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      KCI등재 SCIE SCOPUS

      Cytotoxic Activity Evaluation and QSAR Study of Chromene-based Chalcones

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      https://www.riss.kr/link?id=A104666485

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      다국어 초록 (Multilingual Abstract)

      Chalcone and chromene motifs are synthetic or naturally occurring scaffolds with significant cytotoxic profile. Two types of novel regioisomeric chromene-chalcone hybrids, namely 1-(6-chloro or 6-methoxy-2H-chromen-3-yl)-3-phenylprop-2-en-1-one (Type A) and 3-(6-chloro or 6-methoxy-2H-chromen-3-yl)-1-phenylprop-2-en-1-one (Type B), both with different substituents on the phenyl ring attached to propenone linkage, have been evaluated for their cytotoxic activity against breast cancer cell lines (MCF-7 and MDA-MB-231). The results indicate that type A of chromene-chalcones demonstrated better cytotoxic profile than type B especially in MDA-MB-231 cell line. In addition, the growth inhibitory activity of most of the target compounds is higher than Etoposide as a reference drug. QSAR analysis of these novel compounds demonstrated that topological and geometrical parameters are among the important descriptors that influence the cytotoxic activity profile of compounds.
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      Chalcone and chromene motifs are synthetic or naturally occurring scaffolds with significant cytotoxic profile. Two types of novel regioisomeric chromene-chalcone hybrids, namely 1-(6-chloro or 6-methoxy-2H-chromen-3-yl)-3-phenylprop-2-en-1-one (Type ...

      Chalcone and chromene motifs are synthetic or naturally occurring scaffolds with significant cytotoxic profile. Two types of novel regioisomeric chromene-chalcone hybrids, namely 1-(6-chloro or 6-methoxy-2H-chromen-3-yl)-3-phenylprop-2-en-1-one (Type A) and 3-(6-chloro or 6-methoxy-2H-chromen-3-yl)-1-phenylprop-2-en-1-one (Type B), both with different substituents on the phenyl ring attached to propenone linkage, have been evaluated for their cytotoxic activity against breast cancer cell lines (MCF-7 and MDA-MB-231). The results indicate that type A of chromene-chalcones demonstrated better cytotoxic profile than type B especially in MDA-MB-231 cell line. In addition, the growth inhibitory activity of most of the target compounds is higher than Etoposide as a reference drug. QSAR analysis of these novel compounds demonstrated that topological and geometrical parameters are among the important descriptors that influence the cytotoxic activity profile of compounds.

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      참고문헌 (Reference)

      1 Sharma, G. N., "Various types and management of breast cancer : an overview" 1 : 109-126, 2010

      2 Hadfield, J. A., "Tubulin and microtubules as target for anticancer drugs" 5 : 309-325, 2003

      3 Rojas, J., "The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production" 12 : 1951-1954, 2002

      4 Lawrence, N. J., "The chemistry and biology of antimitotic chalcones and related enone systems" 11 : 1679-1693, 2005

      5 Sivakumar, P. M., "Synthesis, biological evaluation, mechanism of action and quantitative structure-activity relationship studies of chalcones as antibacterial agents" 73 : 403-415, 2009

      6 Mahmoodi, M., "Synthesis and in-vitro cytotoxicity of poly-functionalized 4-(2-arylthiazol-4-yl)-4H-chromenes" 343 : 411-416, 2010

      7 Sashidhara, K. V., "Synthesis and in vitro evaluation of novel coumarin– chalcone hybrids as potential anticancer agents Bioorg" 20 : 7205-7211, 2010

      8 Mao, W., "Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant antiproliferative activity against breast cancer cell lines" 19 : 4570-4573, 2009

      9 Bois, F., "Synthesis and biological activity of 4-alkoxy chalcones : potential hydrophobic modulators of P-glycoprotein-mediated multidrug resistance" 7 : 2691-2695, 1999

      10 Huang, W., "Synthesis and antitumor activity of novel dithiocarbamate substituted chromones" 44 : 3687-3696, 2009

      1 Sharma, G. N., "Various types and management of breast cancer : an overview" 1 : 109-126, 2010

      2 Hadfield, J. A., "Tubulin and microtubules as target for anticancer drugs" 5 : 309-325, 2003

      3 Rojas, J., "The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production" 12 : 1951-1954, 2002

      4 Lawrence, N. J., "The chemistry and biology of antimitotic chalcones and related enone systems" 11 : 1679-1693, 2005

      5 Sivakumar, P. M., "Synthesis, biological evaluation, mechanism of action and quantitative structure-activity relationship studies of chalcones as antibacterial agents" 73 : 403-415, 2009

      6 Mahmoodi, M., "Synthesis and in-vitro cytotoxicity of poly-functionalized 4-(2-arylthiazol-4-yl)-4H-chromenes" 343 : 411-416, 2010

      7 Sashidhara, K. V., "Synthesis and in vitro evaluation of novel coumarin– chalcone hybrids as potential anticancer agents Bioorg" 20 : 7205-7211, 2010

      8 Mao, W., "Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant antiproliferative activity against breast cancer cell lines" 19 : 4570-4573, 2009

      9 Bois, F., "Synthesis and biological activity of 4-alkoxy chalcones : potential hydrophobic modulators of P-glycoprotein-mediated multidrug resistance" 7 : 2691-2695, 1999

      10 Huang, W., "Synthesis and antitumor activity of novel dithiocarbamate substituted chromones" 44 : 3687-3696, 2009

      11 Liu, M., "Structure–activity relationships of antileishmanial and antimalarial chalcones" 11 : 2729-2738, 2003

      12 Yayli, N., "Stereoselective photochemistry of methoxy chalcones in solution and their radical scavenging activity" 28 : 515-521, 2004

      13 Mosmann, T., "Rapid colorimetric assay for cellular growth and survival : Application to proliferation and cytotoxicity assays" 65 : 55-63, 1983

      14 Nazarian, Z., "Novel antileishmanial chalconoids : Synthesis and biological activity of 1-or 3-(6-chloro-2H-chromen-3-yl)propen-1-ones" 45 : 1424-1429, 2010

      15 Reddy, M. V., "New bichalcone analogs as NF-κB inhibitors and as cytotoxic agents inducing Fas/CD95-dependent apoptosis" 19 : 1895-1906, 2011

      16 Sashidhara, K. V., "Neo-tanshinlactone inspired synthesis, in vitro evaluation of novel substituted benzocoumarin derivatives as potent anti-breast cancer agents" 20 : 7127-7131, 2010

      17 Gunatilaka, A. L., "Mechanism-based isolation and structures of some anticancer active natural products" 66 : 2219-2222, 1994

      18 Park, E. J., "Lichochalcone A : an inducer of cell differentiation and cytotoxic agent from Pogostemon cablin" 64 : 464-466, 1998

      19 Alizadeh, B. H., "Isochaihulactone analogues : synthesis and anti-proliferative activity of novel dibenzylbutyrolactones" 45 : 5979-5984, 2010

      20 Nakatani, N., "Induction of apoptosis in human promyelocytic leukemia cell line HL-60 by C-benzylated dihydrochalcones, uvaretin, isouvaretin and diuvaretin" 28 : 83-86, 2005

      21 Frisch, M. J., "Gaussian 98, Revision A. 7" Gaussian, Inc. 1998

      22 Liu, X. L., "Functionalized chalcones as selective inhibitors of P-glycoprotein and breast cancer resistance protein" 16 : 171-180, 2008

      23 Rozmer, Z., "Different effects of two cyclic chalcone analogues on cell cycle of Jurkat T cells" 20 : 1354-1362, 2006

      24 Reddy, M. V., "Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents" 16 : 7358-7370, 2008

      25 Belluti, F., "Design, synthesis and anticancer activities of stilbene-coumarin hybrid compounds : Identification of novel proapoptotic agents" 18 : 3543-3550, 2010

      26 Mayur, Y. C., "Design of new drug molecules to be used in reversing multidrug resistance in cancer cells" 9 : 298-306, 2009

      27 Dimmock, J. R., "Cytotoxic activities of mannich bases of chalcones and related compounds" 4 : 1014-1026, 1998

      28 Zhou, Z. Z., "Construction of a combinatorial library of 2-(4-oxo-4H-1-benzopyran-3-yl)-4-thiazolidinones by microwave-assisted one-pot parallel syntheses" 18 : 381-389, 2007

      29 Foroumadi, A., "Chromene-based synthetic chalcones as potent antileishmanial agents : Synthesis and biological activity" 75 : 590-596, 2010

      30 Heo, S. J., "Chromene induces apoptosis via caspase-3 activation in human leukemia HL-60 cells" 49 : 1998-2004, 2011

      31 Akihisa, T., "Chalcones and other compounds from the exudates of Angelica keiskei and their cancer chemopreventive effects" 69 : 38-42, 2006

      32 Go, M. L., "Chalcones : an update on cytotoxic and chemopretective properties" 12 : 483-499, 2005

      33 Patil, C. B., "Chalcone : A versatile molecule" 1 : 11-22, 2009

      34 Dimmock, J. R., "Bioactivities of chalcones" 6 : 1125-1149, 1999

      35 Liu, Q., "Anti-Coxsackie virus B3 norsesquiterpenoids from the roots of Phyllanthus emblica" 72 : 969-972, 2009

      36 Hughes, G. K., "Alkaloids of the Australian Rutaceae" 162 : 223-224, 1948

      37 Nowakowska, Z., "A review of antiinfective and anti-inflammatory chalcones" 42 : 125-137, 2007

      38 Zhang, Y., "A novel chalcone from Coreopsis tinctoria nutt" 34 : 766-769, 2006

      39 Akbarzadeh, T., "2-Amino-3-cyano-4-(5-arylisoxazol-3-yl)-4H-chromenes : Synthesis and in vitro cytotoxic activity" 345 : 386-392, 2012

      40 Mager, H., ""The problem of multicollinearity in Hansch-type quantitative structure-activity relationships(QSAR)and in chemical linear free energy relationships(LFER)" 38 : 120-128, 1983

      41 Lawrence, N. J., ""The interaction of chalcones with tubulin" 15 : 135-141, 2000

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      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
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