메뉴 건너뛰기




Volumn 1, Issue 4, 1996, Pages 233-240

Novel α-glucosidase inhibitors identified using multiple cyclic peptide combinatorial libraries

Author keywords

Cyclic peptide libraries; Synthetic combinatorial libraries; Glucosidase inhibitors

Indexed keywords

ALPHA GLUCOSIDASE; CYCLOPEPTIDE; DISULFIDE; ENZYME INHIBITOR; LACTAM; PEPTIDE LIBRARY;

EID: 0030202106     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01715527     Document Type: Article
Times cited : (36)

References (34)
  • 3
    • 0028067551 scopus 로고
    • Investigation of antigen-antibody interactions using a soluble nonsupport-boundsynthetic decapeptide library composed of four trillion sequences
    • Pinilla, C., Appel, J.R. Houghten, R.A., Investigation of antigen-antibody interactions using a soluble nonsupport-boundsynthetic decapeptide library composed of four trillion sequences, Biochem. J., 301 (1994) 847-853.
    • (1994) Biochem. J. , vol.301 , pp. 847-853
    • Pinilla, C.1    Appel, J.R.2    Houghten, R.A.3
  • 5
    • 0028100130 scopus 로고
    • Versatility of positional scanning synthetic combinatorial libraries for the identification of individual compounds
    • Pinilla, C., Appel, J.R., Blondelle, S.E., Dooley, C.T., Eichler, J., Ostresh, J.M. Houghten, R.A., Versatility of positional scanning synthetic combinatorial libraries for the identification of individual compounds, Drug Dev. Res., 33 (1994) 133-145.
    • (1994) Drug Dev. Res. , vol.33 , pp. 133-145
    • Pinilla, C.1    Appel, J.R.2    Blondelle, S.E.3    Dooley, C.T.4    Eichler, J.5    Ostresh, J.M.6    Houghten, R.A.7
  • 7
    • 0028064952 scopus 로고
    • Identification of antimicrobial peptides using combinatorial libraries made up of unnatural amino acids
    • Blondelle, S.E., Takahashi, E., Weber, P.A. Houghten, R.A., Identification of antimicrobial peptides using combinatorial libraries made up of unnatural amino acids, Antimicrob. Agents Chemother., 38 (1994) 2280-2286.
    • (1994) Antimicrob. Agents Chemother. , vol.38 , pp. 2280-2286
    • Blondelle, S.E.1    Takahashi, E.2    Weber, P.A.3    Houghten, R.A.4
  • 8
    • 0030047220 scopus 로고    scopus 로고
    • Functionalized protein-like structures from conformationally defined synthetic combinatorial libraries
    • Pérez-Payá, E., Houghten, R.A. Blondelle S.E., Functionalized protein-like structures from conformationally defined synthetic combinatorial libraries, J. Biol. Chem., 271 (1996) 4120.
    • (1996) J. Biol. Chem. , vol.271 , pp. 4120
    • Pérez-Payá, E.1    Houghten, R.A.2    Blondelle, S.E.3
  • 9
    • 0028173391 scopus 로고
    • 'Libraries from libraries': Chemical transformation of combinatorial libraries to extend the range and repertoire of chemical diversity
    • Ostresh, J.M., Husar, G.M., Blondelle, S.E., Dorner, B., Weber, P.A. Houghten, R.A., 'Libraries from libraries': Chemical transformation of combinatorial libraries to extend the range and repertoire of chemical diversity, Proc. Natl. Acad. Sci. USA, 91 (1994) 11138-11142.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 11138-11142
    • Ostresh, J.M.1    Husar, G.M.2    Blondelle, S.E.3    Dorner, B.4    Weber, P.A.5    Houghten, R.A.6
  • 10
    • 0025268863 scopus 로고
    • Potent human renin inhibitors containing novel small cyclic peptides and stable to chymotrypsin degradation
    • Sham, H.L., Rempel, C.A., Stein, H.H. Cohen, J., Potent human renin inhibitors containing novel small cyclic peptides and stable to chymotrypsin degradation, J. Chem. Soc. Chem. Commun., (1990) 666-667.
    • (1990) J. Chem. Soc. Chem. Commun. , pp. 666-667
    • Sham, H.L.1    Rempel, C.A.2    Stein, H.H.3    Cohen, J.4
  • 13
    • 0028535335 scopus 로고
    • Cyclic peptide template combinatorial libraries: Synthesis and identification of chymotrypsin inhibitors
    • Eichler, J., Lucka, A.W. Houghten, R.A., Cyclic peptide template combinatorial libraries: Synthesis and identification of chymotrypsin inhibitors, Pept. Res., 7 (1994) 300-307.
    • (1994) Pept. Res. , vol.7 , pp. 300-307
    • Eichler, J.1    Lucka, A.W.2    Houghten, R.A.3
  • 14
    • 0028808005 scopus 로고
    • Screening of cyclic peptide libraries identifies ligands that bind streptavidin with high affinities
    • Giebel, L.B., Cass, R.T., Milligan, D.L., Young, D.C., Arze, R. Johnson, C.R., Screening of cyclic peptide libraries identifies ligands that bind streptavidin with high affinities, Biochemistry, 34 (1995) 15430-15435.
    • (1995) Biochemistry , vol.34 , pp. 15430-15435
    • Giebel, L.B.1    Cass, R.T.2    Milligan, D.L.3    Young, D.C.4    Arze, R.5    Johnson, C.R.6
  • 15
    • 0027158405 scopus 로고
    • Mimicking of discontinuous epitopes by phage-displayed peptides. I. Epitope mapping of human H ferritin using a phage library of constrained peptides
    • Luzzago, A., Felici, F., Tramontano, A., Pessi, A. Cortese, R., Mimicking of discontinuous epitopes by phage-displayed peptides. I. Epitope mapping of human H ferritin using a phage library of constrained peptides, Gene, 128 (1993) 51-57.
    • (1993) Gene , vol.128 , pp. 51-57
    • Luzzago, A.1    Felici, F.2    Tramontano, A.3    Pessi, A.4    Cortese, R.5
  • 16
    • 0026482552 scopus 로고
    • Oral antidiabetic agents. the emergence of alpha-glucosidase inhibitors
    • Lebovitz, H.E., Oral antidiabetic agents. The emergence of alpha-glucosidase inhibitors, Drugs, 44 (1992) 21-28.
    • (1992) Drugs , vol.44 , pp. 21-28
    • Lebovitz, H.E.1
  • 17
    • 0005207557 scopus 로고
    • Inhibitors of HIV glycosylation enzymes
    • Sandier, M. Smith, J.H. (Eds.) Oxford University Press, Oxford, U.K.
    • Rademacher, T.W., Inhibitors of HIV glycosylation enzymes, In Sandier, M. Smith, J.H. (Eds.) Design of Enzyme Inhibitors as Drugs, Oxford University Press, Oxford, U.K., 1994, pp. 333-343.
    • (1994) Design of Enzyme Inhibitors As Drugs , pp. 333-343
    • Rademacher, T.W.1
  • 18
    • 0028981092 scopus 로고
    • The alpha-glucosidase i inhibitor castanospermine alters endolthelial cell glycosylation, prevents angiogenesis, and inhibits tumor growth
    • Pili, R., Chang, J., Partis, R.A., Mueller, R.A., Chrest, F.J. Passaniti, A., The alpha-glucosidase I inhibitor castanospermine alters endolthelial cell glycosylation, prevents angiogenesis, and inhibits tumor growth, Cancer Res., 55 (1995) 2920-2926.
    • (1995) Cancer Res. , vol.55 , pp. 2920-2926
    • Pili, R.1    Chang, J.2    Partis, R.A.3    Mueller, R.A.4    Chrest, F.J.5    Passaniti, A.6
  • 19
    • 84976512673 scopus 로고
    • Pharmacology of alpha-glucosidase inhibition
    • Bischoff, H., Pharmacology of alpha-glucosidase inhibition, Eur. J. Clin. Invest., 24 Suppl. 3 (1994) 3-10.
    • (1994) Eur. J. Clin. Invest. , vol.24 , Issue.3 SUPPL. , pp. 3-10
    • Bischoff, H.1
  • 21
    • 0023159808 scopus 로고
    • Inhibitors of the biosynthesis and processing of N-linked oligosaccharides
    • Elbein, A.D., Inhibitors of the biosynthesis and processing of N-linked oligosaccharides, Annu. Rev. Biochem., 56 (1987) 497-534.
    • (1987) Annu. Rev. Biochem. , vol.56 , pp. 497-534
    • Elbein, A.D.1
  • 22
    • 53349168468 scopus 로고    scopus 로고
    • Positional scanning combinatorial libraries built around mono- And bicyclic peptide templates
    • Epton, R. (Ed.) Mayflower Worldwide Ltd., Birmingham, U.K.
    • Eichler, J., Lucka, A.W. Houghten, R.A., Positional scanning combinatorial libraries built around mono- and bicyclic peptide templates, In Epton, R. (Ed.) Innovation and Perspectives in Solid-Phase Synthesis, Mayflower Worldwide Ltd., Birmingham, U.K., 1996.
    • (1996) Innovation and Perspectives in Solid-Phase Synthesis
    • Eichler, J.1    Lucka, A.W.2    Houghten, R.A.3
  • 23
    • 0026419319 scopus 로고
    • Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery
    • Houghten, R.A., Pinilla, C., Blondelle, S.E., Appel, J.R., Dooley, C.T. Cuervo, J.H., Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery, Nature, 354(1991) 84-86.
    • (1991) Nature , vol.354 , pp. 84-86
    • Houghten, R.A.1    Pinilla, C.2    Blondelle, S.E.3    Appel, J.R.4    Dooley, C.T.5    Cuervo, J.H.6
  • 24
    • 0000478940 scopus 로고
    • General method for the rapid solid-phase synthesis of large numbers ofpeptides: Specificity of antigen-antibody interaction at the level of individual amino acids
    • Houghten, R.A., General method for the rapid solid-phase synthesis of large numbers ofpeptides: Specificity of antigen-antibody interaction at the level of individual amino acids, Proc. Natl. Acad. Sci. USA, 82(1985) 5131-5135.
    • (1985) Proc. Natl. Acad. Sci. USA , vol.82 , pp. 5131-5135
    • Houghten, R.A.1
  • 25
    • 0027450097 scopus 로고
    • The use of positional scanning synthetic peptide combinatorial libraries for the rapid determination of opioid receptor ligands
    • Dooley, C.T. Houghten, R.A., The use of positional scanning synthetic peptide combinatorial libraries for the rapid determination of opioid receptor ligands, Life Sci., 52 (1993) 1509-1517.
    • (1993) Life Sci. , vol.52 , pp. 1509-1517
    • Dooley, C.T.1    Houghten, R.A.2
  • 26
    • 0000836350 scopus 로고
    • Convenient synthesis of a cyclic peptide disulfide: A type II beta-turn structural model
    • Garcia-Echeverria, C, Albericio, F., Pons, M., Barany, G. Giralt, E., Convenient synthesis of a cyclic peptide disulfide: A type II beta-turn structural model, Tetrahedron Lett., 30 (1989) 2441-2444.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2441-2444
    • Garcia-Echeverria, C.1    Albericio, F.2    Pons, M.3    Barany, G.4    Giralt, E.5
  • 27
    • 13344276445 scopus 로고
    • N2 deprotection of synthetic peptides with a low concentration of HF in dimethyl sulfide: Evidence and application in peptide synthesis
    • N2 deprotection of synthetic peptides with a low concentration of HF in dimethyl sulfide: Evidence and application in peptide synthesis, J. Am. Chem. Soc., 105 (1983) 6442-6455.
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 6442-6455
    • Tam, J.P.1    Heath, W.F.2    Merrifield, R.B.3
  • 28
    • 0022728936 scopus 로고
    • Simplified procedure for carrying out simultaneous multiple hydrogen fluoride cleavages of protected peptide resins
    • Houghten, R.A., Bray, M.K., De Graw, S.T. Kirby, C.J., Simplified procedure for carrying out simultaneous multiple hydrogen fluoride cleavages of protected peptide resins. Int. J. Pept. Protein Res., 27 (1986) 673-678.
    • (1986) Int. J. Pept. Protein Res. , vol.27 , pp. 673-678
    • Houghten, R.A.1    Bray, M.K.2    De Graw, S.T.3    Kirby, C.J.4
  • 29
    • 3042934967 scopus 로고
    • Tissue sulfliydryl groups
    • Ellman, G.L., Tissue sulfliydryl groups, Arch. Biochem. Biophys., 82 (1959) 70-77.
    • (1959) Arch. Biochem. Biophys. , vol.82 , pp. 70-77
    • Ellman, G.L.1
  • 30
    • 0025730051 scopus 로고
    • Synthesis of cyclic peptides on solid support
    • Rovero, P., Quartara, L. Fabbri, G., Synthesis of cyclic peptides on solid support, Tetrahedron Lett., 32 (1991) 2639-2642.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2639-2642
    • Rovero, P.1    Quartara, L.2    Fabbri, G.3
  • 32
    • 0001825241 scopus 로고
    • The purification and properties of an alpha-glucosidase of saccaromyces italicus Y1225
    • Halvorson, H. Ellias, L., The purification and properties of an alpha-glucosidase of saccaromyces italicus Y1225, Biochem. Biophys. Acta, 30 (1958) 28-40.
    • (1958) Biochem. Biophys. Acta , vol.30 , pp. 28-40
    • Halvorson, H.1    Ellias, L.2
  • 33
    • 0002006941 scopus 로고
    • Inhibition of proteolytic enzymes
    • Beynon, R.J. Bond, J.S. (Eds.) IRL Press, Oxford, U.K.
    • Salvesen, G. Nagase, H., Inhibition of proteolytic enzymes, In Beynon, R.J. Bond, J.S. (Eds.) Proteolytic Enzymes - A Practical Approach, IRL Press, Oxford, U.K., 1989, pp. 83-104.
    • (1989) Proteolytic Enzymes - A Practical Approach , pp. 83-104
    • Salvesen, G.1    Nagase, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.