-
2
-
-
0007430054
-
The Electron-Conformational Method of Identification of Pharmacophore and Anti-Pharmacophore Shielding
-
Guner, O. F., Ed.; International University Line: La Jolla
-
Bersuker, I. B.; Bahceci, S.; Boggs, E. J. The Electron-Conformational Method of Identification of Pharmacophore and Anti-Pharmacophore Shielding. In Pharmacophore Perception, Development, and Use in Drug Design; Guner, O. F., Ed.; International University Line: La Jolla, 2000; pp 457-474.
-
(2000)
Pharmacophore Perception, Development, and use in Drug Design
, pp. 457-474
-
-
Bersuker, I.B.1
Bahceci, S.2
Boggs, E.J.3
-
3
-
-
0032790242
-
An Electron-Conformational Method of Identification of Pharmacophore and Anti-Pharmacophore Shielding: Application to Rice Blast Activity
-
Bersuker, I. B.; Bahceci, S.; Boggs, E. J.; Pearlman, R. S. An Electron-Conformational Method of Identification of Pharmacophore and Anti-Pharmacophore Shielding: Application to Rice Blast Activity. J. Comput.-Aided Mol. Des. 1999, 13, 419-434.
-
(1999)
J. Comput.-Aided Mol. Des.
, vol.13
, pp. 419-434
-
-
Bersuker, I.B.1
Bahceci, S.2
Boggs, E.J.3
Pearlman, R.S.4
-
4
-
-
0000459233
-
A Novel Electron-Conformational Approach to Molecular Modeling for QSAR by Identification of Pharmacophore and Anti-Pharmacophore Shielding
-
Bersuker, I. B.; Bahceci, S.; Boggs, E. J.; Pearlman, R. S. A Novel Electron-Conformational Approach to Molecular Modeling for QSAR by Identification of Pharmacophore and Anti-Pharmacophore Shielding. SAR QSAR Environ. Res. 1999, 10, 157-173.
-
(1999)
SAR QSAR Environ. Res.
, vol.10
, pp. 157-173
-
-
Bersuker, I.B.1
Bahceci, S.2
Boggs, E.J.3
Pearlman, R.S.4
-
5
-
-
0000981103
-
The Electron-Topological Approach to the QSAR Problem
-
Lipkowitz, K. B., Boyd, D. B., Eds.; VCH: New York
-
Bersuker, I. B.; Dimoglo, A. S. The Electron-Topological Approach to the QSAR Problem. In Reviews in Computational Chemistry; Lipkowitz, K. B., Boyd, D. B., Eds.; VCH: New York, 1991; Vol. 2, pp 423-460.
-
(1991)
Reviews in Computational Chemistry
, vol.2
, pp. 423-460
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
-
6
-
-
0000128455
-
Origin of Musk Fragrance Activity: The Electron-Topological Approach
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachev, M. Yu.; Vlad, P. F.; Pesaro, M. Origin of Musk Fragrance Activity: The Electron-Topological Approach. New J. Chem. 1991, 15, 307-320.
-
(1991)
New J. Chem.
, vol.15
, pp. 307-320
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
Gorbachev, M.Yu.3
Vlad, P.F.4
Pesaro, M.5
-
7
-
-
84984420123
-
Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461- 473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron- Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1989)
Nahrung-Food
, vol.33
, pp. 405-411
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
Gorbachov, M.Yu.3
Greni, A.I.4
Vysotskaya, L.E.5
Mikhailova, T.V.6
-
8
-
-
84984427220
-
Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461-473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron- Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1988)
Nahrung-Food
, vol.32
, pp. 461-473
-
-
Dimoglo, A.S.1
Gorbachov, M.Yu.2
Bersuker, I.B.3
Greni, A.I.4
Vysotskaya, L.E.5
Stepanova, O.V.6
Lukash, E.Yu.7
-
9
-
-
84984420123
-
The Electron-Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin
-
Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461- 473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1987)
QSAR in Drug Design and Toxicology
, vol.10
, pp. 43-48
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
Gorbachov, M.Yu.3
-
10
-
-
84984420123
-
Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem
-
Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461- 473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron- Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1987)
QSAR in Drug Design and Taxciology
, vol.10
, pp. 340-342
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
Gorbachov, M.Yu.3
Vlad, P.F.4
Koltsa, M.N.5
-
11
-
-
84984420123
-
The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461- 473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron- Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1987)
Bioorgan. Khim.
, vol.13
, pp. 38-44
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
Gorbachov, M.Yu.3
-
12
-
-
84984420123
-
Electron-Topology of Garlic's Biologically Active Thioallyl Compounds
-
Washington, DC
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461- 473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron- Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1990)
First World Congress on the Health Significance of Garlic and Garlic Constituents
-
-
Bersuker, I.B.1
Dimoglo, A.S.2
-
13
-
-
84984420123
-
Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid
-
Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Greni, A. I.; Vysotskaya, L. E.; Mikhailova, T. V. Study of the Electronic and Structural Properties of the Chemical Compounds in Garlic Aroma. Nahrung-Food 1989, 33, 405-411. Dimoglo, A. S.; Gorbachov, M. Yu.; Bersuker, I. B.; Greni, A. I.; Vysotskaya, L. E.; Stepanova, O. V.; Lukash, E. Yu. Structural and Electronic Origin of Meat Odour of Organic Hetero-Atomic Compounds. Nahrung-Food 1988, 32, 461- 473. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron- Topologic Approach to the QSAR Problem Illustrated by Inhibitor Activity for Thymidine Phosphorylase and α-Chymo-Trypsin. In QSAR in Drug Design and Toxicology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 43-48. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu.; Vlad, P. F.; Koltsa, M. N. Structural and Electronic Origin of Odour Properties of Organic Compounds as Revealed by the Electron-Topologic Approach to the QSAR Problem. In QSAR in Drug Design and Taxciology; Hadzi, D., Jerman-Blazic, B., Eds.; Elsevier: Amsterdam, 1987; Vol. 10, pp 340-342. Bersuker, I. B.; Dimoglo, A. S.; Gorbachov, M. Yu. The Electron-Topologic Approach to Structure-Activity Relationships. Inhibition of Thymidine Phosphorylase by Uracil Derivatives. Bioorgan. Khim. 1987, 13, 38-44. Bersuker I. B.; Dimoglo, A. S. Electron-Topology of Garlic's Biologically Active Thioallyl Compounds. In First World Congress on the Health Significance of Garlic and Garlic Constituents; Washington, DC, 1990. Dimoglo, A. S.; Bersuker, I. B.; Popa, D. P.; Kuchkova, K. I. Electron-Topological Study of Plant Growth-Regulator Activity in a Series of Analogs of Abscisic Acid. Theor. Eksp. Khim. 1989, 5, 590.
-
(1989)
Theor. Eksp. Khim.
, vol.5
, pp. 590
-
-
Dimoglo, A.S.1
Bersuker, I.B.2
Popa, D.P.3
Kuchkova, K.I.4
-
14
-
-
0008680532
-
Electron-Topological (ET) Investigation of Structure-Antagonist Activity of a Series of dibenzo-[a,d]cycloalkenimines
-
Guzel, Y.; Saripinar, E.; Yildirim, I. Electron-Topological (ET) Investigation of Structure-Antagonist Activity of a Series of dibenzo-[a,d]cycloalkenimines. J. Mol. Struct. (THEOCHEM) 1997, 418, 83-91. Guzel, Y. Investigation of the Relationship Between the Inhibitory Activity of Glycolic Acid Oxidase and its Chemical Structure: Electron-Topological Approach. J. Mol. Struct. (THEOCHEM) 1996, 366, 131-137 . Dimoglo, A. S.; Beda, A. A.; Shvets, N. M.; Gorbachov, M. Yu.; Kheifits, L. A.; Aulchenko, I. S. Investigation of the Relationship Between Sandalwood Odor and Chemical Structure: Electron-Topological Approach. New. J. Chem. 1995, 19, 149-154. Dimoglo, A. S.; Vlad, P. F.; Shvets, N. M.; Koltsa, M. N.; Guzel, Y.; Saracoglu, M.; Saripinar, E.; Patat, S. Electron-Topological Investigations of the Relationship Between Chemical Structure and Ambergris Odor. New J. Chem. 1995, 19, 1217-1226.
-
(1997)
J. Mol. Struct. (THEOCHEM)
, vol.418
, pp. 83-91
-
-
Guzel, Y.1
Saripinar, E.2
Yildirim, I.3
-
15
-
-
0001668137
-
Investigation of the Relationship between the Inhibitory Activity of Glycolic Acid Oxidase and its Chemical Structure: Electron-Topological Approach
-
Guzel, Y.; Saripinar, E.; Yildirim, I. Electron-Topological (ET) Investigation of Structure-Antagonist Activity of a Series of dibenzo- [a,d]cycloalkenimines. J. Mol. Struct. (THEOCHEM) 1997, 418, 83- 91. Guzel, Y. Investigation of the Relationship Between the Inhibitory Activity of Glycolic Acid Oxidase and its Chemical Structure: Electron-Topological Approach. J. Mol. Struct. (THEOCHEM) 1996, 366, 131-137 . Dimoglo, A. S.; Beda, A. A.; Shvets, N. M.; Gorbachov, M. Yu.; Kheifits, L. A.; Aulchenko, I. S. Investigation of the Relationship Between Sandalwood Odor and Chemical Structure: Electron-Topological Approach. New. J. Chem. 1995, 19, 149-154. Dimoglo, A. S.; Vlad, P. F.; Shvets, N. M.; Koltsa, M. N.; Guzel, Y.; Saracoglu, M.; Saripinar, E.; Patat, S. Electron-Topological Investigations of the Relationship Between Chemical Structure and Ambergris Odor. New J. Chem. 1995, 19, 1217-1226.
-
(1996)
J. Mol. Struct. (THEOCHEM)
, vol.366
, pp. 131-137
-
-
Guzel, Y.1
-
16
-
-
0008680532
-
Investigation of the Relationship between Sandalwood Odor and Chemical Structure: Electron-Topological Approach
-
Guzel, Y.; Saripinar, E.; Yildirim, I. Electron-Topological (ET) Investigation of Structure-Antagonist Activity of a Series of dibenzo- [a,d]cycloalkenimines. J. Mol. Struct. (THEOCHEM) 1997, 418, 83- 91. Guzel, Y. Investigation of the Relationship Between the Inhibitory Activity of Glycolic Acid Oxidase and its Chemical Structure: Electron-Topological Approach. J. Mol. Struct. (THEOCHEM) 1996, 366, 131-137 . Dimoglo, A. S.; Beda, A. A.; Shvets, N. M.; Gorbachov, M. Yu.; Kheifits, L. A.; Aulchenko, I. S. Investigation of the Relationship Between Sandalwood Odor and Chemical Structure: Electron-Topological Approach. New. J. Chem. 1995, 19, 149-154. Dimoglo, A. S.; Vlad, P. F.; Shvets, N. M.; Koltsa, M. N.; Guzel, Y.; Saracoglu, M.; Saripinar, E.; Patat, S. Electron-Topological Investigations of the Relationship Between Chemical Structure and Ambergris Odor. New J. Chem. 1995, 19, 1217-1226.
-
(1995)
New. J. Chem.
, vol.19
, pp. 149-154
-
-
Dimoglo, A.S.1
Beda, A.A.2
Shvets, N.M.3
Gorbachov, M.Yu.4
Kheifits, L.A.5
Aulchenko, I.S.6
-
17
-
-
0008680532
-
Electron-Topological Investigations of the Relationship between Chemical Structure and Ambergris Odor
-
Guzel, Y.; Saripinar, E.; Yildirim, I. Electron-Topological (ET) Investigation of Structure-Antagonist Activity of a Series of dibenzo- [a,d]cycloalkenimines. J. Mol. Struct. (THEOCHEM) 1997, 418, 83- 91. Guzel, Y. Investigation of the Relationship Between the Inhibitory Activity of Glycolic Acid Oxidase and its Chemical Structure: Electron-Topological Approach. J. Mol. Struct. (THEOCHEM) 1996, 366, 131-137 . Dimoglo, A. S.; Beda, A. A.; Shvets, N. M.; Gorbachov, M. Yu.; Kheifits, L. A.; Aulchenko, I. S. Investigation of the Relationship Between Sandalwood Odor and Chemical Structure: Electron-Topological Approach. New. J. Chem. 1995, 19, 149-154. Dimoglo, A. S.; Vlad, P. F.; Shvets, N. M.; Koltsa, M. N.; Guzel, Y.; Saracoglu, M.; Saripinar, E.; Patat, S. Electron-Topological Investigations of the Relationship Between Chemical Structure and Ambergris Odor. New J. Chem. 1995, 19, 1217-1226.
-
(1995)
New J. Chem.
, vol.19
, pp. 1217-1226
-
-
Dimoglo, A.S.1
Vlad, P.F.2
Shvets, N.M.3
Koltsa, M.N.4
Guzel, Y.5
Saracoglu, M.6
Saripinar, E.7
Patat, S.8
-
18
-
-
0004119863
-
-
Springer-Verlag: Berlin
-
Fukui, K. Theory of Orientation and Stereoselection; Springer-Verlag: Berlin, 1975. Klopman, G. The Generalized Perturbation Theory of Chemical Reactivity and its Applications. In Chemical Reactivity and Reaction Paths; Klopman, G., Ed.; Wiley: New York, 1974; pp 55-165.
-
(1975)
Theory of Orientation and Stereoselection
-
-
Fukui, K.1
-
19
-
-
0001901709
-
The Generalized Perturbation Theory of Chemical Reactivity and its Applications
-
Klopman, G., Ed.; Wiley: New York
-
Fukui, K. Theory of Orientation and Stereoselection; Springer- Verlag: Berlin, 1975. Klopman, G. The Generalized Perturbation Theory of Chemical Reactivity and its Applications. In Chemical Reactivity and Reaction Paths; Klopman, G., Ed.; Wiley: New York, 1974; pp 55-165.
-
(1974)
Chemical Reactivity and Reaction Paths
, pp. 55-165
-
-
Klopman, G.1
-
21
-
-
0002379892
-
3D Molecular Structures: Generation and Use in 3D Searching
-
Kubinyi, H., Ed.; ESCOM: Leiden
-
Pearlman, R. S. 3D Molecular Structures: Generation and Use in 3D Searching. In 3D QSAR in Drug Design: Theory, Methods and Application; Kubinyi, H., Ed.; ESCOM: Leiden, 1993; Vol. 1, pp 41-79.
-
(1993)
3D QSAR in Drug Design: Theory, Methods and Application
, vol.1
, pp. 41-79
-
-
Pearlman, R.S.1
-
24
-
-
0003876179
-
-
Mathworks, Inc.
-
MATLAB, Version 5.3; Mathworks, Inc., 1999.
-
(1999)
MATLAB, Version 5.3
-
-
-
26
-
-
0033193464
-
Automated Pharmacophore Identification for Large Chemical Data Sets
-
Chen, X.; Rusinko, A. III; Tropsha, A.; Young, S. S. Automated Pharmacophore Identification for Large Chemical Data Sets. J. Chem. Inf. Comput. Sci. 1999, 39, 887-896.
-
(1999)
J. Chem. Inf. Comput. Sci.
, vol.39
, pp. 887-896
-
-
Chen, X.1
Rusinko A. III2
Tropsha, A.3
Young, S.S.4
-
27
-
-
0042683908
-
Computer-Aided Design and Evaluation of Angiotensin-Converting Enzyme Inhibitors
-
Perun, T. J., Propst, C. L., Eds.; Marcel Dekker: New York
-
Hangauer, D. G. Computer-Aided Design and Evaluation of Angiotensin-Converting Enzyme Inhibitors. In Computer-Aided Drug Design: Methods and Applications; Perun, T. J., Propst, C. L., Eds.; Marcel Dekker: New York, 1989; pp 253-295.
-
(1989)
Computer-Aided Drug Design: Methods and Applications
, pp. 253-295
-
-
Hangauer, D.G.1
-
28
-
-
85012573934
-
Antihypertensive Agents
-
Robertson, D. W., Ed.; Academic Press: New York
-
Petrillo, E. W.; Trippodo, N. C.; DeForrest, J. M. Antihypertensive Agents. In Annual Reports in Medicinal Chemistry; Robertson, D. W., Ed.; Academic Press: New York, 1989; Vol. 25, pp 51-60.
-
(1989)
Annual Reports in Medicinal Chemistry
, vol.25
, pp. 51-60
-
-
Petrillo, E.W.1
Trippodo, N.C.2
DeForrest, J.M.3
-
29
-
-
0022222411
-
Recent Development in the Design of Angiotensin-Converting Enzyme Inhibitors
-
Wyvratt, M. J.; Patchett, A. A. Recent Development in the Design of Angiotensin-Converting Enzyme Inhibitors. Med. Res. Rev. 1985, 5, 483-531.
-
(1985)
Med. Res. Rev.
, vol.5
, pp. 483-531
-
-
Wyvratt, M.J.1
Patchett, A.A.2
-
30
-
-
0021957042
-
Conformational Analysis and Active Site Modelling of Angiotensin-Converting Enzyme Inhibitors
-
Andrews, P. R.; Carson, J. M.; Caselli, A.; Spark, M. J.; Woodsm, R. Conformational Analysis and Active Site Modelling of Angiotensin-Converting Enzyme Inhibitors. J. Med. Chem. 1985, 28, 393-399.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 393-399
-
-
Andrews, P.R.1
Carson, J.M.2
Caselli, A.3
Spark, M.J.4
Woodsm, R.5
-
31
-
-
0027143192
-
Heterocyclic Lactam Derivatives as Dual Angiotensin Converting Enzyme and Neutral Endopeptidase 24.11 Inhibitors
-
Stanton, J. L.; Sperbeck, D. M.; Trapani, A. J.; Cote, D., Sakane, Y.; Berry, C. J.; Ghai, R. D. Heterocyclic Lactam Derivatives as Dual Angiotensin Converting Enzyme and Neutral Endopeptidase 24.11 Inhibitors. J. Med. Chem. 1993, 36, 3829-3833.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3829-3833
-
-
Stanton, J.L.1
Sperbeck, D.M.2
Trapani, A.J.3
Cote, D.4
Sakane, Y.5
Berry, C.J.6
Ghai, R.D.7
-
32
-
-
0026065915
-
Configuration and Preferential Solid-State Conformations of Perintoprilat (S-9780). Comparison with the Crystal Structures of Other ACE Inhibitors and Conclusions Related to Structure-Activity Relationships
-
Pascard, C.; Guilhem, J.; Vincent M.; Remond, G.; Portevin, B.; Laubie, M. Configuration and Preferential Solid-State Conformations of Perintoprilat (S-9780). Comparison with the Crystal Structures of Other ACE Inhibitors and Conclusions Related to Structure-Activity Relationships. J. Med. Chem. 1991, 34, 663-669.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 663-669
-
-
Pascard, C.1
Guilhem, J.2
Vincent, M.3
Remond, G.4
Portevin, B.5
Laubie, M.6
-
33
-
-
0025313586
-
Crystallographic Studies of Angiotensin-Converting Enzyme Inhibitors and Analysis of Preferred Zinc Coordination Geometry
-
Hausian, R. J.; Codding, P. W. Crystallographic Studies of Angiotensin-Converting Enzyme Inhibitors and Analysis of Preferred Zinc Coordination Geometry. J. Med. Chem. 1990, 33, 1940-1947.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 1940-1947
-
-
Hausian, R.J.1
Codding, P.W.2
-
34
-
-
0001217240
-
Angiotensin-Converting Enzyme Inhibitors. 2. Perhydroazepin-2-one Derivatives
-
Yanagisawa, H.; Ishirara, S.; Ando, A.; Kanazaki, T.; Miyamoto, S.; Koike, H.; Iijima, Y.; Oizumi, K.; Matsushita, Y.; Hata, T. Angiotensin-Converting Enzyme Inhibitors. 2. Perhydroazepin-2-one Derivatives. J. Med. Chem. 1988, 31, 422-428.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 422-428
-
-
Yanagisawa, H.1
Ishirara, S.2
Ando, A.3
Kanazaki, T.4
Miyamoto, S.5
Koike, H.6
Iijima, Y.7
Oizumi, K.8
Matsushita, Y.9
Hata, T.10
-
35
-
-
37049109587
-
The Design and Synthesis of New Triazolo. Pyrazolo-, and Pyridazo-pyridazine Derivatives as Inhibitors of Angiotensin-Converting Enzyme
-
Hassall, C. H.; Krohn, A.; Moody, C. J.; Thomas, W. A. The Design and Synthesis of New Triazolo. Pyrazolo-, and Pyridazo-pyridazine Derivatives as Inhibitors of Angiotensin-Converting Enzyme. J. Chem. Soc., Perkin Trans. 1984, 1, 155-164.
-
(1984)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 155-164
-
-
Hassall, C.H.1
Krohn, A.2
Moody, C.J.3
Thomas, W.A.4
-
36
-
-
0020662490
-
(Mercaptopropanoyl)indoline-2-carboxylic Acids and Related Compounds as Potent Angiotensin Converting Enzyme Inhibitors and Antihypertensive Agents
-
Kim, D. H.; Guinosso, C. J.; Buzby, G. C.; Herbst, D. R.; McCaully, R. H.; Wicks, T. C.; Wendt, R. L. (Mercaptopropanoyl)indoline-2-carboxylic Acids and Related Compounds as Potent Angiotensin Converting Enzyme Inhibitors and Antihypertensive Agents. J. Med. Chem., 1983, 26, 394-403.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 394-403
-
-
Kim, D.H.1
Guinosso, C.J.2
Buzby, G.C.3
Herbst, D.R.4
McCaully, R.H.5
Wicks, T.C.6
Wendt, R.L.7
-
37
-
-
0020617280
-
Angiotensin Converting Enzyme Inhibitors: 1-Glutarylindoline-2-carboxylic Acid Derivatives
-
Gruenfeld, N.; Stanton, J. L.; Yuan, A. M.; Ebetino, F. H.; Browne, L. J.; Gude, C.; Huebner, C. F. Angiotensin Converting Enzyme Inhibitors: 1-Glutarylindoline-2-carboxylic Acid Derivatives. J. Med. Chem. 1983.26, 1277-1282.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1277-1282
-
-
Gruenfeld, N.1
Stanton, J.L.2
Yuan, A.M.3
Ebetino, F.H.4
Browne, L.J.5
Gude, C.6
Huebner, C.F.7
-
38
-
-
0020538811
-
Inhibition of Angiotensin-Converting Enzyme by Phosphonic Amides and Phosphonic Acids
-
Galardy, R. E.; Kontoyiannidou-Ostrem, V.; Kortylewicz, Z. P. Inhibition of Angiotensin-Converting Enzyme by Phosphonic Amides and Phosphonic Acids. Biochemistry 1983, 22, 1990-1995.
-
(1983)
Biochemistry
, vol.22
, pp. 1990-1995
-
-
Galardy, R.E.1
Kontoyiannidou-Ostrem, V.2
Kortylewicz, Z.P.3
-
39
-
-
0020027816
-
Angiotensin-Converting Enzyme Inhibitors: Importance of the Amide Carbonyl of Mercaptoacyl Amino Acids for Hydrogen Bonding to the Enzyme
-
Condon, M. E.; Petrillo, E. W.; Ryono, D. E.; Reid, J. A.; Neubeck, R.; Puar, M.; Heikes, J. E.; Sabo, E. F.; Losee, K. A.; Cushman, D. W.; Ondetti, M. A. Angiotensin-Converting Enzyme Inhibitors: Importance of the Amide Carbonyl of Mercaptoacyl Amino Acids for Hydrogen Bonding to the Enzyme. J. Med. Chem. 1982, 25, 250-258.
-
(1982)
J. Med. Chem.
, vol.25
, pp. 250-258
-
-
Condon, M.E.1
Petrillo, E.W.2
Ryono, D.E.3
Reid, J.A.4
Neubeck, R.5
Puar, M.6
Heikes, J.E.7
Sabo, E.F.8
Losee, K.A.9
Cushman, D.W.10
Ondetti, M.A.11
-
40
-
-
0019274399
-
A New Class of Angiotensin-Converting Enzyme Inhibitors
-
Patchett, A. A.; Harris, E.; Tristram, E. W.; Wyvratt, M. J.; Wu, M. T.; Taub, D.; Peterson, E. R.; Ikeler, T. J.; Broeke, J. T.; Payne, L. G.; Ondeyka, D. L.; Thorsett, E. D.; Greenlee, W. J.; Lohr, N. S.; Hoffsommer, R. D.; Joshua, H.; Ruyle, W. V.; Rothrock, J. W.; Aster, S. D.; Maycock, A. L.; Robinson, F. M.; Hirschmann, R. A New Class of Angiotensin-Converting Enzyme Inhibitors. Nature 1980, 288, 280-283.
-
(1980)
Nature
, vol.288
, pp. 280-283
-
-
Patchett, A.A.1
Harris, E.2
Tristram, E.W.3
Wyvratt, M.J.4
Wu, M.T.5
Taub, D.6
Peterson, E.R.7
Ikeler, T.J.8
Broeke, J.T.9
Payne, L.G.10
Ondeyka, D.L.11
Thorsett, E.D.12
Greenlee, W.J.13
Lohr, N.S.14
Hoffsommer, R.D.15
Joshua, H.16
Ruyle, W.V.17
Rothrock, J.W.18
Aster, S.D.19
Maycock, A.L.20
Robinson, F.M.21
Hirschmann, R.22
more..
-
41
-
-
0017578611
-
Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive Agents
-
Ondetti, M. A.; Rubin, B.; Cushman, D. W. Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive Agents. Science 1977, 196, 441-444.
-
(1977)
Science
, vol.196
, pp. 441-444
-
-
Ondetti, M.A.1
Rubin, B.2
Cushman, D.W.3
-
42
-
-
0017584729
-
Design of Potent Competitive Inhibitors of Angiotensin-Converting Enzyme. Carboxyalkanoyl and Mercaptoalkanoyl Amino Acids
-
Cushman, D. W.; Cheung, H. S.; Sabo, E. F.; Ondetti, M. A. Design of Potent Competitive Inhibitors of Angiotensin-Converting Enzyme. Carboxyalkanoyl and Mercaptoalkanoyl Amino Acids. Biochemistry 1977, 25, 5484-5491.
-
(1977)
Biochemistry
, vol.25
, pp. 5484-5491
-
-
Cushman, D.W.1
Cheung, H.S.2
Sabo, E.F.3
Ondetti, M.A.4
-
43
-
-
0027183015
-
3D-QSAR of Angiotensin-Converting Enzyme and Thermolysin Inhibitors: A Comparison of CoMFa Models Based on Deduced and Experimentally Determined Active Site Geometries
-
DePriest, S. A.; Mayer, D.; Naylor, C. B.; Marshall, G. R. 3D-QSAR of Angiotensin-Converting Enzyme and Thermolysin Inhibitors: A Comparison of CoMFA Models Based on Deduced and Experimentally Determined Active Site Geometries. J. Am. Chem. Soc. 1993, 115, 5372-5384.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 5372-5384
-
-
DePriest, S.A.1
Mayer, D.2
Naylor, C.B.3
Marshall, G.R.4
-
44
-
-
0027308233
-
Three-Dimensional Quantitative Structure-Activity Relationship of Angiotensin-Converting Enzyme and Thermolysin Inhibitors. II. a Comparison of CoMFa Models Incorporating Molecular Orbital Fields and Desolvation Free Energies Based on Active-Analog and Complementary-Receptor-Field Alignment Rules
-
Waller, C. L.; Marshall, G. R. Three-Dimensional Quantitative Structure-Activity Relationship of Angiotensin-Converting Enzyme and Thermolysin Inhibitors. II. A Comparison of CoMFA Models Incorporating Molecular Orbital Fields and Desolvation Free Energies Based on Active-Analog and Complementary-Receptor-Field Alignment Rules. J. Med. Chem. 1993, 36, 2390-2403.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2390-2403
-
-
Waller, C.L.1
Marshall, G.R.2
-
45
-
-
0024635625
-
Constrained Search Conformational Hyperspace
-
Dammkoehler, R. A.; Karasek, S. F.; Shands, E. F. B.; Marshall, G. R. Constrained Search Conformational Hyperspace. J. Comput.-Aided Mol. Des. 1989, 3, 3-21.
-
(1989)
J. Comput.-Aided Mol. Des.
, vol.3
, pp. 3-21
-
-
Dammkoehler, R.A.1
Karasek, S.F.2
Shands, E.F.B.3
Marshall, G.R.4
-
46
-
-
0043184933
-
3D-QSAR: Further Studies on Inhibitors of Converting Enzyme
-
Silipo, C., Vittoria, A., Eds.; Elsevier: Amsterdam, The Netherlands
-
DePriest, S. A.; Shands, E. F. B.; Dammkoehler, R. A.; Marshall, G. R. 3D-QSAR: Further Studies on Inhibitors of Converting Enzyme. In QSAR: Rational Approaches to the Design of Bioactive Compounds; Silipo, C., Vittoria, A., Eds.; Elsevier: Amsterdam, The Netherlands, 1991, Vol. 16, pp 405-414.
-
(1991)
QSAR: Rational Approaches to the Design of Bioactive Compounds
, vol.16
, pp. 405-414
-
-
DePriest, S.A.1
Shands, E.F.B.2
Dammkoehler, R.A.3
Marshall, G.R.4
-
47
-
-
0023326161
-
A Unique Geometry of the Active Site of Angiotensin Converting Enzyme Consistent with Structure-Activity Studies
-
Mayer, D.; Naylor, C. B.; Motoc, I.; Marshall, G. R. A Unique Geometry of the Active Site of Angiotensin Converting Enzyme Consistent with Structure-Activity Studies. J. Comput.-Aided Mol. Des. 1987, 1, 3-16.
-
(1987)
J. Comput.-Aided Mol. Des.
, vol.1
, pp. 3-16
-
-
Mayer, D.1
Naylor, C.B.2
Motoc, I.3
Marshall, G.R.4
-
48
-
-
0029811146
-
Three-Dimensional Models of ACE and NEP Inhibitors and Their Use in the Design of Potent Dual ACE/NEP Inhibitors
-
Bohacek, R.; De Lombaert, S.; Priestle, J.; Grutter, M. Three-Dimensional Models of ACE and NEP Inhibitors and Their Use in the Design of Potent Dual ACE/NEP Inhibitors. J. Am. Chem. Soc. 1996, 118, 8231-8249.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 8231-8249
-
-
Bohacek, R.1
De Lombaert, S.2
Priestle, J.3
Grutter, M.4
-
49
-
-
0005491041
-
Modelling, Synthesis and Pharmacological Study of Perindopril (S 9490), an Angiotensin I Converting Enzyme Inhibitor
-
Delaage, M., Ed.; VCH: New York
-
Vincent, M.; Schiavi, P. Modelling, Synthesis and Pharmacological Study of Perindopril (S 9490), an Angiotensin I Converting Enzyme Inhibitor. In Molecular Recognition Mechanism: Delaage, M., Ed.; VCH: New York, 1991; pp 81-112.
-
(1991)
Molecular Recognition Mechanism
, pp. 81-112
-
-
Vincent, M.1
Schiavi, P.2
-
50
-
-
0023379808
-
A Theoretical Study of Angiotensin Converting Enzyme Inhibitors
-
Saunders: M. R.; Tute, M. S.; Webb, G. A. A Theoretical Study of Angiotensin Converting Enzyme Inhibitors. J. Comput.-Aided Mol. Des. 1987, 1, 133-142.
-
(1987)
J. Comput.-Aided Mol. Des.
, vol.1
, pp. 133-142
-
-
Saunders, M.R.1
Tute, M.S.2
Webb, G.A.3
-
51
-
-
0042683904
-
-
(Osawa: MERCK); SGI Release 5.0.0
-
Spartan Conformational Analysis (Osawa: MERCK); SGI Release 5.0.0, 1997.
-
(1997)
Spartan Conformational Analysis
-
-
|