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Volumn 63, Issue , 2013, Pages 256-268

Novel chiral ferrocenylpyrazolo[1,5-a][1,4]diazepin-4-one derivatives-Synthesis, characterization and inhibition against lung cancer cells

Author keywords

Apoptosis; Cell cycle arrest; Chiral diazepinone; Ferrocene; Lung cancer cells; Pyrazole

Indexed keywords

2 FERROCENYL 5 (2 FLUOROPHENETHYL) 7 HYDROXY 5,6,7,8 TETRAHYDRO 4H PYRAZOLO[1,5 A][1,4]DIAZEPINE 4 ONE; 2 FERROCENYL 5 (4 FLUOROPHENETHYL) 7 HYDROXY 5,6,7,8 TETRAHDYRO 4H PYRAZOLO[1,5 A][1,4]DIAZEPINE 4 ONE; 2 FERROCENYL 7 HYDROXY 5 (3 METHOXYPHENETHYL) 5,6,7,8 TETRAHYDRO 4H PYRAZOLO[1,5 A][1,4]DIAZEPIN 4 ONE; 2 FERROCENYL 7 HYDROXY 5 PHENETHYL 5,6,7,8 TETRAHYDRO 4H PYRAZOLO[1,5 A][1,4]DIAZEPIN 4 ONE; 5 (2 FLUOROPHENETHYL) 7 HYDROXY 2 FERROCENYL 5,6,7,8 TETRAHYDRO 4H PYRAZOLO[1,5 A][1,4]DIAZEPINE 4 ONE; 5 ARYLETHYL 2 FERROCENYL 7 HYDROXY 5,6,7,8 TETRAHYDRO 4H PYRAZOLO[1,5 A][1,4]DIAZEPIN 4 ONE; 7 HYDROXY 5 (3 METHOXYPHENETHYL) 2 PHENYL 5,6,7,8 TETRAHYDROPROPYRAZOLO[1,5 A][1,4]DIAZEPIN 4 ONE; ANTINEOPLASTIC AGENT; BENZENE; DIAZEPINE DERIVATIVE; DIETHYL 1,1' [(PHENETHYLAZANEDIYL)BIS(2 HDYROXYPROPANE 3,1 DIYL)]BIS(3 FERROCENYL 1H PYRAZOLE 5 CARBOXYLATE); UNCLASSIFIED DRUG;

EID: 84874941515     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.02.016     Document Type: Article
Times cited : (30)

References (65)
  • 3
    • 77957827162 scopus 로고    scopus 로고
    • Synthesis of new pyrazole derivatives and their anticancer evaluation
    • G.M. Nitulescu, C. Draghici, and A.V. Missir Synthesis of new pyrazole derivatives and their anticancer evaluation Eur. J. Med. Chem. 45 2010 4914 4919
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 4914-4919
    • Nitulescu, G.M.1    Draghici, C.2    Missir, A.V.3
  • 4
    • 77955551619 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of some new thiazole, thiophene and pyrazole derivatives containing benzothiazole moiety
    • S. Bondock, W. Fadaly, and M.A. Metwally Synthesis and antimicrobial activity of some new thiazole, thiophene and pyrazole derivatives containing benzothiazole moiety Eur. J. Med. Chem. 45 2010 3692 3701
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 3692-3701
    • Bondock, S.1    Fadaly, W.2    Metwally, M.A.3
  • 8
    • 72149083045 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a novel series of pyrazole chalcones as anti-inflammatory, antioxidant and antimicrobial agents
    • B.P. Bandgar, S.S. Gawande, R.G. Bodade, N.M. Gawande, and C.N. Khobragade Synthesis and biological evaluation of a novel series of pyrazole chalcones as anti-inflammatory, antioxidant and antimicrobial agents Bioorg. Med. Chem. 17 2009 8168 8173
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 8168-8173
    • Bandgar, B.P.1    Gawande, S.S.2    Bodade, R.G.3    Gawande, N.M.4    Khobragade, C.N.5
  • 11
    • 84861622667 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of a novel series of 1,3,4-oxadiazole bearing N-methyl-4-(trifluoromethyl)phenyl pyrazole moiety as cytotoxic agents
    • P. Puthiyapurayil, B. Poojary, C. Chikkanna, and S.K. Buridipad Design, synthesis and biological evaluation of a novel series of 1,3,4-oxadiazole bearing N-methyl-4-(trifluoromethyl)phenyl pyrazole moiety as cytotoxic agents Eur. J. Med. Chem. 53 2012 203 210
    • (2012) Eur. J. Med. Chem. , vol.53 , pp. 203-210
    • Puthiyapurayil, P.1    Poojary, B.2    Chikkanna, C.3    Buridipad, S.K.4
  • 12
    • 84857921808 scopus 로고    scopus 로고
    • Synthesis and biological validation of novel pyrazole derivatives with anticancer activity guided by 3D-QSAR analysis
    • I. Vujasinović, A. Paravić-Radičević, K. Mlinarić-Majerski, K. Brajša, and B. Bertoša Synthesis and biological validation of novel pyrazole derivatives with anticancer activity guided by 3D-QSAR analysis Bioorg. Med. Chem. 20 2012 2101 2110
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 2101-2110
    • Vujasinović, I.1    Paravić-Radičević, A.2    Mlinarić-Majerski, K.3    Brajša, K.4    Bertoša, B.5
  • 14
    • 84864398952 scopus 로고    scopus 로고
    • Synthesis of ferrocenyl pyrazole-containing chiral aminoethanol derivatives and their inhibition against A549 and H322 lung cancer cells
    • S.L. Shen, J. Zhu, M. Li, B.X. Zhao, and J.Y. Miao Synthesis of ferrocenyl pyrazole-containing chiral aminoethanol derivatives and their inhibition against A549 and H322 lung cancer cells Eur. J. Med. Chem. 54 2012 287 294
    • (2012) Eur. J. Med. Chem. , vol.54 , pp. 287-294
    • Shen, S.L.1    Zhu, J.2    Li, M.3    Zhao, B.X.4    Miao, J.Y.5
  • 16
    • 0016012745 scopus 로고
    • Quantitative assay of pyrazofurin, a new antiviral, antitumor antibiotic
    • J.E. Westhead, and H.D. Price Quantitative assay of pyrazofurin, a new antiviral, antitumor antibiotic Antimicrob. Agents Chemother. 5 1 1974 90 91
    • (1974) Antimicrob. Agents Chemother. , vol.5 , Issue.1 , pp. 90-91
    • Westhead, J.E.1    Price, H.D.2
  • 20
    • 84856637031 scopus 로고    scopus 로고
    • Exploring the chemistry of epoxy amides for the synthesis of the 2″-epi-diazepanone core of liposidomycins and caprazamycins
    • F. Sarabia, C. Vivar-García, C. García-Ruiz, L. Martín-Ortiz, and A. Romero-Carrasco Exploring the chemistry of epoxy amides for the synthesis of the 2″-epi-diazepanone core of liposidomycins and caprazamycins J. Org. Chem. 77 2012 1328 1339
    • (2012) J. Org. Chem. , vol.77 , pp. 1328-1339
    • Sarabia, F.1    Vivar-García, C.2    García-Ruiz, C.3    Martín-Ortiz, L.4    Romero-Carrasco, A.5
  • 21
    • 43049148337 scopus 로고    scopus 로고
    • Structure-activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents
    • S. Hirano, S. Ichikawa, and A. Matsuda Structure-activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents Bioorg. Med. Chem. 16 2008 5123 5133
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 5123-5133
    • Hirano, S.1    Ichikawa, S.2    Matsuda, A.3
  • 22
    • 0014691619 scopus 로고
    • Platinum compounds: A new class of potent antitumour agents
    • B. Rosenberg, L. VanCamp, J.E. Trosko, and V.H. Mansour Platinum compounds: a new class of potent antitumour agents Nature 222 1969 385 386
    • (1969) Nature , vol.222 , pp. 385-386
    • Rosenberg, B.1    Vancamp, L.2    Trosko, J.E.3    Mansour, V.H.4
  • 23
    • 33744486894 scopus 로고    scopus 로고
    • Metal-based antitumour drugs in the post genomic era
    • P.J. Dysona, and G. Sava Metal-based antitumour drugs in the post genomic era Dalton Trans. 16 2006 1929 1933
    • (2006) Dalton Trans. , vol.16 , pp. 1929-1933
    • Dysona, P.J.1    Sava, G.2
  • 25
    • 80052545632 scopus 로고    scopus 로고
    • Gold(I) complexes of water-soluble diphos-type ligands: Synthesis, anticancer activity, apoptosis and thioredoxin reductase inhibition
    • C. Wetzel, P.C. Kunz, M.U. Kassack, A. Hamacher, P. Böhler, W. Watjen, I. Ott, R. Rubbiani, and B. Spingler Gold(I) complexes of water-soluble diphos-type ligands: synthesis, anticancer activity, apoptosis and thioredoxin reductase inhibition Dalton Trans. 40 2011 9212 9220
    • (2011) Dalton Trans. , vol.40 , pp. 9212-9220
    • Wetzel, C.1    Kunz, P.C.2    Kassack, M.U.3    Hamacher, A.4    Böhler, P.5    Watjen, W.6    Ott, I.7    Rubbiani, R.8    Spingler, B.9
  • 26
  • 32
    • 84856718468 scopus 로고    scopus 로고
    • Cytotoxicity and hydrolysis of trans-Ti(IV) complexes of salen ligands: Structure-activity relationship studies
    • A. Tzubery, and E.Y. Tshuva Cytotoxicity and hydrolysis of trans-Ti(IV) complexes of salen ligands: structure-activity relationship studies Inorg. Chem. 51 2012 1796 1804
    • (2012) Inorg. Chem. , vol.51 , pp. 1796-1804
    • Tzubery, A.1    Tshuva, E.Y.2
  • 33
    • 79951698826 scopus 로고    scopus 로고
    • Functionalization of osmium arene anticancer complexes with (poly)arginine: Effect on cellular uptake, internalization, and cytotoxicity
    • S.H. van Rijt, H. Kostrhunova, V. Brabec, and P.J. Sadler Functionalization of osmium arene anticancer complexes with (poly)arginine: effect on cellular uptake, internalization, and cytotoxicity Bioconjug. Chem. 22 2011 218 226
    • (2011) Bioconjug. Chem. , vol.22 , pp. 218-226
    • Van Rijt, S.H.1    Kostrhunova, H.2    Brabec, V.3    Sadler, P.J.4
  • 36
    • 33751332303 scopus 로고
    • A new type of organo-iron compound
    • T.J. Kealy, and P.L. Pauson A new type of organo-iron compound Nature 168 1951 1039 1040
    • (1951) Nature , vol.168 , pp. 1039-1040
    • Kealy, T.J.1    Pauson, P.L.2
  • 37
    • 77955211857 scopus 로고    scopus 로고
    • Organometallic cyclic polyphenols derived from 1,2-(α-keto tri or tetra methylene) ferrocene show strong antiproliferative activity on hormone-independent breast cancer cells
    • D. Plazuk, S. Top, A. Vessières, M.-A. Plamont, M. Huché, J. Zakrzewski, A. Makal, K. Woźniak, and G. Jaouen Organometallic cyclic polyphenols derived from 1,2-(α-keto tri or tetra methylene) ferrocene show strong antiproliferative activity on hormone-independent breast cancer cells Dalton Trans. 39 2010 7444 7450
    • (2010) Dalton Trans. , vol.39 , pp. 7444-7450
    • Plazuk, D.1    Top, S.2    Vessières, A.3    Plamont, M.-A.4    Huché, M.5    Zakrzewski, J.6    Makal, A.7    Woźniak, K.8    Jaouen, G.9
  • 38
    • 48049083798 scopus 로고    scopus 로고
    • Ferrocene conjugates of chloroquine and other antimalarials: The development of ferroquine, a new antimalarial
    • D. Dive, and C. Biot Ferrocene conjugates of chloroquine and other antimalarials: the development of ferroquine, a new antimalarial ChemMedChem 3 2008 383 391
    • (2008) ChemMedChem , vol.3 , pp. 383-391
    • Dive, D.1    Biot, C.2
  • 40
    • 80053211447 scopus 로고    scopus 로고
    • Conjugation of substituted ferrocenyl to thiadiazine as apoptosis-inducing agents targeting the Bax/Bcl-2 pathway
    • R.D. Miao, J. Wei, M.H. Lv, Y. Cai, Y.P. Du, X.P. Hui, and Q. Wang Conjugation of substituted ferrocenyl to thiadiazine as apoptosis-inducing agents targeting the Bax/Bcl-2 pathway Eur. J. Med. Chem. 46 2011 5000 5009
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 5000-5009
    • Miao, R.D.1    Wei, J.2    Lv, M.H.3    Cai, Y.4    Du, Y.P.5    Hui, X.P.6    Wang, Q.7
  • 42
    • 79953225844 scopus 로고    scopus 로고
    • Ferrocenyl-substituted curcumin: Can it influence antioxidant ability to protect DNA?
    • P.Z. Li, and Z.Q. Liu Ferrocenyl-substituted curcumin: can it influence antioxidant ability to protect DNA? Eur. J. Med. Chem. 46 2011 1821 1826
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 1821-1826
    • Li, P.Z.1    Liu, Z.Q.2
  • 44
    • 33750806826 scopus 로고    scopus 로고
    • Design, synthesis, and preliminary biological evaluation of novel ethyl 1-(2′-hydroxy-3′-aroxypropyl)-3-aryl-1H-pyrazole-5-carboxylate
    • F. Wei, B.X. Zhao, B. Huang, L. Zhang, C.H. Sun, W.L. Dong, D.S. Shinc, and J.Y. Miao Design, synthesis, and preliminary biological evaluation of novel ethyl 1-(2′-hydroxy-3′-aroxypropyl)-3-aryl-1H-pyrazole-5-carboxylate Bioorg. Med. Chem. Lett. 16 2006 6342 6347
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 6342-6347
    • Wei, F.1    Zhao, B.X.2    Huang, B.3    Zhang, L.4    Sun, C.H.5    Dong, W.L.6    Shinc, D.S.7    Miao, J.Y.8
  • 45
    • 34548814453 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide derivatives as potential agents against A549 lung cancer cells
    • Y. Xia, Z.W. Dong, B.X. Zhao, X. Ge, N. Meng, D.S. Shin, and J.Y. Miao Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H- pyrazole-5-carbohydrazide derivatives as potential agents against A549 lung cancer cells Bioorg. Med. Chem. 15 2007 6893 6899
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 6893-6899
    • Xia, Y.1    Dong, Z.W.2    Zhao, B.X.3    Ge, X.4    Meng, N.5    Shin, D.S.6    Miao, J.Y.7
  • 46
    • 40649085969 scopus 로고    scopus 로고
    • Synthesis, structure characterization and preliminary biological evaluation of novel 5-alkyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H) -one derivatives
    • Y.S. Xie, X.H. Pan, B.X. Zhao, J.T. Liu, D.S. Shin, J.H. Zhang, L.W. Zheng, J. Zhao, and J.Y. Miao Synthesis, structure characterization and preliminary biological evaluation of novel 5-alkyl-2-ferrocenyl-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives J. Organomet. Chem. 693 2008 1367 1374
    • (2008) J. Organomet. Chem. , vol.693 , pp. 1367-1374
    • Xie, Y.S.1    Pan, X.H.2    Zhao, B.X.3    Liu, J.T.4    Shin, D.S.5    Zhang, J.H.6    Zheng, L.W.7    Zhao, J.8    Miao, J.Y.9
  • 47
    • 53249134365 scopus 로고    scopus 로고
    • 5-Alkyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives inhibit growth of lung cancer A549 cell by inducing apoptosis
    • X.H. Pan, X. Liu, B.X. Zhao, Y.S. Xie, D.S. Shin, S.L. Zhang, J. Zhao, and J.Y. Miao 5-Alkyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives inhibit growth of lung cancer A549 cell by inducing apoptosis Bioorg. Med. Chem. 16 2008 9093 9100
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 9093-9100
    • Pan, X.H.1    Liu, X.2    Zhao, B.X.3    Xie, Y.S.4    Shin, D.S.5    Zhang, S.L.6    Zhao, J.7    Miao, J.Y.8
  • 48
    • 47349110358 scopus 로고    scopus 로고
    • Synthesis and discovery of autophagy inducers for A549 and H460 lung cancer cells, novel 1-(2′-hydroxy-3′-aroxypropyl)-3-aryl-1H- pyrazole-5-carbohydrazide derivatives
    • C.D. Fan, B.X. Zhao, F. Wei, G.H. Zhang, W.L. Dong, and J.Y. Miao Synthesis and discovery of autophagy inducers for A549 and H460 lung cancer cells, novel 1-(2′-hydroxy-3′-aroxypropyl)-3-aryl-1H-pyrazole-5- carbohydrazide derivatives Bioorg. Med. Chem. Lett. 18 2008 3860 3864
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 3860-3864
    • Fan, C.D.1    Zhao, B.X.2    Wei, F.3    Zhang, G.H.4    Dong, W.L.5    Miao, J.Y.6
  • 49
    • 43049115718 scopus 로고    scopus 로고
    • Synthesis and discovery of a novel pyrazole derivative as an inhibitor of apoptosis through modulating integrin β4, ROS, and p53 levels in vascular endothelial cells
    • B.X. Zhao, L. Zhang, X.S. Zhu, M.S. Wan, J. Zhao, Y. Zhang, S.L. Zhang, and J.Y. Miao Synthesis and discovery of a novel pyrazole derivative as an inhibitor of apoptosis through modulating integrin β4, ROS, and p53 levels in vascular endothelial cells Bioorg. Med. Chem. 16 2008 5171 5180
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 5171-5180
    • Zhao, B.X.1    Zhang, L.2    Zhu, X.S.3    Wan, M.S.4    Zhao, J.5    Zhang, Y.6    Zhang, S.L.7    Miao, J.Y.8
  • 50
    • 56349098902 scopus 로고    scopus 로고
    • Synthesis and preliminary biological evaluation of novel pyrazolo[1,5-a] pyrazin-4(5H)-one derivatives as potential agents against A549 lung cancer cells
    • J.H. Zhang, C.D. Fan, B.X. Zhao, D.S. Shin, W.L. Dong, Y.S. Xie, and J.Y. Miao Synthesis and preliminary biological evaluation of novel pyrazolo[1,5-a] pyrazin-4(5H)-one derivatives as potential agents against A549 lung cancer cells Bioorg. Med. Chem. 16 2008 10165 10171
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 10165-10171
    • Zhang, J.H.1    Fan, C.D.2    Zhao, B.X.3    Shin, D.S.4    Dong, W.L.5    Xie, Y.S.6    Miao, J.Y.7
  • 51
    • 54049104981 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide hydrazone derivatives as potential agents against A549 lung cancer cells
    • Y. Xia, C.D. Fan, B.X. Zhao, J. Zhao, D.S. Shin, and J.Y. Miao Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5- carbohydrazide hydrazone derivatives as potential agents against A549 lung cancer cells Eur. J. Med. Chem. 43 2008 2347 2353
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 2347-2353
    • Xia, Y.1    Fan, C.D.2    Zhao, B.X.3    Zhao, J.4    Shin, D.S.5    Miao, J.Y.6
  • 52
    • 61349184617 scopus 로고    scopus 로고
    • Synthesis of novel substituted pyrazole-5-carbohydrazide hydrazone derivatives and discovery of a potent apoptosis inducer in A549 lung cancer cells
    • L.W. Zheng, L.L. Wu, B.X. Zhao, W.L. Dong, and J.Y. Miao Synthesis of novel substituted pyrazole-5-carbohydrazide hydrazone derivatives and discovery of a potent apoptosis inducer in A549 lung cancer cells Bioorg. Med. Chem. 17 2009 1957 1962
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 1957-1962
    • Zheng, L.W.1    Wu, L.L.2    Zhao, B.X.3    Dong, W.L.4    Miao, J.Y.5
  • 53
    • 71749114878 scopus 로고    scopus 로고
    • Synthesis and discovery of pyrazole-5-carbohydrazide N-glycosides as inducer of autophagy in A549 lung cancer cells
    • S. Lian, H. Su, B.X. Zhao, W.Y. Liu, L.W. Zheng, and J.Y. Miao Synthesis and discovery of pyrazole-5-carbohydrazide N-glycosides as inducer of autophagy in A549 lung cancer cells Bioorg. Med. Chem. 17 2009 7085 7092
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 7085-7092
    • Lian, S.1    Su, H.2    Zhao, B.X.3    Liu, W.Y.4    Zheng, L.W.5    Miao, J.Y.6
  • 54
    • 68949114187 scopus 로고    scopus 로고
    • Synthesis of novel pyrazole carboxamide derivatives and discovery of modulators for apoptosis or autophagy in A549 lung cancer cells
    • X.L. Ding, H.Y. Zhang, L. Qi, B.X. Zhao, S. Lian, H.S. Lv, and J.Y. Miao Synthesis of novel pyrazole carboxamide derivatives and discovery of modulators for apoptosis or autophagy in A549 lung cancer cells Bioorg. Med. Chem. Lett. 19 2009 5325 5328
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 5325-5328
    • Ding, X.L.1    Zhang, H.Y.2    Qi, L.3    Zhao, B.X.4    Lian, S.5    Lv, H.S.6    Miao, J.Y.7
  • 55
    • 79958753893 scopus 로고    scopus 로고
    • Synthesis of novel pyrazolo[1,5-a]pyrazin-4(5H)-one derivatives and their inhibition against growth of A549 and H322 lung cancer cells
    • L.W. Zheng, J.H. Shao, B.X. Zhao, and J.Y. Miao Synthesis of novel pyrazolo[1,5-a]pyrazin-4(5H)-one derivatives and their inhibition against growth of A549 and H322 lung cancer cells Bioorg. Med. Chem. Lett. 21 2011 3909 3913
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 3909-3913
    • Zheng, L.W.1    Shao, J.H.2    Zhao, B.X.3    Miao, J.Y.4
  • 56
    • 78649320250 scopus 로고    scopus 로고
    • Synthesis, crystal structure and biological evaluation of novel 2-(5-(hydroxymethyl)-3-phenyl-1H-pyrazol-1-yl)-1-phenylethanol derivatives
    • L.W. Zheng, J. Zhu, B.X. Zhao, Y.H. Huang, J. Ding, and J.Y. Miao Synthesis, crystal structure and biological evaluation of novel 2-(5-(hydroxymethyl)-3-phenyl-1H-pyrazol-1-yl)-1-phenylethanol derivatives Eur. J. Med. Chem. 45 2010 5792 5799
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 5792-5799
    • Zheng, L.W.1    Zhu, J.2    Zhao, B.X.3    Huang, Y.H.4    Ding, J.5    Miao, J.Y.6
  • 57
    • 84855641205 scopus 로고    scopus 로고
    • Synthesis of 5-benzyl-2-phenylpyrazolo[1,5-a]pyrazin-4,6(5H,7H)-dione derivatives and discovery of an apoptosis inducer for H322 lung cancer cells
    • H.S. Lv, X.Q. Kong, Q.Q. Ming, X. Jin, J.Y. Miao, and B.X. Zhao Synthesis of 5-benzyl-2-phenylpyrazolo[1,5-a]pyrazin-4,6(5H,7H)-dione derivatives and discovery of an apoptosis inducer for H322 lung cancer cells Bioorg. Med. Chem. Lett. 22 2012 844 849
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 844-849
    • Lv, H.S.1    Kong, X.Q.2    Ming, Q.Q.3    Jin, X.4    Miao, J.Y.5    Zhao, B.X.6
  • 58
    • 72049098462 scopus 로고    scopus 로고
    • Synthesis, single-crystal characterization and preliminary biological evaluation of novel ferrocenyl pyrazolo[1,5-a]pyrazin-4(5H)-one derivatives
    • Y.S. Xie, H.L. Zhao, H. Su, B.X. Zhao, J.T. Liu, J.K. Li, H.S. Lv, B.S. Wang, D.S. Shin, and J.Y. Miao Synthesis, single-crystal characterization and preliminary biological evaluation of novel ferrocenyl pyrazolo[1,5-a]pyrazin- 4(5H)-one derivatives Eur. J. Med. Chem. 45 2010 210 218
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 210-218
    • Xie, Y.S.1    Zhao, H.L.2    Su, H.3    Zhao, B.X.4    Liu, J.T.5    Li, J.K.6    Lv, H.S.7    Wang, B.S.8    Shin, D.S.9    Miao, J.Y.10
  • 59
    • 0000750790 scopus 로고
    • The structure of triclinic ferrocene at 101, 123 and 148 K
    • P. Seiler, and J.D. Dunitz The structure of triclinic ferrocene at 101, 123 and 148 K Acta Crystallogr. B 35 1979 2020 2032
    • (1979) Acta Crystallogr. B , vol.35 , pp. 2020-2032
    • Seiler, P.1    Dunitz, J.D.2
  • 60
    • 0037137615 scopus 로고    scopus 로고
    • Water stability and cytotoxic activity relationship of a series of ferrocenium derivatives. ESR insights on the radical production during the degradation process
    • G. Tabbì, C. Cassino, G. Cavigiolio, D. Colangelo, A. Ghiglia, I. Viano, and D. Osella Water stability and cytotoxic activity relationship of a series of ferrocenium derivatives. ESR insights on the radical production during the degradation process J. Med. Chem. 45 2002 5786 5796
    • (2002) J. Med. Chem. , vol.45 , pp. 5786-5796
    • Tabbì, G.1    Cassino, C.2    Cavigiolio, G.3    Colangelo, D.4    Ghiglia, A.5    Viano, I.6    Osella, D.7
  • 61
    • 33645521251 scopus 로고    scopus 로고
    • Metal complex SERMs (selective oestrogen receptor modulators). The influence of different metal units on breast cancer cell antiproliferative effects
    • A. Vessières, S. Top, W. Beck, E. Hillard, and G. Jaouen Metal complex SERMs (selective oestrogen receptor modulators). The influence of different metal units on breast cancer cell antiproliferative effects Dalton Trans. 4 2006 529 541
    • (2006) Dalton Trans. , vol.4 , pp. 529-541
    • Vessières, A.1    Top, S.2    Beck, W.3    Hillard, E.4    Jaouen, G.5
  • 63
    • 84867326201 scopus 로고    scopus 로고
    • Ferrocenyl bioconjugates of ampicillin and 6-aminopenicillinic acid-synthesis, electrochemistry and biological activity
    • J. Skiba, A. Rajnisz, K.N. de Oliveira, I. Ott, J. Solecka, and K. Kowalski Ferrocenyl bioconjugates of ampicillin and 6-aminopenicillinic acid-synthesis, electrochemistry and biological activity Eur. J. Med. Chem. 57 2012 234 239
    • (2012) Eur. J. Med. Chem. , vol.57 , pp. 234-239
    • Skiba, J.1    Rajnisz, A.2    De Oliveira, K.N.3    Ott, I.4    Solecka, J.5    Kowalski, K.6


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