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Volumn 56, Issue 22, 2000, Pages 3523-3531

Jozimine B, a constitutionally unsymmetric, antiplasmodial 'dimer' of the naphthylisoquinoline alkaloid ancistrocladine

Author keywords

Antimalarial activity; Dimeric naphthylisoquinolines; Non phenolic oxidative dimerization; Quantum chemical CD calculations

Indexed keywords

ANCISTROCLADINE; ANTIMALARIAL AGENT; JOZIMINE B; NAPHTHYLISOQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034717322     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00272-6     Document Type: Article
Times cited : (18)

References (45)
  • 3
    • 77957089074 scopus 로고
    • Cordell G.A. New York: Academic Press
    • Bringmann G., Pokorny F. Cordell G.A. The Alkaloids. 46:1995;127-271 Academic Press, New York.
    • (1995) The Alkaloids , vol.46 , pp. 127-271
    • Bringmann, G.1    Pokorny, F.2
  • 24
    • 85037951346 scopus 로고    scopus 로고
    • More exactly speaking, such coupling products should be addressed as dehydro-dimers
    • More exactly speaking, such coupling products should be addressed as dehydro-dimers.
  • 25
    • 85037961367 scopus 로고    scopus 로고
    • 32 and were rationalized by a ring current influence of the parallelly stacked naphthalene rings
    • 32 and were rationalized by a ring current influence of the parallelly stacked naphthalene rings.
  • 26
    • 0000981831 scopus 로고
    • 1,2-Dehydroancistrocladine (ancistrocladinine) is also a natural product, isolated i.a. from Ancistrocladus heynanus (Ancistrocladaceae):
    • 1,2-Dehydroancistrocladine (ancistrocladinine) is also a natural product, isolated i.a. from Ancistrocladus heynanus (Ancistrocladaceae): Govindachari, T. R.; Parthasarathy, P. C.; Desai, H. K. Indian J. Chem. 1971, 9, 1421-1422.
    • (1971) Indian J. Chem. , vol.9 , pp. 1421-1422
    • Govindachari, T.R.1    Parthasarathy, P.C.2    Desai, H.K.3
  • 27
    • 85037956536 scopus 로고    scopus 로고
    • Ph.D Thesis, University of Würzburg
    • Wenzel, M. Ph.D Thesis, University of Würzburg, 1999.
    • (1999)
    • Wenzel, M.1
  • 28
    • 0003522539 scopus 로고    scopus 로고
    • P. Schreier, M. Herderich, H.U. Humpf, & W. Schwab. Braunschweig: Vieweg
    • Bringmann G., Busemann S. Schreier P., Herderich M., Humpf H.U., Schwab W. Natural Product Analysis. 1998;195-212 Vieweg, Braunschweig.
    • (1998) Natural Product Analysis , pp. 195-212
    • Bringmann, G.1    Busemann, S.2
  • 31
    • 0343546114 scopus 로고
    • Comprehensive Organic Synthesis. Oxford: Pergamon
    • Trost B.M., Fleming I., Pattenden G. Comprehensive Organic Synthesis:1991;659-703 Pergamon, Oxford.
    • (1991) , pp. 659-703
    • Trost, B.M.1    Fleming, I.2    Pattenden, G.3
  • 33
    • 85037953080 scopus 로고    scopus 로고
    • No substantial activity was found, however, against HIV-1 or HIV-2; details will be reported elsewhere unpublished results).
    • No substantial activity was found, however, against HIV-1 or HIV-2; details will be reported elsewhere (Boyd, M. R. et al., unpublished results).
    • Boyd, M.R.1
  • 37
    • 85037965153 scopus 로고    scopus 로고
    • VAMP 6.5 available from Oxford Molecular Ltd., The Medewar Centre, Oxford Science Park, Sandford-on-Thames, Oxford OX4 4GA, England
    • Rauhut, G.; Chandrasekhar, J.; Alex, A.; Beck, B.; Sauer, W.; Clark, T. VAMP 6.5 available from Oxford Molecular Ltd., The Medewar Centre, Oxford Science Park, Sandford-on-Thames, Oxford OX4 4GA, England.
    • Rauhut, G.1    Chandrasekhar, J.2    Alex, A.3    Beck, B.4    Sauer, W.5    Clark, T.6
  • 38
    • 85037968963 scopus 로고
    • SYBYL: Tripos Associates, St. Hanley Road, Suite 303, St. Louis, MO 63144, USA
    • SYBYL: Tripos Associates, 1699 St. Hanley Road, Suite 303, St. Louis, MO 63144, USA.
    • (1699)
  • 40
    • 85037965696 scopus 로고
    • MM3 Modul (SYBYL), Tripos Associates, St. Hanley Road, Suite 303, St. Louis, MO 63144, USA
    • MM3 Modul (SYBYL), Tripos Associates, 1699 St. Hanley Road, Suite 303, St. Louis, MO 63144, USA.
    • (1699)
  • 43
    • 2142813682 scopus 로고
    • van Gunsteren, W. F.; Berendsen, H. J. C. Angew. Chem. 1990, 102, 1020-1055; Angew. Chem. Int. Ed. Engl. 1990, 29, 992-1023.
    • (1990) Angew. Chem. Int. Ed. Engl. , vol.29 , pp. 992-1023
  • 45
    • 0004303991 scopus 로고    scopus 로고
    • Department of Chemistry and Biochemistry, University of Colorado, Boulder, USA; modified by Fleischhauer, J.; Schleker, W.; Kramer; B., ported to LinuX by Gulden, K.-P.
    • Downing, J. W. Program Packet BDZDO/MCDSPD, Department of Chemistry and Biochemistry, University of Colorado, Boulder, USA; modified by Fleischhauer, J.; Schleker, W.; Kramer; B., ported to LinuX by Gulden, K.-P.
    • Program Packet BDZDO/MCDSPD
    • Downing, J.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.