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Volumn 48, Issue 16, 2005, Pages 5369-5372

Design and synthesis of 4-(α-hydroxymalonyl)phenylalanine as a new phosphotyrosyl mimetic and its use in growth factor receptor bound 2 Src-homology 2 (Grb2 SH2) domain-binding peptides

Author keywords

[No Author keywords available]

Indexed keywords

4 (ALPHA HYDROXYMALONYL)PHENYLALANINE; EPIDERMAL GROWTH FACTOR RECEPTOR 2; ESTER DERIVATIVE; GROWTH FACTOR RECEPTOR; PHENYLALANINE DERIVATIVE; PRODRUG; PROTEIN TYROSINE PHOSPHATASE; SIGNALING LYMPHOCYTE ACTIVATION MOLECULE ASSOCIATED PROTEIN; TRIPEPTIDE; UNCLASSIFIED DRUG;

EID: 23444433256     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm050154v     Document Type: Article
Times cited : (10)

References (12)
  • 2
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    • Structure-based design of compounds inhibiting Grb2-SH2 mediated protein-protein interactions in signal transduction pathways
    • Fretz, H.; Furet, P.; Garcia-Echeverria, C.; Rahuel, J.; Schoepfer, J. Structure-based design of compounds inhibiting Grb2-SH2 mediated protein-protein interactions in signal transduction pathways. Curr. Pharm. Des. 2000, 6, 1777-1796.
    • (2000) Curr. Pharm. Des. , vol.6 , pp. 1777-1796
    • Fretz, H.1    Furet, P.2    Garcia-Echeverria, C.3    Rahuel, J.4    Schoepfer, J.5
  • 4
    • 0034624812 scopus 로고    scopus 로고
    • Inhibition of Grb2 SH2 domain binding by non-phosphate containing ligands. 2. 4-(2-Malonyl)-phenylalanine as a potent phosphotyrosyl mimetic
    • Gao, Y.; Luo, J.; Yao, Z.-J.; Guo, R.; Zou, H.; Kelley, J.; Voigt, J. H.; Yang, D.; Burke, T. R., Jr. 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.
    • (2000) J. Med. Chem. , vol.43 , pp. 911-920
    • Gao, Y.1    Luo, J.2    Yao, Z.-J.3    Guo, R.4    Zou, H.5    Kelley, J.6    Voigt, J.H.7    Yang, D.8    Burke Jr., T.R.9
  • 5
    • 0033955133 scopus 로고    scopus 로고
    • Stereoselective preparation of L-4-(2′-malonyl)phenylalanine suitably protected for Fmoc-based synthesis of potent signal transduction inhibitory ligands
    • Gao, Y.; Burke, T. R., Jr. Stereoselective preparation of L-4-(2′-malonyl)phenylalanine suitably protected for Fmoc-based synthesis of potent signal transduction inhibitory ligands. Synlett 2000, 134-136.
    • (2000) Synlett , pp. 134-136
    • Gao, Y.1    Burke Jr., T.R.2
  • 7
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    • Unreported results
    • Unreported results.
  • 9
    • 0001200405 scopus 로고
    • Ester enolates from a-acetoxy esters. Synthesis of arylmalonic and a-arylalkanoic esters from aryl nucleophiles and α-keto esters
    • Ghosh, S.; Pardo, S. N.; Salomon, R. G. Ester enolates from a-acetoxy esters. Synthesis of arylmalonic and a-arylalkanoic esters from aryl nucleophiles and α-keto esters. J. Org. Chem. 1982, 47, 4692-702.
    • (1982) J. Org. Chem. , vol.47 , pp. 4692-4702
    • Ghosh, S.1    Pardo, S.N.2    Salomon, R.G.3
  • 10
    • 0026326741 scopus 로고
    • Asymmetric synthesis of monosubstituted and α,α-disubstituted α-amino acids via diastereoselective glycine enolate alkylations
    • Williams, R. M.; Im, M. N. Asymmetric synthesis of monosubstituted and α,α-disubstituted α-amino acids via diastereoselective glycine enolate alkylations. J. Am. Chem. Soc. 1991, 113, 9276-86.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9276-9286
    • Williams, R.M.1    Im, M.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.