000 01826naaaa2200301uu 4500
001 https://directory.doabooks.org/handle/20.500.12854/53831
005 20220219195625.0
020 _aintechopen.69830
020 _a9781789233544
020 _a9781789233551
024 7 _a10.5772/intechopen.69830
_cdoi
041 0 _aEnglish
042 _adc
100 1 _aDimitrios P. Vlachakis
_4auth
245 1 0 _aMolecular Docking
260 _bIntechOpen
_c2018
300 _a1 electronic resource (188 p.)
506 0 _aOpen Access
_2star
_fUnrestricted online access
520 _aMolecular docking has always been and will be on the forefront of developments in the eminent field of drug design and medicinal chemistry. At the early days, drug discovery was based on blackboard drawings and expert intuition. However, as times move on, the amount of available information and overall knowledge base that needs to be analyzed cannot be processed manually. This, coupled by the rapid growth in computational infrastructure and processing power, has allowed for the efficient use of molecular docking tools and algorithms to be considered in the greater field of drug discovery. In the postgenomic era, molecular docking has become the key player for the screening of hundreds of thousands of compounds against a repertoire of pharmacological targets.
540 _aAll rights reserved
_4http://oapen.org/content/about-rights
546 _aEnglish
653 _aLife Sciences
653 _aMolecular Biology
653 _aGenetics and Molecular Biology
653 _aBiochemistry
856 4 0 _awww.oapen.org
_uhttps://www.intechopen.com/books/molecular-docking
_70
_zDOAB: download the publication
856 4 0 _awww.oapen.org
_uhttps://directory.doabooks.org/handle/20.500.12854/53831
_70
_zDOAB: description of the publication
999 _c40100
_d40100