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Jezik:
Št. zadetkov: 9
Magistrsko delo
Oznake: tuberkuloza;direktni zaviralci InhA;oksidacija pirola;HPLC;
Tuberkuloza je bakterijska kronična nalezljiva bolezen, ki še vedno predstavlja velik svetovni zdravstveni problem, saj letno povzroča več kot milijon smrti. Čeprav imamo že več let standardno terapijo s peroralnimi kemoterapevtiki, ki je pri večini okuženih učinkovita, se težave pojavijo pri bolnik ...
Leto: 2019 Vir: Fakulteta za farmacijo (UL FFA)
Magistrsko delo
Oznake: Ključne besede: zaviralci kalijevih ionskih kanalov KV1.3;protirakavo delovanje;transportne skupine;tarčna dostava v mitohondrije;
Napetostno odvisne kalijeve ionske kanale KV1.3 uvrščamo v skupino ionskih kanalov, ki se aktivirajo, ko pride do spremembe v napetosti membrane. Povečano izražanje kalijevih ionskih kanalov KV1.3 so odkrili v celični membrani in v notranji membrani mitohondrijev nekaterih vrst rakavih celic, kar po ...
Leto: 2023 Vir: Fakulteta za farmacijo (UL FFA)
Magistrsko delo
Oznake: napetostno odvisni kalijevi kanali;rak;zaviralci;SAR;spojina zadetek;optimizacija spojine zadetka;
Napetostno odvisni kalijevi kanali imajo pomembno vlogo pri delovanju celice, saj v celični membrani vzpostavljajo mirovni membranski potencial in določajo dolžino trajanja akcijskega potenciala. Prav tako so vpleteni v celične procese proliferacije in aktivacije, uravnavanja celičnega volumna in v ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Doktorska disertacija
Oznake:
Voltage-gated potassium channels are proteins found in cell membranes. They include channels KV1.3 and KV10.1 (hEAG1), which are significantly involved in cancer development. High expression of KV10.1 (hEAG1) has been found in more than 70% of human cancers. KV1.3 is directly involved in promoting c ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: KV10.1;ion channels;hERG;pharmacophore modelling;virtual screening;antiproliferative activity;
Background: The voltage-gated potassium channel KV10.1 (Eag1) is considered a near- universal tumour marker and represents a promising new target for the discovery of novel anticancer drugs. (2) Methods: We utilized the ligand-based drug discovery methodology using 3D pharmacophore modelling and med ...
Leto: 2021 Vir: Fakulteta za farmacijo (UL FFA)
Pregledni znanstveni članek
Oznake: KV1.3 channel;design of KV1.3 inhibitors;mitochondrial KV1.3;peptide inhibitors;small-molecule inhibitors;
The KV1.3 voltage gated potassium ion channel is involved in many physiological processes both at the plasma membrane and in the mitochondria, chiefly in the immune and nervous systems. Therapeutic targeting KV1.3 with specific peptides and small molecule inhibitors shows great potential for treatin ...
Leto: 2021 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: KV10.1;ionski kanali;hERG;SAR;antiproliferativno delovanje;ion channels;antiproliferative activity;
Expression of the voltage-gated potassium channel KV10.1 (Eag1) has been detected in over 70% of human cancers, making the channel a promising new target for new anticancer drug discovery. A new structural class of KV10.1 inhibitors was prepared by structural optimisation and exploration of the stru ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: Kv1.3;kalijevi ionski kanali;antiproliferativno delovanje;zdravila proti raku;potassium ion channels;antiproliferative activity;apoptosis;anticancer drugs;
The voltage-gated potassium channel KV1.3 has been recognized as a tumor marker and represents a promising new target for the discovery of new anticancer drugs. We designed a novel structural class of KV1.3 inhibitors through structural optimization of benzamide-based hit compounds and structure-act ...
Leto: 2022 Vir: Fakulteta za farmacijo (UL FFA)
Izvirni znanstveni članek
Oznake: inhibitorji;ionski kanal KV1.3;T-limfocitni imunosupresiv;ion channel;KV1.3 inhibitor;T-lymphocyte;immunosuppressive;
Voltage-gated potassium channel KV1.3 inhibitors have been shown to be effective in preventing T-cell proliferation and activation by affecting intracellular Ca2+ homeostasis. Here, we present the structure-activity relationship, KV1.3 inhibition, and immunosuppressive effects of new thiophene-based ...
Leto: 2023 Vir: Fakulteta za farmacijo (UL FFA)
Št. zadetkov: 9
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