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Volumn 57, Issue , 2012, Pages 283-295

3,6-Bis(3-alkylguanidino)acridines as DNA-intercalating antitumor agents

Author keywords

Acridine; Antitumor activity; Caspase 3; Cytotoxic; Intercalator; Molecular modeling; Topoisomerase I

Indexed keywords

(ACRIDINE 3,6 DIYLDIIMINO)BIS[(BUTYLAMINO)METHANIMINIUM]CHLORIDE; (ACRIDINE 3,6 DIYLDIIMINO)BIS[(ETHYLAMINO)METHANIMINIUM]CHLORIDE; (ACRIDINE 3,6 DIYLDIIMINO)BIS[(N HEXYLAMINO)METHANIMINIUM]CHLORIDE; (ACRIDINE 3,6 DIYLDIIMINO)BIS[(N PENTYLAMINO)METHANIMINIUM]CHLORIDE; ACRIDINE DERIVATIVE; ALKYL GROUP; ANTINEOPLASTIC AGENT; CASPASE 3; DNA; DNA TOPOISOMERASE; GUANIDINE DERIVATIVE; PHOSPHATIDYLSERINE; UNCLASSIFIED DRUG;

EID: 84867286121     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2012.09.020     Document Type: Article
Times cited : (46)

References (79)
  • 2
    • 0033806243 scopus 로고    scopus 로고
    • Intercalative binding of small molecules to nucleic acids
    • D.E. Graves, and L.M. Velea Intercalative binding of small molecules to nucleic acids Curr. Org. Chem. 4 2000 915 929
    • (2000) Curr. Org. Chem. , vol.4 , pp. 915-929
    • Graves, D.E.1    Velea, L.M.2
  • 3
    • 77953126483 scopus 로고    scopus 로고
    • Selective binding of small molecules to DNA: Application and perspectives
    • B. Wang, J. Tan, and L. Zhu Selective binding of small molecules to DNA: application and perspectives Colloids Surf. B 79 2010 1 4
    • (2010) Colloids Surf. B , vol.79 , pp. 1-4
    • Wang, B.1    Tan, J.2    Zhu, L.3
  • 4
    • 34548451133 scopus 로고    scopus 로고
    • Noncovalent interaction with DNA: An overview
    • L. Strekowski, and B. Wilson Noncovalent interaction with DNA: an overview Mut. Res. 623 2007 3 13
    • (2007) Mut. Res. , vol.623 , pp. 3-13
    • Strekowski, L.1    Wilson, B.2
  • 6
    • 0342987251 scopus 로고
    • Design of peptides that bind in the minor groove of DNA at 5′-(A, T)5G(A, T)C(A, T) sequences by a dimeric side-by-side motif
    • W.S. Wade, M. Mrksich, and P.B. Dervan Design of peptides that bind in the minor groove of DNA at 5′-(A, T)5G(A, T)C(A, T) sequences by a dimeric side-by-side motif J. Am. Chem. Soc. 114 1992 8783 8794
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 8783-8794
    • Wade, W.S.1    Mrksich, M.2    Dervan, P.B.3
  • 7
    • 0029662190 scopus 로고
    • Effects of the A·T/T·A degeneracy of pyrrole-imidazole polyamide recognition in the minor groove of DNA
    • S. White, E.E. Baird, and P.B. Dervan Effects of the A·T/ T·A degeneracy of pyrrole-imidazole polyamide recognition in the minor groove of DNA Biochemistry 35 1992 12532 12537
    • (1992) Biochemistry , vol.35 , pp. 12532-12537
    • White, S.1    Baird, E.E.2    Dervan, P.B.3
  • 8
    • 0034830898 scopus 로고    scopus 로고
    • Molecular recognition of DNA by small molecules
    • P.B. Dervan Molecular recognition of DNA by small molecules Bioorg. Med. Chem. 9 2001 2215 2235
    • (2001) Bioorg. Med. Chem. , vol.9 , pp. 2215-2235
    • Dervan, P.B.1
  • 9
    • 0344641913 scopus 로고    scopus 로고
    • Sequence-specific DNA recognition by polyamides
    • P.B. Dervan, and R.W. Burli Sequence-specific DNA recognition by polyamides Curr. Opin. Chem. Biol. 3 1999 688 693
    • (1999) Curr. Opin. Chem. Biol. , vol.3 , pp. 688-693
    • Dervan, P.B.1    Burli, R.W.2
  • 11
    • 67849133724 scopus 로고    scopus 로고
    • Identification and cleavage site analysis of DNA sequences bound strongly by bleomycin
    • Q. Ma, Y. Akiyama, Z. Xu, K. Konishi, and S.M. Hecht Identification and cleavage site analysis of DNA sequences bound strongly by bleomycin J. Am. Chem. Soc. 131 2009 2013 2022
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 2013-2022
    • Ma, Q.1    Akiyama, Y.2    Xu, Z.3    Konishi, K.4    Hecht, S.M.5
  • 12
    • 33646015109 scopus 로고    scopus 로고
    • Major groove recognition of DNA by carbohydrates
    • B. Willis, and D.P. Arya Major groove recognition of DNA by carbohydrates Curr. Org. Chem. 10 2006 663 673
    • (2006) Curr. Org. Chem. , vol.10 , pp. 663-673
    • Willis, B.1    Arya, D.P.2
  • 13
    • 77951023778 scopus 로고    scopus 로고
    • Calorimetric and spectroscopic studies of aminoglycoside binding to AT-rich DNA triple helices
    • H. Xi, S. Kumar, L. Dosen-Micovic, and D.P. Arya Calorimetric and spectroscopic studies of aminoglycoside binding to AT-rich DNA triple helices Biochimie 92 2010 514 529
    • (2010) Biochimie , vol.92 , pp. 514-529
    • Xi, H.1    Kumar, S.2    Dosen-Micovic, L.3    Arya, D.P.4
  • 14
    • 80055014243 scopus 로고    scopus 로고
    • Thermodynamics of nucleic acid "shape readout" by an aminosugar
    • H. Xi, E. Davis, N. Ranjan, L. Xue, D. Hyde-Volpe, and D.P. Arya Thermodynamics of nucleic acid "shape readout" by an aminosugar Biochemistry 50 2011 9088 9113
    • (2011) Biochemistry , vol.50 , pp. 9088-9113
    • Xi, H.1    Davis, E.2    Ranjan, N.3    Xue, L.4    Hyde-Volpe, D.5    Arya, D.P.6
  • 15
    • 79960914931 scopus 로고    scopus 로고
    • Recognition of HIV TAR RNA by triazole linked neomycin dimers
    • S. Kumar, and D.P. Arya Recognition of HIV TAR RNA by triazole linked neomycin dimers Bioorg. Med. Chem. Lett. 21 2011 4788 4792
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 4788-4792
    • Kumar, S.1    Arya, D.P.2
  • 16
    • 79955927721 scopus 로고    scopus 로고
    • Neomycin-neomycin dimer: An all-carbohydrate scaffold with high affinity for AT-rich DNA duplexes
    • S. Kumar, L. Xue, and D.P. Arya Neomycin-neomycin dimer: an all-carbohydrate scaffold with high affinity for AT-rich DNA duplexes J. Am. Chem. Soc. 133 2011 7361 7375
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 7361-7375
    • Kumar, S.1    Xue, L.2    Arya, D.P.3
  • 17
    • 0041932005 scopus 로고    scopus 로고
    • Aminoglycoside (neomycin) preference is for A-form nucleic acids, not just RNA: Results from a competition dialysis study
    • D.P. Arya, L. Xue, and B. Willis Aminoglycoside (neomycin) preference is for A-form nucleic acids, not just RNA: results from a competition dialysis study J. Am. Chem. Soc. 125 2003 10148 10149
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10148-10149
    • Arya, D.P.1    Xue, L.2    Willis, B.3
  • 19
    • 0035177432 scopus 로고    scopus 로고
    • Acridine - A neglected antibacterial chromophore
    • M. Wainwright Acridine - a neglected antibacterial chromophore J. Antimicrob. Chemother. 47 2001 1 13
    • (2001) J. Antimicrob. Chemother. , vol.47 , pp. 1-13
    • Wainwright, M.1
  • 21
    • 0025768698 scopus 로고
    • The genetic toxicology of acridines
    • L.R. Ferguson, and W.A. Denny The genetic toxicology of acridines Mut. Res. 258 1991 123 160
    • (1991) Mut. Res. , vol.258 , pp. 123-160
    • Ferguson, L.R.1    Denny, W.A.2
  • 22
    • 0036024720 scopus 로고    scopus 로고
    • Acridine derivatives as chemotherapeutic agents
    • W. Denny Acridine derivatives as chemotherapeutic agents Curr. Med. Chem. 9 2002 1655 1665
    • (2002) Curr. Med. Chem. , vol.9 , pp. 1655-1665
    • Denny, W.1
  • 23
    • 33745185876 scopus 로고    scopus 로고
    • Intercalation of organic dye molecules into double-stranded DNA-general principles and recent developments
    • H. Ihmels, and D. Otto Intercalation of organic dye molecules into double-stranded DNA-general principles and recent developments Top. Curr. Chem. 258 2005 161 204
    • (2005) Top. Curr. Chem. , vol.258 , pp. 161-204
    • Ihmels, H.1    Otto, D.2
  • 27
    • 0033003394 scopus 로고    scopus 로고
    • Natural guanidine derivatives
    • R.G. Berlinck Natural guanidine derivatives Nat. Prod. Rep. 16 1999 339 365
    • (1999) Nat. Prod. Rep. , vol.16 , pp. 339-365
    • Berlinck, R.G.1
  • 29
    • 0034400884 scopus 로고    scopus 로고
    • The guanidine metabolites of Ptilocaulis spiculifer and related compounds; Isolation and synthesis
    • L. Heys, C.G. Moore, and P.J. Murphy The guanidine metabolites of Ptilocaulis spiculifer and related compounds; isolation and synthesis Chem. Soc. Rev. 29 2000 57 67
    • (2000) Chem. Soc. Rev. , vol.29 , pp. 57-67
    • Heys, L.1    Moore, C.G.2    Murphy, P.J.3
  • 30
    • 0000419336 scopus 로고
    • Synthesis and chemistry of guanidine derivatives
    • S. Patai, Z. Rappoport, John Wiley & Sons Chichester, U.K
    • Y. Yamamoto, and S. Kojima Synthesis and chemistry of guanidine derivatives S. Patai, Z. Rappoport, The Chemistry of Amidines and Imidates 1991 John Wiley & Sons Chichester, U.K 485 526
    • (1991) The Chemistry of Amidines and Imidates , pp. 485-526
    • Yamamoto, Y.1    Kojima, S.2
  • 31
    • 0034709386 scopus 로고    scopus 로고
    • A practical entry to the crambescidin family of guanidine alkaloids. Enantioselective total syntheses of ptilomycalin A, crambescidin 657 and its methyl ester (neofolitispates 2) and crambescidin 800
    • D.S. Coffey, A.I. McDonald, L.E. Overman, M.H. Rabinowitz, and P.A. Renhowe A practical entry to the crambescidin family of guanidine alkaloids. Enantioselective total syntheses of ptilomycalin A, crambescidin 657 and its methyl ester (neofolitispates 2) and crambescidin 800 J. Am. Chem. Soc. 122 2000 4893 4903
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4893-4903
    • Coffey, D.S.1    McDonald, A.I.2    Overman, L.E.3    Rabinowitz, M.H.4    Renhowe, P.A.5
  • 33
    • 70349763292 scopus 로고    scopus 로고
    • Biological activities of guanidine compounds
    • F. Saczewski, and L. Balewski Biological activities of guanidine compounds Exp. Opin. Ther. Patents 10 2009 1417 1448
    • (2009) Exp. Opin. Ther. Patents , vol.10 , pp. 1417-1448
    • Saczewski, F.1    Balewski, L.2
  • 35
    • 0034605221 scopus 로고    scopus 로고
    • Solid-phase of acridine-based threading intercalator peptides
    • C.B. Carlson, and P.A. Beal Solid-phase of acridine-based threading intercalator peptides Bioorg. Med. Chem. Lett. 10 2000 1979 1982
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1979-1982
    • Carlson, C.B.1    Beal, P.A.2
  • 38
    • 11844291970 scopus 로고    scopus 로고
    • The search of DNA-intercalators as antitumoral drugs: What it worked and what did not work
    • R. Martinez, and L. Chacon-Garcia The search of DNA-intercalators as antitumoral drugs: what it worked and what did not work Curr. Med. Chem. 12 2005 127 151
    • (2005) Curr. Med. Chem. , vol.12 , pp. 127-151
    • Martinez, R.1    Chacon-Garcia, L.2
  • 39
    • 0038620773 scopus 로고
    • DNA binding studies and site selective fluorescence sensitization of an anthryl probe
    • C.V. Kumar, and E.H. Asuncion DNA binding studies and site selective fluorescence sensitization of an anthryl probe J. Am. Chem. Soc. 115 1993 8547 8553
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 8547-8553
    • Kumar, C.V.1    Asuncion, E.H.2
  • 40
    • 0031304271 scopus 로고    scopus 로고
    • Optical absorbance and fluorescence techniques for measuring DNA-drug interactions
    • K.R. Fox, Human Press Totowa, New Jersey
    • T.C. Jenkins Optical absorbance and fluorescence techniques for measuring DNA-drug interactions K.R. Fox, Drug-DNA Interaction Protocols 1997 Human Press Totowa, New Jersey 195 218
    • (1997) Drug-DNA Interaction Protocols , pp. 195-218
    • Jenkins, T.C.1
  • 41
    • 0016175370 scopus 로고
    • Theoretical aspects of DNA-protein interactions: Co-operative and non-co-operative binding of large ligands to a one-dimensional homogeneous lattice
    • J.D. McGhee, and P.H. von Hippel Theoretical aspects of DNA-protein interactions: co-operative and non-co-operative binding of large ligands to a one-dimensional homogeneous lattice J. Mol. Biol. 86 1974 469 489
    • (1974) J. Mol. Biol. , vol.86 , pp. 469-489
    • McGhee, J.D.1    Von Hippel, P.H.2
  • 42
    • 79651471870 scopus 로고    scopus 로고
    • Technical University in Košice Košice
    • J. Busa Octave 2006 Technical University in Košice Košice
    • (2006) Octave
    • Busa, J.1
  • 44
    • 33846513983 scopus 로고    scopus 로고
    • Stability and structural features of DNA intercalation with ethidium bromide, acridine orange and methylene blue
    • S. Nafisi, A.A. Saboury, N. Keramat, J.-F. Neault, and H.-A. Tajmir-Riahi Stability and structural features of DNA intercalation with ethidium bromide, acridine orange and methylene blue J. Mol. Struct. 827 2007 35 43
    • (2007) J. Mol. Struct. , vol.827 , pp. 35-43
    • Nafisi, S.1    Saboury, A.A.2    Keramat, N.3    Neault, J.-F.4    Tajmir-Riahi, H.-A.5
  • 45
    • 18844447286 scopus 로고    scopus 로고
    • Study on the interaction of new water-soluble porphyrin with DNA
    • J. Kang, H. Wu, X. Lu, Y. Wang, and L. Zhou Study on the interaction of new water-soluble porphyrin with DNA Spectrochim. Acta A 61 2005 2041 2047
    • (2005) Spectrochim. Acta A , vol.61 , pp. 2041-2047
    • Kang, J.1    Wu, H.2    Lu, X.3    Wang, Y.4    Zhou, L.5
  • 49
    • 23944453324 scopus 로고    scopus 로고
    • Synthesis, DNA affinity and protozoal activity of fused ring dicationic compounds and their prodrugs
    • R.K. Arafa, R. Brun, T. Wenzler, F.A. Tanious, W.D. Wilson, C.E. Stephens, and D.W. Boykin Synthesis, DNA affinity and protozoal activity of fused ring dicationic compounds and their prodrugs J. Med. Chem. 48 2005 5480 5488
    • (2005) J. Med. Chem. , vol.48 , pp. 5480-5488
    • Arafa, R.K.1    Brun, R.2    Wenzler, T.3    Tanious, F.A.4    Wilson, W.D.5    Stephens, C.E.6    Boykin, D.W.7
  • 52
    • 12044256590 scopus 로고
    • Base inclinations in natural and synthetic DNAs
    • P.-J. Chou, and W.C. Johnson Base inclinations in natural and synthetic DNAs J. Am. Chem. Soc. 115 1993 1205 1214
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 1205-1214
    • Chou, P.-J.1    Johnson, W.C.2
  • 53
    • 0029026601 scopus 로고
    • Criteria for the mode of binding of DNA binding agents
    • D. Suh, and J.B. Chaires Criteria for the mode of binding of DNA binding agents Bioorg. Med. Chem. 3 1995 723 728
    • (1995) Bioorg. Med. Chem. , vol.3 , pp. 723-728
    • Suh, D.1    Chaires, J.B.2
  • 54
    • 77955417849 scopus 로고    scopus 로고
    • Thermodynamic and structural study of pyrene-1-carboxaldehyde/DNA interactions by molecular spectroscopy: Probing intercalation and binding properties
    • E. Grueso, and R. Prado-Gotor Thermodynamic and structural study of pyrene-1-carboxaldehyde/DNA interactions by molecular spectroscopy: probing intercalation and binding properties Chem. Phys. 373 2010 186 192
    • (2010) Chem. Phys. , vol.373 , pp. 186-192
    • Grueso, E.1    Prado-Gotor, R.2
  • 55
    • 0035724690 scopus 로고    scopus 로고
    • DNA topoisomerases as targets for anticancer drugs
    • Z. Topcu DNA topoisomerases as targets for anticancer drugs J. Clin. Pharm. Ther. 26 2001 405 416
    • (2001) J. Clin. Pharm. Ther. , vol.26 , pp. 405-416
    • Topcu, Z.1
  • 56
    • 33749658088 scopus 로고    scopus 로고
    • Topoisomerase enzymes as therapeutic targets for cancer chemotherapy
    • G.I. Giles, and R.P. Sharma Topoisomerase enzymes as therapeutic targets for cancer chemotherapy Med. Chem. 1 2005 383 394
    • (2005) Med. Chem. , vol.1 , pp. 383-394
    • Giles, G.I.1    Sharma, R.P.2
  • 57
    • 33749034730 scopus 로고    scopus 로고
    • Topoisomerase i inhibitors: Camptothecins and beyond
    • Y. Pommier Topoisomerase I inhibitors: camptothecins and beyond Nat. Rev. Cancer 6 2006 789 802
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 789-802
    • Pommier, Y.1
  • 58
    • 34249018852 scopus 로고    scopus 로고
    • Synthesis, DNA binding, and Leishmania topoisomerase inhibition activities of a novel series of anthra[1,2-d]imidazole-6,11-dione derivatives
    • P. Chaudhuri, H.K. Majumder, and S. Battacharya Synthesis, DNA binding, and Leishmania topoisomerase inhibition activities of a novel series of anthra[1,2-d]imidazole-6,11-dione derivatives J. Med. Chem. 50 2007 2536 2540
    • (2007) J. Med. Chem. , vol.50 , pp. 2536-2540
    • Chaudhuri, P.1    Majumder, H.K.2    Battacharya, S.3
  • 59
    • 84961983597 scopus 로고    scopus 로고
    • An experimental and computational analysis on the differential role of the positional isomers of symmetric bis-2-(pyridyl)-1H-benzimidazoles as DNA binding agents
    • P. Chaudhuri, B. Ganguly, and S. Battacharya An experimental and computational analysis on the differential role of the positional isomers of symmetric bis-2-(pyridyl)-1H-benzimidazoles as DNA binding agents J. Org. Chem. 72 2007 1912 1923
    • (2007) J. Org. Chem. , vol.72 , pp. 1912-1923
    • Chaudhuri, P.1    Ganguly, B.2    Battacharya, S.3
  • 60
    • 22744457037 scopus 로고    scopus 로고
    • Human DNA topoisomerase I: Relaxation, roles, and damage control
    • J.B. Leppard, and J.J. Champoux Human DNA topoisomerase I: relaxation, roles, and damage control Chromosoma 114 2005 75 85
    • (2005) Chromosoma , vol.114 , pp. 75-85
    • Leppard, J.B.1    Champoux, J.J.2
  • 62
    • 34548391416 scopus 로고    scopus 로고
    • DNA topoisomerase II, genotoxicity, and cancer
    • A.K. McClendon, and N. Osheroff DNA topoisomerase II, genotoxicity, and cancer Mutat. Res. 623 2007 83 97
    • (2007) Mutat. Res. , vol.623 , pp. 83-97
    • McClendon, A.K.1    Osheroff, N.2
  • 63
    • 0032189683 scopus 로고    scopus 로고
    • Mechanism of action of eukaryotic DNA topoisomerase i and drugs targeted to the enzyme
    • Y. Pommier, P. Pourquier, Y. Fan, and D. Strumberg Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme Biochim. Biophys. Acta 1400 1998 83 105
    • (1998) Biochim. Biophys. Acta , vol.1400 , pp. 83-105
    • Pommier, Y.1    Pourquier, P.2    Fan, Y.3    Strumberg, D.4
  • 64
    • 56049085650 scopus 로고    scopus 로고
    • Diazoniapolycyclic ions inhibit the activity of topoisomerase i and the growth of certain tumor cell lines
    • S. Basili, G. Basso, A. Faccio, A. Granzhan, H. Ihmels, S. Moro, and G. Viola Diazoniapolycyclic ions inhibit the activity of topoisomerase I and the growth of certain tumor cell lines ChemMedChem 3 2008 1671 1676
    • (2008) ChemMedChem , vol.3 , pp. 1671-1676
    • Basili, S.1    Basso, G.2    Faccio, A.3    Granzhan, A.4    Ihmels, H.5    Moro, S.6    Viola, G.7
  • 65
    • 79958120468 scopus 로고    scopus 로고
    • GADD45[alpha] and annexin A1 are involved in the apoptosis of HL-60 induced by resveratrol
    • G. Li, S. He, L. Chang, H. Lu, H. Zhang, H. Zhang, and J. Chiu GADD45[alpha] and annexin A1 are involved in the apoptosis of HL-60 induced by resveratrol Phytomedicine 18 2011 704 709
    • (2011) Phytomedicine , vol.18 , pp. 704-709
    • Li, G.1    He, S.2    Chang, L.3    Lu, H.4    Zhang, H.5    Zhang, H.6    Chiu, J.7
  • 66
    • 3142708522 scopus 로고    scopus 로고
    • Investigations on DNA intercalation and surface binding by SYBR green I, its structure determination and methodological implications
    • H. Zipper, H. Brunner, J. Bernhagen, and F. Vitzthum Investigations on DNA intercalation and surface binding by SYBR green I, its structure determination and methodological implications Nucleic Acids Res. 32 2004 e103
    • (2004) Nucleic Acids Res. , vol.32 , pp. 103
    • Zipper, H.1    Brunner, H.2    Bernhagen, J.3    Vitzthum, F.4
  • 67
    • 84871437039 scopus 로고    scopus 로고
    • http://www.chemaxon.com.
  • 68
    • 84871435653 scopus 로고    scopus 로고
    • http://gabedit.sourceforge.net.
  • 70
    • 33947716119 scopus 로고    scopus 로고
    • A semi-empirical free energy force field with charge-based desolvation
    • R. Huey, G.M. Morris, A.J. Olson, and D.S. Goodsell A semi-empirical free energy force field with charge-based desolvation J. Comput. Chem. 28 2007 1145 1152
    • (2007) J. Comput. Chem. , vol.28 , pp. 1145-1152
    • Huey, R.1    Morris, G.M.2    Olson, A.J.3    Goodsell, D.S.4
  • 73
    • 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. Model. 17 1999 57 61
    • (1999) J. Mol. Graph. Model. , vol.17 , pp. 57-61
    • Sanner, M.F.1
  • 75
    • 0001398008 scopus 로고    scopus 로고
    • How well does a restrained electrostatic potential (RESP) model perform in calculating conformational energies of organic and biological molecules?
    • J. Wang, W. Wang, P.A. Kollman, and D.A. Case How well does a restrained electrostatic potential (RESP) model perform in calculating conformational energies of organic and biological molecules? J. Comput. Chem. 21 2000 1049 1074
    • (2000) J. Comput. Chem. , vol.21 , pp. 1049-1074
    • Wang, J.1    Wang, W.2    Kollman, P.A.3    Case, D.A.4
  • 79
    • 0037075120 scopus 로고    scopus 로고
    • DNA cross-linking by azinomycin B: Monte Carlo simulations in the evaluation of sequence selectivity
    • S. Alcaro, F. Ortuso, and R.S. Coleman DNA cross-linking by azinomycin B: Monte Carlo simulations in the evaluation of sequence selectivity J. Med. Chem. 45 2002 861 870
    • (2002) J. Med. Chem. , vol.45 , pp. 861-870
    • Alcaro, S.1    Ortuso, F.2    Coleman, R.S.3


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