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Volumn 114, Issue , 2016, Pages 1-6

Corrigendum to “Structural elucidation and evaluation of multidrug-resistance modulatory capability of Amarissinins A-C, diterpenes derived from Salvia amarissima” [Fitoterapia 114 (2016) 1–6](S0367326X16301861)(10.1016/j.fitote.2016.08.007);Structural elucidation and evaluation of multidrug-resistance modulatory capability of amarissinins A–C, diterpenes derived from Salvia amarissima

Author keywords

Clerodane diterpenes; Cytotoxic; Lamiaceae; MDR modulation; Salvia amarissima

Indexed keywords

AMARISSININ A; AMARISSININ B; AMARISSININ C; CYTOTOXIC AGENT; DITERPENE; PLANT EXTRACT; RESERPINE; UNCLASSIFIED DRUG; VINBLASTINE; ANTINEOPLASTIC AGENT; CLERODANE DERIVATIVE;

EID: 84982296150     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2016.11.001     Document Type: Erratum
Times cited : (25)

References (22)
  • 3
    • 84874108043 scopus 로고    scopus 로고
    • Medicinal plant complexes of Salvia subgenus Calosphace: an ethnobotanical study of new world sages
    • [3] Jenks, A.A., Kim, S.C., Medicinal plant complexes of Salvia subgenus Calosphace: an ethnobotanical study of new world sages. J. Ethnopharmacol. 146 (2013), 214–224.
    • (2013) J. Ethnopharmacol. , vol.146 , pp. 214-224
    • Jenks, A.A.1    Kim, S.C.2
  • 4
    • 84943582416 scopus 로고    scopus 로고
    • Antiamoebic and antigiardial activity of clerodane diterpenes from Mexican Salvia species used to treatment of diarrhea
    • [4] Calzada, F., Bautista, E., Yépez-Mulia, L., García-Hernández, N., Ortega, A., Antiamoebic and antigiardial activity of clerodane diterpenes from Mexican Salvia species used to treatment of diarrhea. Phytother. Res. 29 (2015), 1600–1604.
    • (2015) Phytother. Res. , vol.29 , pp. 1600-1604
    • Calzada, F.1    Bautista, E.2    Yépez-Mulia, L.3    García-Hernández, N.4    Ortega, A.5
  • 5
    • 84899557625 scopus 로고    scopus 로고
    • 5,10-seco-neoclerodanes from Salvia microphylla
    • [5] Bautista, E., Toscano, R.A., Ortega, A., 5,10-seco-neoclerodanes from Salvia microphylla. J. Nat. Prod. 77 (2014), 1088–1092.
    • (2014) J. Nat. Prod. , vol.77 , pp. 1088-1092
    • Bautista, E.1    Toscano, R.A.2    Ortega, A.3
  • 7
    • 84880003634 scopus 로고    scopus 로고
    • Microphyllandiolide, a new diterpene with an unprecedented skeleton from Salvia microphylla
    • [7] Bautista, E., Toscano, R.A., Ortega, A., Microphyllandiolide, a new diterpene with an unprecedented skeleton from Salvia microphylla. Org. Lett. 15 (2013), 3210–3213.
    • (2013) Org. Lett. , vol.15 , pp. 3210-3213
    • Bautista, E.1    Toscano, R.A.2    Ortega, A.3
  • 8
    • 82255164544 scopus 로고    scopus 로고
    • Structure of salvioccidentalin, a diterpenoid with a rearranged neoclerodane skeleton from Salvia occidentalis
    • [8] Jaime-Vasconcelos, M.A., Frontana-Uribe, B.A., Morales-Serna, J.A., Salmón, M., Cárdenas, J., Structure of salvioccidentalin, a diterpenoid with a rearranged neoclerodane skeleton from Salvia occidentalis. Molecules 16 (2011), 9109–9115.
    • (2011) Molecules , vol.16 , pp. 9109-9115
    • Jaime-Vasconcelos, M.A.1    Frontana-Uribe, B.A.2    Morales-Serna, J.A.3    Salmón, M.4    Cárdenas, J.5
  • 9
    • 84861534074 scopus 로고    scopus 로고
    • Neo-clerodane diterpenes from Salvia herbacea
    • [9] Bautista, E., Maldonado, E., Ortega, A., Neo-clerodane diterpenes from Salvia herbacea. J. Nat. Prod. 75 (2012), 951–958.
    • (2012) J. Nat. Prod. , vol.75 , pp. 951-958
    • Bautista, E.1    Maldonado, E.2    Ortega, A.3
  • 10
    • 84928788443 scopus 로고    scopus 로고
    • Pharmacogenomic characterization of cytotoxic compounds from Salvia officinalis in cancer cells
    • [10] Kadioglu, O., Efferth, T., Pharmacogenomic characterization of cytotoxic compounds from Salvia officinalis in cancer cells. J. Nat. Prod. 78 (2015), 762–775.
    • (2015) J. Nat. Prod. , vol.78 , pp. 762-775
    • Kadioglu, O.1    Efferth, T.2
  • 11
    • 84891530348 scopus 로고    scopus 로고
    • Elicitors from the endophytic fungus Trichoderma atroviride promote Salvia miltiorrhiza hairy root growth and tanshinone biosynthesis
    • [11] Ming, Q., Su, C., Zheng, C., Jia, M., Zhang, Q., Zhang, H., Rahman, K., Han, T., Qin, L., Elicitors from the endophytic fungus Trichoderma atroviride promote Salvia miltiorrhiza hairy root growth and tanshinone biosynthesis. J. Exp. Bot. 64 (2013), 5687–5694.
    • (2013) J. Exp. Bot. , vol.64 , pp. 5687-5694
    • Ming, Q.1    Su, C.2    Zheng, C.3    Jia, M.4    Zhang, Q.5    Zhang, H.6    Rahman, K.7    Han, T.8    Qin, L.9
  • 12
    • 13144272132 scopus 로고
    • The diterpenoid constituents of Salvia fulgens and Salvia microphylla
    • [12] Esquivel, B., Cárdenas, J., Rodríguez-Hahn, L., The diterpenoid constituents of Salvia fulgens and Salvia microphylla. J. Nat. Prod. 50 (1987), 738–740.
    • (1987) J. Nat. Prod. , vol.50 , pp. 738-740
    • Esquivel, B.1    Cárdenas, J.2    Rodríguez-Hahn, L.3
  • 13
    • 0346908504 scopus 로고
    • The pimarane-type diterpenoids of Salvia microphylla var. neurepia
    • [13] Esquivel, B., Martínez, N.S., Cárdenas, J., Ramamoorthy, T.P., The pimarane-type diterpenoids of Salvia microphylla var. neurepia. Planta Med. 55 (1989), 62–63.
    • (1989) Planta Med. , vol.55 , pp. 62-63
    • Esquivel, B.1    Martínez, N.S.2    Cárdenas, J.3    Ramamoorthy, T.P.4
  • 14
  • 16
    • 84935049174 scopus 로고    scopus 로고
    • Teotihuacanin, a diterpene with an unnusual spiro-10/6 system from Salvia amarissima with potent modulatory activity of multidrug resistance in cancer cells
    • [16] Bautista, E., Fragoso-Serrano, M., Toscano, R.A., García-Peña, M.R., Ortega, A., Teotihuacanin, a diterpene with an unnusual spiro-10/6 system from Salvia amarissima with potent modulatory activity of multidrug resistance in cancer cells. Org. Lett. 17 (2015), 3280–3282.
    • (2015) Org. Lett. , vol.17 , pp. 3280-3282
    • Bautista, E.1    Fragoso-Serrano, M.2    Toscano, R.A.3    García-Peña, M.R.4    Ortega, A.5
  • 18
  • 21
    • 33745006271 scopus 로고    scopus 로고
    • Precise absolute-structure determination in light-atom crystals
    • [21] Parsons, S., Flack, H., Precise absolute-structure determination in light-atom crystals. Acta Crystallogr., A60, 2004, s61.
    • (2004) Acta Crystallogr. , vol.A60 , pp. s61
    • Parsons, S.1    Flack, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.