In vitro antileishmanial, antiplasmodial and cytotoxic activities of a new ventiloquinone and five known triterpenes from Parinari excelsa

Pharmaceutical Biology

Volumn 50, Issue 7, 2012, Pages 801-806

  Attioua, Barthélemy ^a,b   Yeo, Dodehe ^a   Lagnika, Latifou ^c   Harisolo, Ramiarantsoa ^a   Antheaume, Cyril ^b   Weniger, Bernard ^b   Kaiser, Marcel ^d   Lobstein, Annelise ^b   Vonthron Sénécheau, Catherine ^b  

^a UNIVERSITÉ FÉLIX HOUPHOUËT BOIGNY   (Côte d’Ivoire)

^b UNIVERSITÉ DE STRASBOURG   (France)

^c UNIVERSITY OF ABOMEY CALAVI   (Benin)

^d SWISS TROPICAL AND PUBLIC HEALTH INSTITUTE   (Switzerland)

Author keywords

extraction; isolation; leishmania; malaria; Medicine; plant

Indexed keywords

(3BETA) 3 HYDROXYOLEAN 12 EN 28 OIC ACID; 1 [7 ALLYL 5 (ETHOXYMETHOXY) 8 METHOXY 4,6 BIS(METHOXYMETHOXY)NAPHTHALEN 1 YL]ETHANONE; 16BETA HYDROXYLUPANE 1,20(29) DIEN 3 ONE; 3 O BETA DEXTRO GLUCOPYRANOSYL STIGMASTA 5,11(12) DIENE; 3BETA HYDROXYOLEAN 5,12 DIEN 28 OIC ACID; ANTILEISHMANIAL AGENT; ANTIMALARIAL AGENT; CHLOROGENIC ACID; CHLOROQUINE; DAUCOSTEROL; DICHLOROMETHANE; METHANOL; MILTEFOSINE; PARINARI EXCELSA EXTRACT; PLANT EXTRACT; PLANT MEDICINAL PRODUCT; PODOPHYLLOTOXIN; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG; VENTILOQUINONE;

ANIMAL CELL; ANTILEISHMANIAL ACTIVITY; ANTIPLASMODIAL ACTIVITY; ARTICLE; BARK; CHRYSOBALANACEAE; COLUMN CHROMATOGRAPHY; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; HIGH RESOLUTION ELECTROSPRAY MASS SPECTROMETRY; IC 50; IN VITRO STUDY; INFRARED SPECTROSCOPY; LEISHMANIA DONOVANI; MASS SPECTROMETRY; MYOBLAST; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PARINARI EXCELSA; PHYTOCHEMISTRY; PLANT LEAF; PLANT STEM; PLASMODIUM FALCIPARUM; POWDER; RAT;

ANTIMALARIALS; CHRYSOBALANACEAE; LEISHMANIA DONOVANI; NAPHTHOQUINONES; PLANT BARK; PLANT EXTRACTS; PLANT LEAVES; PLASMODIUM FALCIPARUM; TRITERPENES;

CHRYSOBALANACEAE; LEISHMANIA DONOVANI; PARINARI EXCELSA; PLASMODIUM FALCIPARUM;

EID: 84862000404     PISSN: 13880209     EISSN: 17445116     Source Type: Journal    
DOI: 10.3109/13880209.2011.633270     Document Type: Article

References (32)

1. Ahmed SA, Gogal RM Jr, Walsh JE. (1994). A new rapid and simple non-radioactive assay to monitor and determine the proliferation of lymphocytes: An alternative to [3H]thymidine incorporation assay. J Immunol Methods, 170, 211-224. (Pubitemid 24122510)
2. Bayoumi SA, Rowan MG, Beeching JR, Blagbrough IS. (2010). Constituents and secondary metabolite natural products in fresh and deteriorated cassava roots. Phytochemistry, 71, 598-604.
3. Braca A, Abdel-Razik AF, Mendez J, Morelli I. (2005). A new kaurane diterpene dimer from Parinari campestris. Fitoterapia, 76, 614-619. (Pubitemid 41688376)
4. Camacho MR, Mata R, Castaneda P, Kirby GC, Warhurst DC, Croft SL, Phillipson JD. (2000). Bioactive compounds from Celaenodendron mexicanum. Planta Med, 66, 463-468. (Pubitemid 30413510)
5. Choudhary MI, Ranjit R, Atta-ur-Rahman, Devkota KP, Shrestha TM. (2007). Two new leucosesterterpenes from Leucosceptrum canum. Z. Naturforsch, 62, 587-592.
6. Desjardins RE, Canfield CJ, Haynes JD, Chulay JD. (1979). Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique. Antimicrob Agents Chemother, 16, 710-718. (Pubitemid 10082023)
7. Duarte LP, Figueiredo RC, Faria De SG, Soares DB, Da Silva, Rodrigues SBV, Vasconcelos SFC, Silva GDF, Filho SAV. (2010). Chemical constituents of Salacia elliptica (Celastraceae). Quim. Nova, 33, 900-903.
8. Eyong KO, Folefoc GN, Kuete V, Beng VP, Krohn K, Hussain H, Geraldo de Carvalho M, Candido LFO, Miranda da Costa P, Alves do NI, Braz-Filho R. (2008). Triterpenes acids and saponins isolated from Licania arianeae Prance (Chrysobalanaceae). J Nat Med, 62, 360-361.
9. Gessler MC, Msuya DE, Nkunya MH, Mwasumbi LB, Schär A, Heinrich M, Tanner M. (1995). Traditional healers in Tanzania: The treatment of malaria with plant remedies. J Ethnopharmacol, 48, 131-144.
10. Houghton PJ, Raman A. (1998). Laboratory Handbook for the Fractionation of Natural Extracts. London, UK: Chapman & Hall.
11. Hussain M, Zahra DN, Hussain SM, Ahmed E, Ahmad I, Malik A, Ahmed Z. (2008). Structure determination of new steroids from Abutilon pakistanicum by NMR techniques. Magn Reson Chem, 46, 274-277.
12. Kamanzi Atindehou K, Schmid C, Brun R, Koné MW, Traore D. (2004). Antitrypanosomal and antiplasmodial activity of medicinal plants from Côte d'Ivoire. J Ethnopharmacol, 90, 221-227. (Pubitemid 38180480)
13. Kirandeep K, Meenakshi J, Tarandeep K, Rahul J. (2009). Antimalarials from nature. Bioorg. Med Chem, 17, 3229-3256.
14. Kusaura T. (2010). Chlorogenic acid analog analysis method. Pn. Kokai Tokkyo Koho: JP 2010151529 A 20100708.
15. Laurent D, Jullian V, Parenty A, Knibiehler M, Dorin D, Schmitt S, Lozach O, Lebouvier N, Frostin M, Alby F, Maurel S, Doerig C, Meijer L, Sauvain M. (2006). Antimalarial potential of xestoquinone, a protein kinase inhibitor isolated from a Vanuatu marine sponge Xestospongia sp. Bioorg Med Chem, 14, 4477-4482. (Pubitemid 44250770)
16. Missima F, da Silva Filho AA, Nunes GA, Bueno PC, de Sousa JP, Bastos JK, Sforcin JM. (2007). Effect of Baccharis dracunculifolia D.C. (Asteraceae) extracts and its isolated compounds on macrophage activation. J Pharm Pharmacol, 59, 463-468. (Pubitemid 47050912)
17. Muhammad I, Dunbar DC, Khan SI, Tekwani BL, Bedir E, Takamatsu S, Ferreira D, Walker LA. (2003). Antiparasitic alkaloids from Psychotria klugii. J Nat Prod, 66, 962-967. (Pubitemid 36909844)
18. Murata T, Miyase T, Muregi FW, Naoshima-Ishibashi Y, Umehara K, Warashina T, Kanou S, Mkoji GM, Terada M, Ishih A. (2008). Antiplasmodial triterpenoids from Ekebergia capensis. J Nat Prod, 71, 167-174. (Pubitemid 351362972)
19. Ndiaye M, Diatta W, Sy AN, Dièye AM, Faye B, Bassène E. (2008). Antidiabetic properties of aqueous barks extract of Parinari excelsa in alloxan-induced diabetic rats. Fitoterapia, 79, 267-270.
20. Page B, Page M, Noel C. (1993). A new fluorometric assay for cytotoxicity measurements in vitro. Int J Oncol, 3, 473-476. (Pubitemid 23271916)
21. Ridley RG, Hofheinz W, Matile H, Jaquet C, Dorn A, Masciadri R, Jolidon S, Richter WF, Guenzi A, Girometta MA, Urwyler H, Huber W, Thaithong S, Peters W. (1996). 4-Aminoquinoline analogs of chloroquine with shortened side chains retain activity against chloroquine-resistant Plasmodium falciparum. Antimicrob Agents Chemother, 40, 1846-1854. (Pubitemid 26277804)
22. Rocha LG, Almeida JR, Macêdo RO, Barbosa-Filho JM. (2005). A review of natural products with antileishmanial activity. Phytomedicine, 12, 514-535. (Pubitemid 40755130)
23. Snow RW, Guerra CA, Noor AM, Myint HY, Hay SI. (2005). The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature, 434, 214-217. (Pubitemid 40388051)
24. Sultana N, Nam HL. (2010). A new alkene glycoside from the leaves of Sasa quelpaertensis Nakai. Bull Korean Chem Soc, 31, 1088-1090.
25. Thaithong S, Beale GH. (1981). Resistance of ten Thai isolates of Plasmodium falciparum to chloroquine and pyrimethamine by in vitro tests. Trans R Soc Trop Med Hyg, 75, 271-273.
26. Trager W, Jensen JB. (1976). Human malaria parasites in continuous culture. Science, 193, 673-675.
27. Uys AC, Malan SF, van Dyk S, van Zyl RL. (2002). Antimalarial compounds from Parinari capensis. Bioorg Med Chem Lett, 12, 2167-2169. (Pubitemid 34804391)
28. Wei Y, Ma CM, Chen DY, Hattori M. (2008). Anti-HIV-1 protease triterpenoids from Stauntonia obovatifoliola Hayata subsp. intermedia. Phytochemistry, 69, 1875-1879.
29. Werawattanachai N, Kaewamatawong R. (2010). Chemical constituents from Parinari anamense. Biochem Syst Ecol, 38, 836-838.
30. Huber W, Koella JC. (1993). A comparison of three methods of estimating EC50 in studies of drug resistance of malaria parasites. Acta Trop, 55, 257-261.
31. Xiao-Qiang L, Jing-Lian W, Fei-Hua C, Chong L. (2008). Chemical constituents from leaves of Paulownia fortunei. Zhongyaocai, 31, 850-852.
32. Zhang X, Wu D, Zhou J, Pan R, Liu L, Peng L, Luo Y. (1993). The oleanane type triterpenes from the root of Tripterygium hypoglaucum. Yunnan Zhiwu Yanjiu, 15, 92-96.