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Future Medicinal Chemistry|May 30, 2019
Cyclohexyl amide-based novel bacterial topoisomerase inhibitors with prospective GyrA-binding fragmentsAnja Kolarič, Doroteja Novak, Matjaž Weiss, et al.
European Journal of Medicinal Chemistry|May 20, 2018
Insight into structural requirements for selective and/or dual CXCR3 and CXCR4 allosteric modulatorsAnja Kolarič, Urban Švajger, Tihomir Tomašič, et al.
European Journal of Medicinal Chemistry|February 8, 2023
Amide containing NBTI antibacterials with reduced hERG inhibition, retained antimicrobial activity against gram-positive bacteria and in vivo efficacyMaja Kokot, Matjaž Weiss, Irena Zdovc, et al.
Antibiotics (Basel, Switzerland)|August 6, 2021
A Fine-Tuned Lipophilicity/Hydrophilicity Ratio Governs Antibacterial Potency and Selectivity of Bifurcated Halogen Bond-Forming NBTIsAnja Kolarič, Maja Kokot, Martina Hrast, et al.
International Journal of Molecular Sciences|June 11, 2020
Homology Modeling of the Human P-glycoprotein (ABCB1) and Insights into Ligand Binding through Molecular Docking StudiesLiadys Mora Lagares, Nikola Minovski, Ana Yisel Caballero Alfonso, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 17, 2022
Computational Evolution Protocol for Peptide DesignRodrigo Ochoa, Miguel A Soler, Ivan Gladich, et al.
ACS Medicinal Chemistry Letters|December 18, 2024
Structural Aspects of Mycobacterium tuberculosis DNA Gyrase Targeted by Novel Bacterial Topoisomerase InhibitorsMaja Kokot, Martina Hrast Rambaher, Lipeng Feng, et al.
Nature Communications|January 9, 2021
Potent DNA gyrase inhibitors bind asymmetrically to their target using symmetrical bifurcated halogen bondsAnja Kolarič, Thomas Germe, Martina Hrast, et al.
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