-
1
-
-
0029065615
-
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
-
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
-
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
-
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
-
5
-
-
0026419328
-
A new type of synthetic peptide library for identifying ligand-binding activity
-
b. Lam, K.S., Salmon, S.E., Hersh, E.M., Hruby, V.J., Kazmierski, W.M. and Knapp, R.J., A new type of synthetic peptide library for identifying ligand-binding activity, Nature (London), 354 (1991) 82-84.
-
(1991)
Nature (London)
, vol.354
, pp. 82-84
-
-
Lam, K.S.1
Salmon, S.E.2
Hersh, E.M.3
Hruby, V.J.4
Kazmierski, W.M.5
Knapp, R.J.6
-
6
-
-
0028264809
-
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
-
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
-
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
-
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
-
10
-
-
0027142990
-
Discovery of biologically active peptides in random libraries: Solution-phase testing after staged orthogonal release from resin beads
-
a. Salmon, S.E., Lam, K.S., Lebl, M., Kandola, A., Khattri, P.S., Wade, S., Pátek, M., Kocis, P., Krchnák, V., Thorpe, D. and Felder, S., Discovery of biologically active peptides in random libraries: solution-phase testing after staged orthogonal release from resin beads, Proc. Natl. Acad. Sci. USA, 90 (1993) 11708-11712.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 11708-11712
-
-
Salmon, S.E.1
Lam, K.S.2
Lebl, M.3
Kandola, A.4
Khattri, P.S.5
Wade, S.6
Pátek, M.7
Kocis, P.8
Krchnák, V.9
Thorpe, D.10
Felder, S.11
-
11
-
-
0027367140
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
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