Titlebook: QSAR and Molecular Modeling Studies in Heterocyclic Drugs II; Satya Prakash Gupta Book 2006 Springer-Verlag Berlin Heidelberg 2006 Amine.C

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Chronological

QSAR and Molecular Modeling Studiesof Factor Xa and Thrombin Inhibitors,with enzymes in the coagulation system havebeen pursued over the past few decades. Factor FXa and thrombin are both bound to and are enzymaticallyactive in blood clots. In this article, a brief review is presented on the QSAR and molecularmodelling studies on FXa and thrombin inhibitors reported dur

fleeting

,Structural Information and Drug–Enzyme Interaction of the Non-Nucleoside Reverse Transcriptase Inhive few side effects compared to NRTIs. However,mutation of the HIV-1 virus has caused drug resistance to develop and reduce the efficiency of theseinhibitors for drug therapy. As the association of NNRTIs with the binding pocket of the enzyme isessential for the inhibition process, this interaction

Peculate

QSAR Approach in Study of Mutagenicity of Aromatic and Heteroaromatic Amines,al, E-state, quantum chemical, and empirical descriptors (log.) that are often used in corresponding models. Two case studies are presented in more detail. The conclusion addresses the OECD principles for validation of models that are used for regulatory purposes.

专心

Modeling Reaction Mechanism of Cocaine Hydrolysis and Rational Drug Design for Therapeutic Treatmenine addiction have made the development of aneffective pharmacological treatment a high priority. An ideal anti-cocaine medication wouldaccelerate cocaine metabolism producing biologically inactive metabolites. The main metabolic pathwayof cocaine in the body is hydrolysis at its benzoyl ester group

压倒

,QSAR Studies on Thiazolidines: A Biologically Privileged Scaffold,rential specificities in their biologicalresponses. Amongst the heterocyclic systems, thiazolidine is a biologically important scaffoldknown to be associated with several biological activities. Some of the prominent biological responsesattributed to this skeleton are antiviral, antibacterial, antifu

结构

QSAR Studies on Calcium Channel Blockers,, CCBs have been found to be the most effective drugs. These drugs selectively inhibit . . influx into heart muscles by blocking slow inward channels for Ca. or inhibit Ca. influx into vascular smooth muscles. The result is negative inotropism of smooth muscle relaxation, which is translated into hy

小说

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