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Volumn 78, Issue 2, 2012, Pages 182-185

Phenols with anti-HIV activity from daphne acutiloba

Author keywords

anti HIV activity; Daphne acutiloba; phenols; Thymelaeceae

Indexed keywords

3 HYDROXY 1,5 DIPHENYL 1 PENTANONE; 4,4' DIHYDROXY 3,3' DIMETHOXY 9 ETHOXY 9,9' EPOXYLIGNAN; 7 ETHOXYMATAIRESINOL; ANTIVIRUS AGENT; CAFFEIC ACID N OCTADECYL ESTER; DAPHNENIN; DAPHNENONE 1; DAPHNENONE 2; DAPHNEOLONE; DAPHNETONE; DIHYDROCUBEBIN; EPINORTRACHELOGENIN; HAPLOMYRFOLIN; LIGNAN DERIVATIVE; MATAIRESINOL; UNCLASSIFIED DRUG;

EID: 84856242664     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0031-1280263     Document Type: Article
Times cited : (24)

References (20)
  • 1
    • 84856277392 scopus 로고    scopus 로고
    • Yunnan Institute of Materia Medica Kunming the Nationalities Publishing House of Yunnan
    • Yunnan Institute of Materia Medica. The annals of national medicine in Yunnan. Kunming the Nationalities Publishing House of Yunnan 2009
    • (2009) The Annals of National Medicine in Yunnan
  • 2
    • 0021029323 scopus 로고
    • Plant anticancer agents. XXVII: Antileukemic and cytotoxic constitutents of Dirca occidentalis (Thymelaeaceae)
    • Badawi M M., Handa S S., Kinghorn A D., Cordell G A., Farnsworth N R. Plant anticancer agents XXVII: antileukemic and cytotoxic constituents of Dirca occidentalis (Thymelaeaceae). J Pharm Sci 1983 72 1285-1287 (Pubitemid 14229737)
    • (1983) Journal of Pharmaceutical Sciences , vol.72 , Issue.11 , pp. 1285-1287
    • Badawi, M.M.1    Handa, S.S.2    Kinghorn, A.D.3
  • 8
    • 0032189810 scopus 로고    scopus 로고
    • Two biflavonoids from Daphne acutiloba
    • DOI 10.1016/S0031-9422(98)00181-2, PII S0031942298001812
    • Taniguchi M, Fujiwara A, Baba K, Wang N H. Two biflavonoids from Daphne acutiloba. Phytochemistry 1998 49 863-867 (Pubitemid 28445180)
    • (1998) Phytochemistry , vol.49 , Issue.3 , pp. 863-867
    • Taniguchi, M.1    Fujiwara, A.2    Baba, K.3    Wang, N.-H.4
  • 9
    • 4344706311 scopus 로고    scopus 로고
    • Reactions of the natural lignan hydroxymatairesinol in basic and acidic nucleophilic media: Formation and reactivity of a quinone methide intermediate
    • Eklund P C., Sundell F J., Smeds A I., Sjoeholm R E. Reactions of the natural lignan hydroxymatairesinol in basic and acidic nucleophilic media: formation and reactivity of a quinone methide intermediate. Org Biomol Chem 2004 2 2229-2235
    • (2004) Org Biomol Chem , vol.2 , pp. 2229-2235
    • Eklund, P.C.1    Sundell, F.J.2    Smeds, A.I.3    Sjoeholm, R.E.4
  • 10
    • 58149147451 scopus 로고    scopus 로고
    • Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production
    • Liang S, Shen Y H., Tian J M., Wu Z J., Jin H Z., Zhang W D., Yan S K. Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. J Nat Prod 2008 71 1902-1905
    • (2008) J Nat Prod , vol.71 , pp. 1902-1905
    • Liang, S.1    Shen, Y.H.2    Tian, J.M.3    Wu, Z.J.4    Jin, H.Z.5    Zhang, W.D.6    Yan, S.K.7
  • 12
    • 34548450715 scopus 로고    scopus 로고
    • Antimicrobiological activity of lignan: Effect of benzylic oxygen and stereochemistry of 2,3-dibenzyl-4-butanolide and 3,4-dibenzyltetrahydrofuran lignans on activity
    • DOI 10.1271/bbb.70168
    • Akiyama K, Maruyama M, Yamauchi S, Nakashima Y, Nakato T, Tago R, Sugahara T, Kishida T, Koba Y. Antimicrobiological activity of lignan: effect of benzylic oxygen and stereochemistry of 2,3-dibenzyl-4-butanolide and 3,4-dibenzyltetrahydrofuran lignans on activity. Biosci Biotechnol Biochem 2007 71 1745-1751 (Pubitemid 47358710)
    • (2007) Bioscience, Biotechnology and Biochemistry , vol.71 , Issue.7 , pp. 1745-1751
    • Akiyama, K.1    Maruyama, M.2    Yamauchi, S.3    Nakashima, Y.4    Nakato, T.5    Tago, R.6    Sugahara, T.7    Kishida, T.8    Koba, Y.9
  • 13
    • 0001311379 scopus 로고
    • Haplomyrtin and ()-haplomyrfolin: Two lignans from Haplophyllum myrtifolium
    • Evcim U, Gozler B, Freyer A J., Shamma M. Haplomyrtin and ()-haplomyrfolin: two lignans from Haplophyllum myrtifolium. Phytochemistry 1986 25 1949-1951
    • (1986) Phytochemistry , vol.25 , pp. 1949-1951
    • Evcim, U.1    Gozler, B.2    Freyer, A.J.3    Shamma, M.4
  • 14
    • 70349835635 scopus 로고    scopus 로고
    • Synthesis, anti-virus and anti-tumor activities of dibenzylbutyrolactone lignans and their analogues
    • Xia Y, You J, Zhang Y, Su Z. Synthesis, anti-virus and anti-tumor activities of dibenzylbutyrolactone lignans and their analogues. J Chem Res 2009 565-569
    • (2009) J Chem Res , pp. 565-569
    • Xia, Y.1    You, J.2    Zhang, Y.3    Su, Z.4
  • 15
    • 0035216817 scopus 로고    scopus 로고
    • A new bicoumarin from Stellera chamaejasme L
    • Xu Z H., Qin G W., Xu R S. A new bicoumarin from Stellera chamaejasme L. J Asian Nat Prod Res 2001 3 335-340
    • (2001) J Asian Nat Prod Res , vol.3 , pp. 335-340
    • Xu, Z.H.1    Qin, G.W.2    Xu, R.S.3
  • 16
    • 33646795005 scopus 로고    scopus 로고
    • Dicationic ((-)-sparteine)palladium-catalyzed enantioselective aldol reaction of aldehydes with 1-phenyl-1-trimethylsilyloxyethene, proceeding via a palladium enolate
    • DOI 10.1016/j.tetlet.2006.04.068, PII S0040403906007933
    • Kiyooka S, Takeshita Y, Tanaka Y, Higaki T, Wada Y. Dicationic [()-sparteine]palladium-catalyzed enantioselective aldol reaction of aldehydes with 1-phenyl-1-trimethylsilyloxyethene, proceeding via a palladium enolate. Tetrahedron Lett 2006 47 4453-4456 (Pubitemid 43767586)
    • (2006) Tetrahedron Letters , vol.47 , Issue.26 , pp. 4453-4456
    • Kiyooka, S.-i.1    Takeshita, Y.2    Tanaka, Y.3    Higaki, T.4    Wada, Y.5
  • 20
    • 33745158157 scopus 로고
    • A simple method for estimating fifty percent endpoints
    • Reed L J., Muench H. A simple method for estimating fifty percent endpoints. Am J Hyg 1938 27 493-497
    • (1938) Am J Hyg , vol.27 , pp. 493-497
    • Reed, L.J.1    Muench, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.