader A., Tuccinardi T., Granchi C., Martinelli A., Macchia M., Minutolo F. De Tommasi N., Braca A., 2015. Phenylpropanoids and flavonoids from Phlomis kurdica as inhibitors of human lactate dehydrogenase, Phytochemistry in press (DOI: 10.1016/j.phytochem.2015.03.007)

● Bax A., Subramanian S., 1986. Sensivity-enhanced two-dimensional heteronuclear shift correlation NMR spectroscopy. Journal of Magnetic Resonance, 67, 565-569.

● Bohlmann F., Ates N., 1984. Three prenylted flavonoids from Helichrysum athrixiifolium. Phytochemistry, 3, 1338-1339.

● Bremer B., Manen J.F., 2000. Phylogeny and classification of the subfamily Rubioideae (Rubiaceae). Plant Systematics and Evolution, 225, 43-72.

● Bruni A., Nicoletti M., 2000 “Lezioni di botanica farmaceutica” CISU, Roma.

● Chen Y-H., Chang F-R., Wu. C-C., Yen M-H., Liaw C-C., Huang H-C., Kuo Y-H., Wu Y- C., 2006. New Cytotoxic 6-Oxygenated 8, 9-Dihydrofurocoumarins, Hedyotiscone A-C, from Hedyotis biflora. Planta medica, 72, 75-78.

● Davis D.G., Bax A., 1985. Simplification of

1

H NMR spectra by selective excitation of experimental subspectra. Journal of American Chemical Society, 107, 7197-7198.

● De Feo V., 2003. Ethnomedical field study in northern Peruvian Andes with particular reference to divination practices. Journal of Ethnopharmacology, 85, 243-256.

● De Feo V., Della Valle C., De Simone F., Pizza C., 1992. Chemical constituents and

antibacterial activity of Arcytophyllum nitidum HBK. Annali di chimica, 82, 149-

159.

(2)

Bibliografia

126

● Demirezer L. Ö., Gϋrbϋz F. Gϋvenalp Z. Ströch K., Zeeck A., 2006. Iridoids, Flavonoids and Monoterpene Glycosides from Galium verum subsp. verum.

Turkish Journal Chemistry, 30, 525-534.

● Dewick P.M., 2002. Medicinal natural products. A biosynthetic approach. John Wiley & Sons Ltd, London.

● Garo E, Wolfender JL, Hostettmann K, Hiller W, Antus S, Mavi S., 1998. Prenylated flavanones from Monotes engleri: on-line structure elucidation by LC/UV/NMR.

Helvetica Chimica Acta, 81, 754-763.

● Guffantte Serrano I. D., 2013. Screening de actividad antioxidante y citotόxica en Artemia salina de: Arcythophyllum thymifolium, Salvia squalens, Justicia chlorostachya, Myrcianthes rhopaloides, Dalea mutisii. Escuela superior politècnica de Chimborazo.

● Gϋvenalp Z., Demirezer L. Ö., 2005. Flavonol Glycosides from Asperula arvensis L.

Turkish Journal of Chemistry, 29, 163-169.

● Han Y., Nishibe S., Noguchi Y., Jin Z., 2011. Flavonol glycosides from the stems of Trigonella foenum-graecum. Phytochemistry, 58, 577-580.

● Kay L.E., Keifer P., Saarinen T., 1992. Pure absorption gradient enhanced heteronuclear single quantum correlation spectroscopy with improbe sensivity.

Journal of American Chemical Society, 114, 10663-10665.

● Lee E., Moon B-H., Park Y., Hong S., Lee S., Lee Y., Lim Y., 2008. Effects of Hydroxy and Methoxy Substituents on NMR Data in Flavonols. Bulletin of the Korean Chemical Society, 29(2), 507-510.

● Lerner L., Bax A., 1986. Sensivity-enhanced two-dimensional heteronuclear relayed coherence transfer NMR spectroscopy. Journal of Magnetic Resonance, 69, 375-380.

● Manerba M., 2012. L’inibizione della lattico deidrogenasi: una possibile strategia per migliorare il trattamento farmacologico del carcinoma epatocellulare. Alma Mater Studiorum – Università di Bologna.

● Mena P.V., 1990. A Revision of the Genus Arcytophyllum (Rubiaceae:

Hedyotideae) New York Botanical Garden, New York.

● Mondon A., Callsen H., 1975. Chromone und cumarine aus Cneorum

pulverulentum. Chemische Berichte, 108, 2005-2020.

(3)

Bibliografia

127

● Monigatti M., Bussmann R.V., Weckerle C.S., 2013. Medicinal plant use in two Andean communities located at different altitudes in the Bolívar Province, Peru.

Journal of Ethnopharmacology, 145, 450-464.

● Motta F., 1960. Nel Mondo della Natura, enciclopedia di scienze naturali. Motta editore, Milano.

● Okuyama E., Okamoto Y., Yamazaki M., Satake M., 1996. Pharmacologically Active Components of a Peruvian Plant, Huanarpo (Jatropha cilliata). Chemical &

Pharmaceutical Bulletin, 44(2), 333-336.

● Otsuka H., Yoshimura K., Yamasaki K., Cantoria M-C., 1991. Isolation of 10-O- acyliridoid glycosides from a Philippine medicinal plant, Oldelandia corymbosa L.

(Rubiaceae). Chemical & Pharmaceutical Bulletin, 38, 2049-2052.

● Palmer A.G., Cavanag J., Wright P.E., Rance M., 1991. Sensivity improvement in proton-detected two-dimensional heteronuclear correlation NMR spectroscopy.

Journal of Magnetic Resonance, 93, 151-170

● Sklenář P, Balslev H., 2007. Geographic flora elements in the Ecuadorian superpáramo. Flora, 202, 50–61.

● Treccani G., 1956. Dizionario Enciclopedico Italiano. Istituto poligrafico dello stato, Roma.

● Tsai I-L, Wu M-F, Teng C-M, Ishikawa T, Chen I-S., 1998. Anti-platelet aggregation constituents from formosan Toddalia asiatica. Phytochemistry, 48, 1377-1382.

● Tzakoua O., Mylonasa P., Vagiasa C., Petrakisb P. V., 2007. Iridoid Glucosides with Insecticidal Activity from Galium melanantherum. Zeitschrift für Naturforschung B, A Journal of Chemical Sciences, 62c, 597-602.

● Yue G.G., Kin-Ming Lee J., Cheng L., Chung-Lap Chan B., Jiang L., Fung KP., Leung P.C., Bik-San Lau C., 2012. Reversal of P-glycoprotein-mediated multidrug resistance in human hepatoma cells by hedyotiscone A, a compound isolated from Hedyotis corymbosa. Xenobiotica, 42(6), 562-70.

● Zerback R., Bokel M., Geiger H., Hess D., 1989. A kaempferol 3-glucosylgalactoside

and further flavonoids from pollen of Petunia hybrida. Phytochemistry, 28(3), 897-

899.

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