UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Cathepsin L Inhibitors with Activity against the Liver Fluke Identified From a Focus Library of Quinoxaline 1,4-di- N -Oxide Derivatives

Molecules (Basel, Switzerland), 2019-06, Vol.24 (13), p.2348

2019

Volltextzugriff (PDF)

Identification of Chalcones as Fasciola hepatica Cathepsin L Inhibitors Using a Comprehensive Experimental and Computational Approach

PLoS neglected tropical diseases, 2016-07, Vol.10 (7), p.e0004834-e0004834

2016

Volltextzugriff (PDF)

Novel and Selective Rhipicephalus microplus Triosephosphate Isomerase Inhibitors with Acaricidal Activity

Veterinary sciences, 2018-08, Vol.5 (3), p.74

2018

Volltextzugriff (PDF)

Substrate Specificity of Cysteine Proteases Beyond the S2 Pocket: Mutagenesis and Molecular Dynamics Investigation of Fasciola hepatica Cathepsins L

Frontiers in molecular biosciences, 2018-04, Vol.5, p.40-40

2018

Volltextzugriff (PDF)

Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: Synthesis, biological evaluation, and structure–activity relationships

Bioorganic & medicinal chemistry, 2007-04, Vol.15 (7), p.2768-2781

2007

Volltextzugriff (PDF)

Analgesic and Anti-Inflammatory Properties of Arylnitroalkenes

Inflammation & allergy drug targets, 2015-02, Vol.14 (1), p.19-28

2015

Volltextzugriff (PDF)

Neuroprotective effects of novel nitrones: In vitro and in silico studies

European journal of pharmacology, 2020-03, Vol.871, p.172926-172926, Article 172926

2020

Volltextzugriff (PDF)

Susceptibility and resistance to Echinococcus granulosus infection: Associations between mouse strains and early peritoneal immune responses

Immunobiology (1979), 2016-03, Vol.221 (3), p.418-426

2016

Volltextzugriff (PDF)

Targets for Anti-T. cruzi Drugs in the Post-Genomic Era

Current enzyme inhibition, 2010-12, Vol.6 (4), p.195-210

2010

Volltextzugriff (PDF)

Discovery of Potent EGFR Inhibitors through the Incorporation of a 3D‐Aromatic‐Boron‐Rich‐Cluster into the 4‐Anilinoquinazoline Scaffold: Potential Drugs for Glioma Treatment

Chemistry : a European journal, 2018-03, Vol.24 (13), p.3122-3126

2018

Volltextzugriff (PDF)

4 - Nitrones as Potential Therapeutic Agents Against Neurodegenerative Diseases

Free radical biology & medicine, 2017-11, Vol.112, p.21-21

2017

Volltextzugriff (PDF)

Nitrones as Potential Therapeutic Agents Against Neurodegenerative Diseases

Free radical biology & medicine, 2017-11, Vol.112, p.21

2017

Volltextzugriff (PDF)

Flavonoid‐Quinoxaline Hybrid Compounds as Cathepsin Inhibitors Against Fascioliasis

ChemMedChem, 2024-09, Vol.19 (18), p.e202400305-n/a

2024

Volltextzugriff (PDF)

Insight into the mechanism of action and selectivity of caspase-3 reversible inhibitors through in silico studies

Journal of molecular structure, 2017-11, Vol.1147, p.558-568

2017

Volltextzugriff (PDF)

Molecular docking and molecular dynamics simulation studies of Trypanosoma cruzi triosephosphate isomerase inhibitors. Insights into the inhibition mechanism and selectivity

Journal of molecular graphics & modelling, 2015-05, Vol.58, p.40-49

2015

Volltextzugriff (PDF)

Cover Feature: Discovery of Potent EGFR Inhibitors through the Incorporation of a 3D‐Aromatic‐Boron‐Rich‐Cluster into the 4‐Anilinoquinazoline Scaffold: Potential Drugs for Glioma Treatment (Chem. Eur. J. 13/2018)

Chemistry : a European journal, 2018-03, Vol.24 (13), p.3071-3071

2018

Volltextzugriff (PDF)

Aromatic amine N-oxide organometallic compounds: searching for prospective agents against infectious diseases

Dalton transactions : an international journal of inorganic chemistry, 2015-08, Vol.44 (32), p.14453-14464

2015

Volltextzugriff (PDF)

Expanding the family of heteroleptic oxidovanadium(IV) compounds with salicylaldehyde semicarbazones and polypyridyl ligands showing anti-Trypanosoma cruzi activity

Journal of inorganic biochemistry, 2015-06, Vol.147, p.116-125

2015

Volltextzugriff (PDF)

Novel Imidazo[4,5-c][1,2,6]thiadiazine 2,2-dioxides as antiproliferative trypanosoma cruzi drugs: Computational screening from neural network, synthesis and in vivo biological properties

European journal of medicinal chemistry, 2017-08, Vol.136, p.223-234

2017

Volltextzugriff (PDF)

Homology modeling of T. cruzi and L. major NADH-dependent fumarate reductases: Ligand docking, molecular dynamics validation, and insights on their binding modes

Journal of molecular graphics & modelling, 2014-03, Vol.48, p.47-59

2014

Volltextzugriff (PDF)

Thiosemicarbazones derived from 1-indanones as new anti-Trypanosoma cruzi agents

Bioorganic & medicinal chemistry, 2011-11, Vol.19 (22), p.6818-6826

2011

Volltextzugriff (PDF)

In search of patterns over physicochemical properties and pharmacological activities for a set of [MCl 2(thiosemicarbazone)] complexes (M = Pt/Pd): Support for multiple mechanisms of antichagasic action excluding DNA-bonding in vivo?

European journal of medicinal chemistry, 2011-07, Vol.46 (7), p.2639-2651

2011

Volltextzugriff (PDF)

One pot synthesis of benzyltriphenylphosphonium acetates from the corresponding activated benzylic alcohols

ARKIVOC, 2006-06, Vol.2006 (11), p.128-136

2006

Volltextzugriff (PDF)

Second generation of 2H-benzimidazole 1,3-dioxide derivatives as anti-trypanosomatid agents: Synthesis, biological evaluation, and mode of action studies

European journal of medicinal chemistry, 2009-11, Vol.44 (11), p.4426-4433

2009

Volltextzugriff (PDF)

1 – 25 von 55

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(46)
Mit Volltextzugriff
(51)

Publikationsform

Sprache

Englisch
(55)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Cathepsin L Inhibitors with Activity against the Liver Fluke Identified From a Focus Library of Quinoxaline 1,4-di- N -Oxide Derivatives

Identification of Chalcones as Fasciola hepatica Cathepsin L Inhibitors Using a Comprehensive Experimental and Computational Approach

Novel and Selective Rhipicephalus microplus Triosephosphate Isomerase Inhibitors with Acaricidal Activity

Substrate Specificity of Cysteine Proteases Beyond the S2 Pocket: Mutagenesis and Molecular Dynamics Investigation of Fasciola hepatica Cathepsins L

Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: Synthesis, biological evaluation, and structure–activity relationships

Analgesic and Anti-Inflammatory Properties of Arylnitroalkenes

Neuroprotective effects of novel nitrones: In vitro and in silico studies

Susceptibility and resistance to Echinococcus granulosus infection: Associations between mouse strains and early peritoneal immune responses

Targets for Anti-T. cruzi Drugs in the Post-Genomic Era

Discovery of Potent EGFR Inhibitors through the Incorporation of a 3D‐Aromatic‐Boron‐Rich‐Cluster into the 4‐Anilinoquinazoline Scaffold: Potential Drugs for Glioma Treatment

4 - Nitrones as Potential Therapeutic Agents Against Neurodegenerative Diseases

Nitrones as Potential Therapeutic Agents Against Neurodegenerative Diseases

Flavonoid‐Quinoxaline Hybrid Compounds as Cathepsin Inhibitors Against Fascioliasis

Insight into the mechanism of action and selectivity of caspase-3 reversible inhibitors through in silico studies

Molecular docking and molecular dynamics simulation studies of Trypanosoma cruzi triosephosphate isomerase inhibitors. Insights into the inhibition mechanism and selectivity

Cover Feature: Discovery of Potent EGFR Inhibitors through the Incorporation of a 3D‐Aromatic‐Boron‐Rich‐Cluster into the 4‐Anilinoquinazoline Scaffold: Potential Drugs for Glioma Treatment (Chem. Eur. J. 13/2018)

Aromatic amine N-oxide organometallic compounds: searching for prospective agents against infectious diseases

Expanding the family of heteroleptic oxidovanadium(IV) compounds with salicylaldehyde semicarbazones and polypyridyl ligands showing anti-Trypanosoma cruzi activity

Novel Imidazo[4,5-c][1,2,6]thiadiazine 2,2-dioxides as antiproliferative trypanosoma cruzi drugs: Computational screening from neural network, synthesis and in vivo biological properties

Homology modeling of T. cruzi and L. major NADH-dependent fumarate reductases: Ligand docking, molecular dynamics validation, and insights on their binding modes

Potent and Selective Inhibitors of Trypanosoma cruzi Triosephosphate Isomerase with Concomitant Inhibition of Cruzipain: Inhibition of Parasite Growth through Multitarget Activity

Thiosemicarbazones derived from 1-indanones as new anti-Trypanosoma cruzi agents

In search of patterns over physicochemical properties and pharmacological activities for a set of [MCl 2(thiosemicarbazone)] complexes (M = Pt/Pd): Support for multiple mechanisms of antichagasic action excluding DNA-bonding in vivo?

One pot synthesis of benzyltriphenylphosphonium acetates from the corresponding activated benzylic alcohols

Second generation of 2H-benzimidazole 1,3-dioxide derivatives as anti-trypanosomatid agents: Synthesis, biological evaluation, and mode of action studies

Suchergebnisse filtern