메뉴 건너뛰기




Volumn 71, Issue 12, 1999, Pages 2349-2365

Glossary of terms used in combinatorial chemistry (Technical Report)

Author keywords

[No Author keywords available]

Indexed keywords


EID: 18944378492     PISSN: 00334545     EISSN: 13653075     Source Type: Journal    
DOI: 10.1351/pac199971122349     Document Type: Article
Times cited : (51)

References (113)
  • 1
    • 0033582970 scopus 로고    scopus 로고
    • A photolabile carbamate based dual linker analytical construct for facile monitoring of solid phase chemistry: ‘TLC’ for solid phase?
    • S. C. McKeown, S. P. Watson, R. A. E. Carr, P. Marshall. A photolabile carbamate based dual linker analytical construct for facile monitoring of solid phase chemistry: ‘TLC’ for solid phase? Tetrahedron Lett. 40, 2407–2410 (1999).
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2407-2410
    • McKeown, S.C.1    Watson, S.P.2    Carr, R.A.E.3    Marshall, P.4
  • 3
  • 4
    • 0025194307 scopus 로고
    • Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase
    • C. Tuerk, L. Gold. Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase. Science 249, 505–510 (1990).
    • (1990) Science , vol.249 , pp. 505-510
    • Tuerk, C.1    Gold, L.2
  • 5
    • 0025074907 scopus 로고
    • In vitro selection of RNA molecules that bind specific ligands
    • A. D. Ellington, J. W. Szostak. In vitro selection of RNA molecules that bind specific ligands. Nature 346, 818–822 (1990).
    • (1990) Nature , vol.346 , pp. 818-822
    • Ellington, A.D.1    Szostak, J.W.2
  • 6
    • 0031102380 scopus 로고    scopus 로고
    • Nucleic acid selection and the challenge of combinatorial chemistry
    • S. E. Osborne, A. D. Ellington. Nucleic acid selection and the challenge of combinatorial chemistry. Chem. Rev. 97, 349–370 (1997).
    • (1997) Chem. Rev. , vol.97 , pp. 349-370
    • Osborne, S.E.1    Ellington, A.D.2
  • 8
    • 0022646579 scopus 로고
    • A priori delineation of a peptide which mimics a discontinuous antigenic determinant
    • H. M. Geysen, S. J. Rodda, T. J. Mason. A priori delineation of a peptide which mimics a discontinuous antigenic determinant. Mol. Immunol. 23, 709–715 (1986).
    • (1986) Mol. Immunol. , vol.23 , pp. 709-715
    • Geysen, H.M.1    Rodda, S.J.2    Mason, T.J.3
  • 10
    • 0001070152 scopus 로고    scopus 로고
    • Spatially addressable combinatorial libraries
    • M. C. Pirrung. Spatially addressable combinatorial libraries. Chem. Rev. 97, 473–488 (1997).
    • (1997) Chem. Rev. , vol.97 , pp. 473-488
    • Pirrung, M.C.1
  • 12
    • 0032600672 scopus 로고    scopus 로고
    • Beyond mere diversity: tailoring combinatorial libraries for drug discovery
    • E. J. Martin, R. E. Critchlow. Beyond mere diversity: tailoring combinatorial libraries for drug discovery. J. Comb. Chem. 1, 32–45 (1999).
    • (1999) J. Comb. Chem. , vol.1 , pp. 32-45
    • Martin, E.J.1    Critchlow, R.E.2
  • 14
    • 18944392434 scopus 로고    scopus 로고
    • Instructions to Authors
    • Instructions to Authors. J. Comb. Chem. 1, 11A (1999).
    • (1999) J. Comb. Chem. , vol.1 , pp. 11A
  • 15
    • 0028496956 scopus 로고
    • Similarity searching and clustering of chemical structure databases using molecular property data
    • G. M. Downs, P. Willett, W. Fisanick. Similarity searching and clustering of chemical structure databases using molecular property data. J. Chem. Inf. Comput. Sci. 34, 1094–1102 (1994).
    • (1994) J. Chem. Inf. Comput. Sci. , vol.34 , pp. 1094-1102
    • Downs, G.M.1    Willett, P.2    Fisanick, W.3
  • 16
    • 0342645323 scopus 로고    scopus 로고
    • Use of structure-activity data to compare structure-based clustering methods and descriptors for use in compound selection
    • R. D. Brown, Y. C. Martin. Use of structure-activity data to compare structure-based clustering methods and descriptors for use in compound selection. J. Chem. Inf. Comput. Sci. 36, 572–584 (1996).
    • (1996) J. Chem. Inf. Comput. Sci. , vol.36 , pp. 572-584
    • Brown, R.D.1    Martin, Y.C.2
  • 18
    • 19744377612 scopus 로고    scopus 로고
    • Preparation, structure, and morphology of polymer supports
    • D. C. Sherrington. Preparation, structure, and morphology of polymer supports. Chem. Commun. 2275–2286 (1998).
    • (1998) Chem. Commun. , pp. 2275-2286
    • Sherrington, D.C.1
  • 19
    • 0028833961 scopus 로고
    • Reductive alkylation on a solid phase: synthesis of a piperazinedione combinatorial library
    • D. W. Gordon, J. Steele. Reductive alkylation on a solid phase: synthesis of a piperazinedione combinatorial library. Biorg. Med. Chem. Lett. 5, 47–50 (1995).
    • (1995) Biorg. Med. Chem. Lett. , vol.5 , pp. 47-50
    • Gordon, D.W.1    Steele, J.2
  • 20
    • 0031000559 scopus 로고    scopus 로고
    • A simple procedure for the solid phase synthesis of diketopiperazine and diketomorpholine derivatives
    • A. K. Szardenings, T. S. Burkoth, H. H. Lu, D. W. Tien, D. A. Campbell. A simple procedure for the solid phase synthesis of diketopiperazine and diketomorpholine derivatives. Tetrahedron 53, 6573–6593 (1997).
    • (1997) Tetrahedron , vol.53 , pp. 6573-6593
    • Szardenings, A.K.1    Burkoth, T.S.2    Lu, H.H.3    Tien, D.W.4    Campbell, D.A.5
  • 21
    • 0031151959 scopus 로고    scopus 로고
    • Encoding methods for combinatorial chemistry
    • A. W. Czarnik. Encoding methods for combinatorial chemistry. Curr. Opin. Chem. Biol. 1, 60–66 (1997).
    • (1997) Curr. Opin. Chem. Biol. , vol.1 , pp. 60-66
    • Czarnik, A.W.1
  • 22
    • 0026419319 scopus 로고
    • Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery
    • R. A. Houghten, C. Pinella, S. E. Blondelle, J. R. Appel, C. T. Dooley, J. H. Cuervo. Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery. Nature 354, 84–86 (1991).
    • (1991) Nature , vol.354 , pp. 84-86
    • Houghten, R.A.1    Pinella, C.2    Blondelle, S.E.3    Appel, J.R.4    Dooley, C.T.5    Cuervo, J.H.6
  • 23
    • 0029897237 scopus 로고    scopus 로고
    • Deconvolution of combinatorial libraries for drug discovery: theoretical comparison of pooling strategies
    • D. A. M. Konings, J. R. Wyatt, D. J. Ecker, S. M. Freier. Deconvolution of combinatorial libraries for drug discovery: theoretical comparison of pooling strategies. J. Med. Chem. 39, 2710–2719 (1996).
    • (1996) J. Med. Chem. , vol.39 , pp. 2710-2719
    • Konings, D.A.M.1    Wyatt, J.R.2    Ecker, D.J.3    Freier, S.M.4
  • 26
    • 0242326226 scopus 로고    scopus 로고
    • Dendritic and star polymers: classiication, nomenclature, structure representation, and registration in the DuPont SCION database
    • J. L. Schultz, E. S. Wilks. Dendritic and star polymers: classiication, nomenclature, structure representation, and registration in the DuPont SCION database. J. Chem. Inf. Comput. Sci. 38, 85–99 (1998).
    • (1998) J. Chem. Inf. Comput. Sci. , vol.38 , pp. 85-99
    • Schultz, J.L.1    Wilks, E.S.2
  • 28
    • 0030855324 scopus 로고    scopus 로고
    • Solid-phase dendrimer synthesis and the generation of super-high-loading resin beads for combinatorial chemistry
    • V. Swali, N. J. Wells, G. J. Landley, M. Bradley. Solid-phase dendrimer synthesis and the generation of super-high-loading resin beads for combinatorial chemistry. J. Org. Chem. 62, 4902–4903 (1997).
    • (1997) J. Org. Chem. , vol.62 , pp. 4902-4903
    • Swali, V.1    Wells, N.J.2    Landley, G.J.3    Bradley, M.4
  • 29
    • 0032011516 scopus 로고    scopus 로고
    • DIVSEL and COMPLIB—Strategies for the design and comparison of combinatorial libraries using pharmacophoric descriptors
    • S. D. Pickett, C. Luttmann, V. Guerin, A. Laoui, E. James. DIVSEL and COMPLIB—Strategies for the design and comparison of combinatorial libraries using pharmacophoric descriptors. J. Chem. Inf. Comput. Sci. 38, 144–150 (1998).
    • (1998) J. Chem. Inf. Comput. Sci. , vol.38 , pp. 144-150
    • Pickett, S.D.1    Luttmann, C.2    Guerin, V.3    Laoui, A.4    James, E.5
  • 30
    • 0039700206 scopus 로고    scopus 로고
    • Identification of a preferred set of molecular descriptors for compound classification based on principal components analysis
    • L. Xue, J. Godden, H. Gao, J. Bajorath. Identification of a preferred set of molecular descriptors for compound classification based on principal components analysis. J. Chem. Inf. Comput. Sci. 39, 699–704 (1999).
    • (1999) J. Chem. Inf. Comput. Sci. , vol.39 , pp. 699-704
    • Xue, L.1    Godden, J.2    Gao, H.3    Bajorath, J.4
  • 35
    • 0031960506 scopus 로고    scopus 로고
    • A visual tagging process for mix and sort combinatorial chemistry
    • J. W. Guiles, C. L. Lanter, R. A. Rivero. A visual tagging process for mix and sort combinatorial chemistry. Angew. Chem. Int. Ed. 37, 926–928 (1998).
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 926-928
    • Guiles, J.W.1    Lanter, C.L.2    Rivero, R.A.3
  • 38
    • 0032476782 scopus 로고    scopus 로고
    • Strategies for the dynamic integration of combinatorial synthesis and screening
    • A. Ganesan. Strategies for the dynamic integration of combinatorial synthesis and screening. Angew. Chem. Int. Ed. 37, 2828–2831 (1998).
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2828-2831
    • Ganesan, A.1
  • 39
    • 0031750811 scopus 로고    scopus 로고
    • Use of molecular recognition to drive chemical evolution: mechanisms of an automated genetic algorithm implementation
    • A. V. Eliseev, M. I. Nelen. Use of molecular recognition to drive chemical evolution: mechanisms of an automated genetic algorithm implementation. Chem. Eur. J. 4, 825–834 (1998).
    • (1998) Chem. Eur. J. , vol.4 , pp. 825-834
    • Eliseev, A.V.1    Nelen, M.I.2
  • 40
    • 0033127029 scopus 로고    scopus 로고
    • Pharmocophore fingerprinting 1. Application to QSAR and focused library design
    • M. J. McGregor, S. M. Muskal. Pharmocophore fingerprinting 1. Application to QSAR and focused library design. J. Chem. Inf. Comput. Sci. 39, 569–574 (1999).
    • (1999) J. Chem. Inf. Comput. Sci. , vol.39 , pp. 569-574
    • McGregor, M.J.1    Muskal, S.M.2
  • 41
    • 0000637270 scopus 로고    scopus 로고
    • Flow cytometry: a versatile tool for all stages of drug discovery
    • J. Nolan, S. Laver, E. R. Prossnitz, L. A. Sklar. Flow cytometry: a versatile tool for all stages of drug discovery. Drug Discovery Today 4, 173–180 (1999).
    • (1999) Drug Discovery Today , vol.4 , pp. 173-180
    • Nolan, J.1    Laver, S.2    Prossnitz, E.R.3    Sklar, L.A.4
  • 42
    • 0032978498 scopus 로고    scopus 로고
    • Automated synthesis: new tools for the organic chemist
    • N. W. Hird. Automated synthesis: new tools for the organic chemist. Drug Discovery Today 4, 265–274 (1999).
    • (1999) Drug Discovery Today , vol.4 , pp. 265-274
    • Hird, N.W.1
  • 43
    • 0032543080 scopus 로고    scopus 로고
    • Strategy-level separation in organic synthesis: from planning to practice
    • D. P. Curran. Strategy-level separation in organic synthesis: from planning to practice. Angew. Chem. Int. Ed. 37, 1174–1196 (1998).
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1174-1196
    • Curran, D.P.1
  • 44
    • 0033521531 scopus 로고    scopus 로고
    • Micro-scale frontal affinity chromatography with mass spectrometric detection: a new method for the screening of compound libraries
    • D. C. Schriemer, D. R. Bundle, L. Li, O. Hindsgaul. Micro-scale frontal affinity chromatography with mass spectrometric detection: a new method for the screening of compound libraries. Angew. Chem. Int. Ed. 37, 3383–3387 (1998).
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 3383-3387
    • Schriemer, D.C.1    Bundle, D.R.2    Li, L.3    Hindsgaul, O.4
  • 45
    • 0000628992 scopus 로고
    • Methods for combinatorial organic-synthesis—The use of fast C-13 NMR analysis for gel phase reaction monitoring
    • G. C. Look, C. P. Holmes, J. P. Chinn, M. A. Gallop. Methods for combinatorial organic-synthesis—The use of fast C-13 NMR analysis for gel phase reaction monitoring. J. Org. Chem. 59, 7588–7590 (1994).
    • (1994) J. Org. Chem. , vol.59 , pp. 7588-7590
    • Look, G.C.1    Holmes, C.P.2    Chinn, J.P.3    Gallop, M.A.4
  • 46
    • 2842561522 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of small-molecule libraries
    • J. A. Ellman. Design, synthesis, and evaluation of small-molecule libraries. Acc. Chem. Res. 29, 132–143 (1996).
    • (1996) Acc. Chem. Res. , vol.29 , pp. 132-143
    • Ellman, J.A.1
  • 47
    • 0032087817 scopus 로고    scopus 로고
    • Applications of genetic algorithms in molecular diversity
    • L. Weber. Applications of genetic algorithms in molecular diversity. Curr. Opin. Chem. Biol. 2, 381–385 (1998).
    • (1998) Curr. Opin. Chem. Biol. , vol.2 , pp. 381-385
    • Weber, L.1
  • 48
    • 0029271228 scopus 로고
    • Using a genetic algorithm to suggest combinatorial libraries
    • R. P. Sheridan, S. K. Kearsley. Using a genetic algorithm to suggest combinatorial libraries. J. Chem. Inf. Comput. Sci. 35, 310–320 (1995).
    • (1995) J. Chem. Inf. Comput. Sci. , vol.35 , pp. 310-320
    • Sheridan, R.P.1    Kearsley, S.K.2
  • 49
    • 0028863971 scopus 로고
    • Genetic algorithms in molecular recognition and design
    • P. Willett. Genetic algorithms in molecular recognition and design. Trends Biotech. 13, 516–521 (1995).
    • (1995) Trends Biotech. , vol.13 , pp. 516-521
    • Willett, P.1
  • 50
    • 0032832775 scopus 로고    scopus 로고
    • Drug screening—Beyond the bottleneck
    • A. Dove. Drug screening—Beyond the bottleneck. Nature Biotech. 17, 859–863 (1999).
    • (1999) Nature Biotech. , vol.17 , pp. 859-863
    • Dove, A.1
  • 51
    • 0032502884 scopus 로고    scopus 로고
    • Thermographic selection of effective catalysts from an encoded polymer-bound library
    • S. J. Taylor, J. P. Morken. Thermographic selection of effective catalysts from an encoded polymer-bound library. Science 280, 267–270 (1998).
    • (1998) Science , vol.280 , pp. 267-270
    • Taylor, S.J.1    Morken, J.P.2
  • 52
    • 0014772602 scopus 로고
    • Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides
    • E. Kaiser, R. L. Colescott, C. D. Bossing, P. I. Cook. Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides. Anal. Biochem. 34, 595–598 (1970).
    • (1970) Anal. Biochem. , vol.34 , pp. 595-598
    • Kaiser, E.1    Colescott, R.L.2    Bossing, C.D.3    Cook, P.I.4
  • 53
    • 0019627519 scopus 로고
    • Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction
    • V. K. Sarin, S. B. H. Kent, J. P. Tam, R. B. Merrifield. Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction. Anal. Biochem. 117, 147–157 (1981).
    • (1981) Anal. Biochem. , vol.117 , pp. 147-157
    • Sarin, V.K.1    Kent, S.B.H.2    Tam, J.P.3    Merrifield, R.B.4
  • 54
    • 0001275595 scopus 로고
    • A comparison of acid labile linkage agents for the synthesis of peptide C-terminal amides
    • M. S. Bernatowicz, S. B. Daniels, H. Koster. A comparison of acid labile linkage agents for the synthesis of peptide C-terminal amides. Tetrahedron Lett. 30, 4645–4648 (1989).
    • (1989) Tetrahedron Lett. , vol.30 , pp. 4645-4648
    • Bernatowicz, M.S.1    Daniels, S.B.2    Koster, H.3
  • 55
    • 0011217950 scopus 로고    scopus 로고
    • Oligosaccharide mimetics obtained by novel, rapid screening of carboxylic acid encoded glycopeptide libraries
    • P. M. St. Hilaire, T. L. Lowary, M. Meldal, K. Bock. Oligosaccharide mimetics obtained by novel, rapid screening of carboxylic acid encoded glycopeptide libraries. J. Am. Chem. Soc. 120, 13 312–13320 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , Issue.13 , pp. 312-13320
    • Hilaire, P.M.S.T.1    Lowary, T.L.2    Meldal, M.3    Bock, K.4
  • 56
    • 0028173391 scopus 로고
    • ‘Libraries from libraries’: Chemical transformation of combinatorial libraries to extend the range and repertoire of chemical diversity
    • J. M. Ostresh, G. M. Husar, S. E. Blondelle, B. Dorner, P. A. Weber, R. A. Houghten. ‘Libraries from libraries’: Chemical transformation of combinatorial libraries to extend the range and repertoire of chemical diversity. Proc. Natl. Acad. Sci. USA 91, 11 138–11 142 (1994).
    • (1994) Proc. Natl. Acad. Sci. USA , vol.11 , pp. 142
    • Ostresh, J.M.1    Husar, G.M.2    Blondelle, S.E.3    Dorner, B.4    Weber, P.A.5    Houghten, R.A.6
  • 58
    • 0015529625 scopus 로고
    • Liquid phase synthesis of peptides
    • E. Bayer, M. Mutter. Liquid phase synthesis of peptides. Nature (London) 237, 512–513 (1972).
    • (1972) Nature (London) , vol.237 , pp. 512-513
    • Bayer, E.1    Mutter, M.2
  • 59
    • 0031098534 scopus 로고    scopus 로고
    • Organic synthesis on soluble polymer supports: liquid phase methodologies
    • D. J. Gravert, K. D. Janda. Organic synthesis on soluble polymer supports: liquid phase methodologies. Chem. Rev. 97, 489–510 (1997).
    • (1997) Chem. Rev. , vol.97 , pp. 489-510
    • Gravert, D.J.1    Janda, K.D.2
  • 60
    • 0000012760 scopus 로고    scopus 로고
    • Influence of resin structure, tether length, and solvent upon the high-resolution 1H NMR spectra of solid-phase-synthesis resins
    • P. A. Keifer. Influence of resin structure, tether length, and solvent upon the high-resolution 1H NMR spectra of solid-phase-synthesis resins. J. Org. Chem. 61, 1558–1559 (1996).
    • (1996) J. Org. Chem. , vol.61 , pp. 1558-1559
    • Keifer, P.A.1
  • 62
    • 0029388980 scopus 로고
    • A class of cobalt oxide magnetoresistance materials discovered with combinatorial synthesis
    • G. Briceno, H. Chang, X. Sun, P. G. Schultz, X. D. Xiang. A class of cobalt oxide magnetoresistance materials discovered with combinatorial synthesis. Science 270, 273–275 (1995).
    • (1995) Science , vol.270 , pp. 273-275
    • Briceno, G.1    Chang, H.2    Sun, X.3    Schultz, P.G.4    Xiang, X.D.5
  • 63
    • 20744456789 scopus 로고
    • Solid-Phase Peptide Synthesis. 1. The synthesis of a tetrapeptide
    • R. B. Merrifield. Solid-Phase Peptide Synthesis. 1. The synthesis of a tetrapeptide. J. Am. Chem. Soc. 85, 2149–2154 (1963).
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 2149-2154
    • Merrifield, R.B.1
  • 66
    • 0028037524 scopus 로고
    • Sub-library composition of peptide libraries: potential application in screening
    • A. Furka. Sub-library composition of peptide libraries: potential application in screening. Drug Dev. Res. 33, 90–97 (1994).
    • (1994) Drug Dev. Res. , vol.33 , pp. 90-97
    • Furka, A.1
  • 67
    • 0028794072 scopus 로고
    • Preparation and screening against acetylcholinesterase of a non-peptide ‘indexed’ combinatorial library
    • M. C. Pirrung, J. Chen. Preparation and screening against acetylcholinesterase of a non-peptide ‘indexed’ combinatorial library. J. Am. Chem. Soc. 117, 1240–1245 (1995).
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 1240-1245
    • Pirrung, M.C.1    Chen, J.2
  • 69
    • 0028149989 scopus 로고
    • Recursive deconvolution of combinatorial chemical libraries
    • E. Erb, K. D. Janda, S. Brenner. Recursive deconvolution of combinatorial chemical libraries. Proc. Natl. Acad. Sci. U.S.A. 91, 11 422–11 426 (1994).
    • (1994) Proc. Natl. Acad. Sci. U.S.A. , vol.91 , pp. 11 422-11 426
    • Erb, E.1    Janda, K.D.2    Brenner, S.3
  • 70
    • 0027500111 scopus 로고
    • Multiple release of equimolar amounts of peptides from a polymeric carrier using orthogonal linkage-cleavage chemistry
    • M. Lebl, M. Pátek, P. Kočiš, V. Krchňák, V. J. Hruby, S. E. Salmon, K. S. Lam. Multiple release of equimolar amounts of peptides from a polymeric carrier using orthogonal linkage-cleavage chemistry. Int. J. Peptide Prot. Res. 41, 201–203 (1993).
    • (1993) Int. J. Peptide Prot. Res. , vol.41 , pp. 201-203
    • Lebl, M.1    Pátek, M.2    Kočiš, P.3    Krchňák, V.4    Hruby, V.J.5    Salmon, S.E.6    Lam, K.S.7
  • 71
    • 0029013332 scopus 로고
    • Synthesis of a small molecule combinatorial library encoded with molecular tags
    • J. J. Baldwin, J. J. Burbaum, I. Henderson, M. H. J. Ohlmeyer. Synthesis of a small molecule combinatorial library encoded with molecular tags. J. Am. Chem. Soc. 117, 5588–5589 (1995).
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5588-5589
    • Baldwin, J.J.1    Burbaum, J.J.2    Henderson, I.3    Ohlmeyer, M.H.J.4
  • 72
    • 0000908874 scopus 로고
    • Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by sub-monomer solid-phase synthesis
    • R. N. Zuckerman, J. M. Kerr, S. B. H. Kent, W. H. Moos. Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by sub-monomer solid-phase synthesis. J. Am. Chem. Soc. 114, 10 646–10 647 (1992).
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10 646-10 647
    • Zuckerman, R.N.1    Kerr, J.M.2    Kent, S.B.H.3    Moos, W.H.4
  • 74
    • 0024991625 scopus 로고
    • Peptides on phage: a vast library of peptides for identifying ligands
    • S. Cwirla, E. A. Peters, R. W. Barrett, W. J. Dower. Peptides on phage: a vast library of peptides for identifying ligands. Proc. Natl. Acad. Sci. USA 87, 6378–6382 (1990).
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 6378-6382
    • Cwirla, S.1    Peters, E.A.2    Barrett, R.W.3    Dower, W.J.4
  • 75
    • 0025112794 scopus 로고
    • Searching for peptide ligands with an epitope library
    • J. K. Scott, G. P. Smith. Searching for peptide ligands with an epitope library. Science 249, 386–390 (1990).
    • (1990) Science , vol.249 , pp. 386-390
    • Scott, J.K.1    Smith, G.P.2
  • 77
    • 85026053788 scopus 로고    scopus 로고
    • Glossary of terms used in medicinal chemistry (IUPAC recommendations 1998)
    • C. Wermuth, C. R. Ganellin, P. Lindberg, L. Mitscher. Glossary of terms used in medicinal chemistry (IUPAC recommendations 1998). Pure Appl. Chem. 70, 1129–1143 (1998).
    • (1998) Pure Appl. Chem. , vol.70 , pp. 1129-1143
    • Wermuth, C.1    Ganellin, C.R.2    Lindberg, P.3    Mitscher, L.4
  • 78
    • 0002627226 scopus 로고    scopus 로고
    • Pharmacophore identification
    • (H. Kubinyi, ed.), Escom, Leiden
    • C. Wermuth, T. Langer. Pharmacophore identification. In 3D QSAR in Drug Design (H. Kubinyi, ed.) pp. 117–136. Escom, Leiden (1998).
    • (1998) 3D QSAR in Drug Design , pp. 117-136
    • Wermuth, C.1    Langer, T.2
  • 80
    • 0000577984 scopus 로고    scopus 로고
    • The ‘one-bead-one-compound’ combinatorial library method
    • K. S. Lam, M. Lebl, V. Krchňák. The ‘one-bead-one-compound’ combinatorial library method. Chem. Rev. 97, 411–448 (1997).
    • (1997) Chem. Rev. , vol.97 , pp. 411-448
    • Lam, K.S.1    Lebl, M.2    Krchňák, V.3
  • 86
    • 0000528756 scopus 로고    scopus 로고
    • The effectiveness of reactant pools for generating structurally diverse combinatorial libraries
    • V. J. Gillet, P. Willett, J. Bradshaw. The effectiveness of reactant pools for generating structurally diverse combinatorial libraries. J. Chem. Inf. Comput. Sci. 37, 731–740 (1997).
    • (1997) J. Chem. Inf. Comput. Sci. , vol.37 , pp. 731-740
    • Gillet, V.J.1    Willett, P.2    Bradshaw, J.3
  • 87
    • 0007827457 scopus 로고    scopus 로고
    • Direct infrared spectroscopic analysis of reagent partitioning in polystyrene bead supported solid phase reaction chemistry
    • D. E. Pivonka, D. L. Palmer. Direct infrared spectroscopic analysis of reagent partitioning in polystyrene bead supported solid phase reaction chemistry. J. Comb. Chem. 1, 294–296 (1999).
    • (1999) J. Comb. Chem. , vol.1 , pp. 294-296
    • Pivonka, D.E.1    Palmer, D.L.2
  • 88
    • 0000128084 scopus 로고    scopus 로고
    • Recursive partitioning analysis of a large structure-activity data set using three-dimensional descriptors
    • X. Chen, A. Rusinko III, S.S. Young. Recursive partitioning analysis of a large structure-activity data set using three-dimensional descriptors. J. Chem. Inf. Comput. Sci. 38, 1054–1062 (1998).
    • (1998) J. Chem. Inf. Comput. Sci. , vol.38 , pp. 1054-1062
    • Chen, X.1    Rusinko, A.2    Young, S.S.3
  • 89
  • 90
    • 45949123116 scopus 로고
    • Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin
    • H. Rink. Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin. Tetrahedron Lett. 28, 3787–3790 (1987).
    • (1987) Tetrahedron Lett. , vol.28 , pp. 3787-3790
    • Rink, H.1
  • 91
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • C. Lipinski, F. Lombardo, B. W. Dominy, P. J. Feeney. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug. Deliv. Res. 23, 3–25 (1997).
    • (1997) Adv. Drug. Deliv. Res. , vol.23 , pp. 3-25
    • Lipinski, C.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 92
    • 37049133408 scopus 로고
    • Safety catch principle in solid phase peptide synthesis
    • G. W. Kenner. Safety catch principle in solid phase peptide synthesis. J. Chem. Soc. D. 636–637 (1971).
    • (1971) J. Chem. Soc. D. , pp. 636-637
    • Kenner, G.W.1
  • 93
    • 0001434775 scopus 로고    scopus 로고
    • Safety-catch and multiply cleavable linkers in solid-phase synthesis
    • M. Pátek, M. Lebl. Safety-catch and multiply cleavable linkers in solid-phase synthesis. Biopolymers 47, 353–363 (1998).
    • (1998) Biopolymers , vol.47 , pp. 353-363
    • Pátek, M.1    Lebl, M.2
  • 94
    • 0001176887 scopus 로고    scopus 로고
    • Activation method to prepare a highly reactive acylsulfonamide ‘safety-catch’ linker for solid-phase synthesis
    • B. J. Backes, A. A. Virgilio, J. A. Ellman. Activation method to prepare a highly reactive acylsulfonamide ‘safety-catch’ linker for solid-phase synthesis. J. Am. Chem. Soc. 118, 3055–3056 (1996).
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3055-3056
    • Backes, B.J.1    Virgilio, A.A.2    Ellman, J.A.3
  • 95
    • 0030607141 scopus 로고    scopus 로고
    • Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries
    • S. W. Kaldor, M. G. Siegel, J. E. Fritz, B. A. Deressman, P. J. Hahn. Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries. Tetrahedron Lett. 37, 7193–7196 (1996).
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7193-7196
    • Kaldor, S.W.1    Siegel, M.G.2    Fritz, J.E.3    Deressman, B.A.4    Hahn, P.J.5
  • 96
    • 0030987922 scopus 로고    scopus 로고
    • Polymer-supported quenching reagents for parallel purification
    • R. J. Booth, J. C. Hodges. Polymer-supported quenching reagents for parallel purification. J. Am. Chem. Soc. 119, 4882–4886 (1997).
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4882-4886
    • Booth, R.J.1    Hodges, J.C.2
  • 97
    • 0030952762 scopus 로고    scopus 로고
    • Chemical library purification strategies based on principles of complementary molecular reactivity and molecular recognition
    • D. L. Flynn, J. Z. Crich, R. V. Devraj, S. L. Hockerman, J. J. Parlow, M. S. South, M. S. Woodard. Chemical library purification strategies based on principles of complementary molecular reactivity and molecular recognition. J. Am. Chem. Soc. 119, 4874–4881 (1997).
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4874-4881
    • Flynn, D.L.1    Crich, J.Z.2    Devraj, R.V.3    Hockerman, S.L.4    Parlow, J.J.5    South, M.S.6    Woodard, M.S.7
  • 98
    • 0032948663 scopus 로고    scopus 로고
    • Solid-supported reagent strategies for rapid purification of combinatorial synthesis products
    • R. J. Booth, J. C. Hodges. Solid-supported reagent strategies for rapid purification of combinatorial synthesis products. Acc. Chem. Res. 32, 18–26 (1999).
    • (1999) Acc. Chem. Res. , vol.32 , pp. 18-26
    • Booth, R.J.1    Hodges, J.C.2
  • 99
    • 0030813190 scopus 로고    scopus 로고
    • In situ chemical tagging: tetrafluorophthalic anhydride as a ‘sequestration enabling reagent’ in the purification of solution-phase combinatorial libraries
    • J. J. Parlow, W. Naing, M. S. South, D. L. Flynn. In situ chemical tagging: tetrafluorophthalic anhydride as a ‘sequestration enabling reagent’ in the purification of solution-phase combinatorial libraries. Tetrahedron Lett. 38, 7959–7962 (1997).
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7959-7962
    • Parlow, J.J.1    Naing, W.2    South, M.S.3    Flynn, D.L.4
  • 100
    • 84958233921 scopus 로고    scopus 로고
    • Supports for solid-phase organic synthesis
    • (G. Jung, ed.), VCH, Weinheim
    • M. Winter. Supports for solid-phase organic synthesis. In Combinatorial Peptide and Non-Peptide Libraries (G. Jung, ed.), pp. 465–509. VCH, Weinheim (1996).
    • (1996) Combinatorial Peptide and Non-Peptide Libraries , pp. 465-509
    • Winter, M.1
  • 101
    • 85026064638 scopus 로고    scopus 로고
    • Matrix-assisted synthetic transformations: a mosaic of different contributions. 1. The pattern emerges
    • D. Hudson. Matrix-assisted synthetic transformations: a mosaic of different contributions. 1. The pattern emerges. J. Comb. Chem. 1, 330–360 (1999).
    • (1999) J. Comb. Chem. , vol.1 , pp. 330-360
    • Hudson, D.1
  • 103
    • 0000191614 scopus 로고    scopus 로고
    • Stochastic algorithms for maximizing molecular diversity
    • D. K. Agrafiotis. Stochastic algorithms for maximizing molecular diversity. J. Chem. Inf. Comput. Sci. 37, 841–851 (1997).
    • (1997) J. Chem. Inf. Comput. Sci. , vol.37 , pp. 841-851
    • Agrafiotis, D.K.1
  • 104
    • 0029040208 scopus 로고
    • Deconvolution of combinatorial libraries for drug discovery: a model system
    • S. M. Freier, D. A. M. Konings, J. R. Wyatt, D. J. Ecker. Deconvolution of combinatorial libraries for drug discovery: a model system. J. Med. Chem. 38, 344–352 (1995).
    • (1995) J. Med. Chem. , vol.38 , pp. 344-352
    • Freier, S.M.1    Konings, D.A.M.2    Wyatt, J.R.3    Ecker, D.J.4
  • 105
    • 0000478940 scopus 로고
    • General method for the rapid solid-phase synthesis of large numbers of peptides
    • R. A. Houghten. General method for the rapid solid-phase synthesis of large numbers of peptides. Proc. Natl. Acad. Sci. USA 82, 5131–5135 (1985).
    • (1985) Proc. Natl. Acad. Sci. USA , vol.82 , pp. 5131-5135
    • Houghten, R.A.1
  • 106
    • 84958232329 scopus 로고    scopus 로고
    • PEG grafted polystyrene tentacle polymers: physico-chemical properties and application in chemical synthesis
    • (G. Jung ed.), VCH, Weinheim
    • W. Rapp. PEG grafted polystyrene tentacle polymers: physico-chemical properties and application in chemical synthesis. In Combinatorial Peptide and Non-Peptide Libraries (G. Jung ed.), pp. 425–464. VCH, Weinheim (1996).
    • (1996) Combinatorial Peptide and Non-Peptide Libraries , pp. 425-464
    • Rapp, W.1
  • 107
    • 0026029284 scopus 로고
    • Towards the chemical synthesis of proteins
    • E. Bayer. Towards the chemical synthesis of proteins. Angew. Chem. Int. Ed. Engl. 30, 113–129 (1991).
    • (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 113-129
    • Bayer, E.1
  • 108
    • 0001339949 scopus 로고    scopus 로고
    • Germanium and silicon linking strategies for traceless solid-phase synthesis
    • M. J. Plunkett, J. A. Ellman. Germanium and silicon linking strategies for traceless solid-phase synthesis. J. Org. Chem. 62, 2885–2893 (1997).
    • (1997) J. Org. Chem. , vol.62 , pp. 2885-2893
    • Plunkett, M.J.1    Ellman, J.A.2
  • 109
    • 0032509385 scopus 로고    scopus 로고
    • Selenium-linking strategy for traceless solid-phase synthesis: direct loading, aliphatic C–H bond formation upon cleavage and reaction monitoring by gradient MAS NMR spectroscopy
    • T. Ruhland, K. Andersen, H. Pedersen. Selenium-linking strategy for traceless solid-phase synthesis: direct loading, aliphatic C–H bond formation upon cleavage and reaction monitoring by gradient MAS NMR spectroscopy. J. Org. Chem. 63, 9204–9211 (1998).
    • (1998) J. Org. Chem. , vol.63 , pp. 9204-9211
    • Ruhland, T.1    Andersen, K.2    Pedersen, H.3
  • 110
    • 0001092931 scopus 로고
    • Solid-supported benzotriazoles: synthetic auxiliaries and traceless linkers for the combinatorial synthesis of amine libraries
    • A. Paio, A. Zaramella, R. Ferritto, N. Conti, C. Marchioro, P. Seneci. Solid-supported benzotriazoles: synthetic auxiliaries and traceless linkers for the combinatorial synthesis of amine libraries. J. Comb. Chem. 1, 317–325 (1991).
    • (1991) J. Comb. Chem. , vol.1 , pp. 317-325
    • Paio, A.1    Zaramella, A.2    Ferritto, R.3    Conti, N.4    Marchioro, C.5    Seneci, P.6
  • 112
    • 0015931593 scopus 로고
    • p-Alkoxybenzyl alcohol resin and p-alkoxybenzyloxycarbonylhydrazide resin for solid phase synthesis of protected peptide fragements
    • S. Wang. p-Alkoxybenzyl alcohol resin and p-alkoxybenzyloxycarbonylhydrazide resin for solid phase synthesis of protected peptide fragements. J. Am. Chem. Soc. 95, 1328–1333 (1973).
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 1328-1333
    • Wang, S.1
  • 113
    • 0001057314 scopus 로고    scopus 로고
    • X-ray photoelectron spectroscopy analysis of solid-phase reactions using 3-brominated Wang resin
    • S.-E. Yoo, Y.-D. Gong, J.-S. Seo, M. M. Sung, S. S. Lee, Y. Kim. X-ray photoelectron spectroscopy analysis of solid-phase reactions using 3-brominated Wang resin. J. Comb. Chem. 1, 177–180 (1999).
    • (1999) J. Comb. Chem. , vol.1 , pp. 177-180
    • Yoo, S.-E.1    Gong, Y.-D.2    Seo, J.-S.3    Sung, M.M.4    Lee, S.S.5    Kim, Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.