UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 36

Sortiert nach

An Evolutionary Conservation and Druggability Analysis of Enzymes Belonging to the Bacterial Shikimate Pathway

Antibiotics (Basel), 2022-05, Vol.11 (5), p.675

Frlan, Rok

2022

Link zum Volltext

Verfügbarkeit prüfen

Navigating the Chemical Space of ENR Inhibitors: A Comprehensive Analysis

Antibiotics (Basel), 2024-03, Vol.13 (3), p.252

2024

Link zum Volltext

Verfügbarkeit prüfen

The Synthesis of (2R)-Aziridine-2-carboxylic Acid Containing Dipeptides

Acta chimica Slovenica, 2022-06, Vol.69 (2), p.261-270

2022

Link zum Volltext

Verfügbarkeit prüfen

Application of the N -Dibenzyl Protective Group in the Preparation of β-Lactam Pseudopeptides

Molecules (Basel, Switzerland), 2019-04, Vol.24 (7), p.1261

2019

Link zum Volltext

Verfügbarkeit prüfen

Discovery of a fragment hit compound targeting D-Ala:D-Ala ligase of bacterial peptidoglycan biosynthesis

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.387-397

2023

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of MurA Enzyme from Escherichia coli by Flavonoids and Their Synthetic Analogues

ACS omega, 2023-09, Vol.8 (36), p.33006-33016

2023

Link zum Volltext

Verfügbarkeit prüfen

Using Subcritical Water to Obtain Polyphenol-Rich Extracts with Antimicrobial Properties

Antibiotics (Basel), 2024-04, Vol.13 (4), p.334

2024

Link zum Volltext

Verfügbarkeit prüfen

A New Cell‐Based AI‐2‐Mediated Quorum Sensing Interference Assay in Screening of LsrK‐Targeted Inhibitors

Chembiochem : a European journal of chemical biology, 2020-07, Vol.21 (13), p.1918-1922

2020

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of MurA Enzyme from Escherichia coli and Staphylococcus aureus by Diterpenes from Lepechinia meyenii and Their Synthetic Analogs

Antibiotics (Basel), 2021-12, Vol.10 (12), p.1535

2021

Link zum Volltext

Verfügbarkeit prüfen

Recent Progress in Diaryl Ether Synthesis

Synthesis (Stuttgart), 2006-07, Vol.2006 (14), p.2271-2285

2006

Link zum Volltext

Verfügbarkeit prüfen

Synthesis of ethyl 3-(hydroxyphenoxy)benzyl butylphosphonates as potential antigen 85C inhibitors

Tetrahedron, 2007-10, Vol.63 (43), p.10698-10708

2007

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of US 2016/0115161 A1: isoindoline compounds and methods of their use

Expert opinion on therapeutic patents, 2017-06, Vol.27 (6), p.637-641

2017

Link zum Volltext

Verfügbarkeit prüfen

Design and synthesis of novel N-benzylidenesulfonohydrazide inhibitors of MurC and MurD as potential antibacterial agents

Molecules (Basel, Switzerland), 2008-01, Vol.13 (1), p.11-30

2008

Link zum Volltext

Verfügbarkeit prüfen

DNA-encoded library screening on two validated enzymes of the peptidoglycan biosynthetic pathway

Bioorganic & medicinal chemistry letters, 2022-10, Vol.73, p.128915-128915, Article 128915

2022

Link zum Volltext

Verfügbarkeit prüfen

Pyrimido[1,2-b]indazole derivatives: Selective inhibitors of human monoamine oxidase B with neuroprotective activity

European journal of medicinal chemistry, 2021-01, Vol.209, p.112911-112911, Article 112911

2021

Link zum Volltext

Verfügbarkeit prüfen

Mur ligase F as a new target for the flavonoids quercitrin, myricetin, and (–)-epicatechin

Journal of computer-aided molecular design, 2023-12, Vol.37 (12), p.721-733

2023

Link zum Volltext

Verfügbarkeit prüfen

Mur ligases inhibitors with azastilbene scaffold: Expanding the structure–activity relationship

Bioorganic & medicinal chemistry letters, 2021-05, Vol.40, p.127966-127966, Article 127966

2021

Link zum Volltext

Verfügbarkeit prüfen

Identification of a Novel Structural Class of H V 1 Inhibitors by Structure-Based Virtual Screening

Journal of chemical information and modeling, 2024-06, Vol.64 (12), p.4850-4862

2024

Link zum Volltext

Verfügbarkeit prüfen

Effect of Preparation Temperature in Solvent Evaporation Process on Eudragit RS Microsphere Properties

Chemical and Pharmaceutical Bulletin, 2005, Vol.53(1), pp.143-146

2005

Link zum Volltext

Verfügbarkeit prüfen

Cobalt-Catalyzed Cross-Coupling of Grignards with Allylic and Vinylic Bromides: Use of Sarcosine as a Natural Ligand

Journal of organic chemistry, 2015-08, Vol.80 (15), p.7803-7809

2015

Link zum Volltext

Verfügbarkeit prüfen

Identification of a Novel Structural Class of HV1 Inhibitors by Structure-Based Virtual Screening

Journal of chemical information and modeling, 2024-06, Vol.64 (12), p.4850-4862

2024

Link zum Volltext

Verfügbarkeit prüfen

Indoles and 1-(3-(benzyloxy)benzyl)piperazines: Reversible and selective monoamine oxidase B inhibitors identified by screening an in-house compound library

Bioorganic chemistry, 2022-02, Vol.119, p.105581-105581, Article 105581

2022

Link zum Volltext

Verfügbarkeit prüfen

Fragment-Sized Thiazoles in Fragment-Based Drug Discovery Campaigns: Friend or Foe?

ACS medicinal chemistry letters, 2022-12, Vol.13 (12), p.1905-1910

2022

Link zum Volltext

Verfügbarkeit prüfen

D-Glucosamine in iron-catalysed cross-coupling reactions of Grignards with allylic and vinylic bromides: application to the synthesis of a key sitagliptin precursor

Applied organometallic chemistry, 2015-08, Vol.29 (8), p.528-535

2015

Link zum Volltext

Verfügbarkeit prüfen

Discovery of d-amino acid oxidase inhibitors based on virtual screening against the lid-open enzyme conformation

Bioorganic & medicinal chemistry letters, 2018-06, Vol.28 (10), p.1693-1698

2018

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 36

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(30)
Mit Volltextzugriff
(36)

Publikationsform

Artikel
(36)

Sprache

Englisch
(36)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

An Evolutionary Conservation and Druggability Analysis of Enzymes Belonging to the Bacterial Shikimate Pathway

Navigating the Chemical Space of ENR Inhibitors: A Comprehensive Analysis

The Synthesis of (2R)-Aziridine-2-carboxylic Acid Containing Dipeptides

Application of the N -Dibenzyl Protective Group in the Preparation of β-Lactam Pseudopeptides

Discovery of a fragment hit compound targeting D-Ala:D-Ala ligase of bacterial peptidoglycan biosynthesis

Inhibition of MurA Enzyme from Escherichia coli by Flavonoids and Their Synthetic Analogues

Using Subcritical Water to Obtain Polyphenol-Rich Extracts with Antimicrobial Properties

A New Cell‐Based AI‐2‐Mediated Quorum Sensing Interference Assay in Screening of LsrK‐Targeted Inhibitors

Inhibition of MurA Enzyme from Escherichia coli and Staphylococcus aureus by Diterpenes from Lepechinia meyenii and Their Synthetic Analogs

Recent Progress in Diaryl Ether Synthesis

Synthesis of ethyl 3-(hydroxyphenoxy)benzyl butylphosphonates as potential antigen 85C inhibitors

Evaluation of US 2016/0115161 A1: isoindoline compounds and methods of their use

Design and synthesis of novel N-benzylidenesulfonohydrazide inhibitors of MurC and MurD as potential antibacterial agents

DNA-encoded library screening on two validated enzymes of the peptidoglycan biosynthetic pathway

Pyrimido[1,2-b]indazole derivatives: Selective inhibitors of human monoamine oxidase B with neuroprotective activity

Mur ligase F as a new target for the flavonoids quercitrin, myricetin, and (–)-epicatechin

Mur ligases inhibitors with azastilbene scaffold: Expanding the structure–activity relationship

Identification of a Novel Structural Class of H V 1 Inhibitors by Structure-Based Virtual Screening

Effect of Preparation Temperature in Solvent Evaporation Process on Eudragit RS Microsphere Properties

Cobalt-Catalyzed Cross-Coupling of Grignards with Allylic and Vinylic Bromides: Use of Sarcosine as a Natural Ligand

Identification of a Novel Structural Class of HV1 Inhibitors by Structure-Based Virtual Screening

Indoles and 1-(3-(benzyloxy)benzyl)piperazines: Reversible and selective monoamine oxidase B inhibitors identified by screening an in-house compound library

Fragment-Sized Thiazoles in Fragment-Based Drug Discovery Campaigns: Friend or Foe?

D-Glucosamine in iron-catalysed cross-coupling reactions of Grignards with allylic and vinylic bromides: application to the synthesis of a key sitagliptin precursor

Discovery of d-amino acid oxidase inhibitors based on virtual screening against the lid-open enzyme conformation

Suchergebnisse filtern