UB Paderborn / Katalog / Suche / in CDI

1 – 16 von 16

Sortiert nach

Discovery of Quinazolines as Histamine H4 Receptor Inverse Agonists Using a Scaffold Hopping Approach

Journal of medicinal chemistry, 2008-12, Vol.51 (24), p.7855-7865

2008

Volltextzugriff (PDF)

Pan-KRAS inhibitor disables oncogenic signalling and tumour growth

Nature (London), 2023-07, Vol.619 (7968), p.160-166

2023

Volltextzugriff (PDF)

Fragment Optimization of Reversible Binding to the Switch II Pocket on KRAS Leads to a Potent, In Vivo Active KRASG12C Inhibitor

Journal of medicinal chemistry, 2022-11, Vol.65 (21), p.14614-14629

2022

Volltextzugriff (PDF)

Abstract 1271: In vitro and in vivo characterization of BI 1823911 - a novel KRASG12C selective small molecule inhibitor

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.1271-1271

2021

Volltextzugriff (PDF)

Discovery of Quinazolines as Histamine H 4 Receptor Inverse Agonists Using a Scaffold Hopping Approach

Journal of medicinal chemistry, 2008-12, Vol.51 (24), p.7855-7865

2008

Volltextzugriff (PDF)

Targeted Synthesis of Complex Spiro[3H‐indole‐3,2′‐pyrrolidin]‐2(1H)‐ones by Intramolecular Cyclization of Azomethine Ylides: Highly Potent MDM2–p53 Inhibitors

ChemMedChem, 2019-01, Vol.14 (1), p.88-93

2019

Volltextzugriff (PDF)

Targeted Synthesis of Complex Spiro3H-indole-3,2'-pyrrolidin-2(1H)-ones by Intramolecular Cyclization of Azomethine Ylides: Highly Potent MDM2-p53 Inhibitors

ChemMedChem, 2019-01, Vol.14 (1), p.88

2019

Volltextzugriff (PDF)

Chiral linker 5: scope and limitations of arylsubstituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for diastereoselective syntheses

Tetrahedron: asymmetry, 2009-02, Vol.20 (3), p.273-287

2009

Volltextzugriff (PDF)

Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters

Tetrahedron: asymmetry, 2006-09, Vol.17 (16), p.2413-2429

2006

Volltextzugriff (PDF)

Synthesis of novel chiral hydrobenzoin mono- tert-butyl ethers derived from m-hydrobenzoin and their application as chiral auxiliaries in the diastereoselective reduction of α-keto esters

Tetrahedron: asymmetry, 2005-08, Vol.16 (15), p.2631-2647

2005

Volltextzugriff (PDF)

Multicentre evaluation of a second generation point-of-care assay with an extended range for the determination of N-terminal pro-brain natriuretic peptide

Clinical laboratory (Heidelberg), 2012, Vol.58 (5-6), p.515

2012

Volltextzugriff (PDF)

Stereoselectivity in Pinacol-Homocoupling Mediated by Samarium Diiodide

ChemInform, 2004-04, Vol.35 (15), p.no-no

2004

Volltextzugriff (PDF)

Time-resolved DNA release from an O-antigen–specific Salmonella bacteriophage with a contractile tail

The Journal of biological chemistry, 2019-08, Vol.294 (31), p.11751-11761

2019

Volltextzugriff (PDF)

In Vitro Studies of Lipopolysaccharide-Mediated DNA Release of Podovirus HK620

Viruses, 2018-05, Vol.10 (6), p.289

2018

Volltextzugriff (PDF)

Cultivation of Mycobacterium bovis BCG in bioreactors

Journal of biotechnology, 2002-07, Vol.96 (3), p.259-270

2002

Volltextzugriff (PDF)

Dienstleistungsproduktivität: Band 1: Management, Prozessgestaltung, Kundenperspektive. Forum Dienstleistungsmanagement

1. Aufl., 2011

Volltextzugriff (PDF)

1 – 16 von 16

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(14)
Mit Volltextzugriff
(14)

Publikationsform

Artikel
(15)
Bücher
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Discovery of Quinazolines as Histamine H4 Receptor Inverse Agonists Using a Scaffold Hopping Approach

Pan-KRAS inhibitor disables oncogenic signalling and tumour growth

Fragment Optimization of Reversible Binding to the Switch II Pocket on KRAS Leads to a Potent, In Vivo Active KRASG12C Inhibitor

Abstract 1271: In vitro and in vivo characterization of BI 1823911 - a novel KRASG12C selective small molecule inhibitor

Discovery of Quinazolines as Histamine H 4 Receptor Inverse Agonists Using a Scaffold Hopping Approach

Targeted Synthesis of Complex Spiro[3H‐indole‐3,2′‐pyrrolidin]‐2(1H)‐ones by Intramolecular Cyclization of Azomethine Ylides: Highly Potent MDM2–p53 Inhibitors

Targeted Synthesis of Complex Spiro3H-indole-3,2'-pyrrolidin-2(1H)-ones by Intramolecular Cyclization of Azomethine Ylides: Highly Potent MDM2-p53 Inhibitors

Chiral linker 5: scope and limitations of arylsubstituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for diastereoselective syntheses

Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters

Synthesis of novel chiral hydrobenzoin mono- tert-butyl ethers derived from m-hydrobenzoin and their application as chiral auxiliaries in the diastereoselective reduction of α-keto esters

Multicentre evaluation of a second generation point-of-care assay with an extended range for the determination of N-terminal pro-brain natriuretic peptide

Stereoselectivity in Pinacol-Homocoupling Mediated by Samarium Diiodide

Time-resolved DNA release from an O-antigen–specific Salmonella bacteriophage with a contractile tail

In Vitro Studies of Lipopolysaccharide-Mediated DNA Release of Podovirus HK620

Cultivation of Mycobacterium bovis BCG in bioreactors

Dienstleistungsproduktivität: Band 1: Management, Prozessgestaltung, Kundenperspektive. Forum Dienstleistungsmanagement

Suchergebnisse filtern