메뉴 건너뛰기




Volumn 4, Issue 2, 2013, Pages 274-277

Probing the binding site of Abl tyrosine kinase using in situ click chemistry

Author keywords

Abl tyrosine kinase; click chemistry; drug design synthesis; ligand binding site

Indexed keywords

ABELSON KINASE; ALKYNE; AZIDE; FA 030; PROTEIN TYROSINE KINASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 84873976921     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml300394w     Document Type: Article
Times cited : (35)

References (38)
  • 3
    • 77955122860 scopus 로고    scopus 로고
    • 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
  • 5
    • 58549106791 scopus 로고    scopus 로고
    • 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
  • 7
    • 77949858836 scopus 로고    scopus 로고
    • 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
  • 10
    • 77949786732 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 15
    • 18644384979 scopus 로고    scopus 로고
    • 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
  • 21
    • 77949786732 scopus 로고    scopus 로고
    • 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
  • 24
    • 79960550248 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 27
    • 84861316742 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 35
    • 84861520898 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.