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...

JNJ-77242113, a highly potent, selective peptide targeting the IL-23 receptor, provides robust IL-23 pathway inhibition upon oral dosing in rats and humans

Scientific reports, 2024-07, Vol.14 (1), p.17515-12, Article 17515

2024

Volltextzugriff (PDF)

A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones

Journal of organic chemistry, 2005-04, Vol.70 (9), p.3741-3744

2005

Volltextzugriff (PDF)

Crystal Structure of the Tyrosine Kinase Domain of Colony-stimulating Factor-1 Receptor (cFMS) in Complex with Two Inhibitors

The Journal of biological chemistry, 2007-02, Vol.282 (6), p.4094-4101

2007

Volltextzugriff (PDF)

Design, synthesis and preclinical evaluation of bio-conjugated amylinomimetic peptides as long-acting amylin receptor agonists

European journal of medicinal chemistry, 2022-06, Vol.236, p.114330-114330, Article 114330

2022

Volltextzugriff (PDF)

Indazole-based ligands for estrogen-related receptor α as potential anti-diabetic agents

European journal of medicinal chemistry, 2017-09, Vol.138, p.830-853

2017

Volltextzugriff (PDF)

Discovery of novel potent imidazo[1,2-b]pyridazine PDE10a inhibitors

Bioorganic & medicinal chemistry letters, 2016-09, Vol.26 (17), p.4216-4222

2016

Volltextzugriff (PDF)

Synthesis and evaluation of novel 3,4,6-substituted 2-quinolones as FMS kinase inhibitors

Bioorganic & medicinal chemistry, 2008-03, Vol.18 (6), p.2097-2102

2008

Volltextzugriff (PDF)

2-Hydroxy-4,6-diamino-[1,3,5]triazines: A Novel Class of VEGF-R2 (KDR) Tyrosine Kinase Inhibitors

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.1717-1720

2005

Volltextzugriff (PDF)

Single-Step Syntheses of 2-Amino-7-chlorothiazolo[5,4-d]pyrimidines: Intermediates for Bivalent Thiazolopyrimidines

Journal of organic chemistry, 2005-11, Vol.70 (24), p.10194-10197

2005

Volltextzugriff (PDF)

Potent 2′-aminoanilide inhibitors of cFMS as potential anti-inflammatory agents

Bioorganic & medicinal chemistry, 2007-11, Vol.17 (22), p.6070-6074

2007

Volltextzugriff (PDF)

Identification of 2-acylaminothiophene-3-carboxamides as potent inhibitors of FLT3

Bioorganic & medicinal chemistry letters, 2006-06, Vol.16 (12), p.3282-3286

2006

Volltextzugriff (PDF)

Silver(II) oxide-mediated synthesis of 2,4-diarylquinazolines

Tetrahedron letters, 2018-06, Vol.59 (24), p.2368-2371

2018

Volltextzugriff (PDF)

T-cell receptor ligation by peptide/MHC induces activation of a caspase in immature thymocytes: the molecular basis of negative selection

The EMBO Journal, 1997-05, Vol.16 (9), p.2282-2293

1997

Volltextzugriff (PDF)

Multivalent Templated Saccharides: Convenient Syntheses of Spacer-Linked 1,1‘-Bis -and 1,1‘,1‘‘-Tris-β-glycosides by the Glycal Epoxide Glycosidation Method

Journal of organic chemistry, 1997-03, Vol.62 (5), p.1543-1546

1997

Volltextzugriff (PDF)

Asymmetric synthesis of a potent and selective competitive NMDA antagonist

Journal of organic chemistry, 1993-12, Vol.58 (25), p.7263-7270

1993

Volltextzugriff (PDF)

Possible cerebroprotective and in vivo NMDA antagonist activities of sigma agents

Brain research bulletin, 1991-03, Vol.26 (3), p.461-465

1991

Volltextzugriff (PDF)

(Aminoalkoxy)chromones. Selective .sigma. receptor ligands

Journal of medicinal chemistry, 1992-05, Vol.35 (9), p.1526-1535

1992

Volltextzugriff (PDF)

Epimeric cis-decahydroquinoline-5-carboxylic acids: effects on .gamma.-aminobutyric acid uptake and receptor binding in vitro

Journal of medicinal chemistry, 1981-07, Vol.24 (7), p.788-794

1981

Volltextzugriff (PDF)

Substituted 2-(aminomethyl)piperidines: a novel class of selective protein kinase C inhibitors

Journal of medicinal chemistry, 1991-09, Vol.34 (9), p.2928-2931

1991

Volltextzugriff (PDF)

Neopentyl ester protecting groups for arylsulfonic acids

Tetrahedron letters, 1997-01, Vol.38 (3), p.355-358

1997

Volltextzugriff (PDF)

Stereoselective syntheses of the trans-decahydroquinoline-5-carboxylic acid epimers. Diastereomeric zwitterionic probes of .gamma.-aminobutyric acid-related biological properties in vitro and in vivo

Journal of medicinal chemistry, 1986-01, Vol.29 (1), p.1-8

1986

Volltextzugriff (PDF)

Ifenprodil potently interacts with [ 3H](+)-3-PPP-labeled σ binding sites in guinea pig brain membranes

European journal of pharmacology, 1990-02, Vol.176 (2), p.247-248

1990

Volltextzugriff (PDF)

Lipophilic bis-arylsulfonates as inhibitors of the CD4-gp120 interaction

Bioorganic & medicinal chemistry letters, 1996-12, Vol.6 (24), p.2983-2988

1996

Volltextzugriff (PDF)

Single-Step Syntheses of 2-Amino-7-chlorothiazolo[5,4-d]pyrimidines: Intermediates for Bivalent Thiazolopyrimidines

ChemInform, 2006-04, Vol.37 (14), p.no-no

2006

Volltextzugriff (PDF)

A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones

ChemInform, 2005-09, Vol.36 (38), p.no-no

2005

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(36)

Publikationsform

Artikel
(37)

Sprache

Englisch
(37)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

JNJ-77242113, a highly potent, selective peptide targeting the IL-23 receptor, provides robust IL-23 pathway inhibition upon oral dosing in rats and humans

A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones

Crystal Structure of the Tyrosine Kinase Domain of Colony-stimulating Factor-1 Receptor (cFMS) in Complex with Two Inhibitors

Design, synthesis and preclinical evaluation of bio-conjugated amylinomimetic peptides as long-acting amylin receptor agonists

Indazole-based ligands for estrogen-related receptor α as potential anti-diabetic agents

Discovery of novel potent imidazo[1,2-b]pyridazine PDE10a inhibitors

Synthesis and evaluation of novel 3,4,6-substituted 2-quinolones as FMS kinase inhibitors

2-Hydroxy-4,6-diamino-[1,3,5]triazines: A Novel Class of VEGF-R2 (KDR) Tyrosine Kinase Inhibitors

Single-Step Syntheses of 2-Amino-7-chlorothiazolo[5,4-d]pyrimidines: Intermediates for Bivalent Thiazolopyrimidines

Potent 2′-aminoanilide inhibitors of cFMS as potential anti-inflammatory agents

Identification of 2-acylaminothiophene-3-carboxamides as potent inhibitors of FLT3

Silver(II) oxide-mediated synthesis of 2,4-diarylquinazolines

T-cell receptor ligation by peptide/MHC induces activation of a caspase in immature thymocytes: the molecular basis of negative selection

Multivalent Templated Saccharides: Convenient Syntheses of Spacer-Linked 1,1‘-Bis -and 1,1‘,1‘‘-Tris-β-glycosides by the Glycal Epoxide Glycosidation Method

Asymmetric synthesis of a potent and selective competitive NMDA antagonist

Possible cerebroprotective and in vivo NMDA antagonist activities of sigma agents

(Aminoalkoxy)chromones. Selective .sigma. receptor ligands

Epimeric cis-decahydroquinoline-5-carboxylic acids: effects on .gamma.-aminobutyric acid uptake and receptor binding in vitro

Substituted 2-(aminomethyl)piperidines: a novel class of selective protein kinase C inhibitors

Neopentyl ester protecting groups for arylsulfonic acids

Stereoselective syntheses of the trans-decahydroquinoline-5-carboxylic acid epimers. Diastereomeric zwitterionic probes of .gamma.-aminobutyric acid-related biological properties in vitro and in vivo

Ifenprodil potently interacts with [ 3H](+)-3-PPP-labeled σ binding sites in guinea pig brain membranes

Lipophilic bis-arylsulfonates as inhibitors of the CD4-gp120 interaction

Single-Step Syntheses of 2-Amino-7-chlorothiazolo[5,4-d]pyrimidines: Intermediates for Bivalent Thiazolopyrimidines

A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones

Suchergebnisse filtern