-
1
-
-
84859611140
-
Therapeutic targeting of Chk1 in NSCLC stem cells during chemotherapy
-
M. Bartucci, S. Svensson, P. Romania, R. Dattilo, M. Patrizii, M. Signore, S. Navarra, F. Lotti, M. Biffoni, E. Pilozzi, E. Duranti, S. Martinelli, C. Rinaldo, A. Zeuner, M. Maugeri-Saccà, A. Eramo, and R.D. Maria Therapeutic targeting of Chk1 in NSCLC stem cells during chemotherapy Cell. Death Differ. 19 2012 768 778
-
(2012)
Cell. Death Differ.
, vol.19
, pp. 768-778
-
-
Bartucci, M.1
Svensson, S.2
Romania, P.3
Dattilo, R.4
Patrizii, M.5
Signore, M.6
Navarra, S.7
Lotti, F.8
Biffoni, M.9
Pilozzi, E.10
Duranti, E.11
Martinelli, S.12
Rinaldo, C.13
Zeuner, A.14
Maugeri-Saccà, M.15
Eramo, A.16
Maria, R.D.17
-
3
-
-
77957827162
-
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
-
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
-
5
-
-
34047146536
-
Synthesis, docking studies and anti-inflammatory activity of 4,5,6,7-tetrahydro-2H-indazole derivatives
-
O. Rosati, M. Curini, M.C. Marcotullio, A. Macchiarulo, M. Perfumi, L. Mattioli, F. Rismondob, and G. Cravotto Synthesis, docking studies and anti-inflammatory activity of 4,5,6,7-tetrahydro-2H-indazole derivatives Bioorg. Med. Chem. 15 2007 3463 3473
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 3463-3473
-
-
Rosati, O.1
Curini, M.2
Marcotullio, M.C.3
Macchiarulo, A.4
Perfumi, M.5
Mattioli, L.6
Rismondob, F.7
Cravotto, G.8
-
7
-
-
0021919799
-
3,4-Diphenyl-1H-pyrazole-1-propanamine antidepressants
-
D.M. Bailey, P.E. Hansen, A.G. Hlavac, E.R. Baizman, J. Pear, A.F. DeFelice, and M.E. Feigensonf 3,4-Diphenyl-1H-pyrazole-1-propanamine antidepressants J. Med. Chem. 28 1985 256 260
-
(1985)
J. Med. Chem.
, vol.28
, pp. 256-260
-
-
Bailey, D.M.1
Hansen, P.E.2
Hlavac, A.G.3
Baizman, E.R.4
Pear, J.5
Defelice, A.F.6
Feigensonf, M.E.7
-
8
-
-
72149083045
-
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
-
9
-
-
77649295601
-
Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity
-
S.R. Shih, T.Y. Chu, G.R. Reddy, S.N. Tseng, H.L. Chen, W.F. Tang, M.S. Wu, J.Y. Yeh, Y.S. Chao, J.T. Hsu, H.P. Hsieh, and J.T. Horng Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity J. Biomed. Sci. 17 2010 13
-
(2010)
J. Biomed. Sci.
, vol.17
, pp. 13
-
-
Shih, S.R.1
Chu, T.Y.2
Reddy, G.R.3
Tseng, S.N.4
Chen, H.L.5
Tang, W.F.6
Wu, M.S.7
Yeh, J.Y.8
Chao, Y.S.9
Hsu, J.T.10
Hsieh, H.P.11
Horng, J.T.12
-
10
-
-
84856012562
-
Design, synthesis and biological evaluation of pyrazole derivatives as potential multi-kinase inhibitors in hepatocellular carcinoma
-
E. Strocchi, F. Fornari, M. Minguzzi, L. Gramantieri, M. Milazzo, V. Rebuttini, S. Breviglieri, C.M. Camaggi, E. Locatelli, L. Bolondi, and M. Comes-Franchini Design, synthesis and biological evaluation of pyrazole derivatives as potential multi-kinase inhibitors in hepatocellular carcinoma Eur. J. Med. Chem. 48 2012 391 401
-
(2012)
Eur. J. Med. Chem.
, vol.48
, pp. 391-401
-
-
Strocchi, E.1
Fornari, F.2
Minguzzi, M.3
Gramantieri, L.4
Milazzo, M.5
Rebuttini, V.6
Breviglieri, S.7
Camaggi, C.M.8
Locatelli, E.9
Bolondi, L.10
Comes-Franchini, M.11
-
11
-
-
84861622667
-
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
-
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
-
13
-
-
84860528870
-
Synthesis, characterization, and anticancer activity of ruthenium-pyrazole complexes
-
S. David, R.S. Perkins, F.R. Fronczek, S. Kasiri, S.S. Mandal, and R.S. Srivastava Synthesis, characterization, and anticancer activity of ruthenium-pyrazole complexes J. Inorg. Biochem. 111 2012 33 39
-
(2012)
J. Inorg. Biochem.
, vol.111
, pp. 33-39
-
-
David, S.1
Perkins, R.S.2
Fronczek, F.R.3
Kasiri, S.4
Mandal, S.S.5
Srivastava, R.S.6
-
14
-
-
84864398952
-
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
-
15
-
-
82755189699
-
Platinum(II) and palladium(II) complexes with (N, N′) and (C, N, N′)-ligands derived from pyrazole as anticancer and antimalarial agents: Synthesis, characterization and in vitro activities
-
J. Quirante, D. Ruiz, A. Gonzalez, C. López, M. Cascante, R. Cortés, R. Messeguer, C. Calvis, L. Baldomà, A. Pascual, Y. Guérardel, B. Pradines, M. Font-Bardía, T. Calvet, and C. Biot Platinum(II) and palladium(II) complexes with (N, N′) and (C, N, N′)-ligands derived from pyrazole as anticancer and antimalarial agents: synthesis, characterization and in vitro activities J. Inorg. Biochem. 105 2011 1720 1728
-
(2011)
J. Inorg. Biochem.
, vol.105
, pp. 1720-1728
-
-
Quirante, J.1
Ruiz, D.2
Gonzalez, A.3
López, C.4
Cascante, M.5
Cortés, R.6
Messeguer, R.7
Calvis, C.8
Baldomà, L.9
Pascual, A.10
Guérardel, Y.11
Pradines, B.12
Font-Bardía, M.13
Calvet, T.14
Biot, C.15
-
16
-
-
0016012745
-
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
-
17
-
-
35348865461
-
Efficient synthesis of polyfunctionalised enantiopure diazepanone scaffolds
-
O. Monasson, M. Ginisty, G. Bertho, C. Gravier-Pelletier, and Y.L. Merrer Efficient synthesis of polyfunctionalised enantiopure diazepanone scaffolds Tetrahedron Lett. 48 2007 8149 8152
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8149-8152
-
-
Monasson, O.1
Ginisty, M.2
Bertho, G.3
Gravier-Pelletier, C.4
Merrer, Y.L.5
-
18
-
-
0038264165
-
Caprazamycin B, a novel anti-tuberculosis antibiotic, from Streptomyces sp.
-
M. Igarashi, N. Nakagawa, N. Doi, S. Hattori, H. Naganawa, and M. Hamada Caprazamycin B, a novel anti-tuberculosis antibiotic, from Streptomyces sp. J. Antibiot. (Tokyo) 56 2003 580 583
-
(2003)
J. Antibiot. (Tokyo)
, vol.56
, pp. 580-583
-
-
Igarashi, M.1
Nakagawa, N.2
Doi, N.3
Hattori, S.4
Naganawa, H.5
Hamada, M.6
-
19
-
-
21044451034
-
Caprazamycins, novel lipo-nucleoside antibiotics, from Streptomyces sp.
-
M. Igarashi, Y. Takahashi, T. Shitara, H. Nakamura, H. Naganawa, T. Miyake, and Y. Akamatsu Caprazamycins, novel lipo-nucleoside antibiotics, from Streptomyces sp. J. Antibiot. (Tokyo) 58 2005 327 337
-
(2005)
J. Antibiot. (Tokyo)
, vol.58
, pp. 327-337
-
-
Igarashi, M.1
Takahashi, Y.2
Shitara, T.3
Nakamura, H.4
Naganawa, H.5
Miyake, T.6
Akamatsu, Y.7
-
20
-
-
84856637031
-
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
-
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
-
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
-
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
-
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
-
-
84864199303
-
A spontaneous gold(I)-azide alkyne cycloaddition reaction yields gold-peptide bioconjugates which overcome cisplatin resistance in a p53-mutant cancer cell line
-
S.D. Köster, H. Alborzinia, S. Can, I. Kitanovic, S. Wölfl, R. Rubbiani, I. Ott, P. Riesterer, A. Prokop, K. Merza, and N. Metzler-Nolte A spontaneous gold(I)-azide alkyne cycloaddition reaction yields gold-peptide bioconjugates which overcome cisplatin resistance in a p53-mutant cancer cell line Chem. Sci. 3 2012 2062 2072
-
(2012)
Chem. Sci.
, vol.3
, pp. 2062-2072
-
-
Köster, S.D.1
Alborzinia, H.2
Can, S.3
Kitanovic, I.4
Wölfl, S.5
Rubbiani, R.6
Ott, I.7
Riesterer, P.8
Prokop, A.9
Merza, K.10
Metzler-Nolte, N.11
-
27
-
-
84862522363
-
Cellular impact and selectivity of half-sandwich organorhodium(III) anticancer complexes and their organoiridium(III) and trichloridorhodium(III) counterparts
-
Y. Geldmacher, K. Splith, I. Kitanovic, H. Alborzinia, S. Can, R. Rubbiani, M.A. Nazif, P. Wefelmeier, A. Prokop, I. Ott, S. Wölfl, I. Neundorf, and W.S. Sheldrick Cellular impact and selectivity of half-sandwich organorhodium(III) anticancer complexes and their organoiridium(III) and trichloridorhodium(III) counterparts J. Biol. Inorg. Chem. 17 2012 631 646
-
(2012)
J. Biol. Inorg. Chem.
, vol.17
, pp. 631-646
-
-
Geldmacher, Y.1
Splith, K.2
Kitanovic, I.3
Alborzinia, H.4
Can, S.5
Rubbiani, R.6
Nazif, M.A.7
Wefelmeier, P.8
Prokop, A.9
Ott, I.10
Wölfl, S.11
Neundorf, I.12
Sheldrick, W.S.13
-
28
-
-
77957894713
-
Development of bimetallic titanocene-ruthenium-arene complexes as anticancer agents: Relationships between structural and biological properties
-
F. Pelletier, V. Comte, A. Massard, M. Wenzel, S. Toulot, P. Richard, M. Picquet, P.L. Gendre, O. Zava, F. Edafe, A. Casini, and P.J. Dyson Development of bimetallic titanocene-ruthenium-arene complexes as anticancer agents: relationships between structural and biological properties J. Med. Chem. 53 2010 6923 6933
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6923-6933
-
-
Pelletier, F.1
Comte, V.2
Massard, A.3
Wenzel, M.4
Toulot, S.5
Richard, P.6
Picquet, M.7
Gendre, P.L.8
Zava, O.9
Edafe, F.10
Casini, A.11
Dyson, P.J.12
-
29
-
-
84855679883
-
Maleimide-functionalised organoruthenium anticancer agents and their binding to thiol-containing biomolecules
-
M. Hanif, A.A. Nazarov, A. Legin, M. Groessl, V.B. Arion, M.A. Jakupec, Y.O. Tsybin, P.J. Dyson, B.K. Kepplera, and C.G. Hartinger Maleimide- functionalised organoruthenium anticancer agents and their binding to thiol-containing biomolecules Chem. Commun. 48 2012 1475 1477
-
(2012)
Chem. Commun.
, vol.48
, pp. 1475-1477
-
-
Hanif, M.1
Nazarov, A.A.2
Legin, A.3
Groessl, M.4
Arion, V.B.5
Jakupec, M.A.6
Tsybin, Y.O.7
Dyson, P.J.8
Kepplera, B.K.9
Hartinger, C.G.10
-
30
-
-
77957564933
-
Discovery, structure, and anticancer activity of an iridium complex of diselenobenzoquinone
-
H. Amouri, J. Moussa, A.K. Renfrew, P.J. Dyson, M.N. Rager, and L.-M. Chamoreau Discovery, structure, and anticancer activity of an iridium complex of diselenobenzoquinone Angew. Chem. Int. Ed. 49 2010 7530 7533
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 7530-7533
-
-
Amouri, H.1
Moussa, J.2
Renfrew, A.K.3
Dyson, P.J.4
Rager, M.N.5
Chamoreau, L.-M.6
-
31
-
-
66249093488
-
A new generation of anticancer drugs: Mesoporous materials modified with titanocene complexes
-
D. Pérez-Quintanilla, S. Gómez-Ruiz, Ž. Žižak, I. Sierra, S. Prashar, I. del Hierro, M. Fajardo, Z.D. Juranić, and G.N. Kaluderović A new generation of anticancer drugs: mesoporous materials modified with titanocene complexes Chem. Eur. J. 15 2009 5588 5597
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 5588-5597
-
-
Pérez-Quintanilla, D.1
Gómez-Ruiz, S.2
Žižak, Z.3
Sierra, I.4
Prashar, S.5
Del Hierro, I.6
Fajardo, M.7
Juranić, Z.D.8
Kaluderović, G.N.9
-
32
-
-
84856718468
-
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
-
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
-
34
-
-
84862232784
-
Ferrocenyl catechols: Synthesis, oxidation chemistry and anti-proliferative effects on MDA-MB-231 breast cancer cells
-
Y.L.K. Tan, P. Pigeon, S. Top, E. Labbé, O. Buriez, E.A. Hillard, A. Vessières, C. Amatore, W.K. Leong, and G. Jaouen Ferrocenyl catechols: synthesis, oxidation chemistry and anti-proliferative effects on MDA-MB-231 breast cancer cells Dalton Trans. 41 2012 7537 7549
-
(2012)
Dalton Trans.
, vol.41
, pp. 7537-7549
-
-
Tan, Y.L.K.1
Pigeon, P.2
Top, S.3
Labbé, E.4
Buriez, O.5
Hillard, E.A.6
Vessières, A.7
Amatore, C.8
Leong, W.K.9
Jaouen, G.10
-
35
-
-
79952195036
-
Ferrocene-indole hybrids for cancer and malaria therapy
-
J. Quirante, F. Dubar, A. González, C. Lopez, M. Cascante, R. Cortés, I. Forfar, B. Pradines, and C. Biot Ferrocene-indole hybrids for cancer and malaria therapy J. Organomet. Chem. 696 2011 1011 1017
-
(2011)
J. Organomet. Chem.
, vol.696
, pp. 1011-1017
-
-
Quirante, J.1
Dubar, F.2
González, A.3
Lopez, C.4
Cascante, M.5
Cortés, R.6
Forfar, I.7
Pradines, B.8
Biot, C.9
-
36
-
-
33751332303
-
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
-
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
-
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
-
39
-
-
79955550096
-
Synthesis and in vitro antitubercular activity of ferrocene-based hydrazones
-
A. Mahajan, L. Kremer, S. Louw, Y. Guéradel, K. Chibale, and C. Biot Synthesis and in vitro antitubercular activity of ferrocene-based hydrazones Bioorg. Med. Chem. Lett. 21 2011 2866 2868
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 2866-2868
-
-
Mahajan, A.1
Kremer, L.2
Louw, S.3
Guéradel, Y.4
Chibale, K.5
Biot, C.6
-
40
-
-
80053211447
-
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
-
41
-
-
80052934814
-
Biological evaluation of twenty-eight ferrocenyl tetrasubstituted olefins: Cancer cell growth inhibition, ROS production and hemolytic activity
-
A.C. de Oliveira, E.A. Hillard, P. Pigeon, D.D. Rocha, F.A. Rodrigues, R.C. Montenegro, L.V. Costa-Lotufo, M.O. Goulart, and G. Jaouen Biological evaluation of twenty-eight ferrocenyl tetrasubstituted olefins: cancer cell growth inhibition, ROS production and hemolytic activity Eur. J. Med. Chem. 46 2011 3778 3787
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 3778-3787
-
-
De Oliveira, A.C.1
Hillard, E.A.2
Pigeon, P.3
Rocha, D.D.4
Rodrigues, F.A.5
Montenegro, R.C.6
Costa-Lotufo, L.V.7
Goulart, M.O.8
Jaouen, G.9
-
42
-
-
79953225844
-
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
-
43
-
-
78650512040
-
Synthesis and antimycobacterial activity of a series of ferrocenyl derivatives
-
G.M. Maguene, J. Jakhlal, M. Ladyman, A. Vallin, D.A. Ralambomanana, T. Bousquet, J. Maugein, J. Lebibi, and L. Pélinski Synthesis and antimycobacterial activity of a series of ferrocenyl derivatives Eur. J. Med. Chem. 46 2011 31 38
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 31-38
-
-
Maguene, G.M.1
Jakhlal, J.2
Ladyman, M.3
Vallin, A.4
Ralambomanana, D.A.5
Bousquet, T.6
Maugein, J.7
Lebibi, J.8
Pélinski, L.9
-
44
-
-
33750806826
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
62
-
-
63049088802
-
Synthesis, spectral characterization and electrochemical properties of 1H-3-(o-, m- and p-ferrocenylphenyl)-1-phenylpyrazole-4-carboxaldehydes
-
I. Damljanović, M. Čolović, M. Vukić ević, D. Manojlović, N. Radulović, K. Wurst, G. Laus, Z. Ratković, M. Joksović, and R.D. Vukićević Synthesis, spectral characterization and electrochemical properties of 1H-3-(o-, m- and p-ferrocenylphenyl)-1-phenylpyrazole-4-carboxaldehydes J. Organomet. Chem. 694 2009 1575 1580
-
(2009)
J. Organomet. Chem.
, vol.694
, pp. 1575-1580
-
-
Damljanović, I.1
Čolović, M.2
Vukićević, M.3
Manojlović, D.4
Radulović, N.5
Wurst, K.6
Laus, G.7
Ratković, Z.8
Joksović, M.9
Vukićević, R.D.10
-
63
-
-
84867326201
-
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
|