New terpenoids from Maytenus apurimacensis as MDR reversal agents in the parasite Leishmania

Bioorganic and Medicinal Chemistry

Volumn 16, Issue 3, 2008, Pages 1425-1430

  Delgado Méndez, Paulino ^a   Herrera, Nora ^a   Chávez, Haydee ^b   Estévez Braun, Ana ^a,c   Ravelo, Ángel G ^a,c   Cortes, Fernando ^d   Castanys, Santiago ^d   Gamarro, Francisco ^d  

^a UNIVERSIDAD DE LA LAGUNA   (Spain)

^b Universidad Nacional San Luis Gonzaga   (Peru)

^c HOSPITAL UNIVERSITARIO NUESTRA SEÑORA DE CANDELARIA   (Spain)

^d INSTITUTO DE PARASITOLOGÍA Y BIOMEDICINA LÓPEZ NEYRA   (Spain)

Author keywords

Celastraceae; Dihydro agarofuran sesquiterpenes; Leishmania; Lupanes; Maytenus; MDR; Terpenoids

Indexed keywords

1BETA HYDROXY 3BETA CAFFEATE LUP 20(29) ENE; 8 ACETOXY 1,9 DIBENZOYLOXY 4 HYDROXY 6 NICOTYNOYLOXYDIHYDRO BETA AGAROFURAN; 8 ACETOXY 1,9 DIBENZOYLOXY 6 NICOTYNOYLOXYDIHYDRO BETA AGAROFURAN; TERPENOID; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CIRCULAR DICHROISM; DRUG ISOLATION; DRUG STRUCTURE; LEISHMANIA TROPICA; MAYTENUS APURIMACENSIS; MEDICINAL PLANT; MULTIDRUG RESISTANCE; PLANT ROOT; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS;

ANIMALS; ANTIPROTOZOAL AGENTS; DRUG RESISTANCE, MULTIPLE; LEISHMANIA; MAGNETIC RESONANCE SPECTROSCOPY; MAYTENUS; MOLECULAR STRUCTURE; STRUCTURE-ACTIVITY RELATIONSHIP; TERPENES;

CELASTRACEAE; LEISHMANIA TROPICA; MAYTENUS; PROTOZOA;

EID: 38849125592     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2007.10.071     Document Type: Article

References (37)

1. Newman D.J., Cragg G.M., and Snader K.M. J. Nat. Prod. 70 (2007) 461-477
2. Morel C.M. EMBO Rep. 4 (2003) S35-S38
3. Salem M.M., and Werbovetz K.A. Curr. Med. Chem. 13 (2006) 2571-2598
4. Takahashi M., Fuchino H., Sekita S., and Satake M. Phytother. Res. 18 (2004) 573-578
5. Fournet A., and Munoz V. Curr. Top. Med. Chem. 2 (2002) 1215-1237
6. Germonprez N., Maes L., Puyvelde L.V., Tri M.V., Tuan D.A., and De Kimpe N. J. Med. Chem. 48 (2005) 32-37
7. Wong I.L.K., Chan K.F., Burkett B.A., Zhao Y., Chai Y., Sun H., Chan T.H., and Chow L.M.C. Antimicrob. Agents Chemother. 51 (2007) 930-940
8. Croft S.L., Sundar S., and Fairlamb A.H. Clin. Microbiol. Rev. 19 (2006) 11-126
9. Pérez-Victoria J.M., Tincusi B.M., Jimenez I.A., Bazzocchi I.L., Gupta M.P., Castanys S., Gamarro F., and Ravelo A.G. J. Med. Chem. 42 (1999) 4388-4393
10. Kennedy M.L., Cortés-Selva F., Pérez-Victoria J.M., Jiménez I.A., González A.G., Muñoz O., Gamarro F., Casatanys S., and Ravelo A.G. J. Med. Chem. 44 (2001) 4668-4676
11. Cortés-Selva F.M., Campillo C.P., Reyes I.A., Jiménez S., Castanys I.L., Bazzocchi L., Pardo F., Gamarro A.G., and Ravelo A.G. J. Med. Chem. 47 (2004) 576-587
12. Muñoz-Martínez F., Mendoza C.R., Bazzocchi I.L., Castanys S., Jiménez I.A., and Gamarro F. J. Med. Chem. 48 (2005) 4266-4275
13. Betancor C., Freire R., González A.G., Pascard C., and Prangue T. Phytochemistry 19 (1980) 1989-1993
14. Fieser L.F. Experientia 6 (1950) 312-315
15. Nunez M.J., Lopez M.R., Jimenez I.A., Moujir L.M., Ravelo A.G., and Bazzocchi I.L. Tetrahedron Lett. 45 (2004) 7367-7370
16. Johnson A.P., Juby T., and King S.T. J. Chem. Soc. (1963) 2884
17. Shirota O., Morita H., Takeya K., and Itokawa H. J. Nat. Prod. 60 (1997) 111-115
18. Srivastava R.S., and Kulshreshtha D.K. Phytochemistry 27 (1988) 2378-3575
19. Gonzalez A.G., Gonzalez C.M., Ravelo A.G., Domínguez X.A., and Fraga B.M. J. Nat. Prod. 49 (1996) 148-150
20. González A.G., Ferro E.A., and Ravelo A.G. Phytochemistry 26 (1987) 2785-2787
21. Ganguly A.K., Govindachari T.R., Mohamed P.A., Rahim-Tulla A.D., and Viswanathan N. Tetrahedron 22 (1996) 1513-1519
22. Gamlath C.B., Gunaherath K.B., and Gunatilaka A.A.L. J. Chem. Soc. Perkin Trans. 1 (1987) 2849-2853
23. Shirota O., Morita H., Takeya K., and Itokawa H. J. Nat. Prod. 57 (1994) 1675-1681
24. Monache F., Marini-Bettolo G., Gonzalves de Lima O., D'Alburquerque I., and Barros J. J. Chem. Soc. Perkin Trans. 1 (1973) 2725-2728
25. González A.G., Alvarenga N., Rodríguez F.M., Ravelo A.G., Bazzocchi I., and Gupta M.P. Nat. Prod. Lett. 7 (1995) 209-218
26. Martin J.D. Tetrahedron 29 (1973) 2997-3000
27. Wenkert E., Baddeley G.V., Burfitt I.R., and Moreno L.N. Org. Magn. Reson. 11 (1978) 337-343
28. Chiquero M.J., Perez-Victoria J.M., O'Valle F., Gonzalez-Ros J.M., del Moral R.G., Ferragut J.A., Castanys S., and Gamarro F. Biochem Pharmacol. 55 (1998) 131-139
29. Perez-Victoria J.M., Perez-Victoria F.J., Parodi-Talice A., Jimenez I.A., Ravelo A.G., Castanys S., and Gamarro F. Antimicrob. Agents Chemother. 45 (2001) 2468-2474
30. Muñoz O., Peñaloza A., González A.G., Ravelo A.G., Bazzocchi I.L., and Alvarenga N.L. Studies in Natural Products Chemistry (1996), Elsevier Science Publisher, Amsterdam Vol 18, p 739
31. González A.G., Núñez P.M., Ravelo A.G., Sazatornil J.G., Vázquez J.T., Bazzocchi I.L., Morales E.Q., and Muñoz O. J. Chem. Soc. Perkin Trans 1 (1992) 1437-1441
32. Sugiura K., Shizuri Y., Hirata H., and Yamada K. Tetrahedron 23 (1982) 3465-3469
33. Chumkaev P.S., and Kato K. Chem. Pharm. Bull. 53 (2005) 95-96
34. Spengler I.C., Nogueiras C., Ravelo A.G., Jiménez I.A., and Romeu A.R. Afinidad 59 (2002) 237-241
35. Alvarenga N., and Ferro E. Fitoterapia 71 (2000) 719-721
36. Chen B., Duan H., and Takaishi Y. Phytochemistry 51 (1999) 683-687
37. Pan H., Lundgren L.N., and Andersson R. Phytochemistry 37 (1994) 795-799