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Št. zadetkov: 6
Magistrsko delo
Oznake: ubikvitin;imunoproteasom;beta5i-podenota;dipeptidni zaviralci;1,3,4-oksatiazol-2-on;
Načrtovanje in sinteza dipeptidnih zaviralcev imunoproteasoma
Leto: 2017 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: monociklični ß-laktam;Staudingerjeva [2+2] ciklokondenzacija;cerijev amonijev nitrat;hidrazin hidrat;3-amino-4-substituiran azetidin-2-on;inhibitorna aktivnost;monocyclic ß-lactam;Staudinger [2+2] cyclocondensation;cerium ammonium nitrate;hydrazine hydrate;3-amino-4-substituted azetidin-2-one;inhibitory activities;
Monocyclic ß-lactams (azetidin-2-ones) exhibit a wide range of biological activities, the most important of which are antibacterial, anticancer, and cholesterol absorption inhibitory activities. The synthesis of decorated monocyclic ß-lactams is challenging because their ring is highly constrained a ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Doktorska disertacija
Oznake: penicilin vezoči proteini;MurA;kovalentni zaviralci;monociklični β-laktami;kloracetamidi;
Osredotočili smo se na kovalentne zaviralce encimov, ki sodelujejo v sintezi bakterijskega peptidoglikana. Penicilin vezoči proteini (PBP) sodelujejo v zadnji stopnji sinteze bakterijske celične stene in katalizirajo prečno premreženje peptidoglikana. UDP-N-acetilglukozamin enolpiruvil transferaza ( ...
Leto: 2023 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: thiazoles;hit profiling;promiscuous compounds;frequent hitters;privileged scaffolds;fragments;
Thiazoles exhibit a wide range of biological activities and therefore represent useful and attractive building blocks. To evaluate their usefulness and pinpoint their liabilities in fragment screening campaigns, we assembled a focused library of 49 fragment-sized thiazoles and thiadiazoles with vari ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: antibakterijska sredstva;UDP-N-acetilglukozamin enolpiruvil transferaza;tiolna reaktivnost;antibacterial agents;UDP-N-Acetylglucosamine enolpyruvyl transferase;thiol reactivity;
MurA (UDP-N-acetylglucosamine enolpyruvyl transferase) catalyzes the first committed step in the cytoplasmic part of peptidoglycan biosynthesis and is a validated target enzyme for antibacterial drug discovery; the inhibitor fosfomycin has been used clinically for decades. Like fosfomycin, most MurA ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: kovalentni inhibitor;heterociklični elektrofili;označevanje cisteina;kvaternizacija;MurA;covalent inhibitor;heterocyclic electrophiles;cysteine labelling;quaternization;
Heterocyclic electrophiles as small covalent fragments showed promising inhibitory activity on the antibacterial target MurA (UDP-N-acetylglucosamine 1-carboxyvinyltransferase, EC:2.5.1.7). Here, we report the second generation of heterocyclic electrophiles: the quaternized analogue of the heterocyc ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Št. zadetkov: 6
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