-
1
-
-
0026155124
-
Backbone cyclization: A new method for confering conformational constraint on peptides
-
1. Gilon, C., Halle, D., Chorev, M., Selinger, Z. & Byk, G. (1991) Backbone cyclization: a new method for confering conformational constraint on peptides. Biopolymers 31, 747-750.
-
(1991)
Biopolymers
, vol.31
, pp. 747-750
-
-
Gilon, C.1
Halle, D.2
Chorev, M.3
Selinger, Z.4
Byk, G.5
-
2
-
-
0031259776
-
A comparative molecular dynamics study of the conformations of bradykinin B1 and B2-specific receptor antagonists 6-9430, B-9436, and B-9858
-
2. Sejbal, J., Wang, Y., Cann, J.R., Stewart, J.M., Gera, L. & Kotovych, G. (1997) A comparative molecular dynamics study of the conformations of bradykinin B1 and B2-specific receptor antagonists 6-9430, B-9436, and B-9858. Biopolymers 42, 521-535.
-
(1997)
Biopolymers
, vol.42
, pp. 521-535
-
-
Sejbal, J.1
Wang, Y.2
Cann, J.R.3
Stewart, J.M.4
Gera, L.5
Kotovych, G.6
-
3
-
-
0029924435
-
An NMR, CD, molecular dynamics, and fluorometric study of the conformation of the bradykinin antagonist B-9340 in water and in aqueous micellar solutions
-
3. Sejbal, J., Cann, J.R., Stewart, J.M., Gera, L. & Kotovych, G. (1996) An NMR, CD, molecular dynamics, and fluorometric study of the conformation of the bradykinin antagonist B-9340 in water and in aqueous micellar solutions. J. Med. Chem. 39, 1281-1292.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1281-1292
-
-
Sejbal, J.1
Cann, J.R.2
Stewart, J.M.3
Gera, L.4
Kotovych, G.5
-
4
-
-
0027592967
-
A proton magnetic resonance study of two synthetic agonist-antagonist pairs of bradykinin analogues
-
4. Otter, A., Bigler, P., Stewart, J.M. & Kotovych, G. (1993) A proton magnetic resonance study of two synthetic agonist-antagonist pairs of bradykinin analogues. Biopolymers 33, 769-780.
-
(1993)
Biopolymers
, vol.33
, pp. 769-780
-
-
Otter, A.1
Bigler, P.2
Stewart, J.M.3
Kotovych, G.4
-
5
-
-
0028103947
-
Combined approach of NMR and molecular dynamics within a biphasic membran mimetics: Conformation and orientation of the antagonist HOE 140
-
5. Cuba, W., Haessner, R., Breipohl, G. et al. (1994) Combined approach of NMR and molecular dynamics within a biphasic membran mimetics: conformation and orientation of the antagonist HOE 140. J. Am. Chem. Soc. 116, 7532-7540.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 7532-7540
-
-
Cuba, W.1
Haessner, R.2
Breipohl, G.3
-
6
-
-
0031918953
-
Conformational analysis of the highly potent bradykinin antagonist Hoe-140 by means of two different computational methods
-
6. Filizola, M., Centeno, N.B., Carteni-Farina, M. & Ferez, J.J. (1998) Conformational analysis of the highly potent bradykinin antagonist Hoe-140 by means of two different computational methods. J. Biomol. Struc. Dynamics 15, 639-652.
-
(1998)
J. Biomol. Struc. Dynamics
, vol.15
, pp. 639-652
-
-
Filizola, M.1
Centeno, N.B.2
Carteni-Farina, M.3
Ferez, J.J.4
-
7
-
-
0030175350
-
2 receptor antagonists: Bradykinin analogs with N-alkyl amino acids at position 2
-
2 receptor antagonists: bradykinin analogs with N-alkyl amino acids at position 2. Immunopharmacology 33, 73-80.
-
(1996)
Immunopharmacology
, vol.33
, pp. 73-80
-
-
Reissmann, S.1
Greiner, G.2
Seyfarth, L.3
-
8
-
-
33751391520
-
Building units for N-backbone cyclic peptides. I. Synthesis of protected N-(ω-aminoalkylene) amino acids and their incorpoation into dipeptide units
-
8. Byk, G. & Gilon, C. (1992) Building units for N-backbone cyclic peptides. I. Synthesis of protected N-(ω-aminoalkylene) amino acids and their incorpoation into dipeptide units. J. Org. Chem. 57, 5687-5692.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5687-5692
-
-
Byk, G.1
Gilon, C.2
-
9
-
-
0028677301
-
Design, synthesis and characterization of bradykinin antagonists via cyclization of the modified backbone
-
9. Reissmann, S., Greiner, G., Jezek, J. et al. (1995) Design, synthesis and characterization of bradykinin antagonists via cyclization of the modified backbone. Biomed. Peptide Proteins Nucleic Acids 1, 51-56.
-
(1995)
Biomed. Peptide Proteins Nucleic Acids
, vol.1
, pp. 51-56
-
-
Reissmann, S.1
Greiner, G.2
Jezek, J.3
-
10
-
-
0028234916
-
A new general solid-phase method for the synthesis of backbone-to-backbone cyclized peptides
-
10. Kaljuste, K. & Unden, A. (1994) A new general solid-phase method for the synthesis of backbone-to-backbone cyclized peptides. Int. J. Peptide Protein Res. 43, 505-511.
-
(1994)
Int. J. Peptide Protein Res.
, vol.43
, pp. 505-511
-
-
Kaljuste, K.1
Unden, A.2
-
11
-
-
0029025947
-
Building units for N-backbone cyclic peptides. 2. Synthesis of protected N-(ω-thioalkylene) amino acids and their incorporation into dipeptide units
-
11. Bitan, G. & Gilon, C. (1995) Building units for N-backbone cyclic peptides. 2. Synthesis of protected N-(ω-thioalkylene) amino acids and their incorporation into dipeptide units. Tetrahedron 51, 10513-10522.
-
(1995)
Tetrahedron
, vol.51
, pp. 10513-10522
-
-
Bitan, G.1
Gilon, C.2
-
13
-
-
33748737482
-
Building units for N-backbone cyclic peptides. 4. Synthesis of protected Nα-functionalized alkyl amino acids by reductive alkylation of natural amino acids
-
13. Bitan, G., Muller, D., Kasher, R., Gluhov, E.V. & Gilon, C. (1997) Building units for N-backbone cyclic peptides. 4. Synthesis of protected Nα-functionalized alkyl amino acids by reductive alkylation of natural amino acids. J. Chem Soc., Perkin Trans. 1, 1501-1510.
-
(1997)
J. Chem Soc., Perkin Trans.
, vol.1
, pp. 1501-1510
-
-
Bitan, G.1
Muller, D.2
Kasher, R.3
Gluhov, E.V.4
Gilon, C.5
-
14
-
-
0032705743
-
Synthesis of N-carboxyalkyl and N-aminoalkyl functionalized dipeptide building units for the assembly of backbone cyclic peptides
-
14. Müller, B., Besser, D., Kleinwächter, P., Arad, O. & Reissmann, S. (1999) Synthesis of N-carboxyalkyl and N-aminoalkyl functionalized dipeptide building units for the assembly of backbone cyclic peptides. J. Peptide Res. 54, 383-393.
-
(1999)
J. Peptide Res.
, vol.54
, pp. 383-393
-
-
Müller, B.1
Besser, D.2
Kleinwächter, P.3
Arad, O.4
Reissmann, S.5
-
15
-
-
0029742789
-
Synthesis and biological activity of NK-1 selective N-backbone cyclic analogs of the C-terminal hexapeptide of substance P
-
15. Byk, G., Halle, D., Teltser, I., Bitan, G., Selinger, Z. & Gilon, C. (1996) Synthesis and biological activity of NK-1 selective N-backbone cyclic analogs of the C-terminal hexapeptide of substance P. J. Med. Chem. 39, 3174-3178.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3174-3178
-
-
Byk, G.1
Halle, D.2
Teltser, I.3
Bitan, G.4
Selinger, Z.5
Gilon, C.6
-
16
-
-
0030948998
-
Synthesis and biological activity of novel backbone-bicyclic substance-P analogs containing lactam and disulfide bridges
-
16. Bitan, G., Sukhotinsky, I., Mashriki, Y., Hanani, M., Selinger, Z. & Gilon, C. (1997) Synthesis and biological activity of novel backbone-bicyclic substance-P analogs containing lactam and disulfide bridges. J. Peptide Res. 49, 421-426.
-
(1997)
J. Peptide Res.
, vol.49
, pp. 421-426
-
-
Bitan, G.1
Sukhotinsky, I.2
Mashriki, Y.3
Hanani, M.4
Selinger, Z.5
Gilon, C.6
-
17
-
-
0026783997
-
Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptide oxotycin antagonists related to L-365, 209
-
17. Perlow, D.S., Erb, J.M., Could, N.P. et al. (1992) Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptide oxotycin antagonists related to L-365, 209. J. Org. Chem. 57, 4394-4400.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 4394-4400
-
-
Perlow, D.S.1
Erb, J.M.2
Could, N.P.3
-
18
-
-
0026473072
-
Comparative study of methods to couple hindred peptides
-
18. Spencer, J.R., Antonenko, V.V., Delaet, N.G.J. & Goodman, M. (1992) Comparative study of methods to couple hindred peptides. Int. J. Peptide Protein Res. 40, 282-293.
-
(1992)
Int. J. Peptide Protein Res.
, vol.40
, pp. 282-293
-
-
Spencer, J.R.1
Antonenko, V.V.2
Delaet, N.G.J.3
Goodman, M.4
-
19
-
-
0033041516
-
In situ generation of Fmoc-amino acid chlorides using bis(trichloromethyl)carbonate and its utilization for difficult couplings in solid-phase peptide synthesis
-
19. Falb, E., Yechezkel, T., Salitra, Y. & Gilon, C. (1999) In situ generation of Fmoc-amino acid chlorides using bis(trichloromethyl)carbonate and its utilization for difficult couplings in solid-phase peptide synthesis. J. Peptide Res. 53, 507-517.
-
(1999)
J. Peptide Res.
, vol.53
, pp. 507-517
-
-
Falb, E.1
Yechezkel, T.2
Salitra, Y.3
Gilon, C.4
-
20
-
-
0013692004
-
Synthesis of alternative building units for the assembly of backbone cyclic peptides
-
in press
-
20. Besser, D., Müller, B., Agricola, I. & Reissmann, S. (2000) Synthesis of alternative building units for the assembly of backbone cyclic peptides. J. Peptide Sci., in press.
-
(2000)
J. Peptide Sci.
-
-
Besser, D.1
Müller, B.2
Agricola, I.3
Reissmann, S.4
-
21
-
-
85004872164
-
An efficient synthesis of optically active α-(t-butyloxycarbonylamino)-aldehydes from α-amino acids
-
21. Fehrentz, J.A. & Castro, B. (1983) An efficient synthesis of optically active α-(t-butyloxycarbonylamino)-aldehydes from α-amino acids. Synthesis 676-678.
-
(1983)
Synthesis
, pp. 676-678
-
-
Fehrentz, J.A.1
Castro, B.2
-
22
-
-
0000589494
-
Peptide synthesis via amino acid halides
-
22. Carpino, L. A., Beyermann, M., Wenschuh, H. & Bienert, M. (1996) Peptide synthesis via amino acid halides. Acc. Chem. Res. 29, 268-274.
-
(1996)
Acc. Chem. Res.
, vol.29
, pp. 268-274
-
-
Carpino, L.A.1
Beyermann, M.2
Wenschuh, H.3
Bienert, M.4
-
23
-
-
0013695161
-
Recent aspects of the use of tetramethylfluoroformamidinium hexafluorophosphate (TFFH) as a convinient peptide coupling reagent
-
(Ramage, R., Epton, R., eds). Mayflower Scientific Ltd, Kingswinford
-
23. Triolo, S.A., Ionescu, D., Wenschuh, H. et al. (1998) Recent aspects of the use of tetramethylfluoroformamidinium hexafluorophosphate (TFFH) as a convinient peptide coupling reagent. In Peptides 1996 (Proceedings of the Twenty-Fourth European Peptide Symposium) (Ramage, R., Epton, R., eds). Mayflower Scientific Ltd, Kingswinford, pp. 839-840.
-
(1998)
Peptides 1996 (Proceedings of the Twenty-fourth European Peptide Symposium)
, pp. 839-840
-
-
Triolo, S.A.1
Ionescu, D.2
Wenschuh, H.3
-
24
-
-
0023821882
-
9 bradykinin, a B2 receptor selective agonist which is not broken down by either kinase I or kinase II
-
9] bradykinin, a B2 receptor selective agonist which is not broken down by either kinase I or kinase II. Eur. J. Pharmacol. 155, 193-195.
-
(1988)
Eur. J. Pharmacol.
, vol.155
, pp. 193-195
-
-
Drapeau, G.1
Rhaleh, N.E.2
Dion, S.3
Jukic, D.4
Regoli, D.5
-
25
-
-
0023930502
-
Solid phase reductive alkylation techniques in analogue peptide bond and side chain modification
-
25. Coy, D.H., Hocart, S.J. & Sasaki, Y. (1988) Solid phase reductive alkylation techniques in analogue peptide bond and side chain modification. Tetrahedron 44, 835-841.
-
(1988)
Tetrahedron
, vol.44
, pp. 835-841
-
-
Coy, D.H.1
Hocart, S.J.2
Sasaki, Y.3
-
27
-
-
0028048084
-
2-NH] bond: A positional shift in backbone structure caused by a single dipeptide mimetic
-
2-NH] bond: a positional shift in backbone structure caused by a single dipeptide mimetic. J. Am. Chem. Soc. 116, 7735-7743.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 7735-7743
-
-
Geyer, A.1
Müller, G.2
Kessler, H.3
-
28
-
-
0037768402
-
Optically active N-protected α-amino aldehydes in organic synthesis
-
28. Jurczak, J. & Golebiowski, A. (1989) Optically active N-protected α-amino aldehydes in organic synthesis. Chem Rev. 89, 149-164.
-
(1989)
Chem Rev.
, vol.89
, pp. 149-164
-
-
Jurczak, J.1
Golebiowski, A.2
-
29
-
-
33947459491
-
Acylalkylcarbonates as acylating agents for the synthesis of peptides
-
29. Vaughan, J.R. (1951) Acylalkylcarbonates as acylating agents for the synthesis of peptides. J. Am. Chem. Soc. 73, 3547.
-
(1951)
J. Am. Chem. Soc.
, vol.73
, pp. 3547
-
-
Vaughan, J.R.1
-
30
-
-
0029883018
-
Synthesis of novel (N-famesyl) amino acids and their incorporation into peptides
-
30. Byk, G. & Scherman, D. (1996) Synthesis of novel (N-famesyl) amino acids and their incorporation into peptides. Int. J. Peptide Protein Res. 47, 333-339.
-
(1996)
Int. J. Peptide Protein Res.
, vol.47
, pp. 333-339
-
-
Byk, G.1
Scherman, D.2
|