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1. Wu,P., Chen,W.-S., Hu, T.-S., Yao, Z.-J., Wu, Y.-L. Annonaceous Acetogenin from Annona Atemoya Seeds. J. Asian Nat. Prod. Research2001, 3, 177.
2. Wu, Y.-L., Wu, W.-L., Yao, Z.-J., Li, Y.-L., Wang, Y.-F., Li, J.-C., Sun, X.-L., Peng, Z.-H., Yu, Q., Hu, T.-S., Zeng, B.-B., Wang, X.-Z. Syntheses of Enantiopure Natural Products from Sugars. Chinese J. Org. Chem. 2001, 21, 1051.
3. Atabey, N.; Gao, Y.;Yao, Z.-J.; Brechenridge, D.; Soon, L.; Burke Jr., T.R.; Bottaro, D.P. Potent blockade of hepatocyte growth factor-stimulated cell motility by selective inhibitors of Grb2-c-Met interaction. J. Biol. Chem. 2001, 276, 14308-14314.
4. Burke Jr., T. R., Yao, Z.-J., Ye, B., Miyoshi, K., Otaka, A., Wu., L., Zhang, Z.-Y. Phospho-azatyrosine, a less effective protein-tyrosine phosphatase substrate than phosphotyrosine. Bioorganic & Medicinal Chemistry Letters2001, 11, 1265-8.
5. Burke Jr.,T. R., Yao, Z.-J., Gao, Y., Wu, J. X., Zhu, X., Luo, J. H., Guo, R., Yang, D. N-Terminal Carboxyl and Tetrazole-Containing Amides as Adjuvants to Grb2 SH2 Domain Ligand Binding. Bioorg. Med. Chem.2001, 9, 1439-1445.
6. Burke Jr., T. R., Yao, Z.-J., Liu, D.-G., Voigt, J., Gao, Y. Phosphoryltyrosyl Mimetics in the Design of Peptide-Based Signal Transduction Inhibitors. Biopolymers2001, 60, 32-44.
7. Zhang, Y.-L., Yao, Z.-J., Sarmiento, M., Wu, L., Burke, Jr., T. R., Zhang, Z.-Y. Isothermal Titration Calorimetric Study of Ligand Binding to Protein-Tyrosine Phosphatase 1B and Its Substrate-Trapping Mutants. J. Biol. Chem.2000, 275(44), 34205-34212.
8. Long, Y.-Q., Lung, F.-D. T., Voigt, J. H., Yao, Z.-J., Burke, Jr., T. R., Yang, D., Luo, J. H., Guo, R., King, C. K., Roller, P. P. High affinity nonphosphorylated cyclic peptide inhibitors of Grb2-SH2 / growth factor receptor interactions. In Peptides: Frontier of Peptide Science, Proc. of 16th American Peptide Symposium, Tam, J. P., and Kaumaya, P. T. P. (Eds), ESCOM/Kluwer Acad. Publishers, Dordect, The Netherlands,2000, 568-570.
9. Yao, Z.-J., Barchi, J. J., Burke, Jr., T. R. Design and synthesis of a new tyrosine analogue having c1 and c2 angles constrained to values observed for an SH2 domain-bound phosphotyrosyl residue. In Peptides for the New Millennium: Proc. of 16th American Peptide Symposium, Fields, G. B., Tam, J. P., and Barany, G. (Eds), Kluwer Acad. Publishers, Dordect, The Netherlands,2000, p576-8.
10. Gao, Y., Yao, Z.-J., Voigt, J. H., Luo, J. H., Yang, D., Burke, Jr., T. R. Novel phosphotyrosyl mimetics for the preparation of potent small molecule Grb2 SH2 domain inhibitors. In Peptides for the New Millennium: Proc. of 16th American Peptide Symposium, Fields, G. B., Tam, J. P., and Barany, G. (Eds), Kluwer Acad. Publishers, Dordect, The Netherlands, 2000, p566-7.
11. Gao, Y., Luo, J., Yao, Z.-J., Guo, R., Zou, H., Kelley, J., Voigt, J. H., Yang, D., Burke, Jr., T. R. Inhibition of Grb2 SH2 Domain Binding by Non-Phosphate Containing Ligands 2. 4-(2-Malonyl)phenylalanine as a potent Phosphotyrosyl Mimetic. J. Med. Chem.2000,43, 911-920.
12. Burke Jr., T.R.; Gao, Y.; Yao, Z.-J.; Voigt, J.; Luo, J.; Dajun, Y. Potent non phosphate- containing Grb2 SH2 domain inhibitors. Peptide Chemistry 1999. Proceedings of the 36th Japanese Peptide Symposium, Ed. by N. Fujii,The Japanese Peptide Society, 2000, pp 49-52.
13. Yao, Z.-J., Wu, H.-P., Wu, Y.-L. Polyether Mimics of Natural Occurring Cytotoxic Annonaceous Acetogenins. J. Med. Chem.2000,43, 2484-2487.
14. Liu, D.-G.; Yao, Z.-J.;Gao, Y.; Burke, T.R., Jr. Large scale preparation of cell permeable, non-phosphate containing Grb2 SH2 domain inhibitors. Organic Preparations and Procedures International2000,32, 197-201.
15. Chen, H., Cong, L.-N., Li, Y., Yao, Z.-J., Wu, L., Zhang, Z.-Y., Burke Jr., T. R., Quon, M. J. A Phosphotyrosyl Mimetic Peptide Reverses Impairment of Insulin-stimulated Translocation of Glut4 Caused by Overexpression of PTP1B in Rat Adipose Cells. Biochemistry1999, 38(1), 384-389.
16. Yao, Z.-J., King, C. R., Cao, T., Kelley, J., Milne, G. W. A., Voigt, J. H., Burke Jr., T. R. Potent Inhibition of Grb2 SH2, Domain Binding by Non-Phosphate Cotaining Ligands. J. Med. Chem.1999,42(1), 25-35.
17. Burke Jr., T. R., Luo, J., Yao, Z.-J., Gao, Y., Milne, G. W. A., Voigt, J. H., King, C. R., Yang, D. Monocarboxylic-Based Phosphotyrosyl Mimetics in the Design of Grb2 SH2 Domain Inhibitors. Bioorganic and Medicinal Chemistry Lett. 1999,9, 347-352.
18. Yao, Z.-J., Gao, Y., Voigt, J. H., Ford, Jr., H., Burke Jr., T. R. Synthesis of Fmoc-Protected 4-Carboxydifluoromethyl-L-phenylalanine: A Phosphotyrosyl Mimetic of Potential Use for Signal Transduction Studies. Tetrahedron.1999,55, 2865-2874.
19. Yu, Q., Yao, Z.-J., Chen, X.-G., Wu, Y.-L. Total Synthesis of (10R) and (10S)-corossolin, Determination of the C-10 configuration and the Unexpected Differential Toxicity toward Cancer Cell Caused by the Configuration at C-10. J. Org. Chem.1999, 64, 2440-2445.
20. Long, Y.-Q., Yao, Z.-J., Lung, F.-D. T., Voigt, J. H., King, C. R., Burke, Jr., T. R., Roller, P. P. Overlapping function of amino acids in position-2 and Y0 leading to high affinity nonphosphorylated peptide ligands of Grb2-SH2 domain. Biochem. Biphys. Res. Comm.1999, 264, 902-908.
21. Yao, Z.-J., Gao, Y., Burke, T. R., Jr. Preparation of L-N-Fmoc-Pmp(tBu2)-OH From L-Tyrosine. Tetrahedron: Asymmetry 1999, 10, 3727-3734.
22. Wu, Y.-L., Chen, H.-B., Jiang, K., Li, Y., Shan, F., Wang, D.-Y., Wang, Y.-F., Wu, W.-M., Wu, Y., Yao, Z.-J., Yue, Z.-Y., Zhou, C.-M. Interaction of biomolecules with qinghaosu (artemisinin) and its derivatives in the presence of ferrous ion – an exploration of antimalarial mechanism. Pure Appl. Chem.1999, 71, 1139-1142.
23. Burke, T. R., Jr., Gao, Y., Yao, Z.-J., Voigt, J., Luo, J., Yang, D. Potent non phosphate-containing Grb2 SH2 domain inhibitors.Pept. Sci.1999, 36, 49-52.
24. Wu, W.-M., Wu, Y., Wu, Y.-L., Yao, Z.-J., Zhou, C.-M., Li, Y., Shan, F. Unified Mechanism Framework for the Fe(II)-Induced Cleavage of Qinghaosu and Derivatives /Analogs. The First Spin-Trapping Evidence for the previously Postulated Secondary C-4 Radical. J. Am. Chem. Soc.1998, 120, 3316-3325.
25. Hu, Y.-J., Huang, X.-D., Yao, Z.-J., Wu, Y.-L. Formal Synthesis of 3-Deoxy-D-manno-2-Octulosonic Acid (KDO) via a Highly Double-Stereoselective Hetero Diels-Alder Reaction Directed by a (Salen)Co(II) Catalyst and Chiral Diene. J. Org. Chem.1998, 63, 2456-2461.
26. Yao, Z.-J., Ye, B., Miyoshi, K., Otaka, A., Burke Jr., T. R. Preparation of phospho-L-azatyrosine suitably protected for the solid phase synthesis of signal transduction-related peptides. A correction. Synlett.1998, 428-430.
27. Burke Jr., T. R., Yao, Z.-J., Zhao, H. Enantioselective Synthesis of Nonphosphorous-Containing Phosphotyrosyl Mimetics and Their Use in Peptide Synthesis. Tetrahedron, 1998, 54, 9981-9994.
28. Yao, Z.-J., Ye, B., Wu, X.-W, Wang, S., Wu, L., Zhang, Z.-Y., Burke Jr., T. R. Structure-based design and synthesis of small molecule protein-tyrosine phosphatase 1B inhibitors. Bioorganic and Medicinal Chemistry, 1998, 4, 1799-1810.
29. Tan, H.-T., Chen, W.-S., Yu, Q., Yao, Z.-J., Wu, Y.-L. The Isolation and Structure of Microcarpacin B. Youji Huaxue (Chin. J. Org. Chem.)1998, 18(3), 219.
30. Groves, M. R., Yao, Z.-J., Roller, P. P., Burke Jr., T. R., Barford, D. Structral Basis for Inhibition of the Protein Tyrosine Phosphatase 1B by Phosphotyrosine Peptide Mimetics. Biochemstry1998, 37(51), 17773-17783.
31. Chen, W.-S., Yao, Z.-J., Wu, Y.-L. Annonaceous acetogenins fromUvaria microcarpa Seeds. The isolation and structure of microcarpacin. Acta Chemica Sinica1997, 55, 723-728.
32. Burke Jr., T. R., Yao, Z.-J., Smyth, M. S., Ye, B. Phosphotyrosyl-based motifs in the structure-based design of protein-tyrosine kinase-dependent signal transduction inhibitors. Current Pharmaceutical Design, 1997,3, 291.
33. Ye, B., Yao, Z.-J., Burke Jr., T. R. Synthesis of a new tyrosine analog having X1 and X2 angles constrained to values observed for SH2 domain-bound phosphotyrosyl residue. J. Org. Chem.1997, 62, 5428.
34. Yao, Z.-J., Ye, B., Zhao, H., Yan, X., Wu, L., Barford, D., Wang, S., Zhang, Z.-Y., Burke Jr., T. R. Structure-based design of small molecule protein-tyrosine phosphatase inhibitors. In Peptides: Frontier of Peptide Science, Proc. of 15Th American Peptide Symposium, Tam, J. P., and Kaumaya, P. T. P. (Eds), ESCOM/Kluwer Acad. Publishers, Dordect, The Netherlands, 1997, pp183-185.
35. Chen, W.-S., Yao, Z.-J., Xu, Y.-Z., Zhang, Y.-B., Wu, Y.-L. Study on the annonaceous acetogenins from Annona Atemoya Hort.Youji Huaxue (Chin. J. Org. Chem.) 1996, 16, 145.
36. Yao, Z.-J., Yu, Q., Wu, Y.-L. Two-directional enantioselective synthesis of (+)-ancepsenolide.Synthetic Communication. 1996, 26, 3613.
37. Wu, W.-M., Yao, Z.-J., Wu, Y.-L., Jiang, K., Wang, Y.-F., Chen, H.-B., Shan, F., Li, Y. Ferrous ion induced cleavage of the peroxy bond in qinghaosu and its derivatives and the DNA damage associated with this process. Chemical Communication1996, 2213.
38. Yao, Z.-J., Wu, Y.-L. Synthetic studies toward mono-THF annonaceous acetogenins, an enantioselective and convergent approach to corossolone and (10RS)-corossoline. J. Org. Chem. 1995, 60, 1170.
39. Wu, W.-L., Yao, Z.-J., Li, Y.-L., Li, J.-C., Xia, Y., Wu, Y.-L. Diastereoselective propargylation of -alkoxy aldehyde with propargyl bromide and zinc, a versatile and efficient method for synthesis of chiral oxygenated acyclic natural products. J. Org. Chem. 1995, 60, 3257.
40. Chen, W.-S., Yao, Z.-J., Zhang, Y.-B., Xu, Y.-Z., Wu, Y.-L. Atemoyacin A: a new bis-tetrahydrofuranyl annonaceous acetogenin from Annona Atemoya H. Chinese J. Chem.1995, 13, 263.
41. Chen, W.-S., Yao, Z.-J., Wu, Y.-L. Study on the chemical constituents of Annona glabra Linn. Youji Huaxue (Chin. J. Org. Chem.) 1995, 15, 85.
42. Yao, Z.-J., Wu, Y.-L. Annonaceous acetogenins: Future stars against cancer. Youji Huaxue (Chin. J. Org. Chem.) 1995, 15, 120.
43. Chen, W.-S., Yao, Z.-J., Zhang, Y.-B., Xu, Y.-Z., Wu, Y.-L. Study on the chemical constituents of Annona Atemoya H. and the isolation and the structure of atemoyacin B. Acta Chemica Sinica1995, 53, 516.
44. Li, J.-C., Li, Y.-L., Peng, Z.-H., Sun, X.-L., Wang, Y.-F., Wu, Y.-L.,Yao, Z.-J. Chiral syntheses of acyclic natural products from sugars. J. Chin. Chem. Soc. (Taipei) 1995, 42, 681.
45. Yao, Z.-J., Wu, Y.-L. Total synthesis of (10RS, 15R, 16S, 20S, 34R)-corossoline. Tetrahedron Lett. 1994, 35, 157.
46. Yao, Z.-J., Zhang, Y.-B., Wu, Y.-L. Synthesis of annonaceous acetogenin (4S, 5S) and (4S, 5R)-muricatacin as well as confirmation of absolute configuration of the tetrahydrofuran segment of annonacin. Acta Chim. Sinica1992, 50, 901.