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Volumn 85, Issue , 2014, Pages 65-76

Synthesis, biological evaluation and molecular docking of novel chalcone-coumarin hybrids as anticancer and antimalarial agents

Author keywords

Antimalarial activity; Chalcone; Coumarin; Cytotoxicity; Molecular docking; Triazole

Indexed keywords

4 ((1 (3 (3 (2,3 DIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 4 ((1 (3 (3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 4 ((1 (3 (3 (3,4 DIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 4 ((1 (4 (3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 4 ((1 (4 (3 (3,4,5 TRIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YLL)METHOXY) 2H CHROMEN 2 ONE; 7 ((1 (3 (3 (2,3 DIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 7 ((1 (3 (3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 7 ((1 (3 (3 (3,4 DIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1 H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 7 ((1 (4 (3 (2,3 DIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 7 ((1 (4 (3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; 7 ((1 (4 (3 (3,4,5 TRIMETHOXYPHENYL)ACRYLOYL)PHENYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 2H CHROMEN 2 ONE; ALPHA TUBULIN; ANTIMALARIAL AGENT; ANTINEOPLASTIC AGENT; BETA TUBULIN; CHALCONE DERIVATIVE; COUMARIN DERIVATIVE; ETOPOSIDE; FALCIPAIN 2; UNCLASSIFIED DRUG; 1,2,3 TRIAZOLE DERIVATIVE; 4 [[1 [3 [3 (2,3 DIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 4 [[1 [3 [3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 4 [[1 [3 [3 (3,4 DIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 4 [[1 [4 [3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 4 [[1 [4 [3 (3,4,5 TRIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 7 [[1 [3 [3 (2,3 DIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 7 [[1 [3 [3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 7 [[1 [3 [3 (3,4 DIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 7 [[1 [4 [3 (2,3 DIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 7 [[1 [4 [3 (2,3,4 TRIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; 7 [[1 [4 [3 (3,4,5 TRIMETHOXYPHENYL)ACRYLOYL]PHENYL] 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 2H CHROMEN 2 ONE; COLCHICINE; DIHYDROARTEMISININ; DOXORUBICIN; ELLIPTICINE; N [N (3 CARBOXYOXIRANE 2 CARBONYL)LEUCYL]AGMATINE; TUBULIN; CHALCONE; COUMARIN; CYSTEINE PROTEINASE; TRIAZOLE DERIVATIVE;

EID: 84905161366     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.07.087     Document Type: Article
Times cited : (209)

References (60)
  • 1
    • 84857587699 scopus 로고    scopus 로고
    • Exploring pharmacological significance of chalcone scaffold: A review
    • N.K. Sahu, S.S. Balbhadra, J. Choudhary, and D.V. Kohli Exploring pharmacological significance of chalcone scaffold: a review Curr. Med. Chem. 19 2012 209 225
    • (2012) Curr. Med. Chem. , vol.19 , pp. 209-225
    • Sahu, N.K.1    Balbhadra, S.S.2    Choudhary, J.3    Kohli, D.V.4
  • 3
    • 77950854525 scopus 로고    scopus 로고
    • Trends in utilization of the pharmacological potential of chalcones
    • D.I. Batovska, and I.T. Todorova Trends in utilization of the pharmacological potential of chalcones Curr. Clin. Pharmacol. 5 2010 1 29
    • (2010) Curr. Clin. Pharmacol. , vol.5 , pp. 1-29
    • Batovska, D.I.1    Todorova, I.T.2
  • 5
    • 20144367578 scopus 로고    scopus 로고
    • Chalcones: An update on cytotoxic and chemoprotective properties
    • M.L. Go, X. Wu, and X.L. Liu Chalcones: an update on cytotoxic and chemoprotective properties Curr. Med. Chem. 12 2005 483 499
    • (2005) Curr. Med. Chem. , vol.12 , pp. 483-499
    • Go, M.L.1    Wu, X.2    Liu, X.L.3
  • 6
    • 65549090501 scopus 로고    scopus 로고
    • Antimitotic chalcones and related compounds as inhibitors of tubulin assembly
    • S. Ducki Antimitotic chalcones and related compounds as inhibitors of tubulin assembly Anticancer Agents Med. Chem. 9 2009 336 347
    • (2009) Anticancer Agents Med. Chem. , vol.9 , pp. 336-347
    • Ducki, S.1
  • 7
    • 79954418634 scopus 로고    scopus 로고
    • Inhibitors and promoters of tubulin polymerization: Synthesis and biological evaluation of chalcones and related dienones as potential anticancer agents
    • C. Dyrager, M. Wickström, M. Fridén-Saxin, A. Friberg, K. Dahlén, E.A.A. Wallén, J. Gullbo, M. Grøtli, and K. Luthman Inhibitors and promoters of tubulin polymerization: synthesis and biological evaluation of chalcones and related dienones as potential anticancer agents Bioorg. Med. Chem. 19 2011 2659 2665
    • (2011) Bioorg. Med. Chem. , vol.19 , pp. 2659-2665
    • Dyrager, C.1    Wickström, M.2    Fridén-Saxin, M.3    Friberg, A.4    Dahlén, K.5    Wallén, E.A.A.6    Gullbo, J.7    Grøtli, M.8    Luthman, K.9
  • 8
    • 0028357495 scopus 로고
    • Licochalcone A, a new antimalarial agent, inhibits in vitro growth of the human malaria parasite Plasmodium falciparum and protects mice from P. Yoelii infection
    • M. Chen, T.G. Theander, S.B. Christensen, L. Hviid, L. Zhai, and A. Kharazmi Licochalcone A, a new antimalarial agent, inhibits in vitro growth of the human malaria parasite Plasmodium falciparum and protects mice from P. yoelii infection Antimicrob. Agents Chemother. 38 1994 1470 1475
    • (1994) Antimicrob. Agents Chemother. , vol.38 , pp. 1470-1475
    • Chen, M.1    Theander, T.G.2    Christensen, S.B.3    Hviid, L.4    Zhai, L.5    Kharazmi, A.6
  • 10
    • 77955424412 scopus 로고    scopus 로고
    • Synthesis of novel alpha-pyranochalcones and pyrazoline derivatives as Plasmodium falciparum growth inhibitors
    • G. Wanare, R. Aher, N. Kawathekar, R. Ranjan, N.K. Kaushik, and D. Sahal Synthesis of novel alpha-pyranochalcones and pyrazoline derivatives as Plasmodium falciparum growth inhibitors Bioorg. Med. Chem. Lett. 420 2010 4675 4678
    • (2010) Bioorg. Med. Chem. Lett. , vol.420 , pp. 4675-4678
    • Wanare, G.1    Aher, R.2    Kawathekar, N.3    Ranjan, R.4    Kaushik, N.K.5    Sahal, D.6
  • 12
    • 77949487270 scopus 로고    scopus 로고
    • Comparison of the antiplasmodial and falcipain-2 inhibitory activity of β-amino alcohol thiolactone-chalcone and isatin-chalcone hybrids
    • R.H. Hans, J. Gut, P.J. Rosenthal, and K. Chibale Comparison of the antiplasmodial and falcipain-2 inhibitory activity of β-amino alcohol thiolactone-chalcone and isatin-chalcone hybrids Bioorg. Med. Chem. Lett. 20 2010 2234 2237
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 2234-2237
    • Hans, R.H.1    Gut, J.2    Rosenthal, P.J.3    Chibale, K.4
  • 14
    • 4344668584 scopus 로고    scopus 로고
    • Antiplasmodial chalcones inhibit sorbitol-induced hemolysis of Plasmodium falciparum-infected erythrocytes
    • M.-L. Go, M. Liu, P. Wilairat, P.J. Rosenthal, K.J. Saliba, and K. Kirk Antiplasmodial chalcones inhibit sorbitol-induced hemolysis of Plasmodium falciparum-infected erythrocytes Antimicrob. Agents Chemother. 48 2004 3241 3245
    • (2004) Antimicrob. Agents Chemother. , vol.48 , pp. 3241-3245
    • Go, M.-L.1    Liu, M.2    Wilairat, P.3    Rosenthal, P.J.4    Saliba, K.J.5    Kirk, K.6
  • 16
    • 0035818913 scopus 로고    scopus 로고
    • Antimalarial alkoxylated and hydroxylated chalcones: Structure-activity relationship analysis
    • M. Liu, P. Wilairat, and M.-L. Go Antimalarial alkoxylated and hydroxylated chalcones: structure-activity relationship analysis J. Med. Chem. 44 2001 4443 4452
    • (2001) J. Med. Chem. , vol.44 , pp. 4443-4452
    • Liu, M.1    Wilairat, P.2    Go, M.-L.3
  • 17
    • 15944389028 scopus 로고    scopus 로고
    • Simple coumarins and analogues in medicinal chemistry: Occurrence, synthesis and biological activity
    • F. Borges, F. Roleira, N. Milhazes, L. Santana, and E. Uriarte Simple coumarins and analogues in medicinal chemistry: occurrence, synthesis and biological activity Curr. Med. Chem. 12 2005 887 916
    • (2005) Curr. Med. Chem. , vol.12 , pp. 887-916
    • Borges, F.1    Roleira, F.2    Milhazes, N.3    Santana, L.4    Uriarte, E.5
  • 18
    • 11444268281 scopus 로고    scopus 로고
    • Synthetic and natural coumarins as cytotoxic agents
    • I. Kostova Synthetic and natural coumarins as cytotoxic agents Curr. Med. Chem. Anticancer Agents 5 2005 29 46
    • (2005) Curr. Med. Chem. Anticancer Agents , vol.5 , pp. 29-46
    • Kostova, I.1
  • 19
    • 6944237046 scopus 로고    scopus 로고
    • Studies on coumarins and coumarin-related compounds to determine their therapeutic role in the treatment of cancer
    • A. Lacy, and R. O'Kennedy Studies on coumarins and coumarin-related compounds to determine their therapeutic role in the treatment of cancer Curr. Pharm. Des. 10 2004 3797 3811
    • (2004) Curr. Pharm. Des. , vol.10 , pp. 3797-3811
    • Lacy, A.1    O'Kennedy, R.2
  • 22
    • 84897386255 scopus 로고    scopus 로고
    • Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
    • K. Nepali, S. Sharma, M. Sharma, P.M.S. Bedi, and K.L. Dhar Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids Eur. J. Med. Chem. 77 2014 422 487
    • (2014) Eur. J. Med. Chem. , vol.77 , pp. 422-487
    • Nepali, K.1    Sharma, S.2    Sharma, M.3    Bedi, P.M.S.4    Dhar, K.L.5
  • 23
    • 76749095030 scopus 로고    scopus 로고
    • Next-generation antimalarial drugs: Hybrid molecules as a new strategy in drug design
    • F.W. Muregi, and A. Ishih Next-generation antimalarial drugs: hybrid molecules as a new strategy in drug design Drug Dev. Res. 71 2010 20 32
    • (2010) Drug Dev. Res. , vol.71 , pp. 20-32
    • Muregi, F.W.1    Ishih, A.2
  • 25
    • 84899410430 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of novel 4-(4-(substituted)-1H-1,2,3-triazol- 1-yl)-N-phenethylbenzenesulfonamides
    • R. Pingaew, S. Prachayasittikul, S. Ruchirawat, and V. Prachayasittikul Synthesis and cytotoxicity of novel 4-(4-(substituted)-1H-1,2,3-triazol-1-yl)-N- phenethylbenzenesulfonamides Med. Chem. Res. 23 2014 1768 1780
    • (2014) Med. Chem. Res. , vol.23 , pp. 1768-1780
    • Pingaew, R.1    Prachayasittikul, S.2    Ruchirawat, S.3    Prachayasittikul, V.4
  • 26
    • 78249268250 scopus 로고    scopus 로고
    • Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds
    • E.M. Guantai, K. Ncokazi, T.J. Egan, J. Gut, P.J. Rosenthal, P.J. Smith, and K. Chibale Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds Bioorg. Med. Chem. 18 2010 8243 8256
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 8243-8256
    • Guantai, E.M.1    Ncokazi, K.2    Egan, T.J.3    Gut, J.4    Rosenthal, P.J.5    Smith, P.J.6    Chibale, K.7
  • 27
    • 84865140873 scopus 로고    scopus 로고
    • Synthesis and in vitro evaluation of new chloroquine-chalcone hybrids against chloroquine-resistant strain of Plasmodium falciparum
    • K.V. Sashidhara, S.R. Avula, G.R. Palnati, S.V. Singh, K. Srivastava, S.K. Puri, and J.K. Saxena Synthesis and in vitro evaluation of new chloroquine-chalcone hybrids against chloroquine-resistant strain of Plasmodium falciparum Bioorg. Med. Chem. Lett. 22 2012 5455 5459
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 5455-5459
    • Sashidhara, K.V.1    Avula, S.R.2    Palnati, G.R.3    Singh, S.V.4    Srivastava, K.5    Puri, S.K.6    Saxena, J.K.7
  • 30
    • 84884681758 scopus 로고    scopus 로고
    • Novel N-4-piperazinyl-ciprofloxacin-chalcone hybrids: Synthesis, physicochemical properties, anticancer and topoisomerase i and II inhibitory activity
    • M. Abdel-Aziz, S.-E. Park, G.E.-D.A.A. Abuo-Rahma, M.A. Sayed, and Y. Kwon Novel N-4-piperazinyl-ciprofloxacin-chalcone hybrids: synthesis, physicochemical properties, anticancer and topoisomerase I and II inhibitory activity Eur. J. Med. Chem. 69 2013 427 438
    • (2013) Eur. J. Med. Chem. , vol.69 , pp. 427-438
    • Abdel-Aziz, M.1    Park, S.-E.2    Abuo-Rahma, G.E.-D.A.A.3    Sayed, M.A.4    Kwon, Y.5
  • 31
    • 84855800613 scopus 로고    scopus 로고
    • 1,2,3-Triazole tethered β-lactam-chalcone bifunctional hybrids: Synthesis and anticancer evaluation
    • P. Singh, R. Raj, V. Kumar, M.P. Mahajan, P.M.S. Bedi, T. Kaur, and A.K. Saxena 1,2,3-Triazole tethered β-lactam-chalcone bifunctional hybrids: synthesis and anticancer evaluation Eur. J. Med. Chem. 47 2012 594 600
    • (2012) Eur. J. Med. Chem. , vol.47 , pp. 594-600
    • Singh, P.1    Raj, R.2    Kumar, V.3    Mahajan, M.P.4    Bedi, P.M.S.5    Kaur, T.6    Saxena, A.K.7
  • 33
    • 77955559819 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel hybrid chalcone derivatives as vasorelaxant agents
    • X. Dong, L. Du, Z. Pan, T. Liu, B. Yang, and Y. Hu Synthesis and biological evaluation of novel hybrid chalcone derivatives as vasorelaxant agents Eur. J. Med. Chem. 45 2010 3986 3992
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 3986-3992
    • Dong, X.1    Du, L.2    Pan, Z.3    Liu, T.4    Yang, B.5    Hu, Y.6
  • 38
    • 78449284852 scopus 로고    scopus 로고
    • Synthesis and in vitro evaluation of novel coumarin-chalcone hybrids as potential anticancer agents
    • K.V. Sashidhara, A. Kumar, M. Kumar, J. Sarkar, and S. Sinha Synthesis and in vitro evaluation of novel coumarin-chalcone hybrids as potential anticancer agents Bioorg. Med. Chem. Lett. 20 2010 7205 7211
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 7205-7211
    • Sashidhara, K.V.1    Kumar, A.2    Kumar, M.3    Sarkar, J.4    Sinha, S.5
  • 39
  • 40
    • 80053528741 scopus 로고    scopus 로고
    • Click chemistry: 1,2,3-triazoles as pharmacophores
    • S.G. Agalave, S.R. Maujan, and V.S. Pore Click chemistry: 1,2,3-triazoles as pharmacophores Chem. Asian J. 6 2011 2696 2718
    • (2011) Chem. Asian J. , vol.6 , pp. 2696-2718
    • Agalave, S.G.1    Maujan, S.R.2    Pore, V.S.3
  • 41
    • 61449267734 scopus 로고    scopus 로고
    • Structures of falcipain-2 and falcipain-3 bound to small molecule inhibitors: Implications for substrate specificity
    • I.D. Kerr, J.H. Lee, K.C. Pandey, A. Harrison, M. Sajid, P.J. Rosenthal, and L.S. Brinen Structures of falcipain-2 and falcipain-3 bound to small molecule inhibitors: implications for substrate specificity J. Med. Chem. 52 2009 852 857
    • (2009) J. Med. Chem. , vol.52 , pp. 852-857
    • Kerr, I.D.1    Lee, J.H.2    Pandey, K.C.3    Harrison, A.4    Sajid, M.5    Rosenthal, P.J.6    Brinen, L.S.7
  • 43
    • 82555187401 scopus 로고    scopus 로고
    • Evaluation and discovery of novel synthetic chalcone derivatives as anti-inflammatory agents
    • J. Wu, J. Li, Y. Cai, Y. Pan, F. Ye, Y. Zhang, Y. Zhao, S. Yang, X. Li, and G. Liang Evaluation and discovery of novel synthetic chalcone derivatives as anti-inflammatory agents J. Med. Chem. 54 2011 8110 8123
    • (2011) J. Med. Chem. , vol.54 , pp. 8110-8123
    • Wu, J.1    Li, J.2    Cai, Y.3    Pan, Y.4    Ye, F.5    Zhang, Y.6    Zhao, Y.7    Yang, S.8    Li, X.9    Liang, G.10
  • 44
    • 63849220256 scopus 로고    scopus 로고
    • Synthesis of some 4′-amino chalcones and their antiinflammatory and antimicrobial activity
    • Y.R. Prasad, A.S. Rao, and R. Rambabu Synthesis of some 4′-amino chalcones and their antiinflammatory and antimicrobial activity Asian J. Chem. 21 2009 907 914
    • (2009) Asian J. Chem. , vol.21 , pp. 907-914
    • Prasad, Y.R.1    Rao, A.S.2    Rambabu, R.3
  • 45
    • 33751550874 scopus 로고    scopus 로고
    • Synthesis of coumarin-nucleoside conjugates via Huisgen 1,3-dipolar cycloaddition
    • I. Kosiova, S. Kovackova, and P. Kois Synthesis of coumarin-nucleoside conjugates via Huisgen 1,3-dipolar cycloaddition Tetrahedron 63 2007 312 320
    • (2007) Tetrahedron , vol.63 , pp. 312-320
    • Kosiova, I.1    Kovackova, S.2    Kois, P.3
  • 46
    • 0008749803 scopus 로고
    • Claisen rearrangement of 4-propargloxycoumarins: Formation of 2H,5H-Pyrano[3,2-c][1]benzopyran-5-ones
    • C.P. Rao, and G. Srimannarayana Claisen rearrangement of 4-propargloxycoumarins: formation of 2H,5H-Pyrano[3,2-c][1]benzopyran-5-ones Syn. Comm. 20 1990 535 540
    • (1990) Syn. Comm. , vol.20 , pp. 535-540
    • Rao, C.P.1    Srimannarayana, G.2
  • 47
    • 0023158779 scopus 로고
    • Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of radiosensitivity
    • J. Carmichael, W.G. DeGraff, A.F. Gazdar, J.D. Minna, and J.B. Mitchell Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of radiosensitivity Cancer Res. 47 1987 943 946
    • (1987) Cancer Res. , vol.47 , pp. 943-946
    • Carmichael, J.1    Degraff, W.G.2    Gazdar, A.F.3    Minna, J.D.4    Mitchell, J.B.5
  • 48
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • T. Mosmann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 65 1983 55 63
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 50
    • 0017311840 scopus 로고
    • Human malaria parasites in continuous culture
    • W. Trager, and J.B. Jensen Human malaria parasites in continuous culture Science 193 1976 673 675
    • (1976) Science , vol.193 , pp. 673-675
    • Trager, W.1    Jensen, J.B.2
  • 51
    • 0018606732 scopus 로고
    • Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
    • R.E. Desjardins, C.J. Canfield, J.D. Haynes, and J.D. Chulay Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique Antimicrob. Agents Chemother. 16 1979 710 718
    • (1979) Antimicrob. Agents Chemother. , vol.16 , pp. 710-718
    • Desjardins, R.E.1    Canfield, C.J.2    Haynes, J.D.3    Chulay, J.D.4
  • 52
    • 0033589372 scopus 로고    scopus 로고
    • GFP-expressing mammalian cells for fast, sensitive, noninvasive cell growth assessment in a kinetic mode
    • L. Hunt, M. Jordan, M. De Jesus, and F.M. Wurm GFP-expressing mammalian cells for fast, sensitive, noninvasive cell growth assessment in a kinetic mode Biotechnol. Bioeng. 65 1999 201 205
    • (1999) Biotechnol. Bioeng. , vol.65 , pp. 201-205
    • Hunt, L.1    Jordan, M.2    De Jesus, M.3    Wurm, F.M.4
  • 53
    • 0031718310 scopus 로고    scopus 로고
    • Homology modeling, model and software evaluation: Three related resources
    • R. Rodriguez, G. Chinea, N. Lopez, T. Pons, and G. Vriend Homology modeling, model and software evaluation: three related resources Bioinformatics 14 1998 523 528
    • (1998) Bioinformatics , vol.14 , pp. 523-528
    • Rodriguez, R.1    Chinea, G.2    Lopez, N.3    Pons, T.4    Vriend, G.5
  • 54
    • 0033397980 scopus 로고    scopus 로고
    • Python: A programming language for software integration and development
    • M.F. Sanner Python: a programming language for software integration and development J. Mol. Graph. Mod. 17 1999 57 61
    • (1999) J. Mol. Graph. Mod. , vol.17 , pp. 57-61
    • Sanner, M.F.1
  • 57
    • 70450206724 scopus 로고    scopus 로고
    • (Wallingford, Connecticut)
    • M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G.A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H.P. Hratchian, A.F. Izmaylov, J. Bloino, G. Zheng, J.L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J.A. Montgomery, J.E. Peralta, F. Ogliaro, M. Bearpark, J.J. Heyd, E. Brothers, K.N. Kudin, V.N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J.C. Burant, S.S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J.M. Millam, M. Klene, J.E. Knox, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, R.L. Martin, K. Morokuma, V.G. Zakrzewski, G.A. Voth, P. Salvador, J.J. Dannenberg, S. Dapprich, A.D. Daniels, Farkas, J.B. Foresman, J.V. Ortiz, J. Cioslowski, and D.J. Fox Gaussian 09 2009 (Wallingford, Connecticut)
    • (2009) Gaussian 09
    • Frisch, M.J.1    Trucks, G.W.2    Schlegel, H.B.3    Scuseria, G.E.4    Robb, M.A.5    Cheeseman, J.R.6    Scalmani, G.7    Barone, V.8    Mennucci, B.9    Petersson, G.A.10
  • 59
    • 78249237310 scopus 로고    scopus 로고
    • DeLano Scientific LLC Palo Alto, CA
    • W. Delano PyMOL Release 0.99 2002 DeLano Scientific LLC Palo Alto, CA
    • (2002) PyMOL Release 0.99
    • Delano, W.1
  • 60
    • 78650203607 scopus 로고    scopus 로고
    • Drawing the PDB: Protein-ligand complexes in two dimensions
    • Stierand K.,Rarey M.,Drawing the PDB: Protein-ligand complexes in two dimensions,ACS Med. Chem. Lett., 2010,1, 540-545.
    • (2010) ACS Med. Chem. Lett. , vol.1 , pp. 540-545
    • Stierand, K.1    Rarey, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.