Add to ORKGThis text traces developments in rational drug discovery and combinatorial library design with contributions from 50 leading scientists in academia and industry who offer coverage of basic principles, design strategies, methodologies, software tools and algorithms, and applications. It outlines the fundamentals of pharmacophore modelling and 3D Quantitative Structure-Activity Relationships (QSAR), classical QSAR, and target protein structure-based design methods
Contains fulltext : 190629.pdf (Publisher’s version ) (Open Access)eScience techno...
Structural biologists focus on the structure of biomolecules. Several techniques are available to st...
Structure-based drug design is now a common method used by the pharmaceutical industry to identify a...
This text traces developments in rational drug discovery and combinatorial library design with contr...
AbstractStructure-based drug design uses three-dimensional visualization of drug candidates bound to...
Drug discovery utilizes chemical biology and computational drug design approaches for the efficient ...
699-716The major techniques of drug discovery processes for the past thirty years have been summar...
Structure-based drug design is emerging as one of the key components in drug discovery, with many ap...
Pharmacophoresthree-dimensional (3D) arrangements of essential features enabling a molecule to exert...
Several combinatorial methods have been developed to create focused or diverse chemical libraries wi...
The process for drug discovery and development is challenging, time consuming and expensive. Compute...
In recent years, research area of structure-based drug design is a rising field that has been used t...
Both solid- and liquid-phase combinatorial chemistry have emerged as powerful tools for identifying ...
Drug discovery is a highly complex and costly process, which demands integrated efforts in several r...
The process of processing a drug and reaching to the market consists of various steps. In the early ...
Contains fulltext : 190629.pdf (Publisher’s version ) (Open Access)eScience techno...
Structural biologists focus on the structure of biomolecules. Several techniques are available to st...
Structure-based drug design is now a common method used by the pharmaceutical industry to identify a...
This text traces developments in rational drug discovery and combinatorial library design with contr...
AbstractStructure-based drug design uses three-dimensional visualization of drug candidates bound to...
Drug discovery utilizes chemical biology and computational drug design approaches for the efficient ...
699-716The major techniques of drug discovery processes for the past thirty years have been summar...
Structure-based drug design is emerging as one of the key components in drug discovery, with many ap...
Pharmacophoresthree-dimensional (3D) arrangements of essential features enabling a molecule to exert...
Several combinatorial methods have been developed to create focused or diverse chemical libraries wi...
The process for drug discovery and development is challenging, time consuming and expensive. Compute...
In recent years, research area of structure-based drug design is a rising field that has been used t...
Both solid- and liquid-phase combinatorial chemistry have emerged as powerful tools for identifying ...
Drug discovery is a highly complex and costly process, which demands integrated efforts in several r...
The process of processing a drug and reaching to the market consists of various steps. In the early ...
Contains fulltext : 190629.pdf (Publisher’s version ) (Open Access)eScience techno...
Structural biologists focus on the structure of biomolecules. Several techniques are available to st...
Structure-based drug design is now a common method used by the pharmaceutical industry to identify a...