
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:description xml:lang="srp">Botulinum neurotoksini su najjaĉi poznati prirodni otrovi i izazivaĉi botulizma –
potencijalno smrtonosne neuroparalitiĉke bolesti. U poslednje vreme, sve veći broj
studija je usmeren ka pronalaţenju inhibitora botulinum neurotoksina serotipa A
(BoNT/A) aktivnih unutar ćelije, jer terapija antitelima ima uspeha jedino pre nego što
toksin uĊe u neuron. U okviru ove doktorske disertacije izvršena je sinteza i detaljno
ispitivanje inhibitorne aktivnosti novih steroidnih i benzo[b]tiofenskih derivata
4-aminohinolina prema kratkom nizu (BoNT/A LC) i holotoksinu BoNT/A. U
istraţivanju je korišćen proteolitiĉki in vitro esej i ćelijski esej u motornim neuronima
razvijenim iz embrionalnih matiĉnih ćelija miša (mES-MN). Dodatno, molekulsko
modelovanje i uklapanje novih derivata u aktivno mesto enzima izvršeno je korišćenjem
programa Schr dinger Suite 2016-4.
U in vitro proteolitiĉkom eseju, sintetisana jedinjenja su ostvarila do 85%
inhibicije BoNT/A LC pri koncentraciji 20 μM, dok su IC50 vrednosti bile u opsegu 0,7–
10,2 μM. U preintoksikacionom modelu u motornim neuronima razvijenim iz
embrionalnih matiĉnih ćelija miša (mES-MN) novi derivati su vršili zaštitu proteina
SNAP-25i do 88%, u niskim mikromolarnim koncentracijama i u dozno-zavisnom
reţimu. Najaktivniji derivati su testirani u postintoksikacionom modelu, u kome se
jedinjenja dodaju ćelijskoj kulturi 30 ili 60 minuta posle holotoksina. U oba modela je
uoĉena korelacija procenta zaštite SNAP-25 i primenjene koncentracije jedinjenja.
Jedinjenje 17 (JK141) je pokazalo 99% zaštite SNAP-25 kada se administrira 30 minuta
posle BoNT/A...</dc:description>
  <dc:description xml:lang="eng">Botulinum neurotoxins are the most poisonous (biological) substances known
and causative agents of botulism – serious and potentially fatal neuroparalytic illness.
Recently, the majority of efforts have focused on identification of botulinum neurotoxin
serotype A (BoNT/A) inhibitors with intracellular activity, because antibody-based
treatments are successful only before toxin enters a neuron. In this doctoral dissertation
synthesis and detailed evaluation of inhibitory potencies of new steroidal and
benzo[b]thiophene 4-aminoquinoline derivatives against BoNT/A light chain (LC) and
full length BoNT/A is reported. Both in vitro proteolytic assay and cell-based assay
using mouse embryonic stem cell derived motor neurons (mES-MNs) were employed.
To rationalize the inhibitory potencies of the new derivatives, structure-based docking
simulations were performed using Schr dinger Suite 2016-4 and the modules therein.
Using in vitro HPLC-based assay, the newly synthesized molecules have shown
BoNT/A LC inhibition up to 85% at 20 μM and IC50 values ranging from 0.7–10.2 μM.
Compounds tested during BoNT/A challenge in mES-MNs in preintoxication model
were found to protect SNAP-25 proteinii by up to 88% at low μM concentrations and in
dose-dependent manner. The most effective derivatives were also tested in a postexposure
model, where compounds were added 30 or 60 minutes following holotoxin
administration. In both pre- and postintoxication models, dose-dependent behavior was
observed. Compound 17 (JK141) showed 99% of SNAP-25 cleavage protection when
administrated 30 minutes after BoNT/A...</dc:description>
  <dc:description xml:lang="srp">Prirodne nauke - Organska hemija, medicinska hemija / Life sciences- Organic chemistry, medicinal chemistry  Datum odbrane: 07.05.2018. </dc:description>
  <dc:format>259 listova</dc:format>
  <dc:format>8387474 bytes</dc:format>
  <dc:title xml:lang="srp">Dizajn i sinteza inhibitora botulinum neurotoksina A i parazita Plasmodium falciparum : doktorska disertacija</dc:title>
  <dc:creator>Konstantinović, Jelena M., 1988-</dc:creator>
  <dc:date>2018</dc:date>
  <dc:subject xml:lang="srp">OSNO - Opšta sistematizacija naučnih oblasti, Organska hemija</dc:subject>
  <dc:subject xml:lang="eng">OSNO - Opšta sistematizacija naučnih oblasti, Organska hemija</dc:subject>
  <dc:subject xml:lang="srp">botulinum neurotoksin, mali molekuli kao inhibitori, aminohinolin,steroid, benzotiofen, antimalarici, Plasmodium falciparum, farmakokinetika</dc:subject>
  <dc:subject xml:lang="eng">botulinum neurotoxin, small molecule inhibitors, aminoquinoline, steroid,benzotiophene, antimalarials, Plasmodium falciparum, pharmacokinetics</dc:subject>
  <dc:subject xml:lang="srp">547</dc:subject>
  <dc:rights>http://creativecommons.org/licenses/by-nc-nd/2.0/at/legalcode</dc:rights>
  <dc:contributor>Šolaja, Bogdan A., 1951-</dc:contributor>
  <dc:contributor>Milić, Dragana, 1967-</dc:contributor>
  <dc:contributor>Opsenica, Igor, 1977-</dc:contributor>
  <dc:contributor>Đurković-Đaković, Olgica.</dc:contributor>
  <dc:contributor>Kostić, Vladimir S., 1953-</dc:contributor>
  <dc:contributor>Popsavin, Velimir, 1951-</dc:contributor>
  <dc:type>info:eu-repo/semantics/bachelorThesis</dc:type>
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:18090</dc:identifier>
  <dc:identifier>cobiss:50361871</dc:identifier>
  <dc:identifier>thesis:5940</dc:identifier>
  <dc:language>srp</dc:language>
</oai_dc:dc>
