-
1
-
-
79960192285
-
Phospshoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors: Discovery and structure-activity relationships of a series of quinoline and quinoxaline derivatives
-
N. Nishimura, A. Siegmund, L. Liu, K. Yang, M.C. Bryan, K.L. Andrews, Y. Bo, S.K. Booker, S. Caenepeel, D. Freeman, H. Liao, J. McCarter, E.L. Mullady, T. San Miguel, R. Subramanian, N. Tamayo, L. Wang, D.A. Whittington, L. Zalameda, N. Zhang, P.E. Hughes, M.H. Norman, Phospshoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors: discovery and structure-activity relationships of a series of quinoline and quinoxaline derivatives, J. Med. Chem. 54 (2011) 4735-4751.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4735-4751
-
-
Nishimura, N.1
Siegmund, A.2
Liu, L.3
Yang, K.4
Bryan, M.C.5
Andrews, K.L.6
Bo, Y.7
Booker, S.K.8
Caenepeel, S.9
Freeman, D.10
Liao, H.11
McCarter, J.12
Mullady, E.L.13
San Miguel, T.14
Subramanian, R.15
Tamayo, N.16
Wang, L.17
Whittington, D.A.18
Zalameda, L.19
Zhang, N.20
Hughes, P.E.21
Norman, M.H.22
more..
-
2
-
-
79955628183
-
Synthesis and in vitro antitumor activity of substituted quinazoline and quinoxaline derivatives: Search for anticancer agent
-
M.N. Noolvi, H.M. Patel, V. Bhardwaj, A. Chauhan, Synthesis and in vitro antitumor activity of substituted quinazoline and quinoxaline derivatives: search for anticancer agent, Eur. J. Med. Chem. 46 (2011) 2327-2346.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 2327-2346
-
-
Noolvi, M.N.1
Patel, H.M.2
Bhardwaj, V.3
Chauhan, A.4
-
3
-
-
84924379418
-
Preparation containing 1-diethylaminoethyl-3-quinoxalin-2-one derivatives for treatment cancer
-
CAN
-
C. Grimm, K. Ehrenberger, D. Thurnher, Preparation containing 1-diethylaminoethyl-3-quinoxalin-2-one derivatives for treatment cancer, PTC Int. Appl. WO 2005105098; CAN 143:452851, 2005.
-
(2005)
PTC Int. Appl.
, vol.143
, pp. 452851
-
-
Grimm, C.1
Ehrenberger, K.2
Thurnher, D.3
-
4
-
-
80054880978
-
Synthesis and biological evaluation of novel 2-arylamino-3-(arylsulfonyl)quinoxalines as PI3Ka inhibitors
-
P. Wua, Y. Sub, X. Liub, L. Zhangb, Y. Yea, J. Xua, S. Wenga, Y. Lia, T. Liua, S. Huanga, B. Yangb, Q. Heb, Y. Hua, Synthesis and biological evaluation of novel 2-arylamino-3-(arylsulfonyl)quinoxalines as PI3Ka inhibitors, Eur. J. Med. Chem. 46 (2011) 5540-5548.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 5540-5548
-
-
Wua, P.1
Sub, Y.2
Liub, X.3
Zhangb, L.4
Yea, Y.5
Xua, J.6
Wenga, S.7
Lia, Y.8
Liua, T.9
Huanga, S.10
Yangb, B.11
Heb, Q.12
Hua, Y.13
-
5
-
-
0035865923
-
Structure-activity studies of substituted quinoxalinones as multiple-drug-resistance antagonists
-
D.S. Lawrence, J.E. Copper, C.D. Smith, Structure-activity studies of substituted quinoxalinones as multiple-drug-resistance antagonists, J. Med. Chem. 44 (2001) 594-601.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 594-601
-
-
Lawrence, D.S.1
Copper, J.E.2
Smith, C.D.3
-
6
-
-
0029078874
-
Synthesis and biological evaluation of amino-substituted benzo[f]pyrido[4,3-b] and pyrido[3,4-b]quinoxalines: A new class of antineoplastic agents
-
C.H. Nguyen, E. Fan, J. Riou, M.C. Bissery, P. Vrignaud, F. Lavelle, E. Bisagni, Synthesis and biological evaluation of amino-substituted benzo[f]pyrido[4,3-b] and pyrido[3,4-b]quinoxalines: a new class of antineoplastic agents, Anti-Cancer Drug Des. 10 (1995) 277-297.
-
(1995)
Anti-Cancer Drug Des.
, vol.10
, pp. 277-297
-
-
Nguyen, C.H.1
Fan, E.2
Riou, J.3
Bissery, M.C.4
Vrignaud, P.5
Lavelle, F.6
Bisagni, E.7
-
7
-
-
0032444828
-
5-Substituted 2-bromoindolo[3,2-b]quinoxalines. A class of potential antitumor agents with cdc25 phosphatase inhibitory properties
-
A.H. Abadi, 5-Substituted 2-bromoindolo[3,2-b]quinoxalines. A class of potential antitumor agents with cdc25 phosphatase inhibitory properties, Arch. Pharm. Med. Chem. 331 (1998) 352-358.
-
(1998)
Arch. Pharm. Med. Chem.
, vol.331
, pp. 352-358
-
-
Abadi, A.H.1
-
8
-
-
0038825617
-
Pyrrolo[2,3-h]quinolinones: Synthesis and photo-chemotherapic activity
-
P. Barraja, P. Diana, A. Lauria, A. Montalbano, A.M. Almerico, G. Dattolo, G. Cirrincione, G. Viola, F. Dall'Acqua, Pyrrolo[2,3-h]quinolinones: synthesis and photo-chemotherapic activity, Bioorg. Med. Chem. Lett. 13 (2003) 2809-2811.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2809-2811
-
-
Barraja, P.1
Diana, P.2
Lauria, A.3
Montalbano, A.4
Almerico, A.M.5
Dattolo, G.6
Cirrincione, G.7
Viola, G.8
Dall'Acqua, F.9
-
9
-
-
77954217193
-
Synthesis of pyrrolo[3,2-h]quinolinones with good activity and no DNA damage
-
P. Barraja, L. Caracausi, P. Diana, A. Carbone, A. Montalbano, G. Cirrincione, P. Brun, G. Palù, I. Castagliuolo, F. Dall'Acqua, D. Vedaldi, A. Salvador, Synthesis of pyrrolo[3,2-h]quinolinones with good activity and no DNA damage, Bioorg. Med. Chem. 18 (2010) 4830-4843.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 4830-4843
-
-
Barraja, P.1
Caracausi, L.2
Diana, P.3
Carbone, A.4
Montalbano, A.5
Cirrincione, G.6
Brun, P.7
Palù, G.8
Castagliuolo, I.9
Dall'Acqua, F.10
Vedaldi, D.11
Salvador, A.12
-
10
-
-
79959771599
-
Pyrrolo [3,2-h]quinazolines as photochemotherapeutic agents
-
P. Barraja, L. Caracausi, P. Diana, A. Montalbano, A. Carbone, A. Salvador, P. Brun, I. Castagliuolo, S. Tisi, F. Dall'Acqua, D. Vedaldi, G. Cirrincione, Pyrrolo [3,2-h]quinazolines as photochemotherapeutic agents, Chem Med Chem 6 (2011) 1238-1248.
-
(2011)
Chem Med Chem
, vol.6
, pp. 1238-1248
-
-
Barraja, P.1
Caracausi, L.2
Diana, P.3
Montalbano, A.4
Carbone, A.5
Salvador, A.6
Brun, P.7
Castagliuolo, I.8
Tisi, S.9
Dall'Acqua, F.10
Vedaldi, D.11
Cirrincione, G.12
-
11
-
-
84861527373
-
An efficient synthesis of pyrrolo[3′,2′:4,5]thiopyrano[3,2-b] pyridin-2-one: A new ring system of pharmaceutical interest
-
P. Barraja, P. Diana, V. Spanò, A. Montalbano, A. Carbone, B. Parrino, G. Cirrincione, An efficient synthesis of pyrrolo[3′,2′:4,5]thiopyrano[3,2-b] pyridin-2-one: a new ring system of pharmaceutical interest, Tetrahedron 68 (2012) 5087-5094.
-
(2012)
Tetrahedron
, vol.68
, pp. 5087-5094
-
-
Barraja, P.1
Diana, P.2
Spanò, V.3
Montalbano, A.4
Carbone, A.5
Parrino, B.6
Cirrincione, G.7
-
12
-
-
84875613244
-
Synthesis and antiproliferative activity of 2,5-bis(3′- indolyl)pyrroles, analogues of the marine alkaloid nortopsentin
-
A. Carbone, B. Parrino, P. Barraja, V. Spanò, G. Cirrincione, P. Diana, A. Maier, G. Kelter, H.-H. Fiebig, Synthesis and antiproliferative activity of 2,5-bis(3′- indolyl)pyrroles, analogues of the marine alkaloid nortopsentin, Mar. Drugs 11 (2013) 643-654.
-
(2013)
Mar. Drugs
, vol.11
, pp. 643-654
-
-
Carbone, A.1
Parrino, B.2
Barraja, P.3
Spanò, V.4
Cirrincione, G.5
Diana, P.6
Maier, A.7
Kelter, G.8
Fiebig, H.-H.9
-
13
-
-
33750526864
-
Pyrrolo[2,3-h]quinolinones: A new ring system with potent photoantiproliferative activity
-
P. Barraja, P. Diana, A. Montalbano, G. Dattolo, G. Cirrincione, G. Viola, D. Vedaldi, F. Dall'Acqua, Pyrrolo[2,3-h]quinolinones: a new ring system with potent photoantiproliferative activity, Bioorg. Med. Chem. 14 (2006) 8712-8728.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 8712-8728
-
-
Barraja, P.1
Diana, P.2
Montalbano, A.3
Dattolo, G.4
Cirrincione, G.5
Viola, G.6
Vedaldi, D.7
Dall'Acqua, F.8
-
14
-
-
0036501452
-
Girolamo, Pyrrolo[2,1-c][1,2,4]triazines from 2-diazopyrroles: Synthesis and antiproliferative activity
-
P. Diana, P. Barraja, A. Lauria, A. Montalbano, A.M. Almerico, G. Dattolo, G. Cirrincione, Girolamo, Pyrrolo[2,1-c][1,2,4]triazines from 2-diazopyrroles: synthesis and antiproliferative activity, Eur. J. Med. Chem. 37 (2002) 267-272.
-
(2002)
Eur. J. Med. Chem.
, vol.37
, pp. 267-272
-
-
Diana, P.1
Barraja, P.2
Lauria, A.3
Montalbano, A.4
Almerico, A.M.5
Dattolo, G.6
Cirrincione, G.7
-
15
-
-
84913570543
-
11H-Pyrido[3′,2′:4,5]pyrrolo [3,2-c]cinnoline and Pyrido[3′,2′:4,5]pyrrolo[1,2-c][1,2,3]benzotriazine: Two new ring systems with antitumor activity
-
B. Parrino, A. Carbone, M. Muscarella, V. Spano, A. Montalbano, P. Barraja, A. Salvador, D. Vedaldi, G. Cirrincione, P. Diana, 11H-Pyrido[3′,2′:4,5]pyrrolo [3,2-c]cinnoline and Pyrido[3′,2′:4,5]pyrrolo[1,2-c][1,2,3]benzotriazine: two new ring systems with antitumor activity, J. Med. Chem. 57 (2014) 9495-9511.
-
(2014)
J. Med. Chem.
, vol.57
, pp. 9495-9511
-
-
Parrino, B.1
Carbone, A.2
Muscarella, M.3
Spano, V.4
Montalbano, A.5
Barraja, P.6
Salvador, A.7
Vedaldi, D.8
Cirrincione, G.9
Diana, P.10
-
16
-
-
79959717364
-
Synthesis of triazenoazaindoles: A new class of triazenes with antitumor activity
-
P. Diana, A. Stagno, P. Barraja, A. Carbone, B. Parrino, F. Dall'Acqua, D. Vedaldi, A. Salvador, P. Brun, I. Castagliuolo, O.G. Issinger, G. Cirrincione, Synthesis of triazenoazaindoles: a new class of triazenes with antitumor activity, Chem-Med Chem 6 (2011) 1291-1299.
-
(2011)
Chem-Med Chem
, vol.6
, pp. 1291-1299
-
-
Diana, P.1
Stagno, A.2
Barraja, P.3
Carbone, A.4
Parrino, B.5
Dall'Acqua, F.6
Vedaldi, D.7
Salvador, A.8
Brun, P.9
Castagliuolo, I.10
Issinger, O.G.11
Cirrincione, G.12
-
17
-
-
79955044118
-
Synthesis of the new ring system pyrrolizino[2,3-b]indol- 4(5H)-one
-
P. Diana, A. Stagno, P. Barraja, A. Montalbano, A. Carbone, B. Parrino, G. Cirrincione, Synthesis of the new ring system pyrrolizino[2,3-b]indol- 4(5H)-one, Tetrahedron 67 (2011) 3374-3379.
-
(2011)
Tetrahedron
, vol.67
, pp. 3374-3379
-
-
Diana, P.1
Stagno, A.2
Barraja, P.3
Montalbano, A.4
Carbone, A.5
Parrino, B.6
Cirrincione, G.7
-
18
-
-
84868099229
-
Synthesis and antiproliferative activity of the ring system [1,2]ozaxolo[4,5-g]indole
-
P. Barraja, L. Caracausi, P. Diana, V. Spanò, A. Montalbano, A. Carbone, B. Parrino, G. Cirrincione, Synthesis and antiproliferative activity of the ring system [1,2]ozaxolo[4,5-g]indole, Chem Med Chem 7 (2012) 1901-1904.
-
(2012)
Chem Med Chem
, vol.7
, pp. 1901-1904
-
-
Barraja, P.1
Caracausi, L.2
Diana, P.3
Spanò, V.4
Montalbano, A.5
Carbone, A.6
Parrino, B.7
Cirrincione, G.8
-
19
-
-
33947575977
-
Synthesis and antitumor properties of 2,5-bis(3′-indolyl)thiophenes: Analogues of marine alkaloid nortopsentin
-
P. Diana, A. Carbone, P. Barraja, A. Montalbano, A. Martorana, G. Dattolo, O. Gia, L. Dalla Via, G. Cirrincione, Synthesis and antitumor properties of 2,5-bis(3′-indolyl)thiophenes: analogues of marine alkaloid nortopsentin, Bioorg. Med. Chem. Lett. 17 (2007) 2342-2346.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 2342-2346
-
-
Diana, P.1
Carbone, A.2
Barraja, P.3
Montalbano, A.4
Martorana, A.5
Dattolo, G.6
Gia, O.7
Dalla Via, L.8
Cirrincione, G.9
-
20
-
-
35148824608
-
3,5-Bis(3′-indolyl)pyrazoles, analogues of marine alkaloid nortopsentin: Synthesis and antitumor properties
-
P. Diana, A. Carbone, P. Barraja, A. Martorana, O. Gia, L. Dalla Via, G. Cirrincione, 3,5-Bis(3′-indolyl)pyrazoles, analogues of marine alkaloid nortopsentin: synthesis and antitumor properties, Bioorg. Med. Chem. Lett. 17 (2007) 6134-6137.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 6134-6137
-
-
Diana, P.1
Carbone, A.2
Barraja, P.3
Martorana, A.4
Gia, O.5
Dalla Via, L.6
Cirrincione, G.7
-
21
-
-
77953129279
-
Synthesis and antitumor activity of 2,5-bis(3′-indolyl)-furans and 3,5-bis(3′-indolyl)- isoxazoles, nortopsentin analogues
-
P. Diana, A. Carbone, P. Barraja, G. Kelter, H.-H. Fiebig, G. Cirrincione, Synthesis and antitumor activity of 2,5-bis(3′-indolyl)-furans and 3,5-bis(3′-indolyl)- isoxazoles, nortopsentin analogues, Bioorg. Med. Chem. 18 (2010) 4524-4529.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 4524-4529
-
-
Diana, P.1
Carbone, A.2
Barraja, P.3
Kelter, G.4
Fiebig, H.-H.5
Cirrincione, G.6
-
22
-
-
79959695729
-
Synthesis and antitumor activity of 3- (2-phenyl-1,3-thiazol-4-yl)-1H-indoles and 3-(2-phenyl-1,3-thiazol-4-yl)-1H- 7-azaindoles
-
P. Diana, A. Carbone, P. Barraja, A. Montalbano, B. Parrino, A. Lopergolo, M. Pennati, N. Zaffaroni, G. Cirrincione, Synthesis and antitumor activity of 3- (2-phenyl-1,3-thiazol-4-yl)-1H-indoles and 3-(2-phenyl-1,3-thiazol-4-yl)-1H- 7-azaindoles, Chem Med Chem 6 (2011) 1300-1309.
-
(2011)
Chem Med Chem
, vol.6
, pp. 1300-1309
-
-
Diana, P.1
Carbone, A.2
Barraja, P.3
Montalbano, A.4
Parrino, B.5
Lopergolo, A.6
Pennati, M.7
Zaffaroni, N.8
Cirrincione, G.9
-
23
-
-
84884252001
-
Novel 1H-pyrrolo[2,3-b]pyridine derivatives nortopsentin analogues: Synthesis and antitumor activity in peritoneal mesothelioma experimental models
-
A. Carbone, M. Pennati, B. Parrino, A. Lopergolo, P. Barraja, A. Montalbano, V. Spanò, S. Sbarra, V. Doldi, M. De Cesare, G. Cirrincione, P. Diana, N. Zaffaroni, Novel 1H-pyrrolo[2,3-b]pyridine derivatives nortopsentin analogues: synthesis and antitumor activity in peritoneal mesothelioma experimental models, J. Med. Chem. 56 (2013) 7060-7072.
-
(2013)
J. Med. Chem.
, vol.56
, pp. 7060-7072
-
-
Carbone, A.1
Pennati, M.2
Parrino, B.3
Lopergolo, A.4
Barraja, P.5
Montalbano, A.6
Spanò, V.7
Sbarra, S.8
Doldi, V.9
De Cesare, M.10
Cirrincione, G.11
Diana, P.12
Zaffaroni, N.13
-
24
-
-
84899857869
-
Synthesis and antiproliferative activity of substituted 3[2-(1H-indol-3-yl)-1,3-thiazol-4-yl]-1H-pyrrolo[3,2-b]pyridines, marine alkaloid nortopsentin analogues
-
A. Carbone, M. Pennati, P. Barraja, A. Montalbano, B. Parrino, V. Spanò, A. Lopergolo, S. Sbarra, V. Doldi, N. Zaffaroni, G. Cirrincione, P. Diana, Synthesis and antiproliferative activity of substituted 3[2-(1H-indol-3-yl)-1,3-thiazol-4-yl]-1H-pyrrolo[3,2-b]pyridines, marine alkaloid nortopsentin analogues, Curr. Med. Chem. 21 (2014) 1654-1666.
-
(2014)
Curr. Med. Chem.
, vol.21
, pp. 1654-1666
-
-
Carbone, A.1
Pennati, M.2
Barraja, P.3
Montalbano, A.4
Parrino, B.5
Spanò, V.6
Lopergolo, A.7
Sbarra, S.8
Doldi, V.9
Zaffaroni, N.10
Cirrincione, G.11
Diana, P.12
-
25
-
-
55549147121
-
Nucleophilic reactions in the indole series: Displacement of bromine under phase transfer catalysis
-
P. Barraja, P. Diana, A. Carbone, G. Cirrincione, Nucleophilic reactions in the indole series: displacement of bromine under phase transfer catalysis, Tetrahedron 64 (2008) 11625-11631.
-
(2008)
Tetrahedron
, vol.64
, pp. 11625-11631
-
-
Barraja, P.1
Diana, P.2
Carbone, A.3
Cirrincione, G.4
-
26
-
-
84879201292
-
Synthesis of [1,2]oxazolo[5,4-e]indazoles as antitumour agents
-
P. Barraja, V. Spanò, D. Giallombardo, P. Diana, A. Montalbano, A. Carbone, B. Parrino, G. Cirrincione, Synthesis of [1,2]oxazolo[5,4-e]indazoles as antitumour agents, Tetrahedron 69 (2013) 6474-6477.
-
(2013)
Tetrahedron
, vol.69
, pp. 6474-6477
-
-
Barraja, P.1
Spanò, V.2
Giallombardo, D.3
Diana, P.4
Montalbano, A.5
Carbone, A.6
Parrino, B.7
Cirrincione, G.8
-
27
-
-
84885180946
-
Convenient synthesis of pyrrolo[3,4-g]indazole
-
V. Spanò, A. Montalbano, A. Carbone, B. Parrino, P. Diana, G. Cirrincione, P. Barraja, Convenient synthesis of pyrrolo[3,4-g]indazole, Tetrahedron 69 (2013) 9839-9847.
-
(2013)
Tetrahedron
, vol.69
, pp. 9839-9847
-
-
Spanò, V.1
Montalbano, A.2
Carbone, A.3
Parrino, B.4
Diana, P.5
Cirrincione, G.6
Barraja, P.7
-
28
-
-
61349197002
-
Pyrano[2,3-e]isoindol-2-ones, a new angelicin heteroanalogues
-
P. Barraja, V. Spanò, P. Diana, A. Carbone, G. Cirrincione, D. Vedaldi, A. Salvador, G. Viola, F. Dall'Acqua, Pyrano[2,3-e]isoindol-2-ones, a new angelicin heteroanalogues, Bioorg. Med. Chem. Lett. 19 (2009) 1711-1714.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 1711-1714
-
-
Barraja, P.1
Spanò, V.2
Diana, P.3
Carbone, A.4
Cirrincione, G.5
Vedaldi, D.6
Salvador, A.7
Viola, G.8
Dall'Acqua, F.9
-
29
-
-
68049085688
-
Synthesis of the new ring system 6,8-dihydro-5H-pyrrolo[3,4-h]quinazoline, heteroanalogue of angelicin
-
P. Barraja, V. Spanò, P. Diana, A. Carbone, G. Cirrincione, Synthesis of the new ring system 6,8-dihydro-5H-pyrrolo[3,4-h]quinazoline, heteroanalogue of angelicin, Tetrahedron Lett. 50 (2009) 5389-5391.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 5389-5391
-
-
Barraja, P.1
Spanò, V.2
Diana, P.3
Carbone, A.4
Cirrincione, G.5
-
30
-
-
79953200428
-
Cirrincione, Pyrrolo[3,4-h]quinolinones a new class of photochemotherapeutic agents
-
P. Barraja, P. Diana, A. Montalbano, A. Carbone, G. Viola, G. Basso, A. Salvador, D. Vedaldi, F. Dall'Acqua, Cirrincione, Pyrrolo[3,4-h]quinolinones a new class of photochemotherapeutic agents, Bioorg. Med. Chem. 19 (2011) 2326-2341.
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 2326-2341
-
-
Barraja, P.1
Diana, P.2
Montalbano, A.3
Carbone, A.4
Viola, G.5
Basso, G.6
Salvador, A.7
Vedaldi, D.8
Dall'Acqua, F.9
-
31
-
-
33750942120
-
Isoindolo[2,1-c]benzo[1,2,4]triazines: A new ring system with antiproliferative activity
-
P. Diana, A. Martorana, P. Barraja, A. Lauria, A. Montalbano, A.M. Almerico, G. Dattolo, G. Cirrincione, Isoindolo[2,1-c]benzo[1,2,4]triazines: a new ring system with antiproliferative activity, Bioorg. Med. Chem. 15 (2007) 343-349.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 343-349
-
-
Diana, P.1
Martorana, A.2
Barraja, P.3
Lauria, A.4
Montalbano, A.5
Almerico, A.M.6
Dattolo, G.7
Cirrincione, G.8
-
32
-
-
84893428486
-
Synthesis of a new class of pyrrolo[3,4-h]quinazolines with antimitotic activity
-
V. Spanò, A. Montalbano, A. Carbone, B. Parrino, P. Diana, G. Cirrincione, I. Castagliuolo, P. Brun, O.-G. Issinger, S. Tisi, I. Primac, D. Vedaldi, A. Salvador, P. Barraja, Synthesis of a new class of pyrrolo[3,4-h]quinazolines with antimitotic activity, Eur. J. Med. Chem. 74 (2014) 340-357.
-
(2014)
Eur. J. Med. Chem.
, vol.74
, pp. 340-357
-
-
Spanò, V.1
Montalbano, A.2
Carbone, A.3
Parrino, B.4
Diana, P.5
Cirrincione, G.6
Castagliuolo, I.7
Brun, P.8
Issinger, O.-G.9
Tisi, S.10
Primac, I.11
Vedaldi, D.12
Salvador, A.13
Barraja, P.14
-
33
-
-
43049130352
-
Isoindolo[2,1-A]quinoxaline derivatives, novel potent antitumor agents with dual inhibition of tubulin polymerization and topoisomerase I
-
P. Diana, A. Martorana, P. Barraja, A. Montalbano, G. Dattolo, G. Cirrincione, F. Dall'Acqua, A. Salvador, D. Vedaldi, G. Basso, G. Viola, Isoindolo[2,1-a]quinoxaline derivatives, novel potent antitumor agents with dual inhibition of tubulin polymerization and topoisomerase I, J. Med. Chem. 51 (2008) 2387-2399.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 2387-2399
-
-
Diana, P.1
Martorana, A.2
Barraja, P.3
Montalbano, A.4
Dattolo, G.5
Cirrincione, G.6
Dall'Acqua, F.7
Salvador, A.8
Vedaldi, D.9
Basso, G.10
Viola, G.11
-
35
-
-
0028127430
-
Oxidation of aromatic 1,2-dimethanols by activated dimethyl sulfoxide
-
O. Farooq, Oxidation of aromatic 1,2-dimethanols by activated dimethyl sulfoxide, Synthesis (1994) 1035-1036.
-
(1994)
Synthesis
, pp. 1035-1036
-
-
Farooq, O.1
-
36
-
-
79956087404
-
Aceno[2,1,3]thiadiazoles for field-effect transistors: Synthesis and crystal packing
-
T. Lei, Y. Zhou, C.-Y. Cheng, Y. Cao, Y. Peng, J. Bian, J. Pei, Aceno[2,1,3]thiadiazoles for field-effect transistors: synthesis and crystal packing, Org. Lett. 13 (2011) 2642-2645.
-
(2011)
Org. Lett.
, vol.13
, pp. 2642-2645
-
-
Lei, T.1
Zhou, Y.2
Cheng, C.-Y.3
Cao, Y.4
Peng, Y.5
Bian, J.6
Pei, J.7
-
37
-
-
0344103635
-
Cycloaddition of benzodiazepine nitrones to alkynes: Synthesis and x-ray analysis of some tricyclic quinoxalines
-
G. Capozzi, R. Ottana, G. Romeo, G. Sindona, N. Uccella, G. Valle, Cycloaddition of benzodiazepine nitrones to alkynes: synthesis and x-ray analysis of some tricyclic quinoxalines, J. Chem. Res. S. 7 (1986) 234-235.
-
(1986)
J. Chem. Res. S.
, vol.7
, pp. 234-235
-
-
Capozzi, G.1
Ottana, R.2
Romeo, G.3
Sindona, G.4
Uccella, N.5
Valle, G.6
-
38
-
-
79959772130
-
Pyrroloquinoxaline hydrazones as fluorescent probes for amyloid fibrils
-
S. Gemma, L. Colombo, G. Forloni, L. Savini, C. Fracasso, S. Caccia, M. Salmona, M. Brindisi, B.P. Joshi, P. Tripaldi, G. Giorgi, O. Taglialatela-Scafati, E. Novellino, I. Fiorini, G. Campiani, S. Butini, Pyrroloquinoxaline hydrazones as fluorescent probes for amyloid fibrils, Org. Biomol. Chem. 9 (2011) 5137-5148.
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 5137-5148
-
-
Gemma, S.1
Colombo, L.2
Forloni, G.3
Savini, L.4
Fracasso, C.5
Caccia, S.6
Salmona, M.7
Brindisi, M.8
Joshi, B.P.9
Tripaldi, P.10
Giorgi, G.11
Taglialatela-Scafati, O.12
Novellino, E.13
Fiorini, I.14
Campiani, G.15
Butini, S.16
-
39
-
-
0034020188
-
Oxidative heterocyclization of 2-alkynylbenzaldehydes with 1,2-phenylenediamine
-
G. Dyker, W. Stirner, G. Henkel, Oxidative heterocyclization of 2-alkynylbenzaldehydes with 1,2-phenylenediamine, Eur. J. Org. Chem. 8 (2000) 1433-1441.
-
(2000)
Eur. J. Org. Chem.
, vol.8
, pp. 1433-1441
-
-
Dyker, G.1
Stirner, W.2
Henkel, G.3
-
40
-
-
0025872827
-
Resistance to antimitotic drugs in Chinese hamster ovary cells correlated ovary cells correlates with changes in the level of polymerized tubulin
-
A.M. Minotti, S.B. Barlow, F. Cabral, Resistance to antimitotic drugs in Chinese hamster ovary cells correlated ovary cells correlates with changes in the level of polymerized tubulin, J. Biol. Chem. 266 (1991) 3987-3994.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 3987-3994
-
-
Minotti, A.M.1
Barlow, S.B.2
Cabral, F.3
-
41
-
-
0029778770
-
Brain-derived neurotrophic factor protects neuroblastoma cells from vimblastine toxicity
-
S. Scala, K. Wosikowski, P. Giannakakou, P. Valle, J.L. Biedler, B.A. Spengler, E. Luccarelli, S.E. Bates, C.J. Thiele, Brain-derived neurotrophic factor protects neuroblastoma cells from vimblastine toxicity, Cancer Res. 56 (1996) 3737-3742.
-
(1996)
Cancer Res.
, vol.56
, pp. 3737-3742
-
-
Scala, S.1
Wosikowski, K.2
Giannakakou, P.3
Valle, P.4
Biedler, J.L.5
Spengler, B.A.6
Luccarelli, E.7
Bates, S.E.8
Thiele, C.J.9
-
42
-
-
0028288462
-
Topoisomerase II mediated DNA lesions induced by acridine-4-carboxamide and 2-(4-pyridyl)quinoline-8-carboxamide
-
J.M. Woynarowski, K. McCarthy, B. Reynolds, T.A. Beerman, W.A. Denny, Topoisomerase II mediated DNA lesions induced by acridine-4-carboxamide and 2-(4-pyridyl)quinoline-8-carboxamide, Anticancer Drug Des. 9 (1994) 9-24.
-
(1994)
Anticancer Drug Des.
, vol.9
, pp. 9-24
-
-
Woynarowski, J.M.1
McCarthy, K.2
Reynolds, B.3
Beerman, T.A.4
Denny, W.A.5
-
43
-
-
34247641796
-
Fluorescence-based melting assays for studying quadruplex ligands
-
A. De Cian, L. Guittat, M. Kaiser, B. Saccà, S. Amrane, A. Bourdoncle, P. Alberti, M.P. Teulade-Fichou, L. Lacroix, J.L. Mergny, Fluorescence-based melting assays for studying quadruplex ligands, Methods 42 (2007) 183-195.
-
(2007)
Methods
, vol.42
, pp. 183-195
-
-
De Cian, A.1
Guittat, L.2
Kaiser, M.3
Saccà, B.4
Amrane, S.5
Bourdoncle, A.6
Alberti, P.7
Teulade-Fichou, M.P.8
Lacroix, L.9
Mergny, J.L.10
-
44
-
-
84879934080
-
Structure and circular dichroism of DNA in concentrated polymer solutions
-
C.F. Jordan, L.S. Lerman, J.H. Venable Jr., Structure and circular dichroism of DNA in concentrated polymer solutions, Nat. New Biol. 236 (1972) 67-70.
-
(1972)
Nat. New Biol.
, vol.236
, pp. 67-70
-
-
Jordan, C.F.1
Lerman, L.S.2
Venable, J.H.3
-
45
-
-
84865330936
-
The effects of silver nanoparticles and doxorubicin combination on DNA structure and its antiproliferative effect against T47D and MCF7 cell lines
-
A. Hekmat, A.A. Saboury, A. Divsalar, The effects of silver nanoparticles and doxorubicin combination on DNA structure and its antiproliferative effect against T47D and MCF7 cell lines, J. Biomed. Nanotechnol. 8 (2012) 968-982.
-
(2012)
J. Biomed. Nanotechnol.
, vol.8
, pp. 968-982
-
-
Hekmat, A.1
Saboury, A.A.2
Divsalar, A.3
-
46
-
-
84886626805
-
G-quadruplex structures in the human genome as novel therapeutic targets
-
J. Bidzinska, G. Cimino-Reale, N. Zaffaroni, M. Folini, G-quadruplex structures in the human genome as novel therapeutic targets, Molecules 18 (2013) 12368-12395.
-
(2013)
Molecules
, vol.18
, pp. 12368-12395
-
-
Bidzinska, J.1
Cimino-Reale, G.2
Zaffaroni, N.3
Folini, M.4
-
47
-
-
70449725230
-
Stabilization of quadruplex DNA perturbs telomere replication leading to the activation of an ATR-dependent ATM signaling pathway
-
A. Rizzo, E. Salvati, M. Porru, C. D'Angelo, M.F. Stevens, M. D'Incalci, C. Leonetti, E. Gilson, G. Zupi, A. Biroccio, Stabilization of quadruplex DNA perturbs telomere replication leading to the activation of an ATR-dependent ATM signaling pathway, Nucl. Acids Res. 37 (2009) 5353-5364.
-
(2009)
Nucl. Acids Res.
, vol.37
, pp. 5353-5364
-
-
Rizzo, A.1
Salvati, E.2
Porru, M.3
D'Angelo, C.4
Stevens, M.F.5
D'Incalci, M.6
Leonetti, C.7
Gilson, E.8
Zupi, G.9
Biroccio, A.10
-
48
-
-
84866054725
-
Autophagy acts as a safeguard mechanism against G-quadruplex ligand-mediated DNA damage
-
N.I. Orlotti, G. Cimino-Reale, E. Borghini, M. Pennati, C. Sissi, F. Perrone, M. Palumbo, M.G. Daidone, M. Folini, N. Zaffaroni, Autophagy acts as a safeguard mechanism against G-quadruplex ligand-mediated DNA damage, Autophagy 8 (2012) 1185-1196.
-
(2012)
Autophagy
, vol.8
, pp. 1185-1196
-
-
Orlotti, N.I.1
Cimino-Reale, G.2
Borghini, E.3
Pennati, M.4
Sissi, C.5
Perrone, F.6
Palumbo, M.7
Daidone, M.G.8
Folini, M.9
Zaffaroni, N.10
-
49
-
-
0034671853
-
Interaction of human DNA topoisomerase I with G-quartet structures
-
P.B. Arimondo, J.F. Riou, J.L. Mergny, J. Tazi, J.S. Sun, T. Garestier, C. Hélène, Interaction of human DNA topoisomerase I with G-quartet structures, Nucl. Acids Res. 28 (2000) 4832-4838.
-
(2000)
Nucl. Acids Res.
, vol.28
, pp. 4832-4838
-
-
Arimondo, P.B.1
Riou, J.F.2
Mergny, J.L.3
Tazi, J.4
Sun, J.S.5
Garestier, T.6
Hélène, C.7
-
50
-
-
79954568864
-
DNA damage persistence as determinant of tumor sensitivity to the combination of Topo I inhibitors and telomere-targeting agents
-
A. Biroccio, M. Porru, A. Rizzo, E. Salvati, C. D'Angelo, A. Orlandi, D. Passeri, M. Franceschin, M.F. Stevens, E. Gilson, G. Beretta, G. Zupi, C. Pisano, F. Zunino, C. Leonetti, DNA damage persistence as determinant of tumor sensitivity to the combination of Topo I inhibitors and telomere-targeting agents, Clin. Cancer Res. 17 (2011) 2227-3336.
-
(2011)
Clin. Cancer Res.
, vol.17
, pp. 2227-3336
-
-
Biroccio, A.1
Porru, M.2
Rizzo, A.3
Salvati, E.4
D'Angelo, C.5
Orlandi, A.6
Passeri, D.7
Franceschin, M.8
Stevens, M.F.9
Gilson, E.10
Beretta, G.11
Zupi, G.12
Pisano, C.13
Zunino, F.14
Leonetti, C.15
-
51
-
-
12344264552
-
Copper-catalyzed allylations of zirconocene intermediates generated from o-alkenyl or o-alkynylbenzyl ether derivatives and zirconocene-butene complex
-
Y. Ikeuchi, T. Taguchi, Y. Hanzawa, Copper-catalyzed allylations of zirconocene intermediates generated from o-alkenyl or o-alkynylbenzyl ether derivatives and zirconocene-butene complex, J. Org. Chem. 70 (2005) 756-759.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 756-759
-
-
Ikeuchi, Y.1
Taguchi, T.2
Hanzawa, Y.3
-
52
-
-
78650387403
-
NHC-catalyzed spiro bis-indane formation via domino Stetter-Aldol-Michael and Stetter-Aldol-Aldol reactions
-
E. Sanchez-Larios, J.M. Holmes, C.L. Daschner, M. Gravel, NHC-catalyzed spiro bis-indane formation via domino Stetter-Aldol-Michael and Stetter-Aldol-Aldol reactions, Org. Lett. 12 (2010) 5772-5775.
-
(2010)
Org. Lett.
, vol.12
, pp. 5772-5775
-
-
Sanchez-Larios, E.1
Holmes, J.M.2
Daschner, C.L.3
Gravel, M.4
-
53
-
-
0033179386
-
Tethering a type IB topoisomerase to a DNA site by enzyme fusion to a heterologous site-selective DNA-binding protein domain
-
G.L. Beretta, M. Binaschi, E. Zagni, L. Capuani, G. Capranico, Tethering a type IB topoisomerase to a DNA site by enzyme fusion to a heterologous site-selective DNA-binding protein domain, Cancer Res. 59 (1999) 3689-3697.
-
(1999)
Cancer Res.
, vol.59
, pp. 3689-3697
-
-
Beretta, G.L.1
Binaschi, M.2
Zagni, E.3
Capuani, L.4
Capranico, G.5
-
54
-
-
73149092085
-
Antimitotic effect of the retinoid 4-oxo-fenretinide through inhibition of tubulin polymerization: A novel mechanism of retinoid growth-inhibitory activity
-
V. Appierto, P. Tiberio, E. Cavadini, P. Casalini, G. Cappelletti, F. Formelli, Antimitotic effect of the retinoid 4-oxo-fenretinide through inhibition of tubulin polymerization: a novel mechanism of retinoid growth-inhibitory activity, Mol. Cancer Ther. 8 (2009) 3360-3368.
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 3360-3368
-
-
Appierto, V.1
Tiberio, P.2
Cavadini, E.3
Casalini, P.4
Cappelletti, G.5
Formelli, F.6
|