메뉴 건너뛰기




Volumn 31, Issue 3, 2011, Pages 335-343

Cytotoxic effect of some natural compounds isolated: From Lauraceae plants and synthetic derivatives

Author keywords

Biological products; Diterpenes; In vitro; Lauraceae; Straining

Indexed keywords

LAURACEAE; NECTANDRA AMAZONUM; OCOTEA; PLEUROTHYRIUM CINEREUM;

EID: 84863189382     PISSN: 01204157     EISSN: None     Source Type: Journal    
DOI: 10.7705/biomedica.v31i3.347     Document Type: Article
Times cited : (14)

References (37)
  • 1
    • 63149118507 scopus 로고    scopus 로고
    • Ready for a comeback of natural products in oncology
    • Bailly C. Ready for a comeback of natural products in oncology. Biochem Pharmacol. 2009;77:1447-57.
    • (2009) Biochem Pharmacol , vol.77 , pp. 1447-1457
    • Bailly, C.1
  • 2
    • 0035829014 scopus 로고    scopus 로고
    • In vitro bioassays for anticancer drug screening: Effects of cell concentration and other assay parameters on growth inhibitory activity
    • Lieberman MM, Patterson GM, Moore RE. In vitro bioassays for anticancer drug screening: Effects of cell concentration and other assay parameters on growth inhibitory activity. Cancer Lett. 2001;173:21-9.
    • (2001) Cancer Lett , vol.173 , pp. 21-29
    • Lieberman, M.M.1    Patterson, G.M.2    Moore, R.E.3
  • 3
    • 65049089754 scopus 로고    scopus 로고
    • Natural compounds for cancer treatment and prevention
    • Nobili S, Lippi D, Witort E. Natural compounds for cancer treatment and prevention. Pharmacol Res. 2009;59:365-78.
    • (2009) Pharmacol Res , vol.59 , pp. 365-378
    • Nobili, S.1    Lippi, D.2    Witort, E.3
  • 4
    • 0033920537 scopus 로고    scopus 로고
    • Anti-cancer drug discovery and development in Brazil: Targeted plant collection as a rational strategy to acquire candidate anti-cancer compounds
    • Mans DR, Da Rocha A, Schwartsmann G. Anti-cancer drug discovery and development in Brazil: Targeted plant collection as a rational strategy to acquire candidate anti-cancer compounds. Oncologist. 2000;5:185-99.
    • (2000) Oncologist , vol.5 , pp. 185-199
    • Mans, D.R.1    Da Rocha, A.2    Schwartsmann, G.3
  • 5
    • 84873609726 scopus 로고    scopus 로고
    • Organización Mundial de la Salud. Descriptive note number 297
    • Organización Mundial de la Salud. Descriptive note number 297: Cancer. Geneva: WHO; 2009.
    • (2009) Cancer. Geneva: WHO
  • 6
    • 84873608620 scopus 로고    scopus 로고
    • Instituto Nacional de Cancerología. Anuario estadístico 2005Bogotá: Legis
    • Instituto Nacional de Cancerología. Anuario estadístico 2005: Por el control del cáncer. Volumen 3. Bogotá: Legis; 2007.
    • (2007) Por el control del cáncer , vol.3
  • 7
    • 0001380216 scopus 로고
    • Lignans, neolignans and related compounds
    • Whiting DA. Lignans, neolignans and related compounds. Nat Prod Rep. 1985;2:191-211.
    • (1985) Nat Prod Rep , vol.2 , pp. 191-211
    • Whiting, D.A.1
  • 8
    • 11844249453 scopus 로고    scopus 로고
    • Lignans and neolignans as lead compounds
    • Apers S, Vlietinck A, Pieters L. Lignans and neolignans as lead compounds. Phytochem Rev. 2003;2:201-17.
    • (2003) Phytochem Rev , vol.2 , pp. 201-217
    • Apers, S.1    Vlietinck, A.2    Pieters, L.3
  • 10
    • 0032145353 scopus 로고    scopus 로고
    • Additional cytotoxic neolignans from Persea obovatifolia
    • Tsai IL, Hsieh CF, Duh CY. Additional cytotoxic neolignans from Persea obovatifolia. Phytochemistry. 1998;48:1371-5.
    • (1998) Phytochemistry , vol.48 , pp. 1371-1375
    • Tsai, I.L.1    Hsieh, C.F.2    Duh, C.Y.3
  • 11
    • 11844287538 scopus 로고    scopus 로고
    • Antileishmanial activity, cytotoxicity and QSAR analysis of synthetic dihydrobenzofuran lignans and related benzofurans
    • van Miert S, van Dyck S, Schmidt TJ, Brun R, Vlietinck A, Lemiére G, et al. Antileishmanial activity, cytotoxicity and QSAR analysis of synthetic dihydrobenzofuran lignans and related benzofurans. Bioorg Med Chem. 2005;13:661-9.
    • (2005) Bioorg Med Chem , vol.13 , pp. 661-669
    • van Miert, S.1    van Dyck, S.2    Schmidt, T.J.3    Brun, R.4    Vlietinck, A.5    Lemiére, G.6
  • 13
    • 1342269078 scopus 로고    scopus 로고
    • Antibacterial activity of extracts and neolignans from Piper regnellii (Miq) C. DC. var. pallescens (C. DC.) Yunck
    • Pessini GL, Filho BPD, Nakamura CV, Cortez DA. Antibacterial activity of extracts and neolignans from Piper regnellii (Miq.) C. DC. var. pallescens (C. DC.) Yunck. Mem Inst Oswaldo Cruz. 2003;98:1115-20.
    • (2003) Mem Inst Oswaldo Cruz , vol.98 , pp. 1115-1120
    • Pessini, G.L.1    Filho, B.P.D.2    Nakamura, C.V.3    Cortez, D.A.4
  • 14
    • 0344360434 scopus 로고
    • PAF antagonistic benzofuran neolignans from Piper kadsura
    • Ma Y, Han GQ, Wang YY. PAF antagonistic benzofuran neolignans from Piper kadsura. Acta Pharm Sin. 1993;28:370-3.
    • (1993) Acta Pharm Sin , vol.28 , pp. 370-373
    • Ma, Y.1    Han, G.Q.2    Wang, Y.Y.3
  • 15
    • 0346753438 scopus 로고    scopus 로고
    • The stereoselective synthesis of neolignans
    • Sefkow M. The stereoselective synthesis of neolignans. Synthesis. 2003;17:2595-625.
    • (2003) Synthesis , vol.17 , pp. 2595-2625
    • Sefkow, M.1
  • 16
    • 0345300793 scopus 로고
    • PAF receptor antagonistic principles from Chinese traditional drugs
    • Han G. PAF receptor antagonistic principles from Chinese traditional drugs. Progr Nat Sci. 1995;5:299-306.
    • (1995) Progr Nat Sci , vol.5 , pp. 299-306
    • Han, G.1
  • 17
    • 0000594573 scopus 로고
    • Four phenolic neolignans from Magnolia liliflora
    • Iida T, Ito K. Four phenolic neolignans from Magnolia liliflora. Phytochemistry. 1983;22:763-6.
    • (1983) Phytochemistry , vol.22 , pp. 763-766
    • Iida, T.1    Ito, K.2
  • 18
    • 0032864662 scopus 로고    scopus 로고
    • 2,3-dihydrobenzofuran neolignans from Aristolochia pubescens
    • Nascimento IR, Lopes LM. 2,3-dihydrobenzofuran neolignans from Aristolochia pubescens. Phytochemistry. 1999;52:345-50.
    • (1999) Phytochemistry , vol.52 , pp. 345-350
    • Nascimento, I.R.1    Lopes, L.M.2
  • 19
    • 69249091444 scopus 로고    scopus 로고
    • PAF-antagonistic bicyclo[3 2. 1]octanoid neolignans from leaves of Ocotea macrophylla Kunth. (Lauraceae)
    • Coy-Barrera ED, Cuca-Suárez LE, Sefkow M. PAF-antagonistic bicyclo[3.2.1]octanoid neolignans from leaves of Ocotea macrophylla Kunth. (Lauraceae). Phytochemistry. 2009;70:1309-14.
    • (2009) Phytochemistry , vol.70 , pp. 1309-1314
    • Coy-Barrera, E.D.1    Cuca-Suárez, L.E.2    Sefkow, M.3
  • 20
    • 47349091343 scopus 로고    scopus 로고
    • Chemical constituents from Pleurothyrium cinereum (van der Werff) (Lauraceae) from Colombia
    • Coy ED, Cuca LE. Chemical constituents from Pleurothyrium cinereum (van der Werff) (Lauraceae) from Colombia. Biochem Syst Ecol. 2008;36:674-7.
    • (2008) Biochem Syst Ecol , vol.36 , pp. 674-677
    • Coy, E.D.1    Cuca, L.E.2
  • 21
    • 68049104317 scopus 로고    scopus 로고
    • Macrophyllin-type bicyclo[3 2. 1]octanoid neolignans from the leaves of Pleurothyrium cinereum
    • Coy ED, Cuca LE, Sefkow M. Macrophyllin-type bicyclo[3.2.1]octanoid neolignans from the leaves of Pleurothyrium cinereum. J Nat Prod. 2009;72:1245-8.
    • (2009) J Nat Prod , vol.72 , pp. 1245-1248
    • Coy, E.D.1    Cuca, L.E.2    Sefkow, M.3
  • 23
    • 66949167785 scopus 로고    scopus 로고
    • Three New 7.3' 8. 5'-connected bicyclo[3. 2. 1]octanoids and other neolignans from leaves of Nectandra amazonum NEES. (Lauraceae)
    • Coy ED, Cuca LE. Three New 7.3',8.5'-connected bicyclo[3.2.1]octanoids and other neolignans from leaves of Nectandra amazonum NEES. (Lauraceae). Chem Pharm Bull. 2009;57:639-42.
    • (2009) Chem Pharm Bull , vol.57 , pp. 639-642
    • Coy, E.D.1    Cuca, L.E.2
  • 25
    • 77951825300 scopus 로고    scopus 로고
    • One-pot Pd-catalyzed synthesis of trans-dihydrobenzofurans from o-aminophenols
    • Coy ED, Jovanovic L, Sefkow M. One-pot, Pd-catalyzed synthesis of trans-dihydrobenzofurans from o-aminophenols. Org Lett. 2010;12:1976-9.
    • (2010) Org Lett , vol.12 , pp. 1976-1979
    • Coy, E.D.1    Jovanovic, L.2    Sefkow, M.3
  • 26
    • 0001557536 scopus 로고
    • Diazomethane
    • Collection. New York: Wiley
    • Arndt F. Diazomethane. In: Organic syntheses. Collection Volume 2. New York: Wiley; 1943. p. 165.
    • (1943) Organic syntheses , vol.165 , pp. 2
    • Arndt, F.1
  • 28
    • 39049175269 scopus 로고    scopus 로고
    • Caracterización del perfil de sensibilidad de un panel de líneas celulares para valoración de citotoxicidad in vitro
    • León CJ, Gómez SM, Morantes SJ, Cordero CP, Aristizabal FA. Caracterización del perfil de sensibilidad de un panel de líneas celulares para valoración de citotoxicidad in vitro. Biomédica. 2006;26:161-8.
    • (2006) Biomédica , vol.26 , pp. 161-168
    • León, C.J.1    Gómez, S.M.2    Morantes, S.J.3    Cordero, C.P.4    Aristizabal, F.A.5
  • 29
    • 77951071582 scopus 로고    scopus 로고
    • Comparison of resazurin and MTT methods on studies of citotoxicity in human tumor cell lines
    • Escobar L, Rivera A, Aristizabal F. Comparison of resazurin and MTT methods on studies of citotoxicity in human tumor cell lines. Vitae. 2010;17:67-74.
    • (2010) Vitae , vol.17 , pp. 67-74
    • Escobar, L.1    Rivera, A.2    Aristizabal, F.3
  • 30
    • 77955101324 scopus 로고    scopus 로고
    • Fluorometric assay for cell proliferation in human tumor cell lines application
    • Escobar L, Aristizabal F. Fluorometric assay for cell proliferation in human tumor cell lines application. Vitae. 2010;17:173-80.
    • (2010) Vitae , vol.17 , pp. 173-180
    • Escobar, L.1    Aristizabal, F.2
  • 31
    • 1542750825 scopus 로고    scopus 로고
    • Evaluación preliminar in vitro de citotoxicidad de extractos vegetales sobre líneas derivadas de tumores humanos, empleando dos métodos colorimétricos
    • Cordero CP, Aristizabal FA. Evaluación preliminar in vitro de citotoxicidad de extractos vegetales sobre líneas derivadas de tumores humanos, empleando dos métodos colorimétricos. Rev Colomb Biotecnol. 2002;4:100-6.
    • (2002) Rev Colomb Biotecnol , vol.4 , pp. 100-106
    • Cordero, C.P.1    Aristizabal, F.A.2
  • 33
    • 0035993557 scopus 로고    scopus 로고
    • The cytotoxic and embryotoxic effects of kaurenoic acid, a diterpene isolated from Copaifera langsdorffii oleo-resin
    • Costa-Lotufo LV, Cunha GM, Farias PA, Viana GS, Cunha KM, Pessoa C, et al. The cytotoxic and embryotoxic effects of kaurenoic acid, a diterpene isolated from Copaifera langsdorffii oleo-resin. Toxicon. 2002;40:1231-4.
    • (2002) Toxicon , vol.40 , pp. 1231-1234
    • Costa-Lotufo, L.V.1    Cunha, G.M.2    Farias, P.A.3    Viana, G.S.4    Cunha, K.M.5    Pessoa, C.6
  • 34
    • 37549007617 scopus 로고    scopus 로고
    • Cytotoxic and apoptosis-inducing effect of ent-15-oxo-kaur-16-en-19-oic acid, a derivative of grandiflorolic acid from Espeletia schultzii
    • Ruiz Y, Rodríguez J, Arvelo F, Usubillaga A, Monsalve M, Galindo-Castro I. Cytotoxic and apoptosis-inducing effect of ent-15-oxo-kaur-16-en-19-oic acid, a derivative of grandiflorolic acid from Espeletia schultzii. Phytochemistry. 2008;69:432-8.
    • (2008) Phytochemistry , vol.69 , pp. 432-438
    • Ruiz, Y.1    Rodríguez, J.2    Arvelo, F.3    Usubillaga, A.4    Monsalve, M.5    Galindo-Castro, I.6
  • 35
    • 0036294701 scopus 로고    scopus 로고
    • ent-Kaur-16-en-19-oic acid, a KB cells cytotoxic diterpenoid from Elaeoselinum foetidum
    • Mongelli E, Pomilio AB, Sánchez JB, Guerra FM, Massanet GM. ent-Kaur-16-en-19-oic acid, a KB cells cytotoxic diterpenoid from Elaeoselinum foetidum. Phytother Res. 2002;16:387-8.
    • (2002) Phytother Res , vol.16 , pp. 387-388
    • Mongelli, E.1    Pomilio, A.B.2    Sánchez, J.B.3    Guerra, F.M.4    Massanet, G.M.5
  • 36
    • 77951129499 scopus 로고    scopus 로고
    • The first diastereoselective synthesis of cinerins A-C, PAF-antagonistic macrophyllin-type bicyclo[3.2.1]octane neolignans, using a novel Pd-catalysed oxyarylation
    • Coy ED, Cuca LE, Sefkow M. The first diastereoselective synthesis of cinerins A-C, PAF-antagonistic macrophyllin-type bicyclo[3.2.1]octane neolignans, using a novel Pd-catalysed oxyarylation. Org Biomol Chem. 2010;8:2003-5.
    • (2010) Org Biomol Chem , vol.8 , pp. 2003-2005
    • Coy, E.D.1    Cuca, L.E.2    Sefkow, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.