• HOME
    KOREAN
    CHINESS
    SITE MAP
    JOIN
  • Username (Site Login ID)
  • Password
  • Forgot your password?

  • ÇÐÁ¦°£¿¬±¸ | Interdisciplinary Studies in Gambling | Î¥学Ρ研ϼ

    date : 2015-05-20 01:10|hit : 1364
    Article] Synthesis and biological evaluation of isoflavone analogues from Dalbergia oliveri
    DocNo of ILP: 4033

    Doc. Type: Article

    Title: Synthesis and biological evaluation of isoflavone analogues from Dalbergia oliveri

    Authors: Deesamer, S; Kokpol, U; Chavasiri, W; Douillard, S; Peyrot, V; Vidal, N; Combes, S; Finet, JP

    Full Name of Authors: Deesamer, Sujittra; Kokpol, Udom; Chavasiri, Warinthorn; Douillard, Soazig; Peyrot, Vincent; Vidal, Nicolas; Combes, Sebastien; Finet, Jean-Pierre

    Keywords by Author:

    Keywords Plus: ORGANOLEAD-MEDIATED ARYLATION; SELECTIVE SYNTHESIS; TUBULIN; CHALCONES; DERIVATIVES; PROTEIN; BRAIN

    Abstract: Mucronulatol 1 and violanone 2 isolated from Dalbergia oliveri Gamble, and the corresponding isoflavone 3 were prepared by ligand coupling reactions involving organolead reagent. Biological studies have shown a significant cytotoxic effect against an HBL100 leukemia cell line only for isoflavan 1 with an IC50 value amounting to 5.7 mu M. All the drugs modestly inhibit the in vitro microtubule assembly, independently of the cytotoxic ability. Natural compounds 1 and 2 have no antibacterial activity, but are potent inhibitors of the Fusarium oxysporum phytopathogenic fungal growth. (c) 2007 Elsevier Ltd. All rights reserved.

    Cate of OECD: Chemical sciences

    Year of Publication: 2007

    Business Area: other

    Detail Business: medicine & science

    Country: England

    Study Area: Evaluation, choice, drug

    Name of Journal: TETRAHEDRON

    Language: English

    Country of Authors: [Vidal, Nicolas; Combes, Sebastien; Finet, Jean-Pierre] CNRS, UMR 6517, Case 521, F-13397 Marseille 20, France; [Vidal, Nicolas; Combes, Sebastien; Finet, Jean-Pierre] Aix Marseille Univ, Fac Sci & Tech St Jerome, F-13397 Marseille, France; [Deesamer, Sujittra; Kokpol, Udom; Chavasiri, Warinthorn] Chulalongkorn Univ, Fac Sci, Nat Prod Res Unit, Bangkok 10330, Thailand; [Douillard, Soazig; Peyrot, Vincent] CNRS, FRE 2737, F-13385 Marseille, France; [Douillard, Soazig; Peyrot, Vincent] Aix Marseille Univ, Fac Pharm, F-13385 Marseille 5, France

    Press Adress: Combes, S (reprint author), CNRS, UMR 6517, Case 521, F-13397 Marseille 20, France.

    Email Address: sebastien.combes@up.univ-mrs.fr

    Citaion:

    Funding:

    Lists of Citation: ANDREU JM, 1984, BIOCHEMISTRY-US, V23, P1742, DOI 10.1021/bi00303a025; Bailly C, 2003, J MED CHEM, V46, P5437, DOI 10.1021/jm030903d; BEUTLER JA, 1993, BIOORG MED CHEM LETT, V3, P581, DOI 10.1016/S0960-894X(01)81233-6; Chen HY, 2004, BIOORG MED CHEM LETT, V14, P1417, DOI 10.1016/j.bmcl.2004.01.031; COOKE RG, 1969, AUST J CHEM, V22, P2395; DEICAS E, 1991, MYCOSES, V34, P167; Ding K, 2005, TETRAHEDRON LETT, V46, P3707, DOI 10.1016/j.tetlet.2005.03.143; DONNELLY DMX, 1990, J CHEM SOC PERK T 1, P2851, DOI 10.1039/p19900002851; DONNELLY DMX, 1993, J CHEM SOC PERK T 1, P1729, DOI 10.1039/p19930001729; DONNELLY DM, 1974, PHYTOCHEMISTRY, V13, P2587; DONNELLY DMX, 1995, J CHEM SOC PERK T 1, P1679, DOI 10.1039/p19950001679; DONNELLY DMX, 1993, TETRAHEDRON, V49, P7967, DOI 10.1016/S0040-4020(01)88020-0; EDWARDS ML, 1990, J MED CHEM, V33, P1948, DOI 10.1021/jm00169a021; FARKAS L, 1974, J CHEM SOC PERK T 1, P305, DOI 10.1039/p19740000305; FINET JP, 2000, POLYPHENOLS ACTUALIT, V19, P18; FINET JP, 2006, COMPREHENSIVE ORGANO, V3, P381; FITTON AO, 1962, J CHEM SOC, P4870, DOI 10.1039/jr9620004870; Haidara K, 2006, CANCER LETT, V242, P180, DOI 10.1016/j.canlet.2005.11.017; HAMBURGER MO, 1987, J NAT PROD, V50, P19, DOI 10.1021/np50049a003; Hamel E, 1996, MED RES REV, V16, P207, DOI 10.1002/(SICI)1098-1128(199603)16:2<207::AID-MED4>3.0.CO;2-4; Harborne JB, 2000, PHYTOCHEMISTRY, V55, P481, DOI 10.1016/S0031-9422(00)00235-1; HEUSELE C, 1987, EUR J BIOCHEM, V165, P613, DOI 10.1111/j.1432-1033.1987.tb11484.x; Ito A, 2000, TETRAHEDRON, V56, P6401, DOI 10.1016/S0040-4020(00)00584-6; Ito C, 2003, PHYTOCHEMISTRY, V64, P1265, DOI 10.1016/j.phytochem.2003.08.010; KOZYROD RP, 1985, AUST J CHEM, V38, P1147; KUROSAWA K, 1968, J CHEM SOC CHEM COMM, P1263; Lawrence NJ, 2000, ANTI-CANCER DRUG DES, V15, P135; LEE JC, 1973, J BIOL CHEM, V248, P7253; LICHIUS JJ, 1994, J NAT PROD, V57, P1012, DOI 10.1021/np50109a024; NAYLOR P, 1958, J CHEM SOC, P1190, DOI 10.1039/jr9580001190; Nguyen TL, 2005, J MED CHEM, V48, P6107, DOI 10.1021/jm050502t; Pelter A, 1999, ENVIRON TOXICOL PHAR, V7, P217, DOI 10.1016/S1382-6689(99)00017-4; Ren MQ, 2001, EUR J NUTR, V40, P135, DOI 10.1007/PL00007388; WAHALA K, 1991, J CHEM SOC PERK T 1, P3005, DOI 10.1039/p19910003005; WEISENBE.RC, 1968, BIOCHEMISTRY-US, V7, P4466, DOI 10.1021/bi00852a043

    Number of Citaion: 35

    Publication: PERGAMON-ELSEVIER SCIENCE LTD

    City of Publication: OXFORD

    Address of Publication: THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND

    ISSN: 0040-4020

    29-Character Source Abbreviation: TETRAHEDRON

    ISO Source Abbreviation: Tetrahedron

    Volume: 63

    Version: 52

    Start of File: 12986

    End of File: 12993

    DOI: 10.1016/j.tet.2007.10.030

    Number of Pages: 8

    Web of Science Category: Chemistry, Organic

    Subject Category: Chemistry

    Document Delivery Number: 249NQ

    Unique Article Identifier: WOS:000252235900022

    reply : 0
  • list
  • prev
  • next