-
1
-
-
0034528370
-
Functionalization of peptides and proteins by aldehyde or keto groups
-
Melnyk O, Fehrentz J A, Martinez J, Gras-Masse H Functionalization of peptides and proteins by aldehyde or keto groups. Biopolymers 2000; 55: 165-186.
-
(2000)
Biopolymers
, vol.55
, pp. 165-186
-
-
Melnyk, O.1
Fehrentz, J.A.2
Martinez, J.3
Gras-Masse, H.4
-
2
-
-
0028960723
-
Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone, and thiazolidine linkages
-
Shao J, Tam JP. Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone, and thiazolidine linkages. J. Am. Chem. Soc. 1995; 117: 3893-3899.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 3893-3899
-
-
Shao, J.1
Tam, J.P.2
-
3
-
-
0028231302
-
Facile synthesis of homogeneous artificial proteins
-
Rose K Facile synthesis of homogeneous artificial proteins. J. Am. Chem. Soc. 1994; 116: 30-33.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 30-33
-
-
Rose, K.1
-
4
-
-
77949459317
-
Hydrazone ligation strategy to assemble multifunctional viral nanoparticles for cell imaging and tumor targeting
-
Brunel FM, Lewis JD, Destito G, Steinmetz NF., Manchester M, Stuhlmann H, Dawson PE. Hydrazone ligation strategy to assemble multifunctional viral nanoparticles for cell imaging and tumor targeting. Nano Lett. 2010; 10: 1093-1097.
-
(2010)
Nano Lett.
, vol.10
, pp. 1093-1097
-
-
Brunel, F.M.1
Lewis, J.D.2
Destito, G.3
Steinmetz, N.F.4
Manchester, M.5
Stuhlmann, H.6
Dawson, P.E.7
-
5
-
-
58149099860
-
Rapid oxime and hydrazone ligations with aromatic aldehydes for biomolecular labeling
-
Dirksen A, Dawson PE. Rapid oxime and hydrazone ligations with aromatic aldehydes for biomolecular labeling. Bioconjug. Chem. 2008; 19: 2543-2548.
-
(2008)
Bioconjug. Chem.
, vol.19
, pp. 2543-2548
-
-
Dirksen, A.1
Dawson, P.E.2
-
6
-
-
15244344262
-
Anchorage of synthetic peptides onto liposomes via hydrazone and alpha-oxo hydrazone bonds. Preliminary functional investigations
-
Bourel-Bonnet L, Pécheur EI, Grandjean C, Blanpain A, Baust T, Melnyk O, Hoflack Y, Gras-Masse H. Anchorage of synthetic peptides onto liposomes via hydrazone and alpha-oxo hydrazone bonds. Preliminary functional investigations. Bioconjug. Chem. 2005; 16: 450-457.
-
(2005)
Bioconjug. Chem.
, vol.16
, pp. 450-457
-
-
Bourel-Bonnet, L.1
Pécheur, E.I.2
Grandjean, C.3
Blanpain, A.4
Baust, T.5
Melnyk, O.6
Hoflack, Y.7
Gras-Masse, H.8
-
7
-
-
79952609920
-
Synthesis of thiazolidine thioester peptides and acceleration of native chemical ligation
-
Dheur J, Ollivier N, Melnyk O Synthesis of thiazolidine thioester peptides and acceleration of native chemical ligation. Org. Lett. 2011; 13: 1560-1563.
-
(2011)
Org. Lett.
, vol.13
, pp. 1560-1563
-
-
Dheur, J.1
Ollivier, N.2
Melnyk, O.3
-
8
-
-
0035903508
-
Highly efficient synthesis of peptide-oligonucleotide conjugates: chemoselective oxime and thiazolidine formation
-
Forget D, Boturyn D, Defrancq E, Lhomme J, Dumy P. Highly efficient synthesis of peptide-oligonucleotide conjugates: chemoselective oxime and thiazolidine formation. Chemistry 2001; 7: 3976-3984.
-
(2001)
Chemistry
, vol.7
, pp. 3976-3984
-
-
Forget, D.1
Boturyn, D.2
Defrancq, E.3
Lhomme, J.4
Dumy, P.5
-
9
-
-
0028223433
-
Peptide segment ligation strategy without use of protecting groups
-
Liu CF, Tam JP. Peptide segment ligation strategy without use of protecting groups. Proc. Natl. Acad. Sci. U. S. A. 1994; 91: 6584-6588.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 6584-6588
-
-
Liu, C.F.1
Tam, J.P.2
-
10
-
-
0030250872
-
Natural peptides as building blocks for the synthesis of large protein-like molecules with hydrazone and oxime linkages
-
Rose K, Zeng W, Regamey PO, Chernushevich IV, Standing KG, Gaertner HF. Natural peptides as building blocks for the synthesis of large protein-like molecules with hydrazone and oxime linkages. Bioconjugate Chem. 1996; 7: 552-556.
-
(1996)
Bioconjugate Chem.
, vol.7
, pp. 552-556
-
-
Rose, K.1
Zeng, W.2
Regamey, P.O.3
Chernushevich, I.V.4
Standing, K.G.5
Gaertner, H.F.6
-
11
-
-
54749084565
-
Hydrolytic stability of hydrazones and oximes
-
Kalia J, Raines RT. Hydrolytic stability of hydrazones and oximes. Angew. Chem. Int. Ed. 2008; 47: 7523-7526.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7523-7526
-
-
Kalia, J.1
Raines, R.T.2
-
12
-
-
0029140496
-
Total chemical synthesis of a unique transcription factor-related protein: cMyc. Max
-
Canne LE, Ferré d'Amaré AR, Burley SK, Kent SBH. Total chemical synthesis of a unique transcription factor-related protein: cMyc. Max. J. Am. Chem. Soc. 1995; 117: 2998-3007.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 2998-3007
-
-
Canne, L.E.1
Ferré d'Amaré, A.R.2
Burley, S.K.3
Kent, S.B.H.4
-
13
-
-
0036000120
-
Total chemical synthesis of a 27 kDa TASP protein derived from the MscL ion channel of M.tuberculosis by ketoxime-forming ligation
-
Kochendoerfer GG, Tack JM, Cressman S. Total chemical synthesis of a 27 kDa TASP protein derived from the MscL ion channel of M.tuberculosis by ketoxime-forming ligation. Bioconjugate Chem. 2002; 13: 474-480.
-
(2002)
Bioconjugate Chem.
, vol.13
, pp. 474-480
-
-
Kochendoerfer, G.G.1
Tack, J.M.2
Cressman, S.3
-
14
-
-
2442620150
-
Template assembled cyclopeptides as multimeric system for integrin targeting and endocytosis
-
Boturyn D, Coll JL, Garanger E, Favrot MC, Dumy P. Template assembled cyclopeptides as multimeric system for integrin targeting and endocytosis. J. Am. Chem. Soc. 2004; 126: 5730-5739.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 5730-5739
-
-
Boturyn, D.1
Coll, J.L.2
Garanger, E.3
Favrot, M.C.4
Dumy, P.5
-
15
-
-
57749121492
-
Chemoselective ligation and modification strategies for peptides and proteins
-
Hackenberger CP, Schwarzer D. Chemoselective ligation and modification strategies for peptides and proteins. Angew. Chem. Int. Ed Engl. 2008; 47: 10030-10074.
-
(2008)
Angew. Chem. Int. Ed Engl.
, vol.47
, pp. 10030-10074
-
-
Hackenberger, C.P.1
Schwarzer, D.2
-
16
-
-
0034823319
-
Chemoselective approaches to glycoprotein assembly
-
Hang HC, Bertozzi CR. Chemoselective approaches to glycoprotein assembly. Acc. Chem. Res. 2001; 34: 727-736.
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 727-736
-
-
Hang, H.C.1
Bertozzi, C.R.2
-
17
-
-
0037504266
-
Chemoselectively template-assembled glycoconjugates as mimics for multivalent presentation of carbohydrates
-
Renaudet O, Dumy P. Chemoselectively template-assembled glycoconjugates as mimics for multivalent presentation of carbohydrates. Org. Lett. 2003; 5: 243-246.
-
(2003)
Org. Lett.
, vol.5
, pp. 243-246
-
-
Renaudet, O.1
Dumy, P.2
-
18
-
-
77952811232
-
Recent developments in oligonucleotide conjugation
-
For a review see
-
For a review see: Singh Y, Murat P, Defrancq E. Recent developments in oligonucleotide conjugation. Chem. Soc. Rev. 2010; 39: 2054-2070.
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 2054-2070
-
-
Singh, Y.1
Murat, P.2
Defrancq, E.3
-
20
-
-
0035825038
-
Synthesis of peptide di-aldehyde precursor for successive orthogonal chemoselective ligations via oxime bond
-
Lelièvre D, Buré C, Laot F, Delmas A. Synthesis of peptide di-aldehyde precursor for successive orthogonal chemoselective ligations via oxime bond. Tetrahedron Lett. 2001; 42: 235-238.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 235-238
-
-
Lelièvre, D.1
Buré, C.2
Laot, F.3
Delmas, A.4
-
21
-
-
10944228789
-
Synthesis of branched oxime-linked peptide mimetics of the MUC1 containing a universal T-helper epitope
-
Cremer GA, Bureaud N, Lelièvre D, Piller V, Piller F, Delmas A. Synthesis of branched oxime-linked peptide mimetics of the MUC1 containing a universal T-helper epitope. Chem. Eur. J. 2004; 10: 6353-6360.
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 6353-6360
-
-
Cremer, G.A.1
Bureaud, N.2
Lelièvre, D.3
Piller, V.4
Piller, F.5
Delmas, A.6
-
22
-
-
33749028981
-
Synthesis and biological evaluation of a multiantigenic Tn/TF-containing glycopeptide mimic of the tumor-related MUC1 glycoprotein
-
Cremer GA, Bureaud N, Piller V, Kunz H, Piller F, Delmas AF. Synthesis and biological evaluation of a multiantigenic Tn/TF-containing glycopeptide mimic of the tumor-related MUC1 glycoprotein. Chem. Med. Chem. 2006; 9: 965-968.
-
(2006)
Chem. Med. Chem.
, vol.9
, pp. 965-968
-
-
Cremer, G.A.1
Bureaud, N.2
Piller, V.3
Kunz, H.4
Piller, F.5
Delmas, A.F.6
-
23
-
-
0001239876
-
Equilibria for additions to the carbonyl group
-
Sander EG, Jencks WP. Equilibria for additions to the carbonyl group. J. Am. Chem. Soc. 1968; 90: 6154-6162.
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 6154-6162
-
-
Sander, E.G.1
Jencks, W.P.2
-
24
-
-
77249089970
-
Bioorthogonal chemistry: recent progress and future directions
-
Lim RK, Lin Q. Bioorthogonal chemistry: recent progress and future directions. Chem. Commun. 2010; 46: 1589-1600.
-
(2010)
Chem. Commun.
, vol.46
, pp. 1589-1600
-
-
Lim, R.K.1
Lin, Q.2
-
25
-
-
0032564556
-
Simple and efficient solid-phase synthesis of unprotected peptide aldehyde for peptide segment ligation
-
Lelièvre D, Chabane H, Delmas A. Simple and efficient solid-phase synthesis of unprotected peptide aldehyde for peptide segment ligation. Tetrahedron Lett. 1998; 39: 9675-9678.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9675-9678
-
-
Lelièvre, D.1
Chabane, H.2
Delmas, A.3
-
26
-
-
0036642737
-
Influence of polar support for the synthesis of large C-terminal peptide aldehyde: application to chemoselective ligation
-
Lelièvre D, Turpin O, El Kazzouli S, Delmas A. Influence of polar support for the synthesis of large C-terminal peptide aldehyde: application to chemoselective ligation. Tetrahedron 2002; 58: 5525-5533.
-
(2002)
Tetrahedron
, vol.58
, pp. 5525-5533
-
-
Lelièvre, D.1
Turpin, O.2
El Kazzouli, S.3
Delmas, A.4
-
27
-
-
27644527461
-
Efficient synthesis of C-terminal modified peptide ketones for chemical ligations
-
Marceau P, Buré C, Delmas AF. Efficient synthesis of C-terminal modified peptide ketones for chemical ligations. Bioorg. Med. Chem. Lett. 2005; 15: 5442-5445.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 5442-5445
-
-
Marceau, P.1
Buré, C.2
Delmas, A.F.3
-
28
-
-
0025029968
-
Molecular cloning and expression of human tumor-associated polymorphic epithelial mucin
-
Gendler SJ, Lancaster CA, Taylor-Papadimitriou J, Duhig T, Peat N, Burchell J, Pemberton L, Lalani EN, Wilson D. Molecular cloning and expression of human tumor-associated polymorphic epithelial mucin. J. Biol. Chem. 1990; 265: 15286-15293.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 15286-15293
-
-
Gendler, S.J.1
Lancaster, C.A.2
Taylor-Papadimitriou, J.3
Duhig, T.4
Peat, N.5
Burchell, J.6
Pemberton, L.7
Lalani, E.N.8
Wilson, D.9
-
29
-
-
2942682904
-
MUC1 and the MUCs: a family of human mucins with impact in cancer biology
-
Baldus SE, Engelmann K, Hanisch FG. MUC1 and the MUCs: a family of human mucins with impact in cancer biology. Crit. Rev. Clin. Lab. Sci. 2004; 41: 189-231.
-
(2004)
Crit. Rev. Clin. Lab. Sci.
, vol.41
, pp. 189-231
-
-
Baldus, S.E.1
Engelmann, K.2
Hanisch, F.G.3
-
30
-
-
4043079807
-
Fragmentation study of peptide acetals and aldehydes using in-source collision-induced dissociation
-
Buré C, Le Falher G, Lange C, Delmas A. Fragmentation study of peptide acetals and aldehydes using in-source collision-induced dissociation. J. Mass Spectrom. 2004; 39: 817-823.
-
(2004)
J. Mass Spectrom.
, vol.39
, pp. 817-823
-
-
Buré, C.1
Le Falher, G.2
Lange, C.3
Delmas, A.4
-
31
-
-
9944226776
-
A solid phase linker strategy for the direct synthesis of EDANS-labelled peptide substrates
-
Beythien J, White PD. A solid phase linker strategy for the direct synthesis of EDANS-labelled peptide substrates. Tetrahedron Lett. 2005; 46: 101-104.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 101-104
-
-
Beythien, J.1
White, P.D.2
-
32
-
-
0021159751
-
O-benzotriazolyl-N,N,N',N'-tetramethyluronium hexafluorophosphate as coupling reagent for the synthesis of peptides of biological interest
-
Dourtoglou V, Gross B, Lambropoulou V, Zioudrou C. O-benzotriazolyl-N, N, N', N'-tetramethyluronium hexafluorophosphate as coupling reagent for the synthesis of peptides of biological interest. Synthesis 1984; 7: 572-574.
-
(1984)
Synthesis
, vol.7
, pp. 572-574
-
-
Dourtoglou, V.1
Gross, B.2
Lambropoulou, V.3
Zioudrou, C.4
-
33
-
-
0014772602
-
Color test for detection of free terminal amino groups in solid-phase synthesis of peptides
-
Kaiser E, Colescott RL, Bossinger CD, Cook PI. Color test for detection of free terminal amino groups in solid-phase synthesis of peptides. Anal. Biochem. 1970; 34: 595-598.
-
(1970)
Anal. Biochem.
, vol.34
, pp. 595-598
-
-
Kaiser, E.1
Colescott, R.L.2
Bossinger, C.D.3
Cook, P.I.4
-
34
-
-
12044258245
-
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
-
Carpino LA. 1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive. J. Am. Chem. Soc. 1993; 115: 4397-4398.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 4397-4398
-
-
Carpino, L.A.1
-
35
-
-
0029330768
-
Detection of secondary amines on solid phase
-
Vojkovsky T. Detection of secondary amines on solid phase. Pept. Res. 1995; 8: 236-237.
-
(1995)
Pept. Res.
, vol.8
, pp. 236-237
-
-
Vojkovsky, T.1
-
36
-
-
0035874754
-
Tartric acid-based linker for the solid-phase synthesis of C-terminal peptide alpha-oxo aldehydes
-
Melnyk O, Fruchart JS, Grandjean C, Gras-Masse H. Tartric acid-based linker for the solid-phase synthesis of C-terminal peptide alpha-oxo aldehydes. J. Org. Chem. 2001; 66: 4153-4160.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 4153-4160
-
-
Melnyk, O.1
Fruchart, J.S.2
Grandjean, C.3
Gras-Masse, H.4
-
37
-
-
33747810496
-
Controlling the outcome of overacylation of N-protected aminooxyacetic acid during the synthesis of an aminooxy-peptide for chemical ligation
-
Decostaire IP, Lelièvre D, Zhang HH, Delmas AF. Controlling the outcome of overacylation of N-protected aminooxyacetic acid during the synthesis of an aminooxy-peptide for chemical ligation. Tetrahedron Lett. 2006; 47: 7057-7060.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 7057-7060
-
-
Decostaire, I.P.1
Lelièvre, D.2
Zhang, H.H.3
Delmas, A.F.4
-
38
-
-
34547874240
-
Optimized synthesis of aminooxy-peptides as glycoprobe precursors for surface-based sugar-protein interaction studies
-
Jimenez-Castells C, de la Torre BG, Gallego RG, Andreu D. Optimized synthesis of aminooxy-peptides as glycoprobe precursors for surface-based sugar-protein interaction studies. Bioorg. Med. Chem. Lett. 2007; 17: 5155-5158.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 5155-5158
-
-
Jimenez-Castells, C.1
de la Torre, B.G.2
Gallego, R.G.3
Andreu, D.4
-
39
-
-
78650246909
-
Efficient synthesis of an (aminooxy) acetylated-somatostatin derivative using (aminooxy)acetic acid as a 'carbonyl capture' reagent
-
Mezö G, Szabó I, Kertész I, Hegedüs R, Orbán E, Leurs U, Bösze S, Halmos G, Manea M. Efficient synthesis of an (aminooxy) acetylated-somatostatin derivative using (aminooxy)acetic acid as a 'carbonyl capture' reagent. J. Pept. Sci. 2010; 17: 39-46.
-
(2010)
J. Pept. Sci.
, vol.17
, pp. 39-46
-
-
Mezö, G.1
Szabó, I.2
Kertész, I.3
Hegedüs, R.4
Orbán, E.5
Leurs, U.6
Bösze, S.7
Halmos, G.8
Manea, M.9
-
40
-
-
0033660334
-
Identification by mass spectrometry and tandem mass spectrometry of by-products from an orthogonal peptide ligation by oxime bonds
-
Buré C, Lelièvre D, Delmas A. Identification by mass spectrometry and tandem mass spectrometry of by-products from an orthogonal peptide ligation by oxime bonds. Rapid Commun. Mass Spectrom. 2000; 14: 2158-2164.
-
(2000)
Rapid Commun. Mass Spectrom.
, vol.14
, pp. 2158-2164
-
-
Buré, C.1
Lelièvre, D.2
Delmas, A.3
-
41
-
-
0037369449
-
Correlation analysis between equilibria for addition of semicarbazide and hydroxylamine to several carbonyl compounds and their equilibria for addition of water
-
Malpica A, Calzadilla M. Correlation analysis between equilibria for addition of semicarbazide and hydroxylamine to several carbonyl compounds and their equilibria for addition of water. J. Phys. Org. Chem. 2003; 16: 202-204.
-
(2003)
J. Phys. Org. Chem.
, vol.16
, pp. 202-204
-
-
Malpica, A.1
Calzadilla, M.2
-
42
-
-
0016663345
-
Proton magnetic resonance studies of α-keto acids
-
Cooper AJL, Redfield AG. Proton magnetic resonance studies of α-keto acids. J. Biol. Chem. 1975; 250: 527-532.
-
(1975)
J. Biol. Chem.
, vol.250
, pp. 527-532
-
-
Cooper, A.J.L.1
Redfield, A.G.2
-
43
-
-
0034762195
-
In-source fragmentation of peptide aldehydes and acetals: influence of peptide length and charge state
-
Buré C, Gobert W, Lelièvre D, Delmas A. In-source fragmentation of peptide aldehydes and acetals: influence of peptide length and charge state. J. Mass Spectrom. 2001; 36: 1149-1155.
-
(2001)
J. Mass Spectrom.
, vol.36
, pp. 1149-1155
-
-
Buré, C.1
Gobert, W.2
Lelièvre, D.3
Delmas, A.4
-
44
-
-
18844435152
-
Collision-induced dissociation of peptide thioesters: the influence of peptide length on fragmentation
-
Buré C, Boujard O, Bertrand M, Lange C, Delmas A. Collision-induced dissociation of peptide thioesters: the influence of peptide length on fragmentation. Eur. J. Mass Spectrom. 2005; 11: 31-34.
-
(2005)
Eur. J. Mass Spectrom.
, vol.11
, pp. 31-34
-
-
Buré, C.1
Boujard, O.2
Bertrand, M.3
Lange, C.4
Delmas, A.5
-
45
-
-
0030629686
-
Synthesis and evaluation of fluorescent chemokines labeled at the amino terminal
-
Offord RE, Gaertner HF, Wells TN, Proudfoot AE. Synthesis and evaluation of fluorescent chemokines labeled at the amino terminal. Methods Enzymol. 1997; 287: 348-369.
-
(1997)
Methods Enzymol.
, vol.287
, pp. 348-369
-
-
Offord, R.E.1
Gaertner, H.F.2
Wells, T.N.3
Proudfoot, A.E.4
-
46
-
-
0020399342
-
α-Aminoaldehydes: transition state analogue inhibitors of leucine aminopeptidase
-
Andersson L, Isley TC, Wolfenden R α-Aminoaldehydes: transition state analogue inhibitors of leucine aminopeptidase. Biochemistry 1982; 21: 4177-4180.
-
(1982)
Biochemistry
, vol.21
, pp. 4177-4180
-
-
Andersson, L.1
Isley, T.C.2
Wolfenden, R.3
|