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...

Development of targeted protein degradation therapeutics

Nature chemical biology, 2019-10, Vol.15 (10), p.937-944

2019

Volltextzugriff (PDF)

Accessing Drug Metabolites via Transition-Metal Catalyzed C−H Oxidation: The Liver as Synthetic Inspiration

Angewandte Chemie International Edition, 2016-11, Vol.55 (46), p.14218-14238

International ed. in English, 2016

Volltextzugriff (PDF)

Crystal structure of the SALL4-pomalidomide-cereblon-DDB1 complex

Nature structural & molecular biology, 2020-04, Vol.27 (4), p.319-322

2020

Volltextzugriff (PDF)

SALL4 mediates teratogenicity as a thalidomide-dependent cereblon substrate

Nature chemical biology, 2018-10, Vol.14 (10), p.981-987

2018

Volltextzugriff (PDF)

Quaternary Charge-Transfer Complex Enables Photoenzymatic Intermolecular Hydroalkylation of Olefins

Journal of the American Chemical Society, 2021-01, Vol.143 (1), p.97-102

2021

Volltextzugriff (PDF)

Intermolecular Crossed [2 + 2] Cycloaddition Promoted by Visible-Light Triplet Photosensitization: Expedient Access to Polysubstituted 2‑Oxaspiro[3.3]heptanes

Journal of the American Chemical Society, 2021-03, Vol.143 (10), p.4055-4063

2021

Volltextzugriff (PDF)

Synthetic strategy: natural products on demand

Nature chemistry, 2014-06, Vol.6 (6), p.460

Hamann, Lawrence G

2014

Volltextzugriff (PDF)

Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect

Nature (London), 2010-05, Vol.465 (7294), p.96-100

2010

Volltextzugriff (PDF)

Regioselective Synthesis and Slow-Release Suzuki–Miyaura Cross-Coupling of MIDA Boronate-Functionalized Isoxazoles and Triazoles

Journal of organic chemistry, 2011-12, Vol.76 (24), p.10241-10248

2011

Volltextzugriff (PDF)

Discovery of a novel, highly potent and orally bioavailable pyrrolidinone indole series of irreversible Myeloperoxidase (MPO) inhibitors

Biochemical pharmacology, 2023-03, Vol.209, p.115418, Article 115418

2023

Volltextzugriff (PDF)

Discovery of a novel indole pharmacophore for the irreversible inhibition of myeloperoxidase (MPO)

Bioorganic & medicinal chemistry, 2020-06, Vol.28 (12), p.115548-115548, Article 115548

2020

Volltextzugriff (PDF)

Selective VPS34 inhibitor blocks autophagy and uncovers a role for NCOA4 in ferritin degradation and iron homeostasis in vivo

Nature cell biology, 2014-11, Vol.16 (11), p.1069-1079

2014

Volltextzugriff (PDF)

Die Erschließung von Wirkstoffmetaboliten durch übergangsmetallkatalysierte C-H-Oxidation: die Leber als Inspiration für die Synthese

Angewandte Chemie, 2016-11, Vol.128 (46), p.14430-14451

2016

Volltextzugriff (PDF)

One-Pot Reductive Amination and Suzuki–Miyaura Cross-Coupling of Formyl Aryl and Heteroaryl MIDA Boronates in Array Format

Journal of organic chemistry, 2011-06, Vol.76 (12), p.4930-4940

2011

Volltextzugriff (PDF)

Inhibitors of HIV-1 attachment: The discovery and structure–activity relationships of tetrahydroisoquinolines as replacements for the piperazine benzamide in the 3-glyoxylyl 6-azaindole pharmacophore

Bioorganic & medicinal chemistry letters, 2016-01, Vol.26 (1), p.160-167

2016

Volltextzugriff (PDF)

2-Alkyloxazoles as potent and selective PI4KIIIβ inhibitors demonstrating inhibition of HCV replication

Bioorganic & medicinal chemistry letters, 2014-08, Vol.24 (16), p.3714-3718

2014

Volltextzugriff (PDF)

One-Pot C–N/C–C Cross-Coupling of Methyliminodiacetic Acid Boronyl Arenes Enabled by Protective Enolization

Organic letters, 2012-11, Vol.14 (21), p.5578-5581

2012

Volltextzugriff (PDF)

Synthesis and SAR of azolopyrimidines as potent and selective dipeptidyl peptidase-4 (DPP4) inhibitors for type 2 diabetes

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (15), p.4395-4398

2010

Volltextzugriff (PDF)

Substituted piperidinyl glycinyl 2-cyano-4,5-methano pyrrolidines as potent and stable dipeptidyl peptidase IV inhibitors

Bioorganic & medicinal chemistry letters, 2013-03, Vol.23 (6), p.1622-1625

2013

Volltextzugriff (PDF)

Sensitization of diabetic and obese mice to insulin by retinoid X receptor agonists

Nature (London), 1997-03, Vol.386 (6623), p.407-410

1997

Volltextzugriff (PDF)

Discovery of pyridyl sulfonamide 11-beta-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors for the treatment of metabolic disorders

Bioorganic & medicinal chemistry letters, 2014-11, Vol.24 (21), p.5045-5049

2014

Volltextzugriff (PDF)

Generation of 3,8-substituted 1,2,4-triazolopyridines as potent inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1)

Bioorganic & medicinal chemistry letters, 2011-07, Vol.21 (14), p.4146-4149

2011

Volltextzugriff (PDF)

Mechanism of Gly-Pro-pNA cleavage catalyzed by dipeptidyl peptidase-IV and its inhibition by saxagliptin (BMS-477118)

Archives of biochemistry and biophysics, 2006, Vol.445 (1), p.9-18

2006

Volltextzugriff (PDF)

A scalable synthesis of (1R,3S,5R)-2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid

Tetrahedron letters, 2013-12, Vol.54 (49), p.6722-6724

2013

Volltextzugriff (PDF)

1 – 25 von 102

Suche als RSS-Feed

Aktive Filter

KollektionElektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals

Zeitschrift / SerieJournal Of Medicinal Chemistry

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(84)
Mit Volltextzugriff
(88)

Publikationsform

Sprache

Englisch
(101)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(62)
Chemistry
(42)
Life Sciences & Biomedicine
(40)
Physical Sciences
(39)
Chemistry, Organic
(30)
Humans
(26)
Pharmacology & Pharmacy
(25)
Chemistry, Medicinal
(24)
Biological And Medical Sciences
(21)
Medical Sciences
(21)
Pharmacology. Drug Treatments
(20)
Structure-Activity Relationship
(17)
Animals
(15)
Biochemistry
(10)
Biochemistry & Molecular Biology
(10)
Molecular Structure
(10)
Organic Chemistry
(10)
Technology
(10)
Female
(8)
General And Cellular Metabolism. Vitamins
(8)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Development of targeted protein degradation therapeutics

Accessing Drug Metabolites via Transition-Metal Catalyzed C−H Oxidation: The Liver as Synthetic Inspiration

Crystal structure of the SALL4-pomalidomide-cereblon-DDB1 complex

SALL4 mediates teratogenicity as a thalidomide-dependent cereblon substrate

Quaternary Charge-Transfer Complex Enables Photoenzymatic Intermolecular Hydroalkylation of Olefins

Intermolecular Crossed [2 + 2] Cycloaddition Promoted by Visible-Light Triplet Photosensitization: Expedient Access to Polysubstituted 2‑Oxaspiro[3.3]heptanes

SMN2 splice modulators enhance U1-pre-mRNA association and rescue SMA mice

Synthetic strategy: natural products on demand

Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect

Regioselective Synthesis and Slow-Release Suzuki–Miyaura Cross-Coupling of MIDA Boronate-Functionalized Isoxazoles and Triazoles

Discovery of a novel, highly potent and orally bioavailable pyrrolidinone indole series of irreversible Myeloperoxidase (MPO) inhibitors

Discovery of a novel indole pharmacophore for the irreversible inhibition of myeloperoxidase (MPO)

Selective VPS34 inhibitor blocks autophagy and uncovers a role for NCOA4 in ferritin degradation and iron homeostasis in vivo

Die Erschließung von Wirkstoffmetaboliten durch übergangsmetallkatalysierte C-H-Oxidation: die Leber als Inspiration für die Synthese

One-Pot Reductive Amination and Suzuki–Miyaura Cross-Coupling of Formyl Aryl and Heteroaryl MIDA Boronates in Array Format

Inhibitors of HIV-1 attachment: The discovery and structure–activity relationships of tetrahydroisoquinolines as replacements for the piperazine benzamide in the 3-glyoxylyl 6-azaindole pharmacophore

2-Alkyloxazoles as potent and selective PI4KIIIβ inhibitors demonstrating inhibition of HCV replication

One-Pot C–N/C–C Cross-Coupling of Methyliminodiacetic Acid Boronyl Arenes Enabled by Protective Enolization

Synthesis and SAR of azolopyrimidines as potent and selective dipeptidyl peptidase-4 (DPP4) inhibitors for type 2 diabetes

Substituted piperidinyl glycinyl 2-cyano-4,5-methano pyrrolidines as potent and stable dipeptidyl peptidase IV inhibitors

Sensitization of diabetic and obese mice to insulin by retinoid X receptor agonists

Discovery of pyridyl sulfonamide 11-beta-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors for the treatment of metabolic disorders

Generation of 3,8-substituted 1,2,4-triazolopyridines as potent inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1)

Mechanism of Gly-Pro-pNA cleavage catalyzed by dipeptidyl peptidase-IV and its inhibition by saxagliptin (BMS-477118)

A scalable synthesis of (1R,3S,5R)-2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid

Aktive Filter

Suchergebnisse filtern