UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 977

Sortiert nach

BACE1 (β-secretase) inhibitors for the treatment of Alzheimer's disease

Chemical Society reviews, 2014-10, Vol.43 (19), p.6765-6813

2014

Link zum Volltext

Verfügbarkeit prüfen

Recent Progress in the Development of HIV‑1 Protease Inhibitors for the Treatment of HIV/AIDS

Journal of medicinal chemistry, 2016-06, Vol.59 (11), p.5172-5208

2016

Link zum Volltext

Verfügbarkeit prüfen

Drug Development and Medicinal Chemistry Efforts toward SARS‐Coronavirus and Covid‐19 Therapeutics

ChemMedChem, 2020-06, Vol.15 (11), p.907-932

2020

Link zum Volltext

Verfügbarkeit prüfen

The Curtius rearrangement: mechanistic insight and recent applications in natural product syntheses

Organic & biomolecular chemistry, 2018, Vol.16 (12), p.26-227

2018

Link zum Volltext

Verfügbarkeit prüfen

The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry

ChemMedChem, 2018-11, Vol.13 (22), p.2351-2373

2018

Link zum Volltext

Verfügbarkeit prüfen

Achmatowicz reaction and its application in the syntheses of bioactive molecules

RSC advances, 2016-01, Vol.6 (112), p.111564-111598

2016

Link zum Volltext

Verfügbarkeit prüfen

A small molecule compound with an indole moiety inhibits the main protease of SARS-CoV-2 and blocks virus replication

Nature communications, 2021-01, Vol.12 (1), p.668-12, Article 668

2021

Link zum Volltext

Verfügbarkeit prüfen

Beyond darunavir: recent development of next generation HIV-1 protease inhibitors to combat drug resistance

Chemical communications (Cambridge, England), 2022-10, Vol.58 (84), p.11762-11782

2022

Link zum Volltext

Verfügbarkeit prüfen

Total Syntheses of the Proposed Structure of Iriomoteolide-1a, -1b and Synthesis of Three Derivatives for Structural Studies

Marine drugs, 2022-09, Vol.20 (10), p.587

2022

Link zum Volltext

Verfügbarkeit prüfen

Urea Derivatives in Modern Drug Discovery and Medicinal Chemistry

Journal of medicinal chemistry, 2020-03, Vol.63 (6), p.2751-2788

2020

Link zum Volltext

Verfügbarkeit prüfen

Enantioselective Total Synthesis of (−)-Zampanolide, a Potent Microtubule-Stabilizing Agent

Organic letters, 2011-08, Vol.13 (15), p.4108-4111

2011

Link zum Volltext

Verfügbarkeit prüfen

Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitors

Nature communications, 2021-07, Vol.12 (1), p.4491-4491, Article 4491

2021

Link zum Volltext

Verfügbarkeit prüfen

Enhancing Protein Backbone Binding-A Fruitful Concept for Combating Drug-Resistant HIV

Angewandte Chemie (International ed.), 2012-02, Vol.51 (8), p.1778-1802

International ed. in English, 2012

Link zum Volltext

Verfügbarkeit prüfen

U2 snRNA structure is influenced by SF3A and SF3B proteins but not by SF3B inhibitors

PloS one, 2021-10, Vol.16 (10), p.e0258551-e0258551

2021

Link zum Volltext

Verfügbarkeit prüfen

Enantioselective Syntheses of FR901464 and Spliceostatin A: Potent Inhibitors of Spliceosome

Organic letters, 2013-10, Vol.15 (19), p.5088-5091

2013

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of darunavir-derived HIV-1 protease inhibitors incorporating P2′ amide-derivatives: Synthesis, biological evaluation and structural studies

Bioorganic & medicinal chemistry letters, 2023-03, Vol.83, p.129168-129168, Article 129168

2023

Link zum Volltext

Verfügbarkeit prüfen

Enantioselective Syntheses of (-)-Alloyohimbane and (-)-Yohimbane by an Efficient Enzymatic Desymmetrization Process

European journal of organic chemistry, 2016-12, Vol.2016 (36), p.6001-6009

2016

Link zum Volltext

Verfügbarkeit prüfen

noncovalent class of papain-like protease/deubiquitinase inhibitors blocks SARS virus replication

Proceedings of the National Academy of Sciences - PNAS, 2008-10, Vol.105 (42), p.16119-16124

2008

Link zum Volltext

Verfügbarkeit prüfen

Enantioselective Total Synthesis of (+)-Largazole, a Potent Inhibitor of Histone Deacetylase

Organic letters, 2008-09, Vol.10 (17), p.3907-3909

2008

Link zum Volltext

Verfügbarkeit prüfen

An enantioselective enzymatic desymmetrization route to hexahydro-4H-furopyranol, a high-affinity ligand for HIV-1 protease inhibitors

Tetrahedron letters, 2017-08, Vol.58 (33), p.3230-3233

2017

Link zum Volltext

Verfügbarkeit prüfen

GRL-0920, an Indole Chloropyridinyl Ester, Completely Blocks SARS-CoV-2 Infection

mBio, 2020-08, Vol.11 (4)

2020

Link zum Volltext

Verfügbarkeit prüfen

Deubiquitinating and Interferon Antagonism Activities of Coronavirus Papain-Like Proteases

Journal of Virology, 2010-05, Vol.84 (9), p.4619-4629

2010

Link zum Volltext

Verfügbarkeit prüfen

Design of HIV Protease Inhibitors Targeting Protein Backbone: An Effective Strategy for Combating Drug Resistance

Accounts of chemical research, 2008-01, Vol.41 (1), p.78-86

2008

Link zum Volltext

Verfügbarkeit prüfen

A Stereoselective Synthesis of (+)-Herboxidiene/GEX1A

Organic letters, 2011-01, Vol.13 (1), p.66-69

2011

Link zum Volltext

Verfügbarkeit prüfen

Potent antiviral HIV-1 protease inhibitor combats highly drug resistant mutant PR20

Biochemical and biophysical research communications, 2019-10, Vol.519 (1), p.61-66

2019

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 977

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(778)
Mit Volltextzugriff
(953)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(602)
Physical Sciences
(306)
Life Sciences & Biomedicine
(284)
Chemistry
(277)
Chemistry, Organic
(192)
Humans
(166)
Pharmacology & Pharmacy
(141)
Chemistry, Medicinal
(117)
Organic Chemistry
(109)
Models, Molecular
(86)
Stereoisomerism
(81)
Molecular Structure
(79)
Crystallography, X-Ray
(78)
Technology
(78)
Drug Design
(73)
Animals
(72)
Biological And Medical Sciences
(72)
Hiv Protease Inhibitors - Pharmacology
(72)
Hiv Protease Inhibitors - Chemistry
(71)
Biochemistry & Molecular Biology
(70)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

BACE1 (β-secretase) inhibitors for the treatment of Alzheimer's disease

Recent Progress in the Development of HIV‑1 Protease Inhibitors for the Treatment of HIV/AIDS

Drug Development and Medicinal Chemistry Efforts toward SARS‐Coronavirus and Covid‐19 Therapeutics

The Curtius rearrangement: mechanistic insight and recent applications in natural product syntheses

The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry

Achmatowicz reaction and its application in the syntheses of bioactive molecules

A small molecule compound with an indole moiety inhibits the main protease of SARS-CoV-2 and blocks virus replication

Beyond darunavir: recent development of next generation HIV-1 protease inhibitors to combat drug resistance

Total Syntheses of the Proposed Structure of Iriomoteolide-1a, -1b and Synthesis of Three Derivatives for Structural Studies

Urea Derivatives in Modern Drug Discovery and Medicinal Chemistry

Enantioselective Total Synthesis of (−)-Zampanolide, a Potent Microtubule-Stabilizing Agent

Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitors

Enhancing Protein Backbone Binding-A Fruitful Concept for Combating Drug-Resistant HIV

U2 snRNA structure is influenced by SF3A and SF3B proteins but not by SF3B inhibitors

Enantioselective Syntheses of FR901464 and Spliceostatin A: Potent Inhibitors of Spliceosome

Evaluation of darunavir-derived HIV-1 protease inhibitors incorporating P2′ amide-derivatives: Synthesis, biological evaluation and structural studies

Enantioselective Syntheses of (-)-Alloyohimbane and (-)-Yohimbane by an Efficient Enzymatic Desymmetrization Process

noncovalent class of papain-like protease/deubiquitinase inhibitors blocks SARS virus replication

Enantioselective Total Synthesis of (+)-Largazole, a Potent Inhibitor of Histone Deacetylase

An enantioselective enzymatic desymmetrization route to hexahydro-4H-furopyranol, a high-affinity ligand for HIV-1 protease inhibitors

GRL-0920, an Indole Chloropyridinyl Ester, Completely Blocks SARS-CoV-2 Infection

Deubiquitinating and Interferon Antagonism Activities of Coronavirus Papain-Like Proteases

Design of HIV Protease Inhibitors Targeting Protein Backbone: An Effective Strategy for Combating Drug Resistance

A Stereoselective Synthesis of (+)-Herboxidiene/GEX1A

Potent antiviral HIV-1 protease inhibitor combats highly drug resistant mutant PR20

Suchergebnisse filtern