Egyszerű nézet

dc.contributor.author Baska, Ferenc
dc.contributor.author Szekely ER,
dc.contributor.author Szantai-Kis C,
dc.contributor.author Banhegyi P,
dc.contributor.author Hegymegi-Barakonyi, Bálint
dc.contributor.author Zsákai, Lilian
dc.contributor.author Kéri, György
dc.contributor.author Őrfi, László
dc.date.accessioned 2015-11-23T20:46:27Z
dc.date.available 2015-11-23T20:46:27Z
dc.date.issued 2013
dc.identifier 84888358150
dc.identifier.citation pagination=88-95; journalVolume=83; journalIssueNumber=3; journalTitle=ACTA PHARMACEUTICA HUNGARICA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2389
dc.description.abstract Tuberculosis is considered to be one of the major health problem not only in the less developed countries but in the economically developed countries as well. Roughly one third of the world's population are infected with Mycobacterium tuberculosis and a significant part of them are carriers of latent tuberculosis. From ten percent of these latent infections are developing the active TB disease and fifty percent of them die from the illness without appropriate treatment. The drug-resistant Mycobacterium tuberculosis (MDR-TB, XDR-TB) and TB-HIV co-infection attracted attention to the most serious infectious disease. Inhibition of alternative signaling pathways were an important part of the research strategies for cancer and inflammatory diseases in recent years. In case of Mycobacterium tuberculosis such pathways were also identified, for example, three serine-threonine kinases (PknA, PknB, PknG) which are necessary and essential for bacterial growth. In this paper we summarize our best anti-TB active compounds, their biological effects and structure-activity relationships using in silico modeling, biochemical measurements and tests on active bacteria.
dc.relation.ispartof urn:issn:0001-6659
dc.title Mycobacterium tuberculosis ellenes hatoanyagok fejlesztese es szerkezet-hatas osszefuggeseinek vizsgalata.
dc.type Journal Article
dc.date.updated 2015-11-20T09:50:14Z
dc.language.rfc3066 hu
dc.identifier.mtmt 2488916
dc.identifier.pubmed 24369587
dc.contributor.department Semmelweis Egyetem
dc.contributor.department SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.department SE/AOK/I/OVMBPI/MTA-SE Pathobiokémiai Kutatócsoport
dc.contributor.department SE/GYTK/Gyógyszerészi Kémiai Intézet
dc.contributor.institution Semmelweis Egyetem


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