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Volumn 80, Issue 8-9, 2014, Pages 719-722

Cytotoxic coumarins from toddalia asiatica

Author keywords

antimalarial; coumarin; cytotoxicity; Rutaceae; Toddalia asiatica

Indexed keywords

1,2 SECODIHYDROMETHYLUMBELLIFERONE METHYL ESTER; 4 O GERANYLCONIFERYL ALDEHYDE; 5 METHOXY 8 GERANYLOXYLPSORALEN; 5,7,8 TRIMETHOXYCOUMARIN; 8 GERANYLOXY 5,7 DIMETHYLOXYCOUMARIN; ANTIMALARIAL AGENT; ANTINEOPLASTIC AGENT; ARTANIN; COUMARIN DERIVATIVE; LEPTODACTYLONE; NELUMOL A; NORCHELERYTHRINE; PHELLOPTERIN; PLANT EXTRACT; TODDALOLACTONE; TODDALOLACTONE METHYL ETHER; TODDALOSIN; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

EID: 84903386592     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0034-1368568     Document Type: Article
Times cited : (23)

References (30)
  • 1
    • 80054912467 scopus 로고    scopus 로고
    • Cytotoxicity of chemical constituents from the stems of Dalbergia parviflora
    • Songsiang U., Hahnvajanawong C., Yenjai C. Cytotoxicity of chemical constituents from the stems of Dalbergia parviflora. Fitoterapia: 2011; 82 1169 1174
    • (2011) Fitoterapia , vol.82 , pp. 1169-1174
    • Songsiang, U.1    Hahnvajanawong, C.2    Yenjai, C.3
  • 2
    • 84884206175 scopus 로고    scopus 로고
    • Clauraila e from the roots of Clausena harmandiana and antifungal activity against Pythium insidiosum
    • Sriphana U., Thongsri Y., Prariyachatigul C., Pakawatchai C., Yenjai C. Clauraila E from the roots of Clausena harmandiana and antifungal activity against Pythium insidiosum. Arch Pharm Res: 2013; 36 1078 1083
    • (2013) Arch Pharm Res , vol.36 , pp. 1078-1083
    • Sriphana, U.1    Thongsri, Y.2    Prariyachatigul, C.3    Pakawatchai, C.4    Yenjai, C.5
  • 4
    • 84903398586 scopus 로고    scopus 로고
    • Ethnomedicinal, phytochemical and pharmacological profile of genus Toddalia
    • Kariuki H. N., Mwonjoria J. K. Ethnomedicinal, phytochemical and pharmacological profile of genus Toddalia. Phytopharmacology: 2013; 4 259 268
    • (2013) Phytopharmacology , vol.4 , pp. 259-268
    • Kariuki, H.N.1    Mwonjoria, J.K.2
  • 5
    • 84857115811 scopus 로고    scopus 로고
    • Antimicrobial activity of Ulopterol isolated from Toddalia asiatica (L.) Lam.: A traditional medicinal plant
    • Karunai Raj M., Balachandran C., Duraipandiyan V., Agastian P., Ignacimuthu S. Antimicrobial activity of Ulopterol isolated from Toddalia asiatica (L.) Lam.: a traditional medicinal plant. J Ethnopharm: 2012; 140 161 165
    • (2012) J Ethnopharm , vol.140 , pp. 161-165
    • Karunai Raj, M.1    Balachandran, C.2    Duraipandiyan, V.3    Agastian, P.4    Ignacimuthu, S.5
  • 6
    • 0027145403 scopus 로고
    • Toddaquinoline from Formosan Toddalia asiatica
    • Chen I. S., Tsai I. L., Wu S. J., Sheen W. S. Toddaquinoline from Formosan Toddalia asiatica. Phytochemistry: 1993; 34 1449 1451
    • (1993) Phytochemistry , vol.34 , pp. 1449-1451
    • Chen, I.S.1    Tsai, I.L.2    Wu, S.J.3    Sheen, W.S.4
  • 7
    • 0031127557 scopus 로고    scopus 로고
    • N-Cyclohexyl amides and a dimeric coumarin from Formosan Toddalia asiatica
    • Tsai I. L., Fang S. C., Ishikawa T., Chang C. T., Chen I. S. N -Cyclohexyl amides and a dimeric coumarin from Formosan Toddalia asiatica. Phytochemistry: 1997; 44 1383 1386
    • (1997) Phytochemistry , vol.44 , pp. 1383-1386
    • Tsai, I.L.1    Fang, S.C.2    Ishikawa, T.3    Chang, C.T.4    Chen, I.S.5
  • 9
    • 0032926724 scopus 로고    scopus 로고
    • Antimicrobial activity of the essential oil of Toddalia asiatica
    • Saxena V. K., Sharma R. N. Antimicrobial activity of the essential oil of Toddalia asiatica. Fitoterapia: 1999; 70 64 66
    • (1999) Fitoterapia , vol.70 , pp. 64-66
    • Saxena, V.K.1    Sharma, R.N.2
  • 11
    • 84866032128 scopus 로고    scopus 로고
    • Antidiabetic and antioxidant activities of Toddalia asiatica (L.) Lam. Leaves in streptozotocin induced diabetic rats
    • Irudayaraj S. S., Sunil C., Duraipandiyan V., Ignacimuthu S. Antidiabetic and antioxidant activities of Toddalia asiatica (L.) Lam. leaves in streptozotocin induced diabetic rats. J Ethnopharm: 2012; 143 515 523
    • (2012) J Ethnopharm , vol.143 , pp. 515-523
    • Irudayaraj, S.S.1    Sunil, C.2    Duraipandiyan, V.3    Ignacimuthu, S.4
  • 13
    • 84859834232 scopus 로고    scopus 로고
    • Nelumal A, the active principle from Ligularia nelumbifolia, is a novel farnesoid X receptor agonist
    • Epifano F., Genovese S., Squires E. J., Gray M. A. Nelumal A, the active principle from Ligularia nelumbifolia, is a novel farnesoid X receptor agonist. Bioorg Med Chem Lett: 2012; 22 3130 3135
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 3130-3135
    • Epifano, F.1    Genovese, S.2    Squires, E.J.3    Gray, M.A.4
  • 16
    • 70449670476 scopus 로고    scopus 로고
    • New geranyloxycoumarins from Toddalia asiatica
    • Wang F., Xu Y., Liu J. K. New geranyloxycoumarins from Toddalia asiatica. J Asian Nat Prod Res: 2009; 11 752 756
    • (2009) J Asian Nat Prod Res , vol.11 , pp. 752-756
    • Wang, F.1    Xu, Y.2    Liu, J.K.3
  • 17
    • 33847408822 scopus 로고    scopus 로고
    • Bioactive coumarins from Boenninghausenia sessilicarpa
    • Yang Q. Y., Tian X. Y., Fang W. S. Bioactive coumarins from Boenninghausenia sessilicarpa. J Asian Nat Prod Res: 2007; 9 59 65
    • (2007) J Asian Nat Prod Res , vol.9 , pp. 59-65
    • Yang, Q.Y.1    Tian, X.Y.2    Fang, W.S.3
  • 18
    • 0011237007 scopus 로고
    • The absolute stereochemistries of (+)-toddalolactone and its related chiral coumarins from Toddalia asiatica (L.) Lam. (T. Aculeata Pers.) and their optical purities
    • Ishii H., Kobayashi J. I., Sakurada E., Ishikawa T. The absolute stereochemistries of (+)-toddalolactone and its related chiral coumarins from Toddalia asiatica (L.) Lam. (T. aculeata Pers.) and their optical purities. J Chem Soc Perkin Trans: 1992; 1 1681 1684
    • (1992) J Chem Soc Perkin Trans , vol.1 , pp. 1681-1684
    • Ishii, H.1    Kobayashi, J.I.2    Sakurada, E.3    Ishikawa, T.4
  • 19
    • 57049111621 scopus 로고    scopus 로고
    • The structure-activity relationship between oxycoumarin derivatives showing inhibitory effects on iNOS in mouse macrophage RAW264.7 cells
    • Nakamura T., Kodama N., Oda M., Tsuchiya S., Arai Y., Kumamoto T., Ishikawa T., Ueno K., Yano S. The structure-activity relationship between oxycoumarin derivatives showing inhibitory effects on iNOS in mouse macrophage RAW264.7 cells. J Nat Med: 2009; 63 15 20
    • (2009) J Nat Med , vol.63 , pp. 15-20
    • Nakamura, T.1    Kodama, N.2    Oda, M.3    Tsuchiya, S.4    Arai, Y.5    Kumamoto, T.6    Ishikawa, T.7    Ueno, K.8    Yano, S.9
  • 20
    • 34250161839 scopus 로고    scopus 로고
    • Antiangiogenic versus cytotoxic activity in analogues of aeroplysinin-1
    • Cordoba R., Tormo N. S., Medarde A. F., Plumet J. Antiangiogenic versus cytotoxic activity in analogues of aeroplysinin-1. Bioorg Med Chem: 2007; 15 5300 5315
    • (2007) Bioorg Med Chem , vol.15 , pp. 5300-5315
    • Cordoba, R.1    Tormo, N.S.2    Medarde, A.F.3    Plumet, J.4
  • 21
    • 0032145208 scopus 로고    scopus 로고
    • Anti-platelet aggregation constituents from Formosan Toddalia asiatica
    • Tsai I. L., Wun M. F., Teng C. H., Ishikawa T., Chen I. S. Anti-platelet aggregation constituents from Formosan Toddalia asiatica. Phytochemistry: 1998; 48 1377 1382
    • (1998) Phytochemistry , vol.48 , pp. 1377-1382
    • Tsai, I.L.1    Wun, M.F.2    Teng, C.H.3    Ishikawa, T.4    Chen, I.S.5
  • 22
    • 79959905752 scopus 로고    scopus 로고
    • Growth inhibitory activities of oxyprenylated and non-prenylated naturally occurring phenylpropanoids in cancer cell lines
    • Bruyère C., Genovese S., Lallemand B., Ionescu-Motatu A., Curini M., Kiss R., Epifano F. Growth inhibitory activities of oxyprenylated and non-prenylated naturally occurring phenylpropanoids in cancer cell lines. Bioorg Med Chem Lett: 2011; 21 4174 4179
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 4174-4179
    • Bruyère, C.1    Genovese, S.2    Lallemand, B.3    Ionescu-Motatu, A.4    Curini, M.5    Kiss, R.6    Epifano, F.7
  • 23
    • 84893739634 scopus 로고    scopus 로고
    • Anti-tumor effects of various furocoumarins isolated from the roots, seeds and fruits of Angelica and Cnidium species under ultraviolet A irradiation
    • Sumiyoshi M., Sakanaka M., Taniguchi M., Baba K., Kimura Y. Anti-tumor effects of various furocoumarins isolated from the roots, seeds and fruits of Angelica and Cnidium species under ultraviolet A irradiation. J Nat Med: 2014; 68 83 94
    • (2014) J Nat Med , vol.68 , pp. 83-94
    • Sumiyoshi, M.1    Sakanaka, M.2    Taniguchi, M.3    Baba, K.4    Kimura, Y.5
  • 26
    • 0033856957 scopus 로고    scopus 로고
    • Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity
    • Brien J. O., Wilson I., Orton T., Pognan F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur J Biochem: 2000; 267 5421 5426
    • (2000) Eur J Biochem , vol.267 , pp. 5421-5426
    • Brien, J.O.1    Wilson, I.2    Orton, T.3    Pognan, F.4
  • 27
    • 0033589372 scopus 로고    scopus 로고
    • GFP-expressing mammalian cells for fast, sensitive, noninvasive cell growth assessment in a kinetic mode
    • Hunt L., Jordan M., De Jesus M., Wurm F. M. GFP-expressing mammalian cells for fast, sensitive, noninvasive cell growth assessment in a kinetic mode. Biotechnol Bioeng: 1999; 65 201 205
    • (1999) Biotechnol Bioeng , vol.65 , pp. 201-205
    • Hunt, L.1    Jordan, M.2    De Jesus, M.3    Wurm, F.M.4
  • 28
    • 0017311840 scopus 로고
    • Human malaria parasites in continuous culture
    • Trage W., Jensen J. B. Human malaria parasites in continuous culture. Science: 1976; 193 673 675
    • (1976) Science , vol.193 , pp. 673-675
    • Trage, W.1    Jensen, J.B.2
  • 29
    • 0018606732 scopus 로고
    • Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
    • Desjardins R. E., Canfield C. J., Haynes J. D., Chulay J. D. Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique. Antimicrob Agents Chemother: 1979; 16 710 718
    • (1979) Antimicrob Agents Chemother , vol.16 , pp. 710-718
    • Desjardins, R.E.1    Canfield, C.J.2    Haynes, J.D.3    Chulay, J.D.4
  • 30
    • 0030903133 scopus 로고    scopus 로고
    • Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium
    • Collins L. A., Franzblau S. G. Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium. Antimicrob Agents Chemother: 1997; 41 1004 1009
    • (1997) Antimicrob Agents Chemother , vol.41 , pp. 1004-1009
    • Collins, L.A.1    Franzblau, S.G.2


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