نتایج جستجو برای: protease inhibitors

تعداد نتایج: 221619  

HTLV-1 and HIV-1 are two major causes for severe T-cell leukemia disease and acquired immune deficiency syndrome (AIDS). HTLV-1 protease, a member of aspartic acid protease family, plays important roles in maturation during virus replication cycle. The impairment of these proteases results in uninfectious HTLV-1virions.Similar to HIV-1protease deliberate mutations that confer drug resistance on...

Journal: :iranian journal of pharmaceutical sciences 0
farzaneh lotfipour faculty of pharmacy, tabriz university of medical sciences, tabriz, iran, diseases of aging program, regional protein chemistry center, ottawa health research institute, university of ottawa, ottawa, ontario, canada, mohammad hossein zarrintan faculty of pharmacy, tabriz university of medical sciences, tabriz, iran, jabraeil sherbafi research center for pharmaceutical nanotechnology, tabriz university of medical sciences, tabriz, iran ajoy basak diseases of aging program, regional protein chemistry center, ottawa health research institute, university of ottawa, ottawa, ontario, canada,

furin is a ca 2+ -dependent serine protease which cleaves proprotein substrates at the arg-xaa-(lys/arg)-arg    site to generate biologically active proteins. furin’s critical role in many cellular events associated with health disorders such as hiv, sars, anthrax, and influenza as well as cancer has made inhibitors of this enzyme as therapeutic targets. to this date, the most potent inhibitor ...

Journal: :molecular biology research communications 2016
mitra kheirabadi javad maleki safieh soufian samane hosseini

htlv-1 and hiv-1 are two major causes for severe t-cell leukemia disease and acquired immune deficiency syndrome (aids). htlv-1 protease, a member of aspartic acid protease family, plays important roles in maturation during virus replication cycle. the impairment of these proteases results in uninfectious htlv-1virions.similar to hiv-1protease deliberate mutations that confer drug resistance on...

Journal: :Journal of the Japanese Association for Infectious Diseases 2005

Journal: :Physical Biology 2021

Using as a template the crystal structure of SARS-CoV-2 main protease, we developed pharmacophore model functional centers protease inhibitor-binding pocket. With this model, conducted data mining conformational database FDA-approved drugs. This search brought 64 compounds that can be potential inhibitors protease. The conformations these undergone 3D fingerprint similarity clusterization. Then...

A Shakoori F Kobarfard J Pourahmad

It has already been reported that muscle necrosis induced by various phenylenediamine derivatives are correlated with their autoxidation rate. Now in a more detailed investigation of the cytotoxic mechanism using a model system of isolated hepatocytes and ring-methylated structural isomer durenediamine (DD) we have shown that under aerobic conditions, phenylenediamine induced cytotoxicity and R...

Journal: :iranian journal of pharmaceutical research 0
a shakoori

it has already been reported that muscle necrosis induced by various phenylenediamine derivatives are correlated with their autoxidation rate. now in a more detailed investigation of the cytotoxic mechanism using a model system of isolated hepatocytes and ring-methylated structural isomer durenediamine (dd) we have shown that under aerobic conditions, phenylenediamine induced cytotoxicity and r...

Journal: :avicenna journal of medical biotechnology 0

background: as a drug target and an antigenic agent, hiv-1 protease (hiv-1 pr) is at the center of attention for designing anti-aids inhibitors and diagnostic tests. in previous studies, the production of the recombinant protease has been faced with several difficulties; therefore, the aims of this study were the easy production, purification of the soluble form of protease in e. coli and inves...

Journal: :molecular biology research communications 2012
mahnaz shahbazi hamid reza karbalaei-heidari

kinetics of bacterial growth and protease production were monitored on a novel isolated moderately halophilic bacterium, salinivibrio sp. strain ms-7, and maximum growth and protease activity was achieved after 48 hours at 30°c and 180 rpm. to determine the effect of various carbon sources on protease production, glucose, lactose, sucrose and maltose were investigated and  maximum production of...

Journal: :Nature Biotechnology 1999

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