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Volumn 4, Issue 1, 2009, Pages 43-46

Alkaloids from Lindera aggregata

Author keywords

(+) norboldine acetate; Aporphine alkaloids; Environmental sensitive; Lindera aggregata; NMR assignments

Indexed keywords

ALKALOID; BOLDINE; LAUROTETANINE; LINDERA AGGREGATA EXTRACT; N METHYLLAUROTETANINE; NORBOLDINE; NORBOLDINE ACETATE; PALLIDINE; PLANT EXTRACT; PRONUCIFERIN; RETICULINE; UNCLASSIFIED DRUG;

EID: 66849114836     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x0900400111     Document Type: Article
Times cited : (32)

References (21)
  • 2
    • 26844548140 scopus 로고    scopus 로고
    • An Editorial Committee of the Administration Bureau of Traditional Chinese Medicine. Shanghai Science & Technology Press, Shanghai
    • An Editorial Committee of the Administration Bureau of Traditional Chinese Medicine. (1999) In Chinese Materia Medica (Zhonghua Bencao). Shanghai Science & Technology Press, Shanghai, Vol. 3, pp. 56-59.
    • (1999) Chinese Materia Medica (Zhonghua Bencao) , vol.3 , pp. 56-59
  • 6
    • 0042034263 scopus 로고    scopus 로고
    • A new sesquiterpene from the roots of Lindera strychnifolia
    • (d) Li JB, Ding Y, Li WM. (2002) A new sesquiterpene from the roots of Lindera strychnifolia. Chinese Chemical Letters, 13, 965-967;
    • (2002) Chinese Chemical Letters , vol.13 , pp. 965-967
    • Li, J.B.1    Ding, Y.2    Li, W.M.3
  • 9
    • 77954111349 scopus 로고    scopus 로고
    • Progress of study on pharmacological activities and mechanisms of benzylisoquinoline alkaloids
    • (g) Cheng HX, Lin Q, Cheng WM. (2006) Progress of study on pharmacological activities and mechanisms of benzylisoquinoline alkaloids. Chinese Journal of New Drugs and Clinical Remedies, 25, 392-399.
    • (2006) Chinese Journal of New Drugs and Clinical Remedies , vol.25 , pp. 392-399
    • Cheng, H.X.1    Lin, Q.2    Cheng, W.M.3
  • 13
    • 19544385954 scopus 로고    scopus 로고
    • A formal [3 + 3] cycloaddition reaction. 5. An enantioselective intramolecular formal aza-[3 + 3] cycloaddition reaction promoted by chiral amine salts
    • (b) Gerasyuto AI, Hsung RP, Sydorenko N, Slafer B. (2005) A formal [3 + 3] cycloaddition reaction. 5. An enantioselective intramolecular formal aza-[3 + 3] cycloaddition reaction promoted by chiral amine salts. Journal of Organic Chemistry, 70, 4248-4256.
    • (2005) Journal of Organic Chemistry , vol.70 , pp. 4248-4256
    • Gerasyuto, A.I.1    Hsung, R.P.2    Sydorenko, N.3    Slafer, B.4
  • 14
    • 0001322468 scopus 로고
    • (S)-Norcoclaurine is the central intermediate in benzylisoquinoline alkaloid biosynthesis
    • Stadler R, Kutchan TM, Zenk MH. (1989) (S)-Norcoclaurine is the central intermediate in benzylisoquinoline alkaloid biosynthesis. Phytochemistry, 28, 1083-1086.
    • (1989) Phytochemistry , vol.28 , pp. 1083-1086
    • Stadler, R.1    Kutchan, T.M.2    Zenk, M.H.3
  • 15
    • 34249078535 scopus 로고    scopus 로고
    • Characterization of isoquinoline alkaloids from Neolitsea sericea var. aurata by HPLC-SPE-NMR
    • Lee SS, Lai YC, Chen CK, Tseng LH, Wang CY. (2007) Characterization of isoquinoline alkaloids from Neolitsea sericea var. aurata by HPLC-SPE-NMR. Journal of Natural Products, 70, 637-642.
    • (2007) Journal of Natural Products , vol.70 , pp. 637-642
    • Lee, S.S.1    Lai, Y.C.2    Chen, C.K.3    Tseng, L.H.4    Wang, C.Y.5
  • 17
    • 0037702267 scopus 로고    scopus 로고
    • Oxazine- and oxazole-fused derivatives of the alkaloid boldine and their complete structural and spectral assignments by HMQC and HMBC experiments
    • (a) Sobarzo-Sánchez E, Cassels BK, Saitz-Barría C, Jullian C. (2001) Oxazine- and oxazole-fused derivatives of the alkaloid boldine and their complete structural and spectral assignments by HMQC and HMBC experiments. Magnetic Resonance in Chemistry, 39, 361-366; (Pubitemid 33277094)
    • (2001) Magnetic Resonance in Chemistry , Issue.6 YEAR 39 , pp. 361-366
    • Sobarzo-Sanchez, E.1    Cassels, B.K.2    Saitz-Barria, C.3    Jullian, C.4
  • 19
    • 31544457863 scopus 로고    scopus 로고
    • A convenient, renewable source of the anxiolytic proaporphine alkaloid glaziovine: Duguetia vallicola leaves
    • (c) Pérez EG, Sáez J, Cassels BK. (2005) A convenient, renewable source of the anxiolytic proaporphine alkaloid glaziovine: Duguetia vsllicola leaves. Journal of the Chilean Chemical Society, 50, 553-557; (Pubitemid 43157185)
    • (2005) Journal of the Chilean Chemical Society , vol.50 , Issue.3 , pp. 45-53
    • Perez, E.G.1    Saez, J.2    Cassels, B.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.