Yersinia pestis and Approaches to Targeting its Outer Protein H Protein-Tyrosine Phosphatase (YopH)BAHTA, M; BURKE, T. R.Current medicinal chemistry. 2012, Vol 19, Num 33, pp 5726-5734, issn 0929-8673, 9 p.Article

Potent inhibition of protein-tyrosine phosphatase-1B using the phosphotyrosyl mimetic fluoro-O-malonyl tyrosine (FOMT)ROLLER, P. P; LI WU; ZHANG, Z.-Y et al.Bioorganic & medicinal chemistry letters (Print). 1998, Vol 8, Num 16, pp 2149-2150, issn 0960-894XArticle

Salicylhydrazine-containing inhibitors of HIV-1 integrase : Implication for a selective chelation in the integrase active siteNEAMATI, N; HUIXIAO HONG; OWEN, J. M et al.Journal of medicinal chemistry (Print). 1998, Vol 41, Num 17, pp 3202-3209, issn 0022-2623Article

L-O-(2-malonyl)tyrosine : a new phosphotyrosyl mimetic for the preparation of Src homology 2 domain inhibitory peptidesBIN YE; AKAMATSU, M; SHOELSON, S. E et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 21, pp 4270-4275, issn 0022-2623Article

Bicyclic compounds as ring-constrained inhibitors of protein-tyrosine kinase p56^lck1BURKE, T. R; LIM, B; MARQUEZ, V. E et al.Journal of medicinal chemistry (Print). 1993, Vol 36, Num 4, pp 425-432, issn 0022-2623Article

Deprotection and cleavage methods for protected peptide resins containing 4-[(diethylphosphono)difluoromethyl]-D,L-phenylalanine residuesOTAKA, A; BURKE, T. R; SMYTH, M. S et al.Tetrahedron letters. 1993, Vol 34, Num 44, issn 0040-4039, 6961, 7039-7042 [5 p.]Article

Solid-phase synthesis of viscosin, a cyclic depsipeptide with antibacterial and antiviral propertiesBURKE, T. R; KNIGHT, M; BHASKAR CHANDRASEKHAR et al.Tetrahedron letters. 1989, Vol 30, Num 5, pp 519-522, issn 0040-4039, 4 p.Article

Chicoric acid analogues as HIV-1 integrase inhibitorsZHAIWEI LIN; NEAMATI, N; DEBYSER, Z et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 8, pp 1401-1414, issn 0022-2623Article

Arylamide inhibitors of HIV-1 integraseZHAO, H; NEAMATI, N; MAZUMDER, A et al.Journal of medicinal chemistry (Print). 1997, Vol 40, Num 8, pp 1186-1194, issn 0022-2623Article

Diarylsulfones, a novel class of human immunodeficiency virus type 1 integrase inhibitorsNEAMATI, N; MAZUMDER, A; ZHAO, H et al.Antimicrobial agents and chemotherapy. 1997, Vol 41, Num 2, pp 385-393, issn 0066-4804Article

Enantioselective synthesis of N-Boc and N-Fmoc protected diethyl 4-phosphono(difluoromethyl)-L-phenylalamine ; agents suitable for the solid-phase synthesis of peptides containing nonhydrolyzable analogues of O-phosphotyrosineSMYTH, M. S; BURKE, T. R.Tetrahedron letters. 1994, Vol 35, Num 4, issn 0040-4039, 498, 551-554 [5 p.]Article

Syp (SH-PTP2) is a positive mediator of growth factor-stimulated mitogenic signal transductionSEN XIAO; ROSE, D. W; SASAOKA, T et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 33, pp 21244-21248, issn 0021-9258Article

Synthesis, of 4-phosphono(difluoromethyl)-D,L-phenylalanine and N-boc and N-Fmoc derivatives suitably protected for solid-phase synthesis of nonyhydrolyzable phosphotyrosyl peptide analoguesBURKE, T. R; SMYTH, M. S; OTAKA, A et al.Tetrahedron letters. 1993, Vol 34, Num 26, issn 0040-4039, 4111, 4125-4128 [5 p.]Article

Inhibition of SH2 domain/phosphoprotein association by a nonhydrolyzable phosphonopeptideDOMCHEK, S. M; AUGER, K. R; SWATI CHATTERJEE et al.Biochemistry (Easton). 1992, Vol 31, Num 41, pp 9865-9870, issn 0006-2960Article

Analysis of styryl-based inhibitors of the lymphocyte tyrosine protein kinase p56^lckZHEN-HONG LI; BURKE, T. R; BOLEN, J. B et al.Biochemical and biophysical research communications (Print). 1991, Vol 180, Num 2, pp 1048-1056, issn 0006-291XArticle

Inhibition of Grb2 SH2 domain binding by non-phosphate-containing ligands. 2. 4-(2-malonyl)phenylalanine as a potent phosphotyrosyl mimeticYANG GAO; LUO, J; YAO, Z.-J et al.Journal of medicinal chemistry (Print). 2000, Vol 43, Num 5, pp 911-920, issn 0022-2623Article

Monocarboxylic-based phosphotyrosyl mimetics in the design of GRB2 SH2 domain inhibitorsBURKE, T. R; LUO, J; YAO, Z.-J et al.Bioorganic & medicinal chemistry letters (Print). 1999, Vol 9, Num 3, pp 347-352, issn 0960-894XArticle

4'-O-[2-(2-fluoromalonyl)]-L-tyrosine : a phosphotyrosyl mimic for the preparation of signal transduction inhibitory peptidesBURKE, T. R; BIN YE; AKAMATSU, M et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 5, pp 1021-1027, issn 0022-2623Article

Cell protein cross-linking by erbstatin and related compoundsSTANWELL, C; YE, B; YUSPA, S. H et al.Biochemical pharmacology. 1996, Vol 52, Num 3, pp 475-480, issn 0006-2952Article

Conformationally constrained phosphotyrosyl mimetics designed as monomeric Src homology 2 domain inhibitorsBURKE, T. R; BARCHI, J. J; GEORGE, C et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 8, pp 1386-1396, issn 0022-2623Article

A general method for the preparation of benzylic α,α-difluorophosphonic acids ; non-hydrolyzable mimetics of phosphotyrosineSMYTH, M. S; FORD, H. JR; BURKE, T. R et al.Tetrahedron letters. 1992, Vol 33, Num 29, pp 4137-4140, issn 0040-4039Article

Preparation of 4-[bis(tert-butoxy)phosphorylmethyl]-N-(fluoren-9-ylmethoxycarbonyl)-DL-phenylalanine. A hydrolytically stable analogue of O-phosphotyrosine potentially suitable for peptide synthesisBURKE, T. R; RUSS, P; LIM, B et al.Synthesis (Stuttgart). 1991, Num 11, pp 1019-1020, issn 0039-7881Article

Solvent systems for the countercurrent chromatography of hydrophobic neuropeptide analogs and hydrophilic protein fragmentsKNIGHT, M; PINEDA, J. D; BURKE, T. R et al.Journal of liquid chromatography. 1988, Vol 11, Num 1, pp 119-131, issn 0148-3919, 13 p.Article

Preparative reversed-phase high-performance liquid chromatography in the synthesis of viscosin, a cyclic depsipeptideBURKE, T. R. JR; BHASKAR CHANDRASEKHAR.Journal of chromatography. 1989, Vol 484, pp 293-298, issn 0021-9673Conference Paper

Counter-current chromatographic purification of [D-Ala¹]peptide T amideBURKE, T. R. JR; KNIGHT, M.Journal of chromatography. 1987, Vol 411, pp 431-435, issn 0021-9673Article