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Journal of Computer-Aided Molecular Design
|
June 1, 1991
The computational design of test compounds with potentially specific biological activity: histamine-H2 agonists derived from 5-HT/H2 antagonists
S Topiol, M Sabio
Journal of Combinatorial Chemistry
|
January 10, 2001
Computer Aided Analysis of Split and Mix Combinatorial Libraries
Topiol, Davies, Vijayakumar, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 27, 2015
7TM X-ray structures for class C GPCRs as new drug-discovery tools. 1. mGluR5
Sid Topiol, Michael Sabio
Expert Opinion on Drug Discovery
|
July 28, 2015
The role of experimental and computational structural approaches in 7TM drug discovery
Sid Topiol, Michael Sabio
Chemical Biology & Drug Design
|
October 11, 2008
Driving forces for ligand migration in the leucine transporter
Anne Marie Jørgensen, Sid Topiol
Bioorganic & Medicinal Chemistry Letters
|
October 3, 2008
Use of the X-ray structure of the beta2-adrenergic receptor for drug discovery. Part 2: Identification of active compounds
Michael Sabio, Kenneth Jones, Sid Topiol
Journal of Medicinal Chemistry
|
November 1, 1984
A theoretical investigation of histamine tautomerism
S Topiol, H Weinstein, R Osman
Journal of Medicinal Chemistry
|
November 1, 1986
Molecular determinants for the agonist activity of 2-methylhistamine and 4-methylhistamine at H2-receptors
P Reggio, S Topiol, H Weinstein
Proteins
|
April 5, 2002
Threading with chemostructural restrictions method for predicting fold and functionally significant residues: application to dipeptidylpeptidase IV (DPP-IV)
Boris Reva, Alexei Finkelstein, Sid Topiol
Annals of the New York Academy of Sciences
|
January 1, 1981
Models for active sites of metalloenzymes. II. Interactions with a model substrate
R Osman, H Weinstein, S Topiol
Page
of 5
Search research articles
Search
Showing results (11-20 of 43) with videos related to
Sort By:
Page
of 5
Journal of Computer-Aided Molecular Design
|
June 1, 1991
The computational design of test compounds with potentially specific biological activity: histamine-H2 agonists derived from 5-HT/H2 antagonists
S Topiol, M Sabio
Journal of Combinatorial Chemistry
|
January 10, 2001
Computer Aided Analysis of Split and Mix Combinatorial Libraries
Topiol, Davies, Vijayakumar, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 27, 2015
7TM X-ray structures for class C GPCRs as new drug-discovery tools. 1. mGluR5
Sid Topiol, Michael Sabio
Expert Opinion on Drug Discovery
|
July 28, 2015
The role of experimental and computational structural approaches in 7TM drug discovery
Sid Topiol, Michael Sabio
Chemical Biology & Drug Design
|
October 11, 2008
Driving forces for ligand migration in the leucine transporter
Anne Marie Jørgensen, Sid Topiol
Bioorganic & Medicinal Chemistry Letters
|
October 3, 2008
Use of the X-ray structure of the beta2-adrenergic receptor for drug discovery. Part 2: Identification of active compounds
Michael Sabio, Kenneth Jones, Sid Topiol
Journal of Medicinal Chemistry
|
November 1, 1984
A theoretical investigation of histamine tautomerism
S Topiol, H Weinstein, R Osman
Journal of Medicinal Chemistry
|
November 1, 1986
Molecular determinants for the agonist activity of 2-methylhistamine and 4-methylhistamine at H2-receptors
P Reggio, S Topiol, H Weinstein
Proteins
|
April 5, 2002
Threading with chemostructural restrictions method for predicting fold and functionally significant residues: application to dipeptidylpeptidase IV (DPP-IV)
Boris Reva, Alexei Finkelstein, Sid Topiol
Annals of the New York Academy of Sciences
|
January 1, 1981
Models for active sites of metalloenzymes. II. Interactions with a model substrate
R Osman, H Weinstein, S Topiol
Page
of 5