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...

The Potential of Transient Receptor Potential Vanilloid Type 1 Channel Modulators for the Treatment of Pain

Journal of medicinal chemistry, 2007-05, Vol.50 (11), p.2589-2596

Westaway, Susan M

2007

Volltextzugriff (PDF)

8‑Substituted Pyrido[3,4‑d]pyrimidin-4(3H)‑one Derivatives As Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors

Journal of medicinal chemistry, 2016-02, Vol.59 (4), p.1388-1409

2016

Volltextzugriff (PDF)

Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4‑d]pyrimidin-4(3H)‑one Derivatives

Journal of medicinal chemistry, 2016-02, Vol.59 (4), p.1370-1387

2016

Volltextzugriff (PDF)

The Identification of and Rationale for Drugs Which Act at The Motilin Receptor

Progress in Medicinal Chemistry, 2009, Vol.48, p.31-80

2009

Volltextzugriff (PDF)

Interrogating the Druggability of the 2‑Oxoglutarate-Dependent Dioxygenase Target Class by Chemical Proteomics

ACS chemical biology, 2016-07, Vol.11 (7), p.2002-2010

2016

Volltextzugriff (PDF)

Assessing histone demethylase inhibitors in cells: lessons learned

Epigenetics & chromatin, 2017, Vol.10, p.9

2017

Volltextzugriff (PDF)

Assessing histone demethylase inhibitors in cells: lessons learned

Epigenetics & chromatin, 2017-03, Vol.10 (1), Article 9

2017

Volltextzugriff (PDF)

Design and synthesis of 6-phenylnicotinamide derivatives as antagonists of TRPV1

Bioorganic & medicinal chemistry, 2008-10, Vol.18 (20), p.5609-5613

2008

Volltextzugriff (PDF)

Tetrahydroquinoline derivatives as opioid receptor antagonists

Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (2), p.670-676

2011

Volltextzugriff (PDF)

Discovery of N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate

Journal of medicinal chemistry, 2009-02, Vol.52 (4), p.1180-1189

2009

Volltextzugriff (PDF)

Identification of small molecule agonists of the motilin receptor

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (24), p.6423-6428

2008

Volltextzugriff (PDF)

N-Tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (17), p.4533-4536

2006

Volltextzugriff (PDF)

The discovery and optimisation of benzazepine sulfonamide and sulfones as potent agonists of the motilin receptor

Bioorganic & medicinal chemistry letters, 2009-11, Vol.19 (22), p.6452-6458

2009

Volltextzugriff (PDF)

The discovery of biaryl carboxamides as novel small molecule agonists of the motilin receptor

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (24), p.6429-6436

2008

Volltextzugriff (PDF)

Stereoselective synthesis of conformationally constrained omega-amino acid analogues from pyroglutamic acid

Organic & biomolecular chemistry, 2005-08, Vol.3 (15), p.2872-2882

2005

Volltextzugriff (PDF)

The potential of transient receptor potential vanilloid type 1 channel modulators for the treatment of pain : Recent approaches in the treatment of neuropathic pain

Journal of medicinal chemistry, 2007, Vol.50 (11), p.2589-2596

WESTAWAY, Susan M

2007

Volltextzugriff (PDF)

Palladium-catalysed α-arylation of esters and amides under microwave conditions

Tetrahedron letters, 2004-09, Vol.45 (40), p.7395-7397

2004

Volltextzugriff (PDF)

Efficient Reformatsky Conjugate Additions to Alkylidene Malonates and Malonamides

Synlett, 2007-03, Vol.2007 (5), p.0733-0736

2007

Volltextzugriff (PDF)

Enantioselective synthesis of a putative hexaketide intermediate in the biosynthesis of the squalestatins

Tetrahedron letters, 1997-07, Vol.38 (30), p.5367-5370

1997

Volltextzugriff (PDF)

The Enantioselective Conversion of Three-Membered Ring Sulfoxides (Episulfoxides) into Alkenyl Sulfoxides using Chiral Lithium Amide Bases

Synlett, 1997-08, Vol.1997 (8), p.919-920

1997

Volltextzugriff (PDF)

The Potential of Transient Receptor Potential Vanilloid Type 1 Channel Modulators for the Treatment of Pain

ChemInform, 2007-08, Vol.38 (33), p.no-no

Westaway, Susan M.

2007

Volltextzugriff (PDF)

Concerning the synthesis and enantioselective rearrangements of episulfoxides

Perkin 1 : an international journal of organic and bio-organic chemistry, 2000 (2), p.153-163

2000

Volltextzugriff (PDF)

Efficient Reformatsky Conjugate Additions to Alkylidene Malonates and Malonamides

ChemInform, 2007-07, Vol.38 (29), p.no-no

2007

Volltextzugriff (PDF)

1 – 25 von 34

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(29)
Mit Volltextzugriff
(31)

Publikationsform

Artikel
(34)

Sprache

Englisch
(34)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(26)
Life Sciences & Biomedicine
(19)
Humans
(16)
Animals
(13)
Chemistry
(13)
Chemistry, Organic
(13)
Physical Sciences
(13)
Chemistry, Medicinal
(12)
Pharmacology & Pharmacy
(12)
Biological And Medical Sciences
(10)
Medical Sciences
(9)
Pharmacology. Drug Treatments
(7)
Drug Design
(6)
Structure-Activity Relationship
(6)
Rats
(5)
Receptors, Gastrointestinal Hormone - Agonists
(5)
Receptors, Neuropeptide - Agonists
(5)
Digestive System
(4)
Enzyme Inhibitors - Chemistry
(4)
Enzyme Inhibitors - Pharmacology
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The Potential of Transient Receptor Potential Vanilloid Type 1 Channel Modulators for the Treatment of Pain

8‑Substituted Pyrido[3,4‑d]pyrimidin-4(3H)‑one Derivatives As Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors

Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4‑d]pyrimidin-4(3H)‑one Derivatives

Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 1. 3‑Amino-4-pyridine Carboxylate Derivatives

The Identification of and Rationale for Drugs Which Act at The Motilin Receptor

Interrogating the Druggability of the 2‑Oxoglutarate-Dependent Dioxygenase Target Class by Chemical Proteomics

Assessing histone demethylase inhibitors in cells: lessons learned

Assessing histone demethylase inhibitors in cells: lessons learned

Design and synthesis of 6-phenylnicotinamide derivatives as antagonists of TRPV1

Tetrahydroquinoline derivatives as opioid receptor antagonists

Discovery of N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate

Identification of small molecule agonists of the motilin receptor

N-Tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1

The discovery and optimisation of benzazepine sulfonamide and sulfones as potent agonists of the motilin receptor

The discovery of biaryl carboxamides as novel small molecule agonists of the motilin receptor

Stereoselective synthesis of conformationally constrained omega-amino acid analogues from pyroglutamic acid

The potential of transient receptor potential vanilloid type 1 channel modulators for the treatment of pain : Recent approaches in the treatment of neuropathic pain

Palladium-catalysed α-arylation of esters and amides under microwave conditions

Efficient Reformatsky Conjugate Additions to Alkylidene Malonates and Malonamides

Enantioselective synthesis of a putative hexaketide intermediate in the biosynthesis of the squalestatins

Discovery of N-(3-Fluorophenyl)-1-[4-([(3S)-3-methyl-1-piperazinyl]methyl)phenylacetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate

The Enantioselective Conversion of Three-Membered Ring Sulfoxides (Episulfoxides) into Alkenyl Sulfoxides using Chiral Lithium Amide Bases

The Potential of Transient Receptor Potential Vanilloid Type 1 Channel Modulators for the Treatment of Pain

Concerning the synthesis and enantioselective rearrangements of episulfoxides

Efficient Reformatsky Conjugate Additions to Alkylidene Malonates and Malonamides

Suchergebnisse filtern