Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
1,2,4-Oxadiazole/2-Imidazoline Hybrids : Multi-target-directed Compounds for the Treatment of Infectious Diseases and Cancer. / Shetnev, Anton; Baykov, S.; Kalinin, Stanislav; Belova, Alexandra; Sharoyko, Vladimir; Rozhkov, Anton; Zelenkov, Lev; Tarasenko, Marina; Sadykov, Evgeny; Korsakov, Mikhail; Krasavin, Mikhail.
в: International Journal of Molecular Sciences, Том 20, № 7, 1699, 01.04.2019, стр. 1699.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - 1,2,4-Oxadiazole/2-Imidazoline Hybrids
T2 - Multi-target-directed Compounds for the Treatment of Infectious Diseases and Cancer
AU - Shetnev, Anton
AU - Baykov, S.
AU - Kalinin, Stanislav
AU - Belova, Alexandra
AU - Sharoyko, Vladimir
AU - Rozhkov, Anton
AU - Zelenkov, Lev
AU - Tarasenko, Marina
AU - Sadykov, Evgeny
AU - Korsakov, Mikhail
AU - Krasavin, Mikhail
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Replacement of amide moiety with the 1,2,4-oxadiazole core in the scaffold of recently reported efflux pump inhibitors afforded a novel series of oxadiazole/2-imidazoline hybrids. The latter compounds exhibited promising antibacterial activity on both Gram-positive (Staphylococcus aureus, Bacillus subtilis) and Gram-negative (Escherichia coli, Pseudomonasfluorescens) strains. Furthermore, selected compounds markedly inhibited the growth of certain drug-resistant bacteria. Additionally, the study revealed the antiproliferative activity of several antibacterial frontrunners against pancreas ductal adenocarcinoma (PANC-1) cell line, as well as their type-selective monoamine oxidase (MAO) inhibitory profile.
AB - Replacement of amide moiety with the 1,2,4-oxadiazole core in the scaffold of recently reported efflux pump inhibitors afforded a novel series of oxadiazole/2-imidazoline hybrids. The latter compounds exhibited promising antibacterial activity on both Gram-positive (Staphylococcus aureus, Bacillus subtilis) and Gram-negative (Escherichia coli, Pseudomonasfluorescens) strains. Furthermore, selected compounds markedly inhibited the growth of certain drug-resistant bacteria. Additionally, the study revealed the antiproliferative activity of several antibacterial frontrunners against pancreas ductal adenocarcinoma (PANC-1) cell line, as well as their type-selective monoamine oxidase (MAO) inhibitory profile.
KW - 1,2,4-oxadiazole
KW - 2-imidazolines
KW - Antibacterial
KW - Cytotoxicity
KW - MAO inhibition
KW - DESIGN
KW - VIVO
KW - PERIPHERY
KW - FURAZOLIDONE
KW - OXADIAZOLE CLASS
KW - antibacterial
KW - IDENTIFICATION
KW - DISCOVERY
KW - IN-VITRO
KW - 1,2, 4-oxadiazole
KW - EXPLORATION
KW - INHIBITORS
KW - cytotoxicity
UR - http://www.scopus.com/inward/record.url?scp=85064550277&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/124oxadiazole2imidazoline-hybrids-multitargetdirected-compounds-treatment-infectious-diseases-cancer
U2 - 10.3390/ijms20071699
DO - 10.3390/ijms20071699
M3 - Article
C2 - 30959765
VL - 20
SP - 1699
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
SN - 1422-0067
IS - 7
M1 - 1699
ER -
ID: 41088229