Antiplasmodial phenolic compounds from Piptadenia pervillei

Planta Medica

Volumn 74, Issue 4, 2008, Pages 417-421

  Ramanandraibe, Voahangy ^a   Grellier, Philippe ^b   Martin, Marie Thérèse ^c   Deville, Alexandre ^b   Joyeau, Roger ^b   Ramanitrahasimbola, David ^a   Mouray, Elisabeth ^b   Rasoanaivo, Philippe ^a   Mambu, Lengo ^b  

^a INSTITUT MALGACHE DE RECHERCHES APPLIQUÉES   (Madagascar)

^b MUSÉUM NATIONAL D'HISTOIRE NATURELLE   (France)

^c CNRS   (France)

Author keywords

(+) catechin gallate; Antiplasmodial activity; Fabaceae; Piptadenia pervillei

Indexed keywords

ANTIMALARIAL AGENT; CAMPTOTHECIN; CATECHIN; CATECHIN 3 GALLATE; CATECHIN 5 GALLATE; CHLOROQUINE; GALLIC ACID ETHYL ESTER; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

ANTIMALARIAL ACTIVITY; ARTICLE; CONTROLLED STUDY; CYTOTOXICITY; DRUG DETERMINATION; DRUG INHIBITION; DRUG ISOLATION; DRUG SCREENING; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IC 50; IN VITRO STUDY; LEGUME; LUNG ALVEOLUS CELL; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PIPTADENIA PERVILLEI; PLASMODIUM FALCIPARUM; STRUCTURE ACTIVITY RELATION;

ANIMALS; ANTIMALARIALS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL LINE; FABACEAE; HUMANS; MOLECULAR STRUCTURE; PHENOLS; PLASMODIUM FALCIPARUM;

FABACEAE; PIPTADENIA; PLASMODIUM FALCIPARUM;

EID: 42549099327     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1034328     Document Type: Article

References (23)

1. Hyde JE. Mechanisms of resistance of Plasmodium falciparum to antimalarial drugs. Microbes Infect 2002; 4: 165-74
2. Brinner KM, Kim JM, Habashita H, Gluzman IY, Goldberg DE, Ellman JA. Novel and potent antimalarial agents. Bioorg Med Chem 2001; 10: 3649-61
3. Sullivan DJ. Theories on malaria pigment formation and quinoline action. Int J Parasitol 2002; 32: 1645-53
4. Fitch CD. Ferriprotoporphyrin IX, phospholipids, and the antimalarial actions of quinoline drugs. Life Sci 2004; 74: 1957-72
5. Rasoanaivo P, Ramanitrahasimbola D, Rafatro H, Rakotondramanana D, Robijaona B, Rakotozafy A et al. Screening extracts of Madagascan plants in search of antiplasmodial compounds. Phytother Res 2004; 18: 742-7
6. Villiers JF. Subfamily mimosoideae. In: Du Puy DJ, editor. The Leguminosae of Madagascar. Kew: Royal Botanical Gardens; 2002: 154-293
7. Zelle RE, McClellan WJ. A simple, high-yielding method for the methylenation of catechols. Tetrahedron Lett 1991; 32: 2461-4
8. Cren-Olivé C, Lebrun S, Rolando C. An efficient synthesis of the four mono methylated isomers of (+)-catechin including the major metabolites and of some dimethylated and trimethylated analogues through selective protection of the catechol ring. J Chem Soc Perkin Trans I; 2002: 821-30
9. Tückmantel W, Kozikowski AP, Romanczyk LJ. Studies in polyphenol chemistry and bioactivity. 1. Preparation of building blocks from (+)-catechin. Procyanidin formation. Synthesis of the cancer cell growth inhibitor, 3-O-galloyl-(2R,3R)-epicatechin 4β,8-[3-O- galloyl-(2R,3R)-epicatechin]. J Am Chem Soc 1999; 121: 12073-81
10. Frappier F, Jossang A, Soudan J, Calvo F, Rasoanaivo P, Ratsimamanga-Urverg S et al. Bisbenzylisoquinolines as modulators of chloroquine resistance in Plasmodium falciparum and multidrug resistance in tumor cells. Antimicrob Agents Chemother 1996; 40: 1476-81
11. 13C NMR assignments of some green tea polyphenols. Magn Reson Chem 1996; 34: 887-90
12. Tanaka T, Nonaka GI, Nishioka I. 7-O-Galloyl-(+)-catechin and 3-O-Galloylprocyanidin B-3 from Sanguisorba officinalis. Phytochemistry 1983; 22: 2575-8
13. Malan E. Derivatives of (+)-catechin-5-gallate from the bark of Acacia nilotica. Phytochemistry 1991; 30: 2737-9
14. Calixto JB, Santos ARS, Cechinel V, Yunes RA. A review of the plants of the genus Phyllanthus: their chemistry, pharmacology, and therapeutic potential. Med Res Rev 1998; 18: 225-58
15. Jankun J, Selman SH, Swiercz R, Skrzypczak-Jankun E. Why drinking green tea could prevent cancer. Nature 1997; 387: 561
16. Fraga CG, Martino VS, Ferraro GE, Coussio JD, Boveris A. Flavonoids as antioxidants evaluated by in vitro and in situ liver chemiluminescence. Biochem Pharmacol 1987; 36: 717-20
17. Kayser O, Kiderlin AF, Croft SL. Natural products as potential antiparasitic drugs. In: Atta-ur-Rahman, editor. Studies in natural products chemistry. Bioactive natural products (Part G). Amsterdam: Elsevier; 2002: 26, 779-848
18. Paveto C, Güida MC, Esteva MI, Martino V, Coussio J, Flawià MM et al. Anti-Trypanosoma cruzi activity of Green tea (Camellia sinensis) catechins. Antimicrob Agents Chemother 2004; 48: 69-74
19. Kolodziej H, Kayser O, Kiderlen AF, Ito H, Hatano T, Yoshida T et al. Proanthocyanidins and related compounds: antileishmanial activity and modulatory effects on nitric oxid and tumor necrosis factor-α-release in the murine macrophage-like cell line RAW 264. Biol Pharm Bull 2001; 24: 1016-21
20. Dickii J, Njifutie N, Foyere JA, Basco L, Ringwald P. In vitro antimalarial activity of limonoids from Khaya grandifolia C.D.C. (Meliaceae). J Ethnopharmacol 2000; 60: 27-33
21. Srivastava P, Chandra S, Arif AJ, Singh C, Pandey VC. Metal chelators/antioxidants: approaches to protect erythrocytic oxidative stress injury during Plasmodium berghei infection in Mastomys coucha. Pharmacol Res 1999; 40: 239-41
22. Tasdemir D, Lack G, Brun R, Rüedi P, Scapozza L, Perozzo R. Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. J Med Chem 2006; 49: 3345-53
23. Sannella AR, Messori L, Casini A, Vincieri FF, Bilia AR, Majori G et al. Antimalarial properties of green tea. Biochem Biophys Res Commun 2007; 353: 177-81