-
1
-
-
33645465610
-
Development of Grb2 SH2 domain signaling antagonists: A potential new class of antiproliferative agents
-
Burke, T. R., Jr. Development of Grb2 SH2 domain signaling antagonists: A potential new class of antiproliferative agents. Int. J. Pept. Res. Ther.. 2006, 12, 33-48.
-
(2006)
Int. J. Pept. Res. Ther
, vol.12
, pp. 33-48
-
-
Burke Jr., T.R.1
-
2
-
-
0033581557
-
Mapping the X+1 binding site of the Grb2-SH2 domain with α,α-disubstituted cyclic α-amino acids
-
(a) Garcia-Echeverria. C.; Gay, B.; Rahuel, J.; Furet, P. Mapping the X+1 binding site of the Grb2-SH2 domain with α,α-disubstituted cyclic α-amino acids. Bioorg. Med. Chem. Lett. 1999, 9, 2915-2920.
-
(1999)
Bioorg. Med. Chem. Lett
, vol.9
, pp. 2915-2920
-
-
Garcia-Echeverria, C.1
Gay, B.2
Rahuel, J.3
Furet, P.4
-
3
-
-
0032572836
-
Structure-based design and synthesis of high affinity tripeptide ligands of the Grb2-SH2 domain
-
(b) Furet, P.; Gay, B.; Caravatti, G.; Garcia-Echeverria, C.; Rahuel, J.; Schoepfer, J.; Fretz, H. Structure-based design and synthesis of high affinity tripeptide ligands of the Grb2-SH2 domain. J. Med. Chem. 1998, 41, 3442-3449.
-
(1998)
J. Med. Chem
, vol.41
, pp. 3442-3449
-
-
Furet, P.1
Gay, B.2
Caravatti, G.3
Garcia-Echeverria, C.4
Rahuel, J.5
Schoepfer, J.6
Fretz, H.7
-
4
-
-
13444270389
-
Design and synthesis of conformationally constrained Grb2 SH2 domain binding peptides employing α-methylphenylalanyl based phosphotyrosyl mimetics
-
Oishi, S.; Karki, R. G.; Kang, S.-U.; Wang, X.; Worthy, K. M.; Bindu, L. K.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R., Jr. Design and synthesis of conformationally constrained Grb2 SH2 domain binding peptides employing α-methylphenylalanyl based phosphotyrosyl mimetics. J. Med. Chem. 2005, 48, 764-772.
-
(2005)
J. Med. Chem
, vol.48
, pp. 764-772
-
-
Oishi, S.1
Karki, R.G.2
Kang, S.-U.3
Wang, X.4
Worthy, K.M.5
Bindu, L.K.6
Nicklaus, M.C.7
Fisher, R.J.8
Burke Jr., T.R.9
-
5
-
-
0027502504
-
Recognition of a high-affinity phosphotyrosyl peptide by the Src homology-2 domain of P56(lck)
-
(a) Eck, M. J.; Shoelson, S. E.; Harrison, S. C. Recognition of a high-affinity phosphotyrosyl peptide by the Src homology-2 domain of P56(lck). Nature 1993, 362, 87-91.
-
(1993)
Nature
, vol.362
, pp. 87-91
-
-
Eck, M.J.1
Shoelson, S.E.2
Harrison, S.C.3
-
6
-
-
0027409064
-
Binding of a high affinity phosphotyrosyl peptide the the Src SH2 domain: Crystal structures of the complexed and peptide-free forms
-
(b) Waksman, G.; Shoelson, S. E.; Pant, N.; Cowburn, D.; Kuriyan, J. Binding of a high affinity phosphotyrosyl peptide the the Src SH2 domain: Crystal structures of the complexed and peptide-free forms. Cell 1993, 72, 779-790.
-
(1993)
Cell
, vol.72
, pp. 779-790
-
-
Waksman, G.1
Shoelson, S.E.2
Pant, N.3
Cowburn, D.4
Kuriyan, J.5
-
7
-
-
0037037384
-
Development of a phosphatase-stable phosphotyrosyl mimetic suitably protected for the synthesis of high affinity Grb2 SH2 domain-binding ligands
-
Wei, C.-Q.; Li, B.; Guo, R.; Yang, D.; Burke, T. R., Jr. Development of a phosphatase-stable phosphotyrosyl mimetic suitably protected for the synthesis of high affinity Grb2 SH2 domain-binding ligands. Bioorg. Med. Chem. Lett. 2002, 12, 2781-2784.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 2781-2784
-
-
Wei, C.-Q.1
Li, B.2
Guo, R.3
Yang, D.4
Burke Jr., T.R.5
-
8
-
-
0029838279
-
4-Aminopiperidine-4-carboxylic acid: A cyclic α,α-disubstituted amino acid for preparation of water soluble highly helical peptides
-
Wysong, C. L.; Yokum, T. S.; McLaughlin, M. L.; Hammer, R. P. 4-Aminopiperidine-4-carboxylic acid: A cyclic α,α-disubstituted amino acid for preparation of water soluble highly helical peptides. J. Org. Chem. 1996, 61, 7650-7651.
-
(1996)
J. Org. Chem
, vol.61
, pp. 7650-7651
-
-
Wysong, C.L.1
Yokum, T.S.2
McLaughlin, M.L.3
Hammer, R.P.4
-
9
-
-
0345434814
-
Potent inhibition of Grb2 SH2 domain binding by non-phosphate-containing ligands
-
Yao, Z. J.; King, C. R.; Cao, T.; Kelley, J.; Milne, G. W. A.; Voigt, J. H.; Burke, T. R. Potent inhibition of Grb2 SH2 domain binding by non-phosphate-containing ligands. J. Med. Chem. 1999, 42, 25-35.
-
(1999)
J. Med. Chem
, vol.42
, pp. 25-35
-
-
Yao, Z.J.1
King, C.R.2
Cao, T.3
Kelley, J.4
Milne, G.W.A.5
Voigt, J.H.6
Burke, T.R.7
-
10
-
-
34247240862
-
-
Available from Pharmacore Inc, High Point, NC
-
Available from Pharmacore Inc., High Point, NC.
-
-
-
-
11
-
-
20044370456
-
-
Oishi, S.; Karki, R. G.; Shi, Z.-D.; Worthy, K. M.; Bindu, L.; Chertov, O.; Esposito, D.; Frank, P.; Gillette, W. K.; Maderia, M. A.; Hartley, J.; Nicklaus, M. C.; Barchi, J. J., Jr.; Fisher, R. J.; Burke, T. R., Jr. Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal β-vinyl-substituted phosphotyrosyl mimetic. Bioorg. Med. Chem. 2005, 13, 2431-2438.
-
Oishi, S.; Karki, R. G.; Shi, Z.-D.; Worthy, K. M.; Bindu, L.; Chertov, O.; Esposito, D.; Frank, P.; Gillette, W. K.; Maderia, M. A.; Hartley, J.; Nicklaus, M. C.; Barchi, J. J., Jr.; Fisher, R. J.; Burke, T. R., Jr. Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal β-vinyl-substituted phosphotyrosyl mimetic. Bioorg. Med. Chem. 2005, 13, 2431-2438.
-
-
-
-
12
-
-
0036304080
-
Crystal structures of the SH2 domain of Grb2: Highlight on the binding of a new high-affinity inhibitor
-
(a) Nioche, P.; Liu, W.-Q.; Broutin, I.; Charbonnier, F.; Latreille, M.-T.; Vidal, M.; Roques, B.; Garbay, C.; Ducruix, A. Crystal structures of the SH2 domain of Grb2: Highlight on the binding of a new high-affinity inhibitor. J. Mol. Biol. 2002, 315, 1167-1177.
-
(2002)
J. Mol. Biol
, vol.315
, pp. 1167-1177
-
-
Nioche, P.1
Liu, W.-Q.2
Broutin, I.3
Charbonnier, F.4
Latreille, M.-T.5
Vidal, M.6
Roques, B.7
Garbay, C.8
Ducruix, A.9
-
13
-
-
0033539113
-
Small peptides containing phosphotyrosine and adjacent α-Mephosphotyrosine or its mimetics as highly potent inhibitors of Grb2 SH2 domain
-
(b) Liu, W. Q.; Vidal, M.; Gresh, N.; Rogues, B. P.; Garbay, C. Small peptides containing phosphotyrosine and adjacent α-Mephosphotyrosine or its mimetics as highly potent inhibitors of Grb2 SH2 domain. J. Med. Chem. 1999, 42, 3737-3741.
-
(1999)
J. Med. Chem
, vol.42
, pp. 3737-3741
-
-
Liu, W.Q.1
Vidal, M.2
Gresh, N.3
Rogues, B.P.4
Garbay, C.5
-
14
-
-
1242273804
-
Structure-activity relationships of small phosphopeptides, inhibitors of Grb2 SH2 domain, and their prodrugs
-
(c) Liu, W.-Q.; Vidal, M.; Olszowy, C.; Million, E.; Lenoir, C.; Dhotel, H.; Garbay, C. Structure-activity relationships of small phosphopeptides, inhibitors of Grb2 SH2 domain, and their prodrugs. J. Med. Chem. 2004, 47, 1223-1233.
-
(2004)
J. Med. Chem
, vol.47
, pp. 1223-1233
-
-
Liu, W.-Q.1
Vidal, M.2
Olszowy, C.3
Million, E.4
Lenoir, C.5
Dhotel, H.6
Garbay, C.7
-
15
-
-
34247188354
-
-
Synthetic procedures for the preparation of mimetics A and B are provided in the Supporting Information
-
Synthetic procedures for the preparation of mimetics A and B are provided in the Supporting Information.
-
-
-
-
16
-
-
0037028049
-
Relationships between structure and interaction kinetics for HIV-1 protease inhibitors
-
Markgren, P. O.; Schaal, W.; Hamalainen, M.; Karlen, A.; Hallgerg, A.; Samuelsson, B.; Danielson, U. H. Relationships between structure and interaction kinetics for HIV-1 protease inhibitors. J. Med. Chem. 2002, 45, 5430-5439.
-
(2002)
J. Med. Chem
, vol.45
, pp. 5430-5439
-
-
Markgren, P.O.1
Schaal, W.2
Hamalainen, M.3
Karlen, A.4
Hallgerg, A.5
Samuelsson, B.6
Danielson, U.H.7
|