نتایج جستجو برای: imido v compound

تعداد نتایج: 427234  

Journal: :IET Communications 2009
Mark F. Flanagan Michael McLaughlin Anthony D. Fagan

Compound precoding is a state-of-the-art technique for combining trellis coding and decision-feedback equalisation (DFE) prior to upstream transmission on the telephone-line channel, and is an option in the International Telecommunications Union (ITU)-T V.92 standard. In this paper, we provide a detailed overview of this technique. We demonstrate that compound precoding combines in a straightfo...

Journal: :iranian journal of medical sciences 0
mehran karimi golam reza panahandeh shahraki majid yavarian abdolreza afrasiabi javad dehbozorgian mohammadreza bordbar

normal hemostasis requires balanced regulation of prothrombotic and antithrombotic factors. inherited alteration of factor v and prothrombin gene, the g20210a mutation, increases the resistance of factor v to degradation and booster production of prothrombin respectively. these alterations can increase hypercoagulability leading to thrombotic consequences. we aimed to assess the frequencies of ...

2012
Amal A. I. Mekawey

A fractions obtained from the culture fluids of a seven fungal species identified as Verticillium albo-atrum; V. lecanii; V. bulbillosum; V. dahliae; Fusarium solani; F. oxysporum, and Aspergillus sclerociarum were shown to contain a compounds with a biological activity against twenty two clinical bacterial strains including eleven isolates of gram positive and other were gram negative. Among t...

Journal: :Molecules 2017
Jielu Wei Ding Li Xin Xi Lulu Liu Ximei Zhao Wenjun Wu Jiwen Zhang

Celangulin V (CV), one of dihydroagarofuran sesquiterpene polyesters isolated from Chinese bittersweet (Celastrus angulatus Maxim), is famous natural botanical insecticide. Decades of research suggests that is displays excellent insecticidal activity against some insects, such as Mythimna separata Walker. Recently, it has been validated that the H subunit of V-ATPase is one of the target protei...

Journal: :Organic & biomolecular chemistry 2012
Pedro Mateus Rita Delgado Paula Brandão Vítor Félix

A polyoxapolyaza heteroditopic macrobicyclic compound (btpN(4)O(3)) was synthesized. The acid-base behaviour of the compound as well as its binding ability for zwitterionic amino acids were studied by potentiometry at 298.2 ± 0.1 K in H(2)O-MeOH (50:50 v/v) and at I = 0.10 ± 0.01 M in NMe(4)TsO. The H(n)btpN(4)O(3)(n+) showed preference for amino acids containing tetrahedral anionic groups.

Journal: :The Journal of antimicrobial chemotherapy 2007
A Hombrouck A Hantson B van Remoortel M Michiels J Vercammen D Rhodes V Tetz Y Engelborghs F Christ Z Debyser M Witvrouw

OBJECTIVES We have previously identified the pyranodipyrimidines (PDPs) as a new class of integrase (IN) inhibitors. The most potent congener V-165 inhibits HIV-1 integration at low micromolar concentrations by inhibiting the binding of IN to the DNA. As part of pre-clinical studies with PDP, we wanted to investigate HIV resistance development against V-165 and to further characterize the physi...

Journal: :Synthetic Communications 2023

Maoecrystal V is a highly oxidized and rearranged norterpenoid isolated from the Chinese herb, Isodon eriocalyx. A synthetic route for C/D/E-ring core compound of maoecrystal has been developed. Introduction C1 fragment to D/E-ring was achieved by lithito dithiane attack, C-ring formed deprotective intramolecular hemiacetalization dithiane-alcohol precursor.

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