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Volumn 4, Issue 4, 2006, Pages 659-666

Utilization of 3′-carboxy-containing tyrosine derivatives as a new class of phosphotyrosyl mimetics in the preparation of novel non-phosphorylated cyclic peptide inhibitors of the Grb2-SH2 domain

(4) Song, Yan Li a Tan, Jinzhi a Luo, Xiao Min a Long, Ya Qiu a

a SHANGHAI INSTITUTE OF MATERIA MEDICA (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; AROMATIC COMPOUNDS; PHOSPHORS; RATE CONSTANTS; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

CARBOXY-CONTAINING GROUPS; CHIRAL POOL SYNTHESIS; PHOSPHOTYROSYL (PTYR) MIMETICS; TYROSINE;

POLYPEPTIDES;

BIOMIMETIC MATERIAL; CYCLOPEPTIDE; DRUG DERIVATIVE; GROWTH FACTOR RECEPTOR BOUND PROTEIN 2; LIGAND; TYROSINE;

ARTICLE; BIOMIMETICS; CHEMICAL STRUCTURE; CHEMISTRY; CLASSIFICATION; DRUG ANTAGONISM; METABOLISM; PHOSPHORYLATION; SRC HOMOLOGY DOMAIN; SYNTHESIS;

BIOMIMETIC MATERIALS; BIOMIMETICS; GRB2 ADAPTOR PROTEIN; LIGANDS; MOLECULAR STRUCTURE; PEPTIDES, CYCLIC; PHOSPHORYLATION; SRC HOMOLOGY DOMAINS; TYROSINE;

EID: 32544437397 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/b515432d Document Type: Article

Times cited : (6)

References (28)

1
- 0026729382
- E. J. Lowenstein R. J. Daly W. L. Batzer B. Margolis R. Lanners A. Ulrich E. Y. Skolnick D. Bar-Sagi J. Schlessinger Cell 70 431 442
- Cell , vol.70 , pp. 431-442
- Lowenstein, E.J.¹ Daly, R.J.² Batzer, W.L.³ Margolis, B.⁴ Lanners, R.⁵ Ulrich, A.⁶ Skolnick, E.Y.⁷ Bar-Sagi, D.⁸ Schlessinger, J.⁹

2
- 13244284809
- T. Pawson J. Schlessinger Curr. Biol. 3 434 442
- Curr. Biol. , vol.3 , pp. 434-442
- Pawson, T.¹ Schlessinger, J.²

3
- 0033545371
- A. M. Tari M. C. Hung K. Li G. Lopez-Berestein Oncogene 18 1325 1332
- Oncogene , vol.18 , pp. 1325-1332
- Tari, A.M.¹ Hung, M.C.² Li, K.³ Lopez-Berestein, G.⁴

4
- 7444229834
- J. V. Soriano N. F. Liu Y. Gao Z.-J. Yao T. Ishibashi C. Underhill T. R. Burke D. P. Bottaro Mol. Cancer Ther. 3 1289 1299
- Mol. Cancer Ther. , vol.3 , pp. 1289-1299
- Soriano, J.V.¹ Liu, N.F.² Gao, Y.³ Yao, Z.-J.⁴ Ishibashi, T.⁵ Underhill, C.⁶ Burke, T.R.⁷ Bottaro, D.P.⁸

5
- 0033667937
- H. Fretz P. Furet C. Garcia-Echeverria J. Rahuel J. Schoepfer Curr. Pharm. Des. 6 1777 1796
- Curr. Pharm. Des. , vol.6 , pp. 1777-1796
- Fretz, H.¹ Furet, P.² Garcia-Echeverria, C.³ Rahuel, J.⁴ Schoepfer, J.⁵

6
- 12844283323
- K. Machida B. J. Mayer Biochim. Biophys. Acta 1747 1 25
- Biochim. Biophys. Acta , vol.1747 , pp. 1-25
- MacHida, K.¹ Mayer, B.J.²

7
- 15844398102
- J. Rahuel B. Gay D. Erdmann A. Strauss C. Garcia-Echeverria P. Furet G. Caravatti H. Fretz J. Schoepfer M. G. Grutter Nat. Struct. Biol. 3 586 589
- Nat. Struct. Biol. , vol.3 , pp. 586-589
- Rahuel, J.¹ Gay, B.² Erdmann, D.³ Strauss, A.⁴ Garcia-Echeverria, C.⁵ Furet, P.⁶ Caravatti, G.⁷ Fretz, H.⁸ Schoepfer, J.⁹ Grutter, M.G.¹⁰

8
- 15144350558
- L. Oligino F.-D. T. Lung L. Sastry J. Bigelow T. Cao M. Curran T. R. Burke S.-M. Wang D. Krag P. P. Roller C. R. King J. Biol. Chem. 272 29046 29052
- J. Biol. Chem. , vol.272 , pp. 29046-29052
- Oligino, L.¹ Lung, F.-D.T.² Sastry, L.³ Bigelow, J.⁴ Cao, T.⁵ Curran, M.⁶ Burke, T.R.⁷ Wang, S.-M.⁸ Krag, D.⁹ Roller, P.P.¹⁰ King, C.R.¹¹

9
- 0033517027
- Y.-Q. Long J. H. Voigt F.-D. T. Lung C. R. King P. P. Roller Bioorg. Med. Chem. Lett. 9 2267 2272
- Bioorg. Med. Chem. Lett. , vol.9 , pp. 2267-2272
- Long, Y.-Q.¹ Voigt, J.H.² Lung, F.-D.T.³ King, C.R.⁴ Roller, P.P.⁵

10
- 0033517842
- Y.-Q. Long Z.-J. Yao J. H. Voigt F.-D. T. Lung J. H. Luo T. R. Burke C. R. King D. Yang P. P. Roller Biochem. Biophys. Res. Commun. 264 902 908
- Biochem. Biophys. Res. Commun. , vol.264 , pp. 902-908
- Long, Y.-Q.¹ Yao, Z.-J.² Voigt, J.H.³ Lung, F.-D.T.⁴ Luo, J.H.⁵ Burke, T.R.⁶ King, C.R.⁷ Yang, D.⁸ Roller, P.P.⁹

11
- 0034967501
- F.-D. T. Lung Y.-Q. Long C. R. King J. Varady X.-W. Wu S.-M. Wang P. P. Roller J. Pept. Res. 57 447 454
- J. Pept. Res. , vol.57 , pp. 447-454
- Lung, F.-D.T.¹ Long, Y.-Q.² King, C.R.³ Varady, J.⁴ Wu, X.-W.⁵ Wang, S.-M.⁶ Roller, P.P.⁷

12
- 0043092110
- Y.-Q. Long F.-D. Lung P. P. Roller Bioorg. Med. Chem. 11 3929 3936
- Bioorg. Med. Chem. , vol.11 , pp. 3929-3936
- Long, Y.-Q.¹ Lung, F.-D.² Roller, P.P.³

13
- 0141682143
- Y.-Q. Long R. Guo J. H. Luo D. Yang P. P. Roller Biochem. Biophys. Res. Commun. 310 334 340
- Biochem. Biophys. Res. Commun. , vol.310 , pp. 334-340
- Long, Y.-Q.¹ Guo, R.² Luo, J.H.³ Yang, D.⁴ Roller, P.P.⁵

14
- 2442417484
- Y.-L. Song P. P. Roller Y.-Q. Long Bioorg. Med. Chem. Lett. 14 3205 3208
- Bioorg. Med. Chem. Lett. , vol.14 , pp. 3205-3208
- Song, Y.-L.¹ Roller, P.P.² Long, Y.-Q.³

15
- 0038679457
- T. R. Burke, Jr. K. Lee Acc. Chem. Res. 36 426 433
- Acc. Chem. Res. , vol.36 , pp. 426-433
- Burke Jr., T.R.¹ Lee, K.²

16
- 0034193474
- Y. Gao L. Wu J. H. Luo R. Guo D. Yang Z. Y. Zhang T. R. Burke Bioorg. Med. Chem. Lett. 10 923 927
- Bioorg. Med. Chem. Lett. , vol.10 , pp. 923-927
- Gao, Y.¹ Wu, L.² Luo, J.H.³ Guo, R.⁴ Yang, D.⁵ Zhang, Z.Y.⁶ Burke, T.R.⁷

17
- 0030889523
- M. E. Jung T. I. Lazarova J. Org. Chem. 62 1553 1555
- J. Org. Chem. , vol.62 , pp. 1553-1555
- Jung, M.E.¹ Lazarova, T.I.²

18
- 0003423124
- IRL, Oxford
- E. Atherton and R. C. Sheppard, Solid Phase Peptide Synthesis: A Practical Approach, IRL, Oxford
- Solid Phase Peptide Synthesis: A Practical Approach
- Atherton, E.¹ Sheppard, R.C.²

19
- 0037534034
- P. Li M. Zhang Y.-Q. Long M. L. Peach H. Liu D. Yang M. Nicklaus P. P. Roller Bioorg. Med. Chem. Lett. 13 2173 2177
- Bioorg. Med. Chem. Lett. , vol.13 , pp. 2173-2177
- Li, P.¹ Zhang, M.² Long, Y.-Q.³ Peach, M.L.⁴ Liu, H.⁵ Yang, D.⁶ Nicklaus, M.⁷ Roller, P.P.⁸

20
- 0035415663
- W. C. Shakespeare Curr. Opin. Chem. Biol. 5 409 415
- Curr. Opin. Chem. Biol. , vol.5 , pp. 409-415
- Shakespeare, W.C.¹

21
- 20444405308
- S.-K. Kang Z.-D. Shi K. M. Worthy L. K. Bindu P. G. Dharmawardana S. J. Choyke D. P. Bottaro R. J. Fisher T. R. Burke, Jr. J. Med. Chem. 48 3945 3948
- J. Med. Chem. , vol.48 , pp. 3945-3948
- Kang, S.-K.¹ Shi, Z.-D.² Worthy, K.M.³ Bindu, L.K.⁴ Dharmawardana, P.G.⁵ Choyke, S.J.⁶ Bottaro, D.P.⁷ Fisher, R.J.⁸ Burke Jr., T.R.⁹

22
- 0033602525
- P. Ettmayer D. France J. Gounarides M. Jarosinski M.-S. Martin J.-M. Rondeau M. Sabio S. Topiol B. Weidmann M. Zurini K. W. Bair J. Med. Chem. 42 971 980
- J. Med. Chem. , vol.42 , pp. 971-980
- Ettmayer, P.¹ France, D.² Gounarides, J.³ Jarosinski, M.⁴ Martin, M.-S.⁵ Rondeau, J.-M.⁶ Sabio, M.⁷ Topiol, S.⁸ Weidmann, B.⁹ Zurini, M.¹⁰ Bair, K.W.¹¹

23
- 0028922586
- A. C. Wallace R. A. Laskowski J. M. Thornton Protein Eng. 8 127 134
- Protein Eng. , vol.8 , pp. 127-134
- Wallace, A.C.¹ Laskowski, R.A.² Thornton, J.M.³

24
- 11644261806
- G. M. Morris D. S. Goodsell R. S. Halliday R. Huey W. E. Hart R. K. Belew A. J. Olson J. Comput. Chem. 19 1639 1662
- J. Comput. Chem. , vol.19 , pp. 1639-1662
- Morris, G.M.¹ Goodsell, D.S.² Halliday, R.S.³ Huey, R.⁴ Hart, W.E.⁵ Belew, R.K.⁶ Olson, A.J.⁷

25
- 0011127153
- Molecular Graphics Laboratory, Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA
- G. M. Morris, D. S. Goodsell, R. Huey, W. E. Hart, R. S. Halliday, R. K. Belew and A. J. Olson, Autodock (Version 3.0.3), Molecular Graphics Laboratory, Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA
- Autodock (Version 3.0.3)
- Morris, G.M.¹ Goodsell, D.S.² Huey, R.³ Hart, W.E.⁴ Halliday, R.S.⁵ Belew, R.K.⁶ Olson, A.J.⁷

26
- 0003797555
- Tripos Associates, St. Louis, MO
- Sybyl (Version 6.8), Tripos Associates, St. Louis, MO
- Sybyl (Version 6.8)

27
- 0021757436
- S. J. Weiner P. A. Kollman D. A. Case U. C. Singh C. Ghio G. Alagona S. Profeta P. Weiner J. Am. Chem. Soc. 106 765 784
- J. Am. Chem. Soc. , vol.106 , pp. 765-784
- Weiner, S.J.¹ Kollman, P.A.² Case, D.A.³ Singh, U.C.⁴ Ghio, C.⁵ Alagona, G.⁶ Profeta, S.⁷ Weiner, P.⁸

28
- 49149147973
- J. Gasteiger M. Marsili Tetrahedron 36 3219 3228
- Tetrahedron , vol.36 , pp. 3219-3228
- Gasteiger, J.¹ Marsili, M.²

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