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Volumn 5, Issue 1, 2000, Pages 25-34

A safety-catch linker for amine release under biologically compatible conditions

Author keywords

Amines; Diketopiperazine; Solid phase organic synthesis (SPOS)

Indexed keywords

AMINE; LINK PROTEIN; PIPERAZINEDIONE; RESIN;

EID: 0034445848     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1011355300910     Document Type: Article
Times cited : (7)

References (22)
  • 1
    • 0029065615 scopus 로고
    • Combinatorial synthesis -The design of compound libraries and their application to drug discovery
    • a. Terret, N.K., Gardner, M., Gordon, D.W., Kobylecki, R.J. and Steele, J., Combinatorial synthesis -The design of compound libraries and their application to drug discovery, Tetrahedron, 51 (1995) 8135-8173.
    • (1995) Tetrahedron , vol.51 , pp. 8135-8173
    • Terret, N.K.1    Gardner, M.2    Gordon, D.W.3    Kobylecki, R.J.4    Steele, J.5
  • 2
    • 0000074870 scopus 로고    scopus 로고
    • Strategy and tactics in combinatorial organic synthesis. Applications to drug discovery
    • b. Gordon, E.M., Gallop, M.A. and Patel, D.V., Strategy and tactics in combinatorial organic synthesis. Applications to drug discovery. Acc. Chem. Res., 29 (1996) 144-154.
    • (1996) Acc. Chem. Res. , vol.29 , pp. 144-154
    • Gordon, E.M.1    Gallop, M.A.2    Patel, D.V.3
  • 3
    • 0000577984 scopus 로고    scopus 로고
    • The 'one-bead-one-compound' combinatorial library method
    • c. Lam, K.S., Lebl, M. and Krchnák, V., The 'one-bead-one-compound' combinatorial library method, Chem. Rev., 97 (1997) 411-448.
    • (1997) Chem. Rev. , vol.97 , pp. 411-448
    • Lam, K.S.1    Lebl, M.2    Krchnák, V.3
  • 4
    • 2842605870 scopus 로고    scopus 로고
    • Discovery of sequence-selective peptide binding by synthetic receptors using encoded combinatorial libraries
    • a. Still, W.C., Discovery of sequence-selective peptide binding by synthetic receptors using encoded combinatorial libraries, Ace. Chem. Res., 29 (1996) 155-170.
    • (1996) Ace. Chem. Res. , vol.29 , pp. 155-170
    • Still, W.C.1
  • 6
    • 0028264809 scopus 로고
    • Portion-mixing peptide libraries of quenched fluorogenic substrates for complete subsite mapping of endoprotease specificity
    • c. Meldal, M., Svendsen, I., Breddam, K. and Auzanneau, F.-I., Portion-mixing peptide libraries of quenched fluorogenic substrates for complete subsite mapping of endoprotease specificity, Proc. Natl. Acad. Sci. USA, 91 (1994) 3314-3318.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 3314-3318
    • Meldal, M.1    Svendsen, I.2    Breddam, K.3    Auzanneau, F.-I.4
  • 7
    • 0029109073 scopus 로고
    • Generation and screening of combinatorial peptide libraries designed for rapid sequencing by mass spectroscopy
    • d. Youngquist, R.S., Fuentes, G.R., Lacey, M.P. and Keough, T., Generation and screening of combinatorial peptide libraries designed for rapid sequencing by mass spectroscopy, J. Am. Chem. Soc., 117 (1995) 3900-3906.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 3900-3906
    • Youngquist, R.S.1    Fuentes, G.R.2    Lacey, M.P.3    Keough, T.4
  • 8
    • 0033574590 scopus 로고    scopus 로고
    • Linkers for solid phase organic synthesis
    • a. James, I.W., Linkers for solid phase organic synthesis, Tetrahedron, 55 (1999) 4855-4946.
    • (1999) Tetrahedron , vol.55 , pp. 4855-4946
    • James, I.W.1
  • 9
    • 0033683359 scopus 로고    scopus 로고
    • Linkers and cleavage strategies in solid-phase organic synthesis and combinatorial chemistry
    • b. Guillier, F., Orain, D. and Bradley, M., Linkers and cleavage strategies in solid-phase organic synthesis and combinatorial chemistry, Chem. Rev., 100 (2000) 2091-2157.
    • (2000) Chem. Rev. , vol.100 , pp. 2091-2157
    • Guillier, F.1    Orain, D.2    Bradley, M.3
  • 11
    • 0027367140 scopus 로고
    • Symmetrical structure allowing the selective multiple release of a defined quantity of peptide from a single bead of polymeric support
    • b. Kočiš, P., Krchňák, V. and Lebl, M., Symmetrical structure allowing the selective multiple release of a defined quantity of peptide from a single bead of polymeric support, Tetrahedron Lett., 34 (1993) 7251-7252.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 7251-7252
    • Kočiš, P.1    Krchňák, V.2    Lebl, M.3
  • 12
    • 0001434775 scopus 로고    scopus 로고
    • Safety-catch and multiply cleavable linkers in solid phase synthesis
    • c. Pátek, M. and Lebl, M., Safety-catch and multiply cleavable linkers in solid phase synthesis, Biopolymers, 47 (1998) 353-363.
    • (1998) Biopolymers , vol.47 , pp. 353-363
    • Pátek, M.1    Lebl, M.2
  • 13
    • 0034696103 scopus 로고    scopus 로고
    • High-loading resin beads for solid-phase synthesis using triple branching symmetrical dendrimers
    • a. Fromont, C. and Bradley, M., High-loading resin beads for solid-phase synthesis using triple branching symmetrical dendrimers, Chem. Commun., (2000) 283-284.
    • (2000) Chem. Commun. , pp. 283-284
    • Fromont, C.1    Bradley, M.2
  • 14
    • 0000314198 scopus 로고    scopus 로고
    • Solid-phase dendrimer synthesis
    • b. Wells, N.J., Basso, A. and Bradley, M., Solid-phase dendrimer synthesis, Biopolymers, 47 (1998) 231-396.
    • (1998) Biopolymers , vol.47 , pp. 231-396
    • Wells, N.J.1    Basso, A.2    Bradley, M.3
  • 15
    • 0030855324 scopus 로고    scopus 로고
    • Solid-phase dendrimer synthesis and generation of super-high-loading resin beads for combinatorial chemistry
    • c. Swali, V., Wells, N.J., Langley, G.J. and Bradley, M., Solid-phase dendrimer synthesis and generation of super-high-loading resin beads for combinatorial chemistry, J. Org. Chem., 62 (1997) 4902-4903.
    • (1997) J. Org. Chem. , vol.62 , pp. 4902-4903
    • Swali, V.1    Wells, N.J.2    Langley, G.J.3    Bradley, M.4
  • 16
    • 0001689141 scopus 로고
    • Direct cleavage of peptides from solid support into aqueous buffer. Application in simultaneous multiple peptide synthesis
    • Bray, A.M., Maeji, N.J., Valerio, R.M, Campbell, R.A. and Geysen, H.M., Direct cleavage of peptides from solid support into aqueous buffer. Application in simultaneous multiple peptide synthesis, J. Org. Chem., 56 (1991) 6659-6666.
    • (1991) J. Org. Chem. , vol.56 , pp. 6659-6666
    • Bray, A.M.1    Maeji, N.J.2    Valerio, R.M.3    Campbell, R.A.4    Geysen, H.M.5
  • 17
    • 1542677609 scopus 로고    scopus 로고
    • A pH cleavable linker for zone diffusion assays and single bead solution screens in combinatorial chemistry
    • Atrash, B. and Bradley, M., A pH cleavable linker for zone diffusion assays and single bead solution screens in combinatorial chemistry, Chem. Commun., (1997) 1397-1398.
    • (1997) Chem. Commun. , pp. 1397-1398
    • Atrash, B.1    Bradley, M.2
  • 18
    • 0000786829 scopus 로고
    • Chlorotrimethylsilane mediated formation of ω-allylesters of aspartic and glutamic acids
    • Beishaw, P.J., Mzengeza, S. and Lajoie, G.A., Chlorotrimethylsilane mediated formation of ω-allylesters of aspartic and glutamic acids, Synth. Commun., 20 (1990) 3157-3160.
    • (1990) Synth. Commun. , vol.20 , pp. 3157-3160
    • Beishaw, P.J.1    Mzengeza, S.2    Lajoie, G.A.3
  • 19
    • 0003162777 scopus 로고
    • Studies on bitter peptides from casein hydrolyzate XIV Bitter taste of synthetic analogs of octapeptides, Arg-Gly-Pro-Phe-Pro-Ile-Ile-Val, corresponding to the C-terminal portion of β-casein
    • Nakatami, M., Nakata, T., Kouge, K. and Okei, H., Studies on bitter peptides from casein hydrolyzate XIV Bitter taste of synthetic analogs of octapeptides, Arg-Gly-Pro-Phe-Pro-Ile-Ile-Val, corresponding to the C-terminal portion of β-casein, Bull. Soc. Chim. Jap., 67 (1994) 438-444.
    • (1994) Bull. Soc. Chim. Jap. , vol.67 , pp. 438-444
    • Nakatami, M.1    Nakata, T.2    Kouge, K.3    Okei, H.4
  • 20
    • 0030959257 scopus 로고    scopus 로고
    • Solution phase combinatorial synthesis. Discovery of novel polyazapyridinophanes with potent antibacterial activity by a solution phase simultaneous addition of functionalities approach
    • An, H., Cummins, L.L., Griffey, R.H., Bharadwaj, R., Haly, B.D., Fraser, A.S., Wilson-Lingardo, L., Risen, L.M., Wyatt, J.R. and Cook, P.D., Solution phase combinatorial synthesis. Discovery of novel polyazapyridinophanes with potent antibacterial activity by a solution phase simultaneous addition of functionalities approach, J. Am. Chem. Soc., 119 (1997) 3696-3708.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 3696-3708
    • An, H.1    Cummins, L.L.2    Griffey, R.H.3    Bharadwaj, R.4    Haly, B.D.5    Fraser, A.S.6    Wilson-Lingardo, L.7    Risen, L.M.8    Wyatt, J.R.9    Cook, P.D.10
  • 21
    • 0033155999 scopus 로고    scopus 로고
    • Comparison of resin and solution screening methodologies in combinatorial chemistry and the identification of a 100 nM inhibitor of trypanothione reductase
    • a. Smith, H.K. and Bradley, M., Comparison of resin and solution screening methodologies in combinatorial chemistry and the identification of a 100 nM inhibitor of trypanothione reductase, J. Comb. Chem., 1 (1999) 326-332.
    • (1999) J. Comb. Chem. , vol.1 , pp. 326-332
    • Smith, H.K.1    Bradley, M.2
  • 22
    • 0030781746 scopus 로고    scopus 로고
    • Solid phase synthesis of polyamine conjugates for the study of trypanothione reductase
    • b. Marsh, I.R. and Bradley, M., Solid phase synthesis of polyamine conjugates for the study of trypanothione reductase, Tetrahedron, 53 (1997) 17317-17334.
    • (1997) Tetrahedron , vol.53 , pp. 17317-17334
    • Marsh, I.R.1    Bradley, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.