-
1
-
-
0021923153
-
76. Peptide Conformations. The Conformation of Cyclosporin A in the Crystal and in Solution
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1985)
Helv. Chim. Acta
, vol.68
, pp. 682-704
-
-
Loosli, H.R.1
Kessler, H.2
Oschkinat, H.3
Petcher, H.P.4
Weber, T.J.5
Widmer, A.6
-
2
-
-
0025054575
-
164. Reinvestigation of the Conformatin of Cyclosporin A in Chloroform
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1990)
Helv. Chim. Acta
, vol.73
, pp. 1818-1832
-
-
Kessler, H.1
Köck, M.2
Wein, T.3
Gehrke, M.4
-
3
-
-
0025835156
-
The NMR Structure of Cyclosporin A Bound to Cyclophilin in Aqueous Solution
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1991)
Biochemistry
, vol.30
, pp. 6563-6574
-
-
Weber, C.1
Wider, G.2
Von Freyberg, B.3
Traber, R.4
Braun, W.5
Widmer, H.6
Wüthrich, K.7
-
4
-
-
0025868159
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1991)
Biochemistry
, vol.30
, pp. 6574-6583
-
-
Fesik, S.W.1
Gampe, R.T.2
Eaton, H.L.3
Gemmecker, G.4
Olejniczak, E.T.5
Neri, P.6
Holzman, T.F.7
Egan, D.A.8
Edalji, R.9
Simmer, R.10
Helfrich, R.11
Hochloewski, J.12
Jackson, M.13
-
5
-
-
0025596913
-
Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 9434-9436
-
-
Karuso, P.1
Kessler, H.2
Mierke, D.F.3
-
6
-
-
0024442393
-
A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1989)
Nature
, vol.341
, pp. 755-757
-
-
Siekerka, J.J.1
Hung, S.H.Y.2
Poe, M.3
Lin, C.S.4
Sigal, N.H.5
-
7
-
-
0025826967
-
Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex
-
13C]Cyclosporin A Bound to Cyclophilin: Bound Conformation and Portions of Cyclosporin Involved in Binding. Biochemistry 1991, 30, 6574-6583. FK506. Solution and X-ray: (e) Karuso, P.; Kessler, H.; Mierke, D. F. Solution Structure of FK506 from Nuclear Magnetic Resonance and Molecular Dynamics. J. Am. Chem. Soc. 1990, 112, 9434-9436. (f) Siekerka, J. J.; Hung, S. H. Y.; Poe, M.; Lin, C. S.; Sigal, N. H. A Cytosolic Binding Protein for the Immunosuppressant FK506 has Peptidyl-Prolyl Isomerase Activity but is Distinct from Cyclophilin. Nature 1989, 341, 755-757. Complex: (g) van Duyne, G. D.; Standaert, R. F.; Karplus, P. A.; Schreiber, S. L.; Clardy, J. Atomic Structure of FKBP-FK506, an Immunophilin Immunosuppressant Complex. Science 1991, 252, 839-842.
-
(1991)
Science
, vol.252
, pp. 839-842
-
-
Van Duyne, G.D.1
Standaert, R.F.2
Karplus, P.A.3
Schreiber, S.L.4
Clardy, J.5
-
8
-
-
0020163940
-
NMR-spektroskopishe Methoden Zur Konformationanayse von Peptiden
-
(a) Kessler, H. NMR-spektroskopishe Methoden Zur Konformationanayse von Peptiden. (Conformations and Biological Activity of Cyclic Peptides.) Angew. Chem., Int. Ed. Engl. 1982, 21, 512-523.
-
(1982)
Angew. Chem., Int. Ed. Engl.
, vol.21
, pp. 512-523
-
-
Kessler, H.1
-
9
-
-
0019958979
-
Conformational Restrictions of Biologically Active Peptides via Amino Acid Side Chain Groups
-
(b) Hruby, V. J. Conformational Restrictions of Biologically Active Peptides via Amino Acid Side Chain Groups. Life Sci. 1982, 31, 189-199.
-
(1982)
Life Sci
, vol.31
, pp. 189-199
-
-
Hruby, V.J.1
-
10
-
-
0025370346
-
Conformationally Restricted Peptides Through Short-Range Cyclizations
-
(c) Toniolo, C. Conformationally Restricted Peptides Through Short-Range Cyclizations. Int. J. Pept. Protein Res. 1990, 35, 287-300.
-
(1990)
Int. J. Pept. Protein Res.
, vol.35
, pp. 287-300
-
-
Toniolo, C.1
-
11
-
-
0000788606
-
Peptide Backbone Modifications: A Structure-Activity Analysis of Peptides Containing Amide Bond Surrogates. Conformational Constraints, and Related Backbone Replacements
-
Weinstein, B., Ed.; Marcel Dekker, New York
-
(a) Spatola, A. F. Peptide Backbone Modifications: A Structure-Activity Analysis of Peptides Containing Amide Bond Surrogates. Conformational Constraints, and Related Backbone Replacements. In Chemistry and Biochemistry of Amino Acids, Peptides, and Proteins; Weinstein, B., Ed.; Marcel Dekker, New York, 1983; Vol. 7, pp 267-357.
-
(1983)
Chemistry and Biochemistry of Amino Acids, Peptides, and Proteins
, vol.7
, pp. 267-357
-
-
Spatola, A.F.1
-
12
-
-
0025336463
-
Emerging Approaches in the Molecular Design of Receptor-Selective Peptide Ligands: Conformational, Topographical and Dynamic Considerations
-
(b) Hruby, B. J.; Al-Obeidi, F.; Kazmierski, W., Emerging Approaches in the Molecular Design of Receptor-Selective Peptide Ligands: Conformational, Topographical and Dynamic Considerations. Biochem. J. 1990, 268, 249-262.
-
(1990)
Biochem. J.
, vol.268
, pp. 249-262
-
-
Hruby, B.J.1
Al-Obeidi, F.2
Kazmierski, W.3
-
13
-
-
0027423502
-
Concepts and Progress in the Development of Peptides Mimics
-
(c) Olson, G. L.; Bolin, D. R.; Bonner, M. P.; Bös, M.; Cook, C. M.; Fry, D. C.; Graves, B. J.; Hatada, M.; Hill, D. E.; Kahn, M.; Madison, V. S.; Ruisiecki, V. K.; Sarabu, R.; Sepinwall, J.; Vincent, G. P.; Voss, M. E. Concepts and Progress in the Development of Peptides Mimics. J. Med. Chem. 1993, 36, 3039-3049.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3039-3049
-
-
Olson, G.L.1
Bolin, D.R.2
Bonner, M.P.3
Bös, M.4
Cook, C.M.5
Fry, D.C.6
Graves, B.J.7
Hatada, M.8
Hill, D.E.9
Kahn, M.10
Madison, V.S.11
Ruisiecki, V.K.12
Sarabu, R.13
Sepinwall, J.14
Vincent, G.P.15
Voss, M.E.16
-
14
-
-
33745502124
-
Peptidomimetics for Receptor Ligands. Discovery, Development, and Medical Perspectives
-
(d) Giannis, A.; Kolter, T. Peptidomimetics for Receptor Ligands. Discovery, Development, and Medical Perspectives. Angew. Chem., Int. Ed. Eng. 1993, 32, 1244-1267.
-
(1993)
Angew. Chem., Int. Ed. Eng.
, vol.32
, pp. 1244-1267
-
-
Giannis, A.1
Kolter, T.2
-
15
-
-
0028038601
-
Peptidomimetics-Tailored Enzyme Inhibitors
-
(e) Gante, J. Peptidomimetics-Tailored Enzyme Inhibitors. Angew. Chem., Int. Ed. Eng. 1994, 33, 1699-1720.
-
(1994)
Angew. Chem., Int. Ed. Eng.
, vol.33
, pp. 1699-1720
-
-
Gante, J.1
-
16
-
-
0027478912
-
Peptidomimetics Derived from Natural-Products
-
(f) Wiley, R. A.; Rich, D. H. Peptidomimetics Derived from Natural-Products. Med. Res. Rev. 1993, 13, 327-384.
-
(1993)
Med. Res. Rev.
, vol.13
, pp. 327-384
-
-
Wiley, R.A.1
Rich, D.H.2
-
17
-
-
0005449318
-
Case Histories of Peptidomimetics. Progression from Peptides to Drugs
-
(g) Adang, A. E. P.; Hermkens, P. H. H.; Linders, J. T. M.; Ottenheijm, H. C. J.; van Staveren, C. J. Case Histories of Peptidomimetics. Progression from Peptides to Drugs. Recl. Trav. Chim. Pays-Bas 1994, 113, 63-78.
-
(1994)
Recl. Trav. Chim. Pays-Bas
, vol.113
, pp. 63-78
-
-
Adang, A.E.P.1
Hermkens, P.H.H.2
Linders, J.T.M.3
Ottenheijm, H.C.J.4
Van Staveren, C.J.5
-
18
-
-
0025409471
-
Conformational Constraints: Nonpeptide β-Turn Mimics
-
(a) Ball, J. B.; Alewood, P. F. Conformational Constraints: Nonpeptide β-Turn Mimics. J. Mol. Recognit. 1990, 3, 55-64.
-
(1990)
J. Mol. Recognit.
, vol.3
, pp. 55-64
-
-
Ball, J.B.1
Alewood, P.F.2
-
19
-
-
77957079236
-
Peptide Secondary Structure Mimetics: Recent Advances and Future Challenges
-
(b) Kahn, M. Peptide Secondary Structure Mimetics: Recent Advances and Future Challenges. SynLett. 1993, 821-826.
-
(1993)
SynLett
, pp. 821-826
-
-
Kahn, M.1
-
20
-
-
0005923704
-
Building Blocks for the Induction or Fixation of Peptide Conformations
-
Testa, B., Fuhrer, W., Kyburz, E., Giger, R., Eds.; VCH: Weinheim, Germany
-
Mueller, K.; Obrecht, D.; Knierzinger, A.; Stankovic, C.; Spiegler, C.; Bannwarth, W.; Trzeciak, A; Englert, G.; Labhardt, A. M.; Schönholzer, P. Building Blocks for the Induction or Fixation of Peptide Conformations. In Perspectives in Medicinal Chemistry; Testa, B., Fuhrer, W., Kyburz, E., Giger, R., Eds.; VCH: Weinheim, Germany, 1993; pp 513-532.
-
(1993)
Perspectives in Medicinal Chemistry
, pp. 513-532
-
-
Mueller, K.1
Obrecht, D.2
Knierzinger, A.3
Stankovic, C.4
Spiegler, C.5
Bannwarth, W.6
Trzeciak, A.7
Englert, G.8
Labhardt, A.M.9
Schönholzer, P.10
-
21
-
-
85023346540
-
Vinylogous Polypeptides: An Alternative Peptide Backbone
-
For example, see: (a) Hagihara, M.; Anthony, N. J.; Stout, T. J.; Clardy, J.; Schreiber, S. L. Vinylogous Polypeptides: An Alternative Peptide Backbone. J. Am. Chem. Soc. 1992, 114, 6568-6570. (b) Smith, A. B., III; Keenan, T. P.; Holcomb, R. C.; Sprengeler, P. A.; Guzman, M. C.; Wood, J. L.; Carroll, P. J.; Hirschmann, R. Design, Synthesis, and Crystal Structure of a Pyrrolinone-Based Peptidomimetic Possessing the Conformation of a β-Strand: Potential Application to the Design of Novel Inhibitors of Proteolytic Enzymes, J. Am. Chem. Soc. 1992, 114, 10672-10674. (c) Chen, L.; Trilles, R. V. Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide. Tetrahedron Lett. 1992, 36, 8715-8718. (d) Boumendjel, A.; Roberts, J. C.; Hu, E.; Pallai, P. V.; Rebek, J., Jr. Design and Asymmetric Synthesis of β-Strand Peptidomimetics. J. Org. Chem. 1996, 61, 4434-4438. (e) Janetka, J. W.; Raman, P.; Satyshur, K.; Flentke, G. R.; Rich, D. H. Novel Cyclic Biphenyl Ether Peptide β-Strand Mimetics and HIV-Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 441-442.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 6568-6570
-
-
Hagihara, M.1
Anthony, N.J.2
Stout, T.J.3
Clardy, J.4
Schreiber, S.L.5
-
22
-
-
0027081659
-
Design, Synthesis, and Crystal Structure of a Pyrrolinone-Based Peptidomimetic Possessing the Conformation of a β-Strand: Potential Application to the Design of Novel Inhibitors of Proteolytic Enzymes
-
For example, see: (a) Hagihara, M.; Anthony, N. J.; Stout, T. J.; Clardy, J.; Schreiber, S. L. Vinylogous Polypeptides: An Alternative Peptide Backbone. J. Am. Chem. Soc. 1992, 114, 6568-6570. (b) Smith, A. B., III; Keenan, T. P.; Holcomb, R. C.; Sprengeler, P. A.; Guzman, M. C.; Wood, J. L.; Carroll, P. J.; Hirschmann, R. Design, Synthesis, and Crystal Structure of a Pyrrolinone-Based Peptidomimetic Possessing the Conformation of a β-Strand: Potential Application to the Design of Novel Inhibitors of Proteolytic Enzymes, J. Am. Chem. Soc. 1992, 114, 10672-10674. (c) Chen, L.; Trilles, R. V. Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide. Tetrahedron Lett. 1992, 36, 8715-8718. (d) Boumendjel, A.; Roberts, J. C.; Hu, E.; Pallai, P. V.; Rebek, J., Jr. Design and Asymmetric Synthesis of β-Strand Peptidomimetics. J. Org. Chem. 1996, 61, 4434-4438. (e) Janetka, J. W.; Raman, P.; Satyshur, K.; Flentke, G. R.; Rich, D. H. Novel Cyclic Biphenyl Ether Peptide β-Strand Mimetics and HIV-Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 441-442.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10672-10674
-
-
Smith III, A.B.1
Keenan, T.P.2
Holcomb, R.C.3
Sprengeler, P.A.4
Guzman, M.C.5
Wood, J.L.6
Carroll, P.J.7
Hirschmann, R.8
-
23
-
-
0028856986
-
Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide
-
For example, see: (a) Hagihara, M.; Anthony, N. J.; Stout, T. J.; Clardy, J.; Schreiber, S. L. Vinylogous Polypeptides: An Alternative Peptide Backbone. J. Am. Chem. Soc. 1992, 114, 6568-6570. (b) Smith, A. B., III; Keenan, T. P.; Holcomb, R. C.; Sprengeler, P. A.; Guzman, M. C.; Wood, J. L.; Carroll, P. J.; Hirschmann, R. Design, Synthesis, and Crystal Structure of a Pyrrolinone-Based Peptidomimetic Possessing the Conformation of a β-Strand: Potential Application to the Design of Novel Inhibitors of Proteolytic Enzymes, J. Am. Chem. Soc. 1992, 114, 10672-10674. (c) Chen, L.; Trilles, R. V. Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide. Tetrahedron Lett. 1992, 36, 8715-8718. (d) Boumendjel, A.; Roberts, J. C.; Hu, E.; Pallai, P. V.; Rebek, J., Jr. Design and Asymmetric Synthesis of β-Strand Peptidomimetics. J. Org. Chem. 1996, 61, 4434-4438. (e) Janetka, J. W.; Raman, P.; Satyshur, K.; Flentke, G. R.; Rich, D. H. Novel Cyclic Biphenyl Ether Peptide β-Strand Mimetics and HIV-Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 441-442.
-
(1992)
Tetrahedron Lett
, vol.36
, pp. 8715-8718
-
-
Chen, L.1
Trilles, R.V.2
-
24
-
-
0030037766
-
Design and Asymmetric Synthesis of β-Strand Peptidomimetics
-
For example, see: (a) Hagihara, M.; Anthony, N. J.; Stout, T. J.; Clardy, J.; Schreiber, S. L. Vinylogous Polypeptides: An Alternative Peptide Backbone. J. Am. Chem. Soc. 1992, 114, 6568-6570. (b) Smith, A. B., III; Keenan, T. P.; Holcomb, R. C.; Sprengeler, P. A.; Guzman, M. C.; Wood, J. L.; Carroll, P. J.; Hirschmann, R. Design, Synthesis, and Crystal Structure of a Pyrrolinone-Based Peptidomimetic Possessing the Conformation of a β-Strand: Potential Application to the Design of Novel Inhibitors of Proteolytic Enzymes, J. Am. Chem. Soc. 1992, 114, 10672-10674. (c) Chen, L.; Trilles, R. V. Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide. Tetrahedron Lett. 1992, 36, 8715-8718. (d) Boumendjel, A.; Roberts, J. C.; Hu, E.; Pallai, P. V.; Rebek, J., Jr. Design and Asymmetric Synthesis of β-Strand Peptidomimetics. J. Org. Chem. 1996, 61, 4434-4438. (e) Janetka, J. W.; Raman, P.; Satyshur, K.; Flentke, G. R.; Rich, D. H. Novel Cyclic Biphenyl Ether Peptide β-Strand Mimetics and HIV-Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 441-442.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4434-4438
-
-
Boumendjel, A.1
Roberts, J.C.2
Hu, E.3
Pallai, P.V.4
Rebek Jr., J.5
-
25
-
-
0031055496
-
Novel Cyclic Biphenyl Ether Peptide β-Strand Mimetics and HIV-Protease Inhibitors
-
For example, see: (a) Hagihara, M.; Anthony, N. J.; Stout, T. J.; Clardy, J.; Schreiber, S. L. Vinylogous Polypeptides: An Alternative Peptide Backbone. J. Am. Chem. Soc. 1992, 114, 6568-6570. (b) Smith, A. B., III; Keenan, T. P.; Holcomb, R. C.; Sprengeler, P. A.; Guzman, M. C.; Wood, J. L.; Carroll, P. J.; Hirschmann, R. Design, Synthesis, and Crystal Structure of a Pyrrolinone-Based Peptidomimetic Possessing the Conformation of a β-Strand: Potential Application to the Design of Novel Inhibitors of Proteolytic Enzymes, J. Am. Chem. Soc. 1992, 114, 10672-10674. (c) Chen, L.; Trilles, R. V. Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide. Tetrahedron Lett. 1992, 36, 8715-8718. (d) Boumendjel, A.; Roberts, J. C.; Hu, E.; Pallai, P. V.; Rebek, J., Jr. Design and Asymmetric Synthesis of β-Strand Peptidomimetics. J. Org. Chem. 1996, 61, 4434-4438. (e) Janetka, J. W.; Raman, P.; Satyshur, K.; Flentke, G. R.; Rich, D. H. Novel Cyclic Biphenyl Ether Peptide β-Strand Mimetics and HIV-Protease Inhibitors. J. Am. Chem. Soc. 1997, 119, 441-442.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 441-442
-
-
Janetka, J.W.1
Raman, P.2
Satyshur, K.3
Flentke, G.R.4
Rich, D.H.5
-
26
-
-
15144343551
-
Synthesis and Conformational Studies of Enkephalin-like Cyclic Peptides and Depsipeptides
-
Deber, C. M., Hruby, V. J., Kopple, K. D., Eds.; Pierce Chemical Co.: Rockford, IL
-
For the fixation of the side chain orientation of Phe see (a) Zechel, C.; Kessler, H.; Geiger, R. Synthesis and Conformational Studies of Enkephalin-like Cyclic Peptides and Depsipeptides. In Peptides, Structure and Function (Proceedings of the 9th American Peptide Symposium); Deber, C. M., Hruby, V. J., Kopple, K. D., Eds.; Pierce Chemical Co.: Rockford, IL, 1985; pp 507-510. (b) Tourwe, D.; Verschueren, K.; Frycia, A.; Davis, P.; Porreca, F.; Hruby, V. J.; Toth, G.; Jaspers, H.; Verheyden, P.; van Binst, G. Conformational Restriction of Tyr and Phe Side Chains in Opioid Peptides: Information About Preferred and Bioactive Side-Chain Topology. Biopolymers 1996, 38, 1-12.
-
(1985)
Peptides, Structure and Function (Proceedings of the 9th American Peptide Symposium)
, pp. 507-510
-
-
Zechel, C.1
Kessler, H.2
Geiger, R.3
-
27
-
-
0030027103
-
Conformational Restriction of Tyr and Phe Side Chains in Opioid Peptides: Information about Preferred and Bioactive Side-Chain Topology
-
For the fixation of the side chain orientation of Phe see (a) Zechel, C.; Kessler, H.; Geiger, R. Synthesis and Conformational Studies of Enkephalin-like Cyclic Peptides and Depsipeptides. In Peptides, Structure and Function (Proceedings of the 9th American Peptide Symposium); Deber, C. M., Hruby, V. J., Kopple, K. D., Eds.; Pierce Chemical Co.: Rockford, IL, 1985; pp 507-510. (b) Tourwe, D.; Verschueren, K.; Frycia, A.; Davis, P.; Porreca, F.; Hruby, V. J.; Toth, G.; Jaspers, H.; Verheyden, P.; van Binst, G. Conformational Restriction of Tyr and Phe Side Chains in Opioid Peptides: Information About Preferred and Bioactive Side-Chain Topology. Biopolymers 1996, 38, 1-12.
-
(1996)
Biopolymers
, vol.38
, pp. 1-12
-
-
Tourwe, D.1
Verschueren, K.2
Frycia, A.3
Davis, P.4
Porreca, F.5
Hruby, V.J.6
Toth, G.7
Jaspers, H.8
Verheyden, P.9
Van Binst, G.10
-
28
-
-
0025074114
-
Cyclopropane Amino Acids (2,3- and 3,4-Methanoamino Acids)
-
For reviews, see: (a) Stammer, C. H. Cyclopropane Amino Acids (2,3- and 3,4-Methanoamino Acids). Tetrahedron 1990, 46, 2231-2254. (b) Burgess, K.; Ho, K.-K.; Moye-Sherman, D. Asymmetric Syntheses of 2,3-Methanoamino Acids. SynLett. 1994, 575-583.
-
(1990)
Tetrahedron
, vol.46
, pp. 2231-2254
-
-
Stammer, C.H.1
-
29
-
-
84949065308
-
Asymmetric Syntheses of 2,3-Methanoamino Acids
-
For reviews, see: (a) Stammer, C. H. Cyclopropane Amino Acids (2,3- and 3,4-Methanoamino Acids). Tetrahedron 1990, 46, 2231-2254. (b) Burgess, K.; Ho, K.-K.; Moye-Sherman, D. Asymmetric Syntheses of 2,3-Methanoamino Acids. SynLett. 1994, 575-583.
-
(1994)
SynLett
, pp. 575-583
-
-
Burgess, K.1
Ho, K.-K.2
Moye-Sherman, D.3
-
30
-
-
0025105049
-
1′ Transition State Analogues. Synthesis of 1(R), 3(R) [1(S), 2(S)] 3-[3-Cyclohexyl-2-[(Boc)amino]-1-hydroxypropyl]-2,2-dimethylcyclopropane Carboxylic Acids
-
1′ Transition State Analogues. Synthesis of 1(R), 3(R) [1(S), 2(S)] 3-[3-Cyclohexyl-2-[(Boc)amino]-1-hydroxypropyl]-2,2-dimethylcyclopropane Carboxylic Acids. Tetrahedron Lett. 1990, 31, 961-964.
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 961-964
-
-
Melnick, M.J.1
Bisaha, S.N.2
Gammill, R.B.3
-
31
-
-
2742587400
-
The Crystal Structure of Cyclopropanecarbohydrazide
-
(a) Chesnut, D. B.; Marsh, R. E. The Crystal Structure of Cyclopropanecarbohydrazide. Acta Crystallogr. 1958, 11, 413-419.
-
(1958)
Acta Crystallogr
, vol.11
, pp. 413-419
-
-
Chesnut, D.B.1
Marsh, R.E.2
-
32
-
-
0001269834
-
The Crystal and Molecular Structure of Cyclopropanecarboxamide
-
(b) Long, R. E.; Maddox, H.; Trueblood, K. N. The Crystal and Molecular Structure of Cyclopropanecarboxamide. Acta Crystallogr. 1969, B25, 2083-2094.
-
(1969)
Acta Crystallogr
, vol.B25
, pp. 2083-2094
-
-
Long, R.E.1
Maddox, H.2
Trueblood, K.N.3
-
33
-
-
0007854289
-
Determination of the Absolute Configuration of a Novel Dipeptide Isostere
-
(c) Lynch, V. M.; Austin, R. E.; Martin, S. F.; George, T. Determination of the Absolute Configuration of a Novel Dipeptide Isostere. Acta Crystallogr. 1991, C47, 1345-1347.
-
(1991)
Acta Crystallogr
, vol.C47
, pp. 1345-1347
-
-
Lynch, V.M.1
Austin, R.E.2
Martin, S.F.3
George, T.4
-
34
-
-
0000768284
-
Preference of cis-Amide Structure in N-Acyl-N-methylanilines
-
(d) Itai, A; Toriumi, Y.; Saito, S.; Kagechika, H.; Shudo, K. Preference of cis-Amide Structure in N-Acyl-N-methylanilines. J. Am. Chem. Soc. 1992, 114, 10649-100650.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10649-100650
-
-
Itai, A.1
Toriumi, Y.2
Saito, S.3
Kagechika, H.4
Shudo, K.5
-
35
-
-
0015101706
-
Entropie Contributions to Rate Accelerations in Enzymatic and Intramolecular Reactions and the Chelate Effect
-
(a) Page, M. I.; Jencks, W. P. Entropie Contributions to Rate Accelerations in Enzymatic and Intramolecular Reactions and the Chelate Effect. Proc. Natl. Acad. Sci. U.S.A. 1971, 68, 1678-1683.
-
(1971)
Proc. Natl. Acad. Sci. U.S.A.
, vol.68
, pp. 1678-1683
-
-
Page, M.I.1
Jencks, W.P.2
-
36
-
-
0019407381
-
On the Attribution and Additivity of Binding Energies
-
(b) Jencks, W. P. On the Attribution and Additivity of Binding Energies. Proc. Natl. Acad. Sci. U.S.A. 1981, 78, 4046-4050.
-
(1981)
Proc. Natl. Acad. Sci. U.S.A.
, vol.78
, pp. 4046-4050
-
-
Jencks, W.P.1
-
37
-
-
9644258919
-
The Cost of Conformational Order: Entropy Changes in Molecular Associations
-
(c) Searle, M. S.; Williams, D. H. The Cost of Conformational Order: Entropy Changes in Molecular Associations. J. Am. Chem. Soc. 1992, 114, 10690-10697.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10690-10697
-
-
Searle, M.S.1
Williams, D.H.2
-
38
-
-
0027241298
-
The Free Energy Change of Restricting a Bond Rotation in the Binding of Peptide Analogues to Vancomycin Group Antibiotics
-
and references therein
-
(d) Gerhard, U.; Searle, M. S.; Williams, D. H. The Free Energy Change of Restricting a Bond Rotation in the Binding of Peptide Analogues to Vancomycin Group Antibiotics. BioMed. Chem. Lett. 1993, 3, 803-808 and references therein.
-
(1993)
BioMed. Chem. Lett.
, vol.3
, pp. 803-808
-
-
Gerhard, U.1
Searle, M.S.2
Williams, D.H.3
-
39
-
-
33646195474
-
The Hydrogen Bond in Molecular Recognition
-
(a) Fersht, A. R., The Hydrogen Bond in Molecular Recognition. Trends Biol. Sci. 1987, 12, 301-304.
-
(1987)
Trends Biol. Sci.
, vol.12
, pp. 301-304
-
-
Fersht, A.R.1
-
40
-
-
0027054352
-
Partitioning of Free Energy Contributions in the Estimation of Binding Constants: Residual Motions and Consequences for Amide-Amide Hydrogen Bond Strengths
-
(b) Searle, M. S.; Williams, D. H.; Gerhard, U. Partitioning of Free Energy Contributions in the Estimation of Binding Constants: Residual Motions and Consequences for Amide-Amide Hydrogen Bond Strengths. J. Am. Chem. Soc. 1992, 114, 10697-10704.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10697-10704
-
-
Searle, M.S.1
Williams, D.H.2
Gerhard, U.3
-
41
-
-
0028821544
-
Hydrogen Bonding in Water Using Synthetic Receptors
-
(c) Kato, Y.; Conn, M. M.; Rebek, Jr., J. Hydrogen Bonding in Water Using Synthetic Receptors. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 1208-1212.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 1208-1212
-
-
Kato, Y.1
Conn, M.M.2
Rebek Jr., J.3
-
42
-
-
0026642037
-
1,2,3-Trisubstituted Cyclopropanes as Conformationally Restricted Peptide Isosteres: Application to the Design and Synthesis of Novel Renin Inhibitors
-
(a) Martin, S. F.; Austin, R. E.; Oalmann, C. J.; Baker, W. R.; Condon, S. L.; DeLara, E.; Rosenberg, S. H.; Spina, K. P.; Stein, H. H.; Cohen, J.; Kleinert, H. D. 1,2,3-Trisubstituted Cyclopropanes as Conformationally Restricted Peptide Isosteres: Application to the Design and Synthesis of Novel Renin Inhibitors. J. Med. Chem. 1992, 35, 1710-1721.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1710-1721
-
-
Martin, S.F.1
Austin, R.E.2
Oalmann, C.J.3
Baker, W.R.4
Condon, S.L.5
Delara, E.6
Rosenberg, S.H.7
Spina, K.P.8
Stein, H.H.9
Cohen, J.10
Kleinert, H.D.11
-
43
-
-
0026494850
-
3 Amino Acid Replacement
-
3 Amino Acid Replacement. Bioorg. Med. Chem. Lett. 1992, 2, 1405.
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 1405
-
-
Baker, W.R.1
Jae, H.S.2
Martin, S.F.3
Condon, S.L.4
Stein, H.H.5
Cohen, J.6
Kleinert, H.D.7
-
44
-
-
0027207873
-
Cyclopropanes as Conformationally Restricted Peptide Isosteres. Design and Synthesis of Novel Collagenase Inhibitors
-
Martin, S. F.; Oalmann, C. J.; Liras, S. Cyclopropanes as Conformationally Restricted Peptide Isosteres. Design and Synthesis of Novel Collagenase Inhibitors, Tetrahedron 1993, 49, 3521-3532.
-
(1993)
Tetrahedron
, vol.49
, pp. 3521-3532
-
-
Martin, S.F.1
Oalmann, C.J.2
Liras, S.3
-
45
-
-
0028506740
-
Design of Orally, Active, Non-Peptide Fibrinogen Receptor Antagonists. An Evolutionary Process from the RGD Sequence to Novel Anti-Platelet Aggregation Agents
-
Bovy, P. R.; Tjoeng, F. S.; Rico, J. G.; Rogers, T. E.; Lindmark, R. J.; Zablocki, J. A.; Garland, R. B.; McMackins, D. E.; Dayringer, H.; Toth, M. V.; Zupec, M. E.; Rao, S.; Panzer-Knodle, S. G.; Nicholson, N. S.; Salyers, A.; Taite, B. B.; Herin, M.; Miyano, M.; Feigen, L. P.; Adams, S. P. Design of Orally, Active, Non-Peptide Fibrinogen Receptor Antagonists. An Evolutionary Process from the RGD Sequence to Novel Anti-Platelet Aggregation Agents. Bioorg. Med. Chem. 1994, 2, 881-895.
-
(1994)
Bioorg. Med. Chem.
, vol.2
, pp. 881-895
-
-
Bovy, P.R.1
Tjoeng, F.S.2
Rico, J.G.3
Rogers, T.E.4
Lindmark, R.J.5
Zablocki, J.A.6
Garland, R.B.7
McMackins, D.E.8
Dayringer, H.9
Toth, M.V.10
Zupec, M.E.11
Rao, S.12
Panzer-Knodle, S.G.13
Nicholson, N.S.14
Salyers, A.15
Taite, B.B.16
Herin, M.17
Miyano, M.18
Feigen, L.P.19
Adams, S.P.20
more..
-
46
-
-
0025952925
-
HIV Protease: A Novel Chemotherapeutic Target for AIDS
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1991)
J. Med Chem.
, vol.34
, pp. 2305-2314
-
-
Huff, J.R.1
-
47
-
-
0026663760
-
Hydroxyethylene Isostere Inhibitors of Human Immunodeficiency Virus-1 Protease: Structure-Activity Analysis Using Enzyme Kinetics, X-ray Crystallography, and Infected T-Cell Assays
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1992)
Biochemistry
, vol.31
, pp. 6646-6659
-
-
Dreyer, G.B.1
Lambert, D.M.2
Meek, T.D.3
Carr, T.J.4
Tomaszek Jr., T.A.5
Fernandez, A.V.6
Bartus, H.7
Cacciavillani, E.8
Hasseil, A.M.9
Minnich, M.10
Petteway Jr., S.R.11
Metcalf, B.W.12
-
48
-
-
0026627809
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1685-1701
-
-
Thompson, W.J.1
Fitzgerald, P.M.D.2
Holloway, M.K.3
Emini, E.A.4
Drake, P.L.5
McKeever, B.M.6
Schleif, W.A.7
Quintero, J.C.8
Zugay, J.A.9
Tucker, T.J.10
Schwering, J.E.11
Homnick, C.F.12
Nunberg, J.13
Springer, J.P.14
Huff, J.R.15
-
49
-
-
0027405931
-
Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 320-330
-
-
Kempf, D.J.1
Codacovi, L.2
Wang, X.C.3
Kohlbrenner, W.E.4
Wideburg, N.E.5
Saldivar, A.6
Vasavanonda, S.7
March, K.C.8
Bryant, P.9
Sham, H.L.10
Green, B.E.11
Betebenner, D.A.12
Erickson, J.13
Norbeck, D.W.14
-
50
-
-
0027189618
-
Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 941-952
-
-
Thaisrivongs, S.1
Turner, S.R.2
Strohbach, J.W.3
Tenbrink, R.E.4
Tarpley, W.G.5
McQuade, T.J.6
Heinrikson, R.L.7
Tomasselli, A.G.8
Hui, J.O.9
Howe, W.J.10
-
51
-
-
0027762073
-
Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 4152-4160
-
-
Waller, C.L.1
Oprea, T.I.2
Giolitti, A.3
Marshall, G.R.4
-
52
-
-
0028057975
-
Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors
-
1′ Phenyl Substituents: X-ray Crystal Structure Assisted Design. J. Med. Chem. 1992, 35, 1685-1701. (d) Kempf, D. J.; Codacovi, L.; Wang, X. C.; Kohlbrenner, W. E.; Wideburg, N. E.; Saldivar, A.; Vasavanonda, S.; March, K. C.; Bryant, P.; Sham, H. L.; Green, B. E.; Betebenner, D. A.; Erickson, J.; Norbeck, D. W. Symmetry-Based Inhibitors of HIV Protease. Structure-activity Studies of Acylated 2,4-Diamino-1,5-diphenyl-3-hydroxypentane and 2,5-Diamino-1,6-diphenylheane-3,4-diol. J. Med. Chem. 1993, 36, 320-330. (e) Thaisrivongs, S.; Turner, S. R.; Strohbach, J. W.; TenBrink, R. E.; Tarpley, W. G.; McQuade, T. J.; Heinrikson, R. L.; Tomasselli, A. G.; Hui, J. O.; Howe, W. J. Inhibitors of the Protease from Human Immunodeficiency Virus: Synthesis, Enzyme Inhibition, and Antiviral Activity of a Series of Compounds Containing the Dihydroxyethylene Transition-State Isostere. J. Med. Chem. 1993, 36, 941-952. (f) Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160. (g) Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bacheler, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C.; Jackson, D. A.; Sharpe, T. R.; Erickson-Viitanen, S. Rational Design of Potent, Bioavailable, Nonpeptide Cyclic Ureas as HIV Protease Inhibitors. Science 1994, 263, 380-384.
-
(1994)
Science
, vol.263
, pp. 380-384
-
-
Lam, P.Y.S.1
Jadhav, P.K.2
Eyermann, C.J.3
Hodge, C.N.4
Ru, Y.5
Bacheler, L.T.6
Meek, J.L.7
Otto, M.J.8
Rayner, M.M.9
Wong, Y.N.10
Chang, C.-H.11
Weber, P.C.12
Jackson, D.A.13
Sharpe, T.R.14
Erickson-Viitanen, S.15
-
53
-
-
0028882977
-
A. Pyrrolinone-Based HIV Protease Inhibitors. Design, Synthesis and Antiviral Activity: Evidence for Improved Transport
-
(h) Smith, A. B., III; Hirschmann, R.; Pasternak, A.; Guzman, M. C.; Yokoyama, A.; Sprengeler, P. A.; Darke, P. L.; Emini, E. A.; Schleif, W. A. Pyrrolinone-Based HIV Protease Inhibitors. Design, Synthesis and Antiviral Activity: Evidence for Improved Transport. J. Am. Chem. Soc. 1995, 117, 11113-11123.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 11113-11123
-
-
Smith III, A.B.1
Hirschmann, R.2
Pasternak, A.3
Guzman, M.C.4
Yokoyama, A.5
Sprengeler, P.A.6
Darke, P.L.7
Emini, E.A.8
Schleif, W.9
-
54
-
-
15144359184
-
X-ray Analysis of HIV-1 Protease and Its Complexes with Inhibitors
-
Pearl, L., Ed; Macmillan Press: New York
-
2 Symmetry-Based Diol Inhibitors of HIV-1 Protease. J. Am. Chem. Soc. 1994, 116, 847-855. (e) Smith, A. B., III; Hirschmann, R.; Pasternak, A.; Yao, W. Sprengeler, P. A.; Holloway, M. K.; Kuo, L. C.; Chen, Z.; Darke, P. L.; Schleif, W. A. An Orally Bioavailable Pyrrolinone Inhibitor of HIV-1 Protrease: Computational Analysis and X-ray Crystal Structure of the Enzyme Complex. J. Med. Chem. 1997, 40, 2440-2444.
-
(1990)
Retroviral Proteases: Control of Maturation and Morphogenesis
, pp. 93-106
-
-
Miller, M.1
Swain, A.L.2
Jaskolski, M.3
Sathyanarayana, B.K.4
Marshall, G.R.5
Rich, D.H.6
Kent, S.B.H.7
Wlodawer, A.8
-
55
-
-
0027218692
-
Structure-Based Inhibitors of HIV-1 Protease
-
2 Symmetry-Based Diol Inhibitors of HIV-1 Protease. J. Am. Chem. Soc. 1994, 116, 847-855. (e) Smith, A. B., III; Hirschmann, R.; Pasternak, A.; Yao, W. Sprengeler, P. A.; Holloway, M. K.; Kuo, L. C.; Chen, Z.; Darke, P. L.; Schleif, W. A. An Orally Bioavailable Pyrrolinone Inhibitor of HIV-1 Protrease: Computational Analysis and X-ray Crystal Structure of the Enzyme Complex. J. Med. Chem. 1997, 40, 2440-2444.
-
(1993)
Annu. Rev. Biochem.
, vol.62
, pp. 543-585
-
-
Wlodawer, A.1
Erickson, J.W.2
-
56
-
-
0027411473
-
A Symmetric Inhibitor Binds HIV-1 Protease Asymmetrically
-
2 Symmetry-Based Diol Inhibitors of HIV-1 Protease. J. Am. Chem. Soc. 1994, 116, 847-855. (e) Smith, A. B., III; Hirschmann, R.; Pasternak, A.; Yao, W. Sprengeler, P. A.; Holloway, M. K.; Kuo, L. C.; Chen, Z.; Darke, P. L.; Schleif, W. A. An Orally Bioavailable Pyrrolinone Inhibitor of HIV-1 Protrease: Computational Analysis and X-ray Crystal Structure of the Enzyme Complex. J. Med. Chem. 1997, 40, 2440-2444.
-
(1993)
Biochemistry
, vol.32
, pp. 937-947
-
-
Dreyer, G.B.1
Boehm, J.C.2
Chenera, B.3
Desjarlais, R.L.4
Hassell, A.M.5
Meek, T.D.6
Tomaszek Jr., T.A.7
-
57
-
-
0028328704
-
2 Symmetry-Based Diol Inhibitors of HIV-1 Protease
-
2 Symmetry-Based Diol Inhibitors of HIV-1 Protease. J. Am. Chem. Soc. 1994, 116, 847-855. (e) Smith, A. B., III; Hirschmann, R.; Pasternak, A.; Yao, W. Sprengeler, P. A.; Holloway, M. K.; Kuo, L. C.; Chen, Z.; Darke, P. L.; Schleif, W. A. An Orally Bioavailable Pyrrolinone Inhibitor of HIV-1 Protrease: Computational Analysis and X-ray Crystal Structure of the Enzyme Complex. J. Med. Chem. 1997, 40, 2440-2444.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 847-855
-
-
Hosur, M.V.1
Bhat, T.N.2
Kempf, D.J.3
Baldwin, E.T.4
Liu, B.5
Gulnik, S.6
Wideburg, N.E.7
Norbeck, D.W.8
Appelt, K.9
Erickson, J.W.10
-
58
-
-
0030806489
-
An Orally Bioavailable Pyrrolinone Inhibitor of HIV-1 Protrease: Computational Analysis and X-ray Crystal Structure of the Enzyme Complex
-
2 Symmetry-Based Diol Inhibitors of HIV-1 Protease. J. Am. Chem. Soc. 1994, 116, 847-855. (e) Smith, A. B., III; Hirschmann, R.; Pasternak, A.; Yao, W. Sprengeler, P. A.; Holloway, M. K.; Kuo, L. C.; Chen, Z.; Darke, P. L.; Schleif, W. A. An Orally Bioavailable Pyrrolinone Inhibitor of HIV-1 Protrease: Computational Analysis and X-ray Crystal Structure of the Enzyme Complex. J. Med. Chem. 1997, 40, 2440-2444.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2440-2444
-
-
Smith III, A.B.1
Hirschmann, R.2
Pasternak, A.3
Yao, W.4
Sprengeler, P.A.5
Holloway, M.K.6
Kuo, L.C.7
Chen, Z.8
Darke, P.L.9
Schleif, W.A.10
-
59
-
-
0026460702
-
2-Symmetric Diamino Alcohols and Diols for Use in HIV Protease Inhibitors
-
2-Symmetric Diamino Alcohols and Diols for Use in HIV Protease Inhibitors. J. Org. Chem. 1992, 57, 5692-5700.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5692-5700
-
-
Kempf, D.J.1
Sowin, T.J.2
Doherty, E.M.3
Hannick, S.M.4
Codavoci, L.5
Henry, R.F.6
Green, B.E.7
Spanton, S.G.8
Norbeck, D.W.9
-
60
-
-
0001733040
-
High Enantioselectivity in the Intramolecular Cyclopropanation of Allyl Diazoacetates Using a Novel Rhodium(II) Catalyst
-
(a) Doyle, M. P.; Pieters, R. J.; Martin, S. F.; Austin, R. E.; Oalmann, C. J.; Müller, P. High Enantioselectivity in the Intramolecular Cyclopropanation of Allyl Diazoacetates Using a Novel Rhodium(II) Catalyst. J. Am. Chem. Soc. 1991, 113, 1423-1424.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 1423-1424
-
-
Doyle, M.P.1
Pieters, R.J.2
Martin, S.F.3
Austin, R.E.4
Oalmann, C.J.5
Müller, P.6
-
61
-
-
0001649755
-
Enantio- and Diastereoselectivity in the Intramolecular Cyclopropanation of Secondary Allylic Diazoacetates
-
(b) Martin, S. F.; Spaller, M. R.; Liras, S.; Hartmann, B. Enantio- and Diastereoselectivity in the Intramolecular Cyclopropanation of Secondary Allylic Diazoacetates. J. Am. Chem. Soc. 1994, 116, 4493-4494.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4493-4494
-
-
Martin, S.F.1
Spaller, M.R.2
Liras, S.3
Hartmann, B.4
-
62
-
-
0001080522
-
Enantioselective Intramolecular Cyclopropanations of Allylic and Homoallylic Diazoacetates and Diazoacetamides Using Chiral Dirhodium (II) Carboxamide Catalysts
-
(c) Doyle, M. P.; Austin, R. E.; Bailey, A. S.; Dwyer, M. P.; Dyatkin, A. B.; Kalinin, A. V.; Kwan, M. M. Y.; Liras, S.; Oalmann, C. J.; Pieters, R. J.; Protopopova, M. N.; Raab, C. E.; Roos, G. H. P.; Zhou, Q.-L.; Martin, S. F. Enantioselective Intramolecular Cyclopropanations of Allylic and Homoallylic Diazoacetates and Diazoacetamides Using Chiral Dirhodium (II) Carboxamide Catalysts. J. Am. Chem. Soc. 1995, 117, 5763-5775.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 5763-5775
-
-
Doyle, M.P.1
Austin, R.E.2
Bailey, A.S.3
Dwyer, M.P.4
Dyatkin, A.B.5
Kalinin, A.V.6
Kwan, M.M.Y.7
Liras, S.8
Oalmann, C.J.9
Pieters, R.J.10
Protopopova, M.N.11
Raab, C.E.12
Roos, G.H.P.13
Zhou, Q.-L.14
Martin, S.F.15
-
63
-
-
0000180605
-
Efficient Synthesis and Intramolecular Cyclopropanation of Unsaturated Diazoacetic Esters
-
Corey, E. J.; Myers, A. G. Efficient Synthesis and Intramolecular Cyclopropanation of Unsaturated Diazoacetic Esters. Tetrahedron Lett. 1984, 23, 3559-3562.
-
(1984)
Tetrahedron Lett.
, vol.23
, pp. 3559-3562
-
-
Corey, E.J.1
Myers, A.G.2
-
64
-
-
49349137641
-
A Mild, General Method for Conversion of Esters to Amides
-
(a) Basha, A.; Lipton, M.; Weinreb, S. M. A Mild, General Method for Conversion of Esters to Amides. Tetrahedron Lett. 1977, 4171-4174.
-
(1977)
Tetrahedron Lett
, pp. 4171-4174
-
-
Basha, A.1
Lipton, M.2
Weinreb, S.M.3
-
65
-
-
21144468068
-
Chemistry of AT-Methoxy-TV-Methylamides. Application in Synthesis. A Review
-
(b) Sibi, M. P. Chemistry of AT-Methoxy-TV-Methylamides. Application in Synthesis. A Review. Org. Prep. Proc. Int. 1993, 25, 15-40.
-
(1993)
Org. Prep. Proc. Int.
, vol.25
, pp. 15-40
-
-
Sibi, M.P.1
-
66
-
-
15144342495
-
-
This mixture of 18c and 20 could not be readily separated, but the corresponding carboxylic acids could be easily separated by flash chromatography
-
This mixture of 18c and 20 could not be readily separated, but the corresponding carboxylic acids could be easily separated by flash chromatography.
-
-
-
-
67
-
-
85006911915
-
A Theorem Relating Cross Relaxation and Hartmann-Hahn Transfer in Multiple-Pulse Sequences. Optimal Suppression of TOCSY Transfer in ROESY
-
Schleucher, J.; Quant, J.; Glaser, S. J.; Griesinger, C. A Theorem Relating Cross Relaxation and Hartmann-Hahn Transfer in Multiple-Pulse Sequences. Optimal Suppression of TOCSY Transfer in ROESY. J. Magn. Reson. A 1995, 112, 144-151.
-
(1995)
J. Magn. Reson. A
, vol.112
, pp. 144-151
-
-
Schleucher, J.1
Quant, J.2
Glaser, S.J.3
Griesinger, C.4
-
68
-
-
33646746207
-
Scalar Coupling Constants- Their Analysis and Their Application for the Elucidation of Structures
-
Eberstadt, M; Gemmecker, G.; Mierke, D. F.; Kessler, H. Scalar Coupling Constants- Their Analysis and Their Application for the Elucidation of Structures. Angew. Chem., Int. Ed. Engl. 1995, 34, 1671-1695.
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 1671-1695
-
-
Eberstadt, M.1
Gemmecker, G.2
Mierke, D.F.3
Kessler, H.4
-
69
-
-
0025613125
-
Motional Properties of Acyl Carrier Protein: Effects on NMR Structural Data
-
Kim Y.; Prestegard, J. H. Motional Properties of Acyl Carrier Protein: Effects on NMR Structural Data. Proteins Struct. Fund. Genet. 1990, 8, 377-385.
-
(1990)
Proteins Struct. Fund. Genet.
, vol.8
, pp. 377-385
-
-
Kim, Y.1
Prestegard, J.H.2
-
70
-
-
0027626054
-
Improved Molecular Dynamics Simulations for the Determination of Peptide Structures
-
Mierke, D. F.; Kessler, H. Improved Molecular Dynamics Simulations for the Determination of Peptide Structures. Biopolymers 1993, 33, 1003-1017.
-
(1993)
Biopolymers
, vol.33
, pp. 1003-1017
-
-
Mierke, D.F.1
Kessler, H.2
-
71
-
-
0026939435
-
Combined Use of Homo- and Heteronuclear Coupling Constants as Restraints in Molecular Dynamics Simulations
-
Mierke, D. F.; Kessler, H. Combined Use of Homo- and Heteronuclear Coupling Constants as Restraints in Molecular Dynamics Simulations. Biopolymers 1992, 32, 1277-1282.
-
(1992)
Biopolymers
, vol.32
, pp. 1277-1282
-
-
Mierke, D.F.1
Kessler, H.2
-
73
-
-
0021095743
-
Sequential Resonance Assignments in Protein Proton Nuclear Magnetic Resonanace Spectra. Computation of Sterically Allowed Proton-Proton Distances and Statistical Analysis of Proton-Proton Distances in Single-Crystal Protein Conformations
-
Wüthrich, K.; Billeter, M.; Braun, W. Sequential Resonance Assignments in Protein Proton Nuclear Magnetic Resonanace Spectra. Computation of Sterically Allowed Proton-Proton Distances and Statistical Analysis of Proton-Proton Distances in Single-Crystal Protein Conformations. J. Mol. Biol. 1983, 169, 946-961.
-
(1983)
J. Mol. Biol.
, vol.169
, pp. 946-961
-
-
Wüthrich, K.1
Billeter, M.2
Braun, W.3
-
74
-
-
0003176324
-
-
Grant, D. M., Harris, R. K., Eds.; John Wiley & Sons: Chichester, England
-
Kessler, H.; Schmitt, W. in Encyclopedia of Nuclear Magnetic Resonance; Grant, D. M., Harris, R. K., Eds.; John Wiley & Sons: Chichester, England, 1996; Vol. 6, pp 3527-3537.
-
(1996)
Encyclopedia of Nuclear Magnetic Resonance
, vol.6
, pp. 3527-3537
-
-
Kessler, H.1
Schmitt, W.2
-
75
-
-
49749206569
-
Nuclear Magnetic Resonance (NMR) Study of Some α-Amino Acids. I. Coupling Constants in Alkaline and Acid Medium
-
(a) Pachler, K. G. R. Nuclear Magnetic Resonance (NMR) Study of Some α-Amino Acids. I. Coupling Constants in Alkaline and Acid Medium. Spektochim. Acta 1963, 19, 2085-2092.
-
(1963)
Spektochim. Acta
, vol.19
, pp. 2085-2092
-
-
Pachler, K.G.R.1
-
76
-
-
4243567363
-
Nuclear Magnetic Resonance Study of Some α-Amino Acids. II. Rotational Isomerism
-
(b) Pachler, K. G. R. Nuclear Magnetic Resonance Study of Some α-Amino Acids. II. Rotational Isomerism. Spektochim. Acta 1964, 20, 581-587.
-
(1964)
Spektochim. Acta
, vol.20
, pp. 581-587
-
-
Pachler, K.G.R.1
-
78
-
-
0000189651
-
Universality in the Peroxidase-Oxidase Reaction: Period Doublings, Chaos, Period Three, and Unstable Limit Cycles
-
Becke, A. D. Universality in the Peroxidase-Oxidase Reaction: Period Doublings, Chaos, Period Three, and Unstable Limit Cycles. J. Phys. Chem. 1993, 98, 5648-5642.
-
(1993)
J. Phys. Chem.
, vol.98
, pp. 5648-15642
-
-
Becke, A.D.1
-
79
-
-
0345491105
-
Various Functionals for the Kinetic Energy Density of an Atom or Molecule
-
Lee, C.; Yang, W.; Parr, R. G. Various Functionals for the Kinetic Energy Density of an Atom or Molecule. Phys. Rev. 1988, B37, 785-789.
-
(1988)
Phys. Rev.
, vol.B37
, pp. 785-789
-
-
Lee, C.1
Yang, W.2
Parr, R.G.3
-
80
-
-
0029644939
-
Structure of HIV-1 Protease with KN-272, a Tight Binding Allophenylnorstatine
-
Baldwin, E. T.; Bhat, T. N.; Gulnik, S. V.; Liu, B.; Topol, I. A.; Kiso, Y.; Mimoto, T.; Mitsuya, H.; Erickson, J. W. Structure of HIV-1 Protease with KN-272, a Tight Binding Allophenylnorstatine. Structure 1995, 3, 581-590.
-
(1995)
Structure
, vol.3
, pp. 581-590
-
-
Baldwin, E.T.1
Bhat, T.N.2
Gulnik, S.V.3
Liu, B.4
Topol, I.A.5
Kiso, Y.6
Mimoto, T.7
Mitsuya, H.8
Erickson, J.W.9
-
81
-
-
0029782278
-
Solution Conformations of KNI272, a Tripeptide HIV Protease Inhibitor Designed on the Basis of Substrate Transition State: Determinated by NMR Spectroscopy and Simulated Annealing Calculations
-
Ohno, Y.; Kiso, Y.; Kobayashi, Y. Solution Conformations of KNI272, a Tripeptide HIV Protease Inhibitor Designed on the Basis of Substrate Transition State: Determinated by NMR Spectroscopy and Simulated Annealing Calculations. Bioorg. Med. Chem. 1996, 4, 1565-1572.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1565-1572
-
-
Ohno, Y.1
Kiso, Y.2
Kobayashi, Y.3
-
82
-
-
0343672469
-
C-Glucoside Durch Direkte 1-CLithiierung von 2-Phenylsulfmyl Aktiviertem D-Glucal. (C-Glycosides from Direct C(1)-Lithiation of 2-Phenylsulfinyl Activated D-Glucals.)
-
Preuss, R.; Schmidt, R. R. C-Glucoside Durch Direkte 1-CLithiierung von 2-Phenylsulfmyl Aktiviertem D-Glucal. (C-Glycosides from Direct C(1)-Lithiation of 2-Phenylsulfinyl Activated D-Glucals.) Liebigs Ann. Chem. 1989, 429-434.
-
(1989)
Liebigs Ann. Chem.
, pp. 429-434
-
-
Preuss, R.1
Schmidt, R.R.2
-
83
-
-
37049098093
-
Rotational Isomerism in 2,3-Dinitro-2,3-dimethylbutane
-
Tan, B.; Chia, L. H. L.; Huang, H.; Kuok, M.; Tang, S. Rotational Isomerism in 2,3-Dinitro-2,3-dimethylbutane. J. Chem. Soc., Perkin Trans. 1984, 2, 1407-1415.
-
(1984)
J. Chem. Soc., Perkin Trans.
, vol.2
, pp. 1407-1415
-
-
Tan, B.1
Chia, L.H.L.2
Huang, H.3
Kuok, M.4
Tang, S.5
-
84
-
-
15144350006
-
-
unpublished results
-
Topol, I. A., unpublished results.
-
-
-
Topol, I.A.1
-
85
-
-
0000662936
-
Bonding Properties of Cyclopropane and Their Chemical Consequences
-
(a) de Meijere, A. Bonding Properties of Cyclopropane and Their Chemical Consequences. Angew. Chem., Int. Ed. Eng. 1979, 18, 809-826.
-
(1979)
Angew. Chem., Int. Ed. Eng.
, vol.18
, pp. 809-826
-
-
De Meijere, A.1
-
86
-
-
0006074021
-
Cyclopropyl Conjugation in Olefinic Esters. Conformational Effects on Ultraviolet Absorption
-
(b) Jorgenson, M. J.; Leung, T. Cyclopropyl Conjugation in Olefinic Esters. Conformational Effects on Ultraviolet Absorption. J. Am. Chem. Soc. 1968, 90, 3769-3774.
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 3769-3774
-
-
Jorgenson, M.J.1
Leung, T.2
-
87
-
-
0026640040
-
Flexible Molecules with Defined Shape-Conformational Design
-
Hoffmann, R. W. Flexible Molecules with Defined Shape-Conformational Design. Angew. Chem., Int. Ed. Engl. 1992, 31, 1124-1134.
-
(1992)
Angew. Chem., Int. Ed. Engl.
, vol.31
, pp. 1124-1134
-
-
Hoffmann, R.W.1
-
88
-
-
0028483655
-
Crystal-Structure of a Tethered Dimer of HIV-1 Proteinase Complexed with an Inhibitor
-
Bhat, T. N.; Baldwin, E. T.; Liu, B.; Cheng, Y.-S. E.; Erickson, J. W. Crystal-Structure of a Tethered Dimer of HIV-1 Proteinase Complexed with an Inhibitor. Nat. Struct. Biol. 1994, 1, 552-556.
-
(1994)
Nat. Struct. Biol.
, vol.1
, pp. 552-556
-
-
Bhat, T.N.1
Baldwin, E.T.2
Liu, B.3
Cheng, Y.-S.E.4
Erickson, J.W.5
-
89
-
-
0029151345
-
Kinetic Characterization and Cross-Resistance Patterns of HIV-1 Protease Mutants Selected under Drug Pressure
-
Gulnik, S. V.; Suvorov, L. I.; Liu, B.; Anderson, B.; Mitsuya, H., Erickson, J. W. Kinetic Characterization and Cross-Resistance Patterns of HIV-1 Protease Mutants Selected under Drug Pressure. Biochemistry 1995, 34, 9282-9287.
-
(1995)
Biochemistry
, vol.34
, pp. 9282-9287
-
-
Gulnik, S.V.1
Suvorov, L.I.2
Liu, B.3
Anderson, B.4
Mitsuya, H.5
Erickson, J.W.6
-
90
-
-
0027474739
-
Invitro Anti-Human-Immunodeficiency-Virus (HIV) Activities of Transition-State HIV Protease Inhibitors Containing Allophenylnorstatine
-
Kageyama, S.; Mimoto, T.; Murakawa, Y.; Nomizu, M.; Ford, H., Jr.; Shirasaka, T.; Gulnik, S.; Erickson, J.; Takada, K.; Hayashi, H.; Broder, S.; Kiso, Y.; Mitsuya, H. Invitro Anti-Human-Immunodeficiency-Virus (HIV) Activities of Transition-State HIV Protease Inhibitors Containing Allophenylnorstatine. Antimicrob. Agents Chemother. 1993, 37, 810-817.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 810-817
-
-
Kageyama, S.1
Mimoto, T.2
Murakawa, Y.3
Nomizu, M.4
Ford Jr., H.5
Shirasaka, T.6
Gulnik, S.7
Erickson, J.8
Takada, K.9
Hayashi, H.10
Broder, S.11
Kiso, Y.12
Mitsuya, H.13
-
91
-
-
84990113699
-
Two-Dimensional NMR Spectroscopy: Background and Overview of the Experiments
-
Kessler, H.; Gehrke, M.; Griesinger, C. Two-Dimensional NMR Spectroscopy: Background and Overview of the Experiments. Angew. Chem., Int. Ed. Engl. 1988, 27, 490-536.
-
(1988)
Angew. Chem., Int. Ed. Engl.
, vol.27
, pp. 490-536
-
-
Kessler, H.1
Gehrke, M.2
Griesinger, C.3
-
93
-
-
0001240703
-
Frequency Offset Effects and Their Elimination in NMR Rotating-Frame Cross-Relaxation Spectroscopy
-
Griesinger, C.; Ernst, R. R. Frequency Offset Effects and Their Elimination in NMR Rotating-Frame Cross-Relaxation Spectroscopy. J. Magn. Reson. 1987, 75, 261-271.
-
(1987)
J. Magn. Reson.
, vol.75
, pp. 261-271
-
-
Griesinger, C.1
Ernst, R.R.2
-
94
-
-
0025252231
-
Heteronuclear Filters in Two-Dimensional [Proton-Proton ]-NMR Spectroscopy: Combined Use with Isotope Labelling for Studies of Macromolecular Conformation and Intermolecular Interactions
-
Otting, G.; Wüthrich, K. Heteronuclear Filters in Two-Dimensional [Proton-Proton ]-NMR Spectroscopy: Combined Use with Isotope Labelling for Studies of Macromolecular Conformation and Intermolecular Interactions. Q. Rev. Biophys. 1990, 23, 39-96.
-
(1990)
Q. Rev. Biophys.
, vol.23
, pp. 39-96
-
-
Otting, G.1
Wüthrich, K.2
-
95
-
-
45249128810
-
Measurement of Vicinal Couplings from Cross Peaks in COSY Spectra
-
Kim, Y.; Prestegard, J. H. Measurement of Vicinal Couplings from Cross Peaks in COSY Spectra. J. Magn. Reson. 1989, 84, 9-13.
-
(1989)
J. Magn. Reson.
, vol.84
, pp. 9-13
-
-
Kim, Y.1
Prestegard, J.H.2
-
96
-
-
0000960167
-
A Convenient Technique for the Measurement and Assignment of Long-Range Carbon-13 Proton Coupling Constants
-
Keeler, J.; Neuhaus, D.; Titman J. J. A Convenient Technique for the Measurement and Assignment of Long-Range Carbon-13 Proton Coupling Constants. J. Chem. Phys. 1988, 146, 545-548.
-
(1988)
J. Chem. Phys.
, vol.146
, pp. 545-548
-
-
Keeler, J.1
Neuhaus, D.2
Titman, J.J.3
-
97
-
-
6344256147
-
Consistent Force Field Studies on Intramolecular Forces in Hydrogen-Bonded Crystals. 2. A Benchmark for the Objective Comparison of Alternative Force Fields
-
(a) Hagler, A. T.; Lifson, S.; Dauber, P. Consistent Force Field Studies on Intramolecular Forces in Hydrogen-Bonded Crystals. 2. A Benchmark for the Objective Comparison of Alternative Force Fields. J. Am. Chem. Soc. 1979, 101, 5122-5130.
-
(1979)
J. Am. Chem. Soc.
, vol.101
, pp. 5122-5130
-
-
Hagler, A.T.1
Lifson, S.2
Dauber, P.3
-
98
-
-
0003841205
-
-
Biosym Technologies, 10065 Barnes Canyon Road, San Diego, CA 92121, USA
-
(b) DISCOVER Version 95.0, Biosym Technologies, 10065 Barnes Canyon Road, San Diego, CA 92121, USA.
-
DISCOVER Version 95.0
-
-
-
99
-
-
4243876410
-
Structure of Two Cyclopropane Derivatives: Cis-and trans-Caronic Acid
-
Jessen, S. M. Structure of Two Cyclopropane Derivatives: cis-and trans-Caronic Acid. Acta Crystallogr., C 1992, 48, 106-116.
-
(1992)
Acta Crystallogr., C
, vol.48
, pp. 106-116
-
-
Jessen, S.M.1
-
100
-
-
0000961089
-
Theoretical Determination of Molecular Structure and Conformation. 20. Reevaluation of the Strain Energies of Cyclopropane and Cyclobutane-CC and CH Bond Energies, 1,3 Interactions, and σ-Aromticity
-
(a) Cremer, D.; Gauss, J. Theoretical Determination of Molecular Structure and Conformation. 20. Reevaluation of the Strain Energies of Cyclopropane and Cyclobutane-CC and CH Bond Energies, 1,3 Interactions, and σ-Aromticity. J. Am. Chem. Soc. 1986, 108, 7467-7477.
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 7467-7477
-
-
Cremer, D.1
Gauss, J.2
-
101
-
-
33845379593
-
Theoretical Determination of Molecular Structure and Conformation. 16. Substituted Cyclopropanes-An Electron Density Model of Substituent-Ring Interactions
-
(b) Cremer, D.; Gauss, J. Theoretical Determination of Molecular Structure and Conformation. 16. Substituted Cyclopropanes-An Electron Density Model of Substituent-Ring Interactions. J. Am. Chem. Soc. 1985, 107, 3811-3819.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 3811-3819
-
-
Cremer, D.1
Gauss, J.2
-
102
-
-
49349130990
-
Spin-Spin Coupling and the Conformational States of Peptide Systems
-
(a) Bystrov, V. F. Spin-Spin Coupling and the Conformational States of Peptide Systems. Prog. Nucl. Magn. Reson. Spectrosc. 1976, 10, 41-81.
-
(1976)
Prog. Nucl. Magn. Reson. Spectrosc.
, vol.10
, pp. 41-81
-
-
Bystrov, V.F.1
-
103
-
-
0001669510
-
Peptide Conformations. 42. Conformation of Side Chains in Peptides Using Heteronuclear Coupling Constants Obtained by Two-Dimensional NMR Spectroscopy
-
(b) Kessler, H.; Griesinger, C.; Wagner, K. Peptide Conformations. 42. Conformation of Side Chains in Peptides Using Heteronuclear Coupling Constants Obtained by Two-Dimensional NMR Spectroscopy. J. Am. Chem. Soc. 1987, 109, 6927-6933.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 6927-6933
-
-
Kessler, H.1
Griesinger, C.2
Wagner, K.3
-
104
-
-
0001501991
-
15N-Enriched Human Ubiquitin
-
15N-Enriched Human Ubiquitin. J. Am. Chem. Soc. 1995, 117, 1810-1813.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 1810-1813
-
-
Wang, A.C.1
Bax, A.2
-
105
-
-
0029879363
-
Determination of the Backbone Dihedral Angles ø in Human Ubiquitin from Reparameterixed Emperical Karplus Equations
-
(d) Wang, A. C.; Bax, A. Determination of the Backbone Dihedral Angles ø in Human Ubiquitin from Reparameterixed Emperical Karplus Equations. J. Am. Chem. Soc. 1996, 118, 2483-2494.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 2483-2494
-
-
Wang, A.C.1
Bax, A.2
-
106
-
-
0001425970
-
Molecular Dynamics with Dimethyl Sulfoxide as a Solvent. Conformation of a Cyclic Hexapeptide
-
Mierke, D. F.; Kessler, H. Molecular Dynamics with Dimethyl Sulfoxide as a Solvent. Conformation of a Cyclic Hexapeptide. J. Am. Chem. Soc. 1991, 113, 9466-9470.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 9466-9470
-
-
Mierke, D.F.1
Kessler, H.2
-
107
-
-
0026751476
-
Conformation of Cyclic Analogues of Substance P: NMR and Molecular Dynamics in Dimethyl Sulfoxide
-
Saulitis, J.; Mierke, D. F.; Byk, G.; Gilon, C.; Kessler, H. Conformation of Cyclic Analogues of Substance P: NMR and Molecular Dynamics in Dimethyl Sulfoxide. J. Am. Chem. Soc. 1992, 114, 4818-4827.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 4818-4827
-
-
Saulitis, J.1
Mierke, D.F.2
Byk, G.3
Gilon, C.4
Kessler, H.5
-
108
-
-
0028128838
-
A Novel Nonpeptide HIV-1 Protease Inhibitor: Elucidation of the Binding Mode and Its Application in the Design of Related Analogs
-
Lunney, E. A.; Hagen, S. E. Domagala, J. M.; Humblet, C.; Kosinski, J.; Tait, B. D.; Warmus, J. S.; Wilson, M.; Ferguson, D.; Hupe, D.; Tummino, P. J.; Baldwin, E. T.; Bhat, T. N.; Liu, B.; Erickson, J. W. A Novel Nonpeptide HIV-1 Protease Inhibitor: Elucidation of the Binding Mode and Its Application in the Design of Related Analogs. J. Med. Chem. 1994, 37, 2664-2677.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2664-2677
-
-
Lunney, E.A.1
Hagen, S.E.2
Domagala, J.M.3
Humblet, C.4
Kosinski, J.5
Tait, B.D.6
Warmus, J.S.7
Wilson, M.8
Ferguson, D.9
Hupe, D.10
Tummino, P.J.11
Baldwin, E.T.12
Bhat, T.N.13
Liu, B.14
Erickson, J.W.15
-
109
-
-
0027520575
-
Aspects of Protein Energetics and Dynamics
-
Rashin, A. A. Aspects of Protein Energetics and Dynamics. Prog. Biophys. Mol. Biol. 1993, 70, 73-200.
-
(1993)
Prog. Biophys. Mol. Biol.
, vol.70
, pp. 73-200
-
-
Rashin, A.A.1
|