-
1
-
-
80052577975
-
Identification of potent c-Src inhibitors strongly affecting the proliferation of human neuroblastoma cells
-
Radi, M.; Brullo, C.; Crespan, E.; Tintori, C.; Musumeci, F.; Biava, M.; Schenone, S.; Dreassi, E.; Zamperini, C.; Maga, G.; Pagano, D.; Angelucci, A.; Bologna, M.; Botta, M. Identification of potent c-Src inhibitors strongly affecting the proliferation of human neuroblastoma cells Bioorg. Med. Chem. Lett. 2011, 21, 5928-5933
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 5928-5933
-
-
Radi, M.1
Brullo, C.2
Crespan, E.3
Tintori, C.4
Musumeci, F.5
Biava, M.6
Schenone, S.7
Dreassi, E.8
Zamperini, C.9
Maga, G.10
Pagano, D.11
Angelucci, A.12
Bologna, M.13
Botta, M.14
-
2
-
-
79955395152
-
Design, Synthesis, Biological Activity, and ADME Properties of Pyrazolo[3,4- d ]pyrimidines Active in Hypoxic Human Leukemia Cells: A Lead Optimization Study
-
Radi, M.; Dreassi, E.; Brullo, C.; Crespan, E.; Tintori, C.; Bernardo, V.; Valoti, M.; Zamperini, C.; Daigl, H.; Musumeci, F.; Carraro, F.; Naldini, A.; Fillipi, I.; Maga, G.; Schenone, S.; Botta, M. Design, Synthesis, Biological Activity, and ADME Properties of Pyrazolo[3,4- d ]pyrimidines Active in Hypoxic Human Leukemia Cells: A Lead Optimization Study J. Med. Chem. 2011, 54, 2610-2626
-
(2011)
J. Med. Chem.
, vol.54
, pp. 2610-2626
-
-
Radi, M.1
Dreassi, E.2
Brullo, C.3
Crespan, E.4
Tintori, C.5
Bernardo, V.6
Valoti, M.7
Zamperini, C.8
Daigl, H.9
Musumeci, F.10
Carraro, F.11
Naldini, A.12
Fillipi, I.13
Maga, G.14
Schenone, S.15
Botta, M.16
-
3
-
-
77955122860
-
Design and Synthesis of Thiadiazoles and Thiazoles Targeting the Bcr-Abl T315I Mutant: From Docking False Positives to ATP-Noncompetitive Inhibitors
-
Radi, M.; Crespan, E.; Falchi, F.; Bernardo, V.; Zanoli, S.; Manetti, F.; Schenone, S.; Maga, G.; Botta, M. Design and Synthesis of Thiadiazoles and Thiazoles Targeting the Bcr-Abl T315I Mutant: from Docking False Positives to ATP-Noncompetitive Inhibitors ChemMedChem 2010, 5, 1226-1231
-
(2010)
ChemMedChem
, vol.5
, pp. 1226-1231
-
-
Radi, M.1
Crespan, E.2
Falchi, F.3
Bernardo, V.4
Zanoli, S.5
Manetti, F.6
Schenone, S.7
Maga, G.8
Botta, M.9
-
4
-
-
38749093340
-
Discovery and SAR of 1,3,4-thiadiazole derivatives as potent Abl tyrosine kinase inhibitors and cytodifferentiating agents
-
Radi, M.; Crespan, E.; Botta, G.; Falchi, F.; Maga, G.; Manetti, F.; Corradi, V.; Mancini, M.; Santucci, M. A.; Schenone, S.; Botta, M. Discovery and SAR of 1,3,4-thiadiazole derivatives as potent Abl tyrosine kinase inhibitors and cytodifferentiating agents Bioorg. Med. Chem. Lett. 2008, 18, 1207-1211
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 1207-1211
-
-
Radi, M.1
Crespan, E.2
Botta, G.3
Falchi, F.4
Maga, G.5
Manetti, F.6
Corradi, V.7
Mancini, M.8
Santucci, M.A.9
Schenone, S.10
Botta, M.11
-
5
-
-
58549106791
-
C6-unsubstituted pyrazolo[3,4-d]pyrimidines are dual Src/Abl inhibitors effective against imatinib mesylate resistant chronic myeloid leukemia cell lines
-
Santucci, M. A.; Corradi, V.; Mancini, M.; Manetti, F.; Radi, M.; Schenone, S.; Botta, M. C6-unsubstituted pyrazolo[3,4-d]pyrimidines are dual Src/Abl inhibitors effective against imatinib mesylate resistant chronic myeloid leukemia cell lines ChemMedChem 2009, 4, 118-126
-
(2009)
ChemMedChem
, vol.4
, pp. 118-126
-
-
Santucci, M.A.1
Corradi, V.2
Mancini, M.3
Manetti, F.4
Radi, M.5
Schenone, S.6
Botta, M.7
-
6
-
-
80055001778
-
N -[2-Methyl-5-(triazol-1-yl)phenyl]pyrimidin-2-amine as a Scaffold for the Synthesis of Inhibitors of Bcr-Abl
-
Arioli, F.; Borrelli, S.; Colombo, F.; Falchi, F.; Fillipi, I.; Crespan, E.; Naldini, A.; Scalia, G.; Silvani, A.; Maga, G.; Carraro, F.; Botta, M.; Passarella, D. N -[2-Methyl-5-(triazol-1-yl)phenyl]pyrimidin-2-amine as a Scaffold for the Synthesis of Inhibitors of Bcr-Abl ChemMedChem 2011, 6, 2009-2018
-
(2011)
ChemMedChem
, vol.6
, pp. 2009-2018
-
-
Arioli, F.1
Borrelli, S.2
Colombo, F.3
Falchi, F.4
Fillipi, I.5
Crespan, E.6
Naldini, A.7
Scalia, G.8
Silvani, A.9
Maga, G.10
Carraro, F.11
Botta, M.12
Passarella, D.13
-
7
-
-
77949858836
-
Kinetic target-guided synthesis
-
Hu, X.; Manetsch, R. Kinetic target-guided synthesis Chem. Soc. Rev. 2010, 39, 1316-1324
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1316-1324
-
-
Hu, X.1
Manetsch, R.2
-
8
-
-
33645509492
-
Thiocolchicine-Podophyllotoxin Conjugates: Dynamic Libraries Based on Disulfide Exchange Reaction
-
Danieli, B.; Giardini, A.; Lesma, G.; Passarella, D.; Peretto, B.; Sacchetti, A.; Silvani, A.; Pratesi, G.; Zunino, F. Thiocolchicine- Podophyllotoxin Conjugates: Dynamic Libraries Based on Disulfide Exchange Reaction J. Org. Chem. 2006, 71, 2848-2853
-
(2006)
J. Org. Chem.
, vol.71
, pp. 2848-2853
-
-
Danieli, B.1
Giardini, A.2
Lesma, G.3
Passarella, D.4
Peretto, B.5
Sacchetti, A.6
Silvani, A.7
Pratesi, G.8
Zunino, F.9
-
9
-
-
80051781198
-
Tubulin-guided dynamic combinatorial library of thiocolchicine- podophyllotoxin conjugates
-
Cappelletti, G.; Cartelli, D.; Peretto, B.; Ventura, M.; Riccioli, M.; Colombo, F.; Snaith, J. S.; Borrelli, S.; Passarella, D. Tubulin-guided dynamic combinatorial library of thiocolchicine-podophyllotoxin conjugates Tetrahedron 2011, 67, 7354-7357
-
(2011)
Tetrahedron
, vol.67
, pp. 7354-7357
-
-
Cappelletti, G.1
Cartelli, D.2
Peretto, B.3
Ventura, M.4
Riccioli, M.5
Colombo, F.6
Snaith, J.S.7
Borrelli, S.8
Passarella, D.9
-
10
-
-
77949786732
-
In situ click chemistry: Probing the binding landscapes of biological molecules
-
Mamidyala, S. K.; Finn, M. G. In situ click chemistry: probing the binding landscapes of biological molecules Chem. Soc. Rev. 2010, 39, 1252-1261
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1252-1261
-
-
Mamidyala, S.K.1
Finn, M.G.2
-
11
-
-
0000096835
-
Click Chemistry: Diverse Chemical Function from a Few Good Reactions
-
Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click Chemistry: Diverse Chemical Function from a Few Good Reactions Angew. Chem., Int. Ed. 2001, 40, 2004-2021
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
12
-
-
0037087516
-
Click Chemistry in Situ: Acetylcholinesterase as a Reaction Vessel for the Selective Assembly of a Femtomolar Inhibitor from an Array of Building Blocks
-
Lewis, W. G.; Grenn, L. G.; Grynszpan, F.; Radić, Z.; Carlier, P. R.; Taylor, P.; Finn, M. G.; Sharpless, K. B. Click Chemistry In Situ: Acetylcholinesterase as a Reaction Vessel for the Selective Assembly of a Femtomolar Inhibitor from an Array of Building Blocks Angew. Chem., Int. Ed. 2002, 41, 1053-1057
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 1053-1057
-
-
Lewis, W.G.1
Grenn, L.G.2
Grynszpan, F.3
Radić, Z.4
Carlier, P.R.5
Taylor, P.6
Finn, M.G.7
Sharpless, K.B.8
-
13
-
-
5644276317
-
In Situ Click Chemistry: Enzyme Inhibitors Made to Their Own Specifications
-
Manetsch, R.; Krasiński, A.; Radić, Z.; Raushel, J.; Taylor, P.; Sharpless, K. B.; Kolb, H. C. In Situ Click Chemistry: Enzyme Inhibitors Made to Their Own Specifications J. Am. Chem. Soc. 2004, 126, 12809-12818
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 12809-12818
-
-
Manetsch, R.1
Krasiński, A.2
Radić, Z.3
Raushel, J.4
Taylor, P.5
Sharpless, K.B.6
Kolb, H.C.7
-
14
-
-
11244252206
-
In Situ Click Chemistry: Enzyme-Generated Inhibitors of Carbonic Anhydrase II
-
Mocharla, V. P.; Colasson, B.; Lee, L. V.; Röper, S.; Sharpless, K. B.; Wong, C. H.; Kolb, H. C. In Situ Click Chemistry: Enzyme-Generated Inhibitors of Carbonic Anhydrase II Angew. Chem., Int. Ed. 2005, 44, 116-120
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 116-120
-
-
Mocharla, V.P.1
Colasson, B.2
Lee, L.V.3
Röper, S.4
Sharpless, K.B.5
Wong, C.H.6
Kolb, H.C.7
-
15
-
-
18644384979
-
In Situ Selection of Lead Compounds by Click Chemistry: Target-Guided Optimization of Acetylcholinesterase Inhibitors
-
Krasiński, A.; Radić, Z.; Manetsch, R.; Raushel, J.; Taylor, P.; Sharpless, K. B.; Kolb, H. C. In Situ Selection of Lead Compounds by Click Chemistry: Target-Guided Optimization of Acetylcholinesterase Inhibitors J. Am. Chem. Soc. 2005, 127, 6686-6692
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 6686-6692
-
-
Krasiński, A.1
Radić, Z.2
Manetsch, R.3
Raushel, J.4
Taylor, P.5
Sharpless, K.B.6
Kolb, H.C.7
-
16
-
-
33746210083
-
Inhibitors of HIV-1 Protease by Using in Situ Click Chemistry
-
Whiting, M.; Muldoon, J.; Lin, Y. C.; Silverman, S. M.; Lindstrom, W.; Olson, A. J.; Kolb, H. C.; Finn, M. G.; Sharpless, K. B.; Elder, J. H.; Fokin, V. V. Inhibitors of HIV-1 Protease by Using In Situ Click Chemistry Angew. Chem., Int. Ed. 2006, 45, 1435-1439
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 1435-1439
-
-
Whiting, M.1
Muldoon, J.2
Lin, Y.C.3
Silverman, S.M.4
Lindstrom, W.5
Olson, A.J.6
Kolb, H.C.7
Finn, M.G.8
Sharpless, K.B.9
Elder, J.H.10
Fokin, V.V.11
-
17
-
-
33747890087
-
Integrated Microfluidics for Parallel Screening of an in Situ Click Chemistry Library
-
Wang, J.; Sui, G.; Mocharla, V. P.; Lin, R. J.; Phelps, M. E.; Kolb, H. C.; Tseng, H. R. Integrated Microfluidics for Parallel Screening of an In Situ Click Chemistry Library Angew. Chem., Int. Ed. 2006, 45, 5276-5281
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 5276-5281
-
-
Wang, J.1
Sui, G.2
Mocharla, V.P.3
Lin, R.J.4
Phelps, M.E.5
Kolb, H.C.6
Tseng, H.R.7
-
18
-
-
70349964290
-
Iterative in Situ Click Chemistry Creates Antibody-like Protein-Capture Agents
-
Agnew, H. D.; Rohde, R. D.; Millward, S. W.; Nag, A.; Yeo, W. S.; Hein, J. E.; Pitram, S. M.; Tariq, A. A.; Burns, V. M.; Krom, R. J.; Fokin, V. V.; Sharpless, K. B.; Heath, J. R. Iterative In Situ Click Chemistry Creates Antibody-like Protein-Capture Agents Angew. Chem., Int. Ed. 2009, 48, 4944-4948
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 4944-4948
-
-
Agnew, H.D.1
Rohde, R.D.2
Millward, S.W.3
Nag, A.4
Yeo, W.S.5
Hein, J.E.6
Pitram, S.M.7
Tariq, A.A.8
Burns, V.M.9
Krom, R.J.10
Fokin, V.V.11
Sharpless, K.B.12
Heath, J.R.13
-
19
-
-
77955316501
-
A Fragment-Based in Situ Combinatorial Approach to Identify High-Affinity Ligands for Unknown Binding Sites
-
Shelke, S. V.; Cutting, B.; Jiang, X.; Koliwer-Brandl, H.; Strasser, D. S.; Schwardt, O.; Kelm, S.; Ernst, B. A Fragment-Based In Situ Combinatorial Approach To Identify High-Affinity Ligands for Unknown Binding Sites Angew. Chem., Int. Ed. 2010, 49, 5721-5725
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 5721-5725
-
-
Shelke, S.V.1
Cutting, B.2
Jiang, X.3
Koliwer-Brandl, H.4
Strasser, D.S.5
Schwardt, O.6
Kelm, S.7
Ernst, B.8
-
20
-
-
78649645179
-
Exploring Drug Target Flexibility Using in Situ Click Chemistry: Application to a Mycobacterial Transcriptional Regulator
-
Willand, N.; Desroses, M.; Toto, P.; Dirié, B.; Lens, Z.; Villeret, V.; Rucktooa, P.; Locht, C.; Baulard, A.; Deprez, B. Exploring Drug Target Flexibility Using in Situ Click Chemistry: Application to a Mycobacterial Transcriptional Regulator ACS Chem. Biol. 2010, 5, 1007-1013
-
(2010)
ACS Chem. Biol.
, vol.5
, pp. 1007-1013
-
-
Willand, N.1
Desroses, M.2
Toto, P.3
Dirié, B.4
Lens, Z.5
Villeret, V.6
Rucktooa, P.7
Locht, C.8
Baulard, A.9
Deprez, B.10
-
21
-
-
77949786732
-
In situ click chemistry: Probing the binding landscapes of biological molecules
-
Mamidyala, S. K.; Finn, M. G. In situ click chemistry: Probing the binding landscapes of biological molecules Chem. Soc. Rev. 2010, 39, 1252-1261
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1252-1261
-
-
Mamidyala, S.K.1
Finn, M.G.2
-
22
-
-
77956609618
-
An Unexpected Example of Protein-Templated Click Chemistry
-
Suzuki, T.; Ota, Y.; Kasuya, Y.; Mutsuga, M.; Kawamura, Y.; Tsumoto, H.; Nakagawa, H.; Finn, M. G.; Miyata, N. An Unexpected Example of Protein-Templated Click Chemistry Angew. Chem., Int. Ed. 2010, 49, 6817-6820
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 6817-6820
-
-
Suzuki, T.1
Ota, Y.2
Kasuya, Y.3
Mutsuga, M.4
Kawamura, Y.5
Tsumoto, H.6
Nakagawa, H.7
Finn, M.G.8
Miyata, N.9
-
23
-
-
80755172538
-
Iterative in Situ Click Chemistry Assembles a Branched Capture Agent and Allosteric Inhibitor for Akt1
-
Millward, S. W.; Henning, R. K.; Kwong, G. A.; Pitram, S.; Agnew, H. D.; Deyle, K. M.; Nag, A.; Hein, J.; Lee, S. S.; Lim, J.; Pfeilsticker, J. A.; Sharpless, K. B.; Heath, J. R. Iterative in Situ Click Chemistry Assembles a Branched Capture Agent and Allosteric Inhibitor for Akt1 J. Am. Chem. Soc. 2011, 133, 18280-18288
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 18280-18288
-
-
Millward, S.W.1
Henning, R.K.2
Kwong, G.A.3
Pitram, S.4
Agnew, H.D.5
Deyle, K.M.6
Nag, A.7
Hein, J.8
Lee, S.S.9
Lim, J.10
Pfeilsticker, J.A.11
Sharpless, K.B.12
Heath, J.R.13
-
24
-
-
79960550248
-
Screening of Protein-Protein Interaction Modulators via Sulfo-Click Kinetic Target-Guided Synthesis
-
Kulkarni, S. S.; Hu, X.; Doi, K.; Wang, H. G.; Manetsch, R. Screening of Protein-Protein Interaction Modulators via Sulfo-Click Kinetic Target-Guided Synthesis ACS Chem. Biol. 2011, 6, 724-732
-
(2011)
ACS Chem. Biol.
, vol.6
, pp. 724-732
-
-
Kulkarni, S.S.1
Hu, X.2
Doi, K.3
Wang, H.G.4
Manetsch, R.5
-
25
-
-
79955768215
-
Stereo- and Regioselective Azide/Alkyne Cycloadditions in Carbonic Anhydrase II via Tethering, Monitored by Crystallography and Mass Spectrometry
-
Schulze Wischer, J.; Sun, D.; Sandner, N. U.; Linne, U.; Heine, A.; Koert, U.; Klebe, G. Stereo- and Regioselective Azide/Alkyne Cycloadditions in Carbonic Anhydrase II via Tethering, Monitored by Crystallography and Mass Spectrometry Chem.-Eur. J. 2011, 17, 5842-5851
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 5842-5851
-
-
Schulze Wischer, J.1
Sun, D.2
Sandner, N.U.3
Linne, U.4
Heine, A.5
Koert, U.6
Klebe, G.7
-
26
-
-
84859994538
-
Generation of Candidate Ligands for Nicotinic Acetylcholine Receptors via in situ Click Chemistry with a Soluble Acetylcholine Binding Protein Template
-
Grimster, N. P.; Stump, B.; Fotsing, J. R.; Weide, T.; Talley, T. T.; Yamauchi, J. G.; Nemecz, A.; Kim, C.; Ho, K. Y.; Sharpless, K. B.; Taylor, P.; Fokin, V. V. Generation of Candidate Ligands for Nicotinic Acetylcholine Receptors via in situ Click Chemistry with a Soluble Acetylcholine Binding Protein Template J. Am. Chem. Soc. 2012, 134, 6732-6740
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 6732-6740
-
-
Grimster, N.P.1
Stump, B.2
Fotsing, J.R.3
Weide, T.4
Talley, T.T.5
Yamauchi, J.G.6
Nemecz, A.7
Kim, C.8
Ho, K.Y.9
Sharpless, K.B.10
Taylor, P.11
Fokin, V.V.12
-
27
-
-
84861316742
-
In Situ Hetero End-Functionalized Polythiophene and Subsequent "click" Chemistry with DNA
-
Lee, J. K.; Ko, S.; Bao, Z. In Situ Hetero End-Functionalized Polythiophene and Subsequent "Click" Chemistry With DNA Macromol. Rapid Commun. 2012, 33, 938-942
-
(2012)
Macromol. Rapid Commun.
, vol.33
, pp. 938-942
-
-
Lee, J.K.1
Ko, S.2
Bao, Z.3
-
28
-
-
84859609311
-
Synthesis of Amphiphilic Rod-Coil P3HT- b -P4VP Carrying a Long Conjugated Block Using NMRP and Click Chemistry
-
Lohwasser, R. H.; Thelakkat, M. Synthesis of Amphiphilic Rod-Coil P3HT- b -P4VP Carrying a Long Conjugated Block Using NMRP and Click Chemistry Macromolecules 2012, 45, 3070-3077
-
(2012)
Macromolecules
, vol.45
, pp. 3070-3077
-
-
Lohwasser, R.H.1
Thelakkat, M.2
-
29
-
-
84861153498
-
Design, Synthesis and Biological Evaluation of Potent Azadipeptide Nitrile Inhibitors and Activity-Based Probes as Promising Anti- Trypanosoma brucei Agents
-
Yang, P. Y.; Wang, M.; Li, L.; Wu, H.; He, C. Y.; Yao, S. Q. Design, Synthesis and Biological Evaluation of Potent Azadipeptide Nitrile Inhibitors and Activity-Based Probes as Promising Anti- Trypanosoma brucei Agents Chem.-Eur. J. 2012, 18, 6528-6541
-
(2012)
Chem. - Eur. J.
, vol.18
, pp. 6528-6541
-
-
Yang, P.Y.1
Wang, M.2
Li, L.3
Wu, H.4
He, C.Y.5
Yao, S.Q.6
-
30
-
-
84863781029
-
Synthesis of a monolithic, micro-immobilised enzyme reactor via click-chemistry
-
Çelebi, B.; Bayraktar, A.; Tuncel, A. Synthesis of a monolithic, micro-immobilised enzyme reactor via click-chemistry Anal. Bioanal. Chem. 2012, 403, 2655-2663
-
(2012)
Anal. Bioanal. Chem.
, vol.403
, pp. 2655-2663
-
-
Cìelebi, B.1
Bayraktar, A.2
Tuncel, A.3
-
31
-
-
84866064789
-
In situ synthesis of fluorescent membrane lipids (ceramides) using click chemistry
-
Garrido, M.; Abad, J. L.; Alonso, A.; Goñi, F. M.; Delgado, A.; Montes, L. R. In situ synthesis of fluorescent membrane lipids (ceramides) using click chemistry J. Chem. Biol. 2012, 5, 119-123
-
(2012)
J. Chem. Biol.
, vol.5
, pp. 119-123
-
-
Garrido, M.1
Abad, J.L.2
Alonso, A.3
Goñi, F.M.4
Delgado, A.5
Montes, L.R.6
-
32
-
-
84856718283
-
Huisgen click cycloadditions from a copper(II)-tren precatalyst without external sacrificial reductant
-
Harmand, L.; Lescure, M. H.; Candelon, N.; Duttine, M.; Lastécouères, D.; Vincent, J. M. Huisgen click cycloadditions from a copper(II)-tren precatalyst without external sacrificial reductant Tetrahedron Lett. 2012, 53, 1417-1420
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 1417-1420
-
-
Harmand, L.1
Lescure, M.H.2
Candelon, N.3
Duttine, M.4
Lastécouères, D.5
Vincent, J.M.6
-
33
-
-
84860658359
-
CuAAC Click Chemistry Accelerates the Discovery of Novel Chemical Scaffolds as Promising Protein Tyrosine Phosphatases Inhibitors
-
He, X. P.; Xie, J.; Tang, Y.; Li, J.; Chen, G. R. CuAAC Click Chemistry Accelerates the Discovery of Novel Chemical Scaffolds as Promising Protein Tyrosine Phosphatases Inhibitors Curr. Med. Chem. 2012, 19, 2399-2405
-
(2012)
Curr. Med. Chem.
, vol.19
, pp. 2399-2405
-
-
He, X.P.1
Xie, J.2
Tang, Y.3
Li, J.4
Chen, G.R.5
-
34
-
-
12144289984
-
Glide: A New Approach for Rapid, Accurate Docking and Scoring. 1. Method and Assessment of Docking Accuracy
-
Friesner, R. A.; Banks, J. L.; Halgren, T. A.; Klicic, J. J.; Mainz, D. T.; Repasky, M. P.; Knoll, E. H.; Shaw, D. E.; Shelley, M.; Perry, J. K.; Francis, P.; Shenkin, P. S. Glide: A New Approach for Rapid, Accurate Docking and Scoring. 1. Method and Assessment of Docking Accuracy J. Med. Chem. 2004, 47, 1739-1749
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1739-1749
-
-
Friesner, R.A.1
Banks, J.L.2
Halgren, T.A.3
Klicic, J.J.4
Mainz, D.T.5
Repasky, M.P.6
Knoll, E.H.7
Shaw, D.E.8
Shelley, M.9
Perry, J.K.10
Francis, P.11
Shenkin, P.S.12
-
35
-
-
84861520898
-
Spatial regulation of receptor tyrosine kinases in development and cancer
-
Casaletto, J. B.; McClatchey, A. J. Spatial regulation of receptor tyrosine kinases in development and cancer Nat. Rev. Cancer 2012, 12, 387-400
-
(2012)
Nat. Rev. Cancer
, vol.12
, pp. 387-400
-
-
Casaletto, J.B.1
McClatchey, A.J.2
-
36
-
-
0036139884
-
Receptor tyrosine kinases as targets for anticancer drugs
-
Zwick, E.; Bange, J.; Ullrich, A. Receptor tyrosine kinases as targets for anticancer drugs Trends Mol. Med. 2002, 8, 17-23
-
(2002)
Trends Mol. Med.
, vol.8
, pp. 17-23
-
-
Zwick, E.1
Bange, J.2
Ullrich, A.3
-
37
-
-
2342591455
-
The discovery of receptor tyrosine kinases: Targets for cancer therapy
-
Gschwind, A.; Fischer, O. M.; Ullrich, A. The discovery of receptor tyrosine kinases: Targets for cancer therapy Nat. Rev. Cancer 2004, 4, 361-370
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 361-370
-
-
Gschwind, A.1
Fischer, O.M.2
Ullrich, A.3
-
38
-
-
0036372960
-
Receptor Tyrosine Kinases as Target for Anti-Cancer Therapy
-
Brunelleschi, S.; Penengo, L.; Santoro, M. M.; Gaudino, G. Receptor Tyrosine Kinases as Target for Anti-Cancer Therapy Curr. Pharm. Des. 2002, 8, 1959-1972
-
(2002)
Curr. Pharm. Des.
, vol.8
, pp. 1959-1972
-
-
Brunelleschi, S.1
Penengo, L.2
Santoro, M.M.3
Gaudino, G.4
|