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Volumn 12, Issue 5, 2014, Pages 2515-2525

Four new jacaranone analogs from the fruits of a Beibu Gulf mangrove Avicennia marina

Author keywords

Antioxidant; Avicennia marina; Chlorocornoside; Cornoside; Jacaranone analogs; Marinoid

Indexed keywords

ANTIOXIDANT; AVICENNIA MARINA EXTRACT; CHLOROCORNOSIDE; DRUG METABOLITE; HALOGEN; JACARANONE DERIVATIVE; MARINOID F; MARINOID G; MARINOID H; MARINOID I; PLANT EXTRACT; QUERCETIN; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; BENZOQUINONE DERIVATIVE; JACARANONE;

EID: 84901402071     PISSN: None     EISSN: 16603397     Source Type: Journal    
DOI: 10.3390/md12052515     Document Type: Article
Times cited : (19)

References (26)
  • 1
    • 48549107460 scopus 로고    scopus 로고
    • Structure elucidation of five new iridoid glucosides from the leaves of Avicennia marina
    • Sun, Y.; Ouyang, J.; Deng, Z.W.; Li, Q.S.; Lin, W.H. Structure elucidation of five new iridoid glucosides from the leaves of Avicennia marina. Magn. Reson. Chem. 2008, 46, 638-642.
    • (2008) Magn. Reson. Chem. , vol.46 , pp. 638-642
    • Sun, Y.1    Ouyang, J.2    Deng, Z.W.3    Li, Q.S.4    Lin, W.H.5
  • 2
    • 0027321663 scopus 로고
    • Phenylpropanoid glycosides from Avicennia marina
    • Fauvel, M.T.; Taoubi, K.; Gleye, J.; Fourasté, I. Phenylpropanoid glycosides from Avicennia marina. Planta Med. 1993, 59, 387. (Pubitemid 23238240)
    • (1993) Planta Medica , vol.59 , Issue.4 , pp. 387
    • Fauvel, M.T.1    Taoubi, K.2    Gleye, J.3    Fouraste, I.4
  • 3
    • 0000133843 scopus 로고
    • Iridoid glucosides in Avicennia marina
    • Konig, G.; Rimpler, H. Iridoid glucosides in Avicennia marina. Phytochemistry 1985, 24, 1245-1248.
    • (1985) Phytochemistry , vol.24 , pp. 1245-1248
    • Konig, G.1    Rimpler, H.2
  • 4
    • 33746867914 scopus 로고    scopus 로고
    • Iridoid glucosides and flavones from the aerial parts of Avicennia marina
    • Feng, Y.; Li, X.M.; Duan, X.J.; Wang, B.G. Iridoid glucosides and flavones from the aerial parts of Avicennia marina. Chem. Biodivers. 2006, 3, 799-806.
    • (2006) Chem. Biodivers. , vol.3 , pp. 799-806
    • Feng, Y.1    Li, X.M.2    Duan, X.J.3    Wang, B.G.4
  • 6
    • 0034071005 scopus 로고    scopus 로고
    • Chemical constituents of Avicennia alba. Isolation and structural elucidation of new naphthoquinones and their analogues
    • Ito, C.; Katsuno, S.; Kondo, Y.; Tan, H.T.W.; Furukawa, H. Chemical constituents of Avicennia alba. Isolation and structural elucidation of new naphthoquinones and their analogues. Chem. Pharm. Bull. 2000, 48, 339-343. (Pubitemid 30187245)
    • (2000) Chemical and Pharmaceutical Bulletin , vol.48 , Issue.3 , pp. 339-343
    • Ito, C.1    Katsuno, S.2    Kondo, Y.3    Tan, H.T.-W.4    Furukawa, H.5
  • 8
    • 0034213978 scopus 로고    scopus 로고
    • New flavonoids from Avicennia marina
    • DOI 10.1016/S0367-326X(99)00169-0, PII S0367326X99001690
    • Sharaf, M.; El-Ansari, M.A.; Saleh, N.A.M. New flavonoids from Avicennia marina. Fitoterapia 2000, 71, 274-277. (Pubitemid 30323678)
    • (2000) Fitoterapia , vol.71 , Issue.3 , pp. 274-277
    • Sharaf, M.1    El-Ansari, M.A.2    Saleh, N.A.M.3
  • 9
    • 42549172226 scopus 로고    scopus 로고
    • New abietane diterpenoids from the mangrove Avicennia marina
    • DOI 10.1055/s-2008-1034318
    • Han, L.; Huang, X.S.; Dahse, H.M.; Moellmann, U.; Grabley, S.; Lin, W.H.; Sattler, I. New abietane diterpenoids from the mangrove Avicennia marina. Planta Med. 2008, 74, 432-437. (Pubitemid 351578804)
    • (2008) Planta Medica , vol.74 , Issue.4 , pp. 432-437
    • Han, L.1    Huang, X.2    Dahse, H.-M.3    Moellmann, U.4    Grabley, S.5    Lin, W.6    Sattler, I.7
  • 10
    • 0343619705 scopus 로고
    • Regiospecific nucleophilic aromatic-substitution - Conjugate addition of active methylene-compounds to quinone monoacetals and aromatization of the adducts
    • Parker, K.A.; Kang, S.K. Regiospecific nucleophilic aromatic-substitution - Conjugate addition of active methylene-compounds to quinone monoacetals and aromatization of the adducts. J. Org. Chem. 1980, 45, 1218-1224.
    • (1980) J. Org. Chem. , vol.45 , pp. 1218-1224
    • Parker, K.A.1    Kang, S.K.2
  • 11
    • 84987265531 scopus 로고
    • Carbon magnetic-resonance spectra of α, β, γ, σ- and α, β, α′, β′-unsaturated-ketones
    • Hollenst, R.; Philipsb, W.V. Carbon magnetic-resonance spectra of α, β, γ, σ- and α, β, α′, β′-unsaturated-ketones. Helv. Chim. Acta 1972, 55, 2030-2044.
    • (1972) Helv. Chim. Acta , vol.55 , pp. 2030-2044
    • Hollenst, R.1    Philipsb, W.V.2
  • 13
    • 0021738437 scopus 로고
    • Structures of rengyol, rengyoxide, and rengyolone, new cyclohexylethane derivatives from Forsythia suspensa fruits
    • Endo, K.; Hikino, H. Structures of rengyol, rengyoxide, and rengyolone, new cyclohexylethane derivatives from Forsythia suspensa fruits. Can. J. Chem. 1984, 62, 2011-2014. (Pubitemid 15220201)
    • (1984) Canadian Journal of Chemistry , vol.62 , Issue.10 , pp. 2011-2014
    • Endo, K.1    Hikino, H.2
  • 14
    • 0000925209 scopus 로고
    • Isolation of cornoside from Olea europaea and its transformation into halleridone
    • Bianco, A.; Scalzo, R.L.; Scarpati, M.L. Isolation of cornoside from Olea europaea and its transformation into halleridone. Phytochemistry 1993, 32, 445-457.
    • (1993) Phytochemistry , vol.32 , pp. 445-457
    • Bianco, A.1    Scalzo, R.L.2    Scarpati, M.L.3
  • 15
    • 0000133193 scopus 로고
    • A quinol glucoside isolated from Cornus species
    • Jensen, S.R.; Kjaer, A.; Nielsen, B.J. A quinol glucoside isolated from Cornus species. Acta Chem. Scand. 1973, 27, 367-369.
    • (1973) Acta Chem. Scand. , vol.27 , pp. 367-369
    • Jensen, S.R.1    Kjaer, A.2    Nielsen, B.J.3
  • 16
    • 85011186779 scopus 로고
    • The glycosides of Martynia louisiana Mill. A new phenylpropanoid glycoside, martynoside
    • Sasaki, H.; Taguchi, H.; Endo, T.; Yosioka, I. The glycosides of Martynia louisiana Mill. A new phenylpropanoid glycoside, martynoside. Chem. Pharm. Bull. 1978, 26, 2111-2121.
    • (1978) Chem. Pharm. Bull. , vol.26 , pp. 2111-2121
    • Sasaki, H.1    Taguchi, H.2    Endo, T.3    Yosioka, I.4
  • 18
    • 33947094112 scopus 로고
    • Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance sepctroscopy
    • Seo, S.; Tomita, Y.; Tori, K.; Yoshimura, Y. Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance sepctroscopy. J. Am. Chem. Soc. 1978, 100, 3331-3339.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 3331-3339
    • Seo, S.1    Tomita, Y.2    Tori, K.3    Yoshimura, Y.4
  • 22
    • 84861181399 scopus 로고    scopus 로고
    • Cellular antioxidant activity of Feijoada whole meal coupled with an in vitro digestion
    • Faller, A.L.K.; Fialho, E.; Liu, R.H. Cellular antioxidant activity of Feijoada whole meal coupled with an in vitro digestion. J. Agric. Food Chem. 2012, 60, 4826-4832.
    • (2012) J. Agric. Food Chem. , vol.60 , pp. 4826-4832
    • Faller, A.L.K.1    Fialho, E.2    Liu, R.H.3
  • 25
    • 36148987289 scopus 로고    scopus 로고
    • Cellular antioxidant activity (CAA) assay for assessing antioxidants, foods, and dietary supplements
    • Wolfe, K.L.; Liu, R.H. Cellular antioxidant activity (CAA) assay for assessing antioxidants, foods, and dietary supplements. J. Agric. Food Chem. 2007, 55, 8896-8907.
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 8896-8907
    • Wolfe, K.L.1    Liu, R.H.2
  • 26
    • 67651171248 scopus 로고    scopus 로고
    • A modified methylene blue assay for accurate cell counting
    • Felice, D.L.; Sun, J.; Liu, R.H. A modified methylene blue assay for accurate cell counting. J. Funct. Foods 2009, 1, 109-118.
    • (2009) J. Funct. Foods , vol.1 , pp. 109-118
    • Felice, D.L.1    Sun, J.2    Liu, R.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.