oleksandr brazhko (5 risultati)

Taschenbuch. Condizione: Neu. Neuware -Scientists of the ZNU Chemistry Department have developed a new software called QuS (abbrv. for QSAR Server), that is designed to integrate and coordinate the work of other software that performs certain stages of QSAR-analysis. QuS is defined by the application of the concept of in silico latest chemometric technologies for drug search. The formation of databases plays a vital role in revealling the laws of SAR / QSAR. The database is a new and necessary connection in solving the problem of predicting the biological activity and toxicity of chemical compounds. Various quinoline derivatives are used as synthons in organic synthesis and molecular design, as well as effective biologically active compounds. In addition, for a significant number of biologically active derivatives of nitrogen-containing heterocycles, there are limited or no systematic studies of 'structure-activity-toxicity', which was the main reason for studying the quinoline derivatives' databases, finding descriptors of their structure which are important for QSAR models as systems for assessing the biological effects of compounds and obtaining promising lead-compoundsBooks on Demand GmbH, Überseering 33, 22297 Hamburg 72 pp. Englisch.

Taschenbuch. Condizione: Neu. Modern Aspects of Drugs Creation Based on QuS-Program Development | Oleksandr Brazhko (u. a.) | Taschenbuch | Englisch | 2020 | LAP LAMBERT Academic Publishing | EAN 9786202923194 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Scientists of the ZNU Chemistry Department have developed a new software called QuS (abbrv. for QSAR Server), that is designed to integrate and coordinate the work of other software that performs certain stages of QSAR-analysis. QuS is defined by the application of the concept of in silico latest chemometric technologies for drug search. The formation of databases plays a vital role in revealling the laws of SAR / QSAR. The database is a new and necessary connection in solving the problem of predicting the biological activity and toxicity of chemical compounds. Various quinoline derivatives are used as synthons in organic synthesis and molecular design, as well as effective biologically active compounds. In addition, for a significant number of biologically active derivatives of nitrogen-containing heterocycles, there are limited or no systematic studies of 'structure-activity-toxicity', which was the main reason for studying the quinoline derivatives' databases, finding descriptors of their structure which are important for QSAR models as systems for assessing the biological effects of compounds and obtaining promising lead-compounds 72 pp. Englisch.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Brazhko OleksandrBrazhko Oleksandr was born in Melitopol, Ukraine. He graduated from Zaporizhia Medical Institute in 1986. He is a Doctor of Biological Sciences (2005), Ph.D. (2007), and a leading expert in the development of bioregu.

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Scientists of the ZNU Chemistry Department have developed a new software called QuS (abbrv. for QSAR Server), that is designed to integrate and coordinate the work of other software that performs certain stages of QSAR-analysis. QuS is defined by the application of the concept of in silico latest chemometric technologies for drug search. The formation of databases plays a vital role in revealling the laws of SAR / QSAR. The database is a new and necessary connection in solving the problem of predicting the biological activity and toxicity of chemical compounds. Various quinoline derivatives are used as synthons in organic synthesis and molecular design, as well as effective biologically active compounds. In addition, for a significant number of biologically active derivatives of nitrogen-containing heterocycles, there are limited or no systematic studies of 'structure-activity-toxicity', which was the main reason for studying the quinoline derivatives' databases, finding descriptors of their structure which are important for QSAR models as systems for assessing the biological effects of compounds and obtaining promising lead-compounds.