Dejan M Opsenica - JoVE Visualize

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Chemico-Biological Interactions|May 18, 2019

Structural aspects of 4-aminoquinolines as reversible inhibitors of human acetylcholinesterase and butyrylcholinesteraseAnita Bosak, Dejan M Opsenica, Goran Šinko, et al.

ACS Chemical Biology|March 29, 2017

Long-Chain 4-Aminoquinolines as Quorum Sensing Inhibitors in Serratia marcescens and Pseudomonas aeruginosaIvana Aleksić, Sandra Šegan, Filip Andrić, et al.

ACS Chemical Biology|October 25, 2019

<i>N</i>-Benzyl Derivatives of Long-Chained 4-Amino-7-chloro-quionolines as Inhibitors of Pyocyanin Production in <i>Pseudomonas aeruginosa</i>Ivana Aleksic, Jelena Jeremic, Dusan Milivojevic, et al.

Bioorganic & Medicinal Chemistry|June 14, 2008

Mixed tetraoxanes containing the acetone subunit as antimalarialsDejan M Opsenica, Natasa Terzić, Philip L Smith, et al.

Molecules (Basel, Switzerland)|November 27, 2024

Derivatives of Amodiaquine as Potent Human Cholinesterases Inhibitors: Implication for Treatment of Alzheimer's DiseaseAna Matošević, Dejan M Opsenica, Marija Bartolić, et al.

Chemico-Biological Interactions|July 5, 2023

Evaluation of 4-aminoquinoline derivatives with an n-octylamino spacer as potential multi-targeting ligands for the treatment of Alzheimer's diseaseAna Matošević, Dejan M Opsenica, Marta Spasić, et al.

Pharmaceutics|June 24, 2022

4-Aminoquinoline-Based Adamantanes as Potential Anticholinesterase Agents in Symptomatic Treatment of Alzheimer's DiseaseKatarina Komatović, Ana Matošević, Nataša Terzić-Jovanović, et al.

European Journal of Medicinal Chemistry|August 14, 2010

An alignment independent 3D QSAR study of the antiproliferative activity of 1,2,4,5-tetraoxanesIlija N Cvijetić, Zeljko P Zizak, Tatjana P Stanojković, et al.

Journal of Medicinal Chemistry|April 19, 2014

Second generation steroidal 4-aminoquinolines are potent, dual-target inhibitors of the botulinum neurotoxin serotype A metalloprotease and P. falciparum malariaMilica Videnović, Dejan M Opsenica, James C Burnett, et al.

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Showing results (1-10 of 9) with videos related to

Sort By:

Pageof 1

Chemico-Biological Interactions|May 18, 2019

Structural aspects of 4-aminoquinolines as reversible inhibitors of human acetylcholinesterase and butyrylcholinesteraseAnita Bosak, Dejan M Opsenica, Goran Šinko, et al.

ACS Chemical Biology|March 29, 2017

Long-Chain 4-Aminoquinolines as Quorum Sensing Inhibitors in Serratia marcescens and Pseudomonas aeruginosaIvana Aleksić, Sandra Šegan, Filip Andrić, et al.

ACS Chemical Biology|October 25, 2019

<i>N</i>-Benzyl Derivatives of Long-Chained 4-Amino-7-chloro-quionolines as Inhibitors of Pyocyanin Production in <i>Pseudomonas aeruginosa</i>Ivana Aleksic, Jelena Jeremic, Dusan Milivojevic, et al.

Bioorganic & Medicinal Chemistry|June 14, 2008

Mixed tetraoxanes containing the acetone subunit as antimalarialsDejan M Opsenica, Natasa Terzić, Philip L Smith, et al.

Molecules (Basel, Switzerland)|November 27, 2024

Derivatives of Amodiaquine as Potent Human Cholinesterases Inhibitors: Implication for Treatment of Alzheimer's DiseaseAna Matošević, Dejan M Opsenica, Marija Bartolić, et al.

Chemico-Biological Interactions|July 5, 2023

Evaluation of 4-aminoquinoline derivatives with an n-octylamino spacer as potential multi-targeting ligands for the treatment of Alzheimer's diseaseAna Matošević, Dejan M Opsenica, Marta Spasić, et al.

Pharmaceutics|June 24, 2022

4-Aminoquinoline-Based Adamantanes as Potential Anticholinesterase Agents in Symptomatic Treatment of Alzheimer's DiseaseKatarina Komatović, Ana Matošević, Nataša Terzić-Jovanović, et al.

European Journal of Medicinal Chemistry|August 14, 2010

An alignment independent 3D QSAR study of the antiproliferative activity of 1,2,4,5-tetraoxanesIlija N Cvijetić, Zeljko P Zizak, Tatjana P Stanojković, et al.

Journal of Medicinal Chemistry|April 19, 2014

Second generation steroidal 4-aminoquinolines are potent, dual-target inhibitors of the botulinum neurotoxin serotype A metalloprotease and P. falciparum malariaMilica Videnović, Dejan M Opsenica, James C Burnett, et al.

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