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...

Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists: binding to a common chemokine receptor motif within the helical bundle

The Journal of biological chemistry, 2000-08, Vol.275 (33), p.25562-25571

2000

Volltextzugriff (PDF)

D3R Grand Challenge 3: blind prediction of protein–ligand poses and affinity rankings

Journal of computer-aided molecular design, 2019-01, Vol.33 (1), p.1-18

2019

Volltextzugriff (PDF)

Sequence Analyses of G-Protein-Coupled Receptors: Similarities to Rhodopsin

Biochemistry (Easton), 2003-03, Vol.42 (10), p.2759-2767

2003

Volltextzugriff (PDF)

Substrate-dependent inhibition or stimulation of HIV RNase H activity by non-nucleoside reverse transcriptase inhibitors (NNRTIs)

Biochemical and biophysical research communications, 2007-01, Vol.352 (2), p.341-350

2007

Volltextzugriff (PDF)

Identification of Residues in the Monocyte Chemotactic Protein-1 That Contact the MCP-1 Receptor, CCR2

Biochemistry (Easton), 1999-10, Vol.38 (40), p.13013-13025

1999

Volltextzugriff (PDF)

Rational design of 6-methylsulfonylindoles as selective cyclooxygenase-2 inhibitors

Bioorganic & medicinal chemistry letters, 2004-09, Vol.14 (18), p.4741-4745

2004

Volltextzugriff (PDF)

Lactams as EP4 Prostanoid Receptor Agonists. 3. Discovery of N-Ethylbenzoic Acid 2-Pyrrolidinones as Subtype Selective Agents

Journal of medicinal chemistry, 2004-12, Vol.47 (25), p.6124-6127

2004

Volltextzugriff (PDF)

Possible Role of the 11-cis-Retinyl Conformation in Controlling the Dual Decay Processes of Excited Rhodopsin

Proceedings of the National Academy of Sciences - PNAS, 2005-08, Vol.102 (31), p.10783-10787

2005

Volltextzugriff (PDF)

Synthesis and Sar of bulky 1-azabicyclo[2.2.1]-3-one oximes as muscarinic receptor subtype selective agonists

Life sciences (1973), 1993, Vol.52 (5), p.505-511

1993

Volltextzugriff (PDF)

Design of Annulated Pyrazoles As Inhibitors of HIV-1 Reverse Transcriptase

Journal of medicinal chemistry, 2009-05, Vol.51 (23)

2009

Volltextzugriff (PDF)

Sequence Analyses of G-Protein-Coupled Receptors: Similarities to Rhodopsin

Biochemistry (Easton), 2003-04, Vol.42 (14), p.4310-4310

2003

Volltextzugriff (PDF)

CI-1017, a functionally M1-selective muscarinic agonist: design, synthesis, and preclinical pharmacology

Pharmaceutica acta Helvetiae, 2000-03, Vol.74 (2-3), p.141-148

2000

Volltextzugriff (PDF)

(±)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-methyl-5-aryl-2-penten-4-ynyl) oximes: Potent muscarinic agonists

Bioorganic & medicinal chemistry letters, 1995-03, Vol.5 (6), p.637-642

1995

Volltextzugriff (PDF)

A rationale for the design and synthesis of m1 selective muscarinic agonists

Bioorganic & medicinal chemistry letters, 1992-08, Vol.2 (8), p.821-826

1992

Volltextzugriff (PDF)

Crystal Structure of Phenylmethanesulfonyl Fluoride-Treated Human Chymase at 1.9 Å

Biochemistry (Easton), 1997-11, Vol.36 (47), p.14318-14324

1997

Volltextzugriff (PDF)

Z-(±)-1-azabicyclo[2.2.1]heptan-3-one, O-(3-aryl-2-propynyl) oximes as potential m1-subtype selective muscarinic agonists

Bioorganic & medicinal chemistry letters, 1995-03, Vol.5 (6), p.631-636

1995

Volltextzugriff (PDF)

Substitution of Lysine-181 to Aspartic Acid in the Third Transmembrane Region of the Endothelin (ET) Type B Receptor Selectively Reduces Its High-Affinity Binding with ET-3 Peptide

Journal of cardiovascular pharmacology, 1992, Vol.20 Suppl 12, p.S5-S7

1992

Volltextzugriff (PDF)

Isomers, visual pigment, and bacteriorhodopsin analogs of 3,7,13-trimethyl-10-isopropyl-2,4,6,8,10-tetradecapentaenal and 3,7,11-trimethyl-10-isopropyl-2,4,6,8,10-dodecapentaenal (two ring open retinal analogs)

Bioorganic chemistry, 1989-06, Vol.17 (2), p.217-223

1989

Volltextzugriff (PDF)

Design and Synthesis of m1-Selective Muscarinic Agonists: (R)-(−)-(Z)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-(3‘-Methoxyphenyl)-2-propynyl)- oxime Maleate (CI-1017), a Functionally m1-Selective Muscarinic Agonist

Journal of medicinal chemistry, 1998-07, Vol.41 (14), p.2524-2536

1998

Volltextzugriff (PDF)

Azulenic retinoids: novel nonbenzenoid aromatic retinoids with anticancer activity

Journal of medicinal chemistry, 1993-10, Vol.36 (21), p.3137-3147

1993

Volltextzugriff (PDF)

Replacement of lysine-181 by aspartic acid in the third transmembrane region of endothelin type B receptor reduces its affinity to endothelin peptides and sarafotoxin 6c without affecting G protein coupling

Journal of cellular biochemistry, 1992-10, Vol.50 (2), p.159-164

1992

Volltextzugriff (PDF)

Mutations of aspartate 103 in the Hm2 receptor and alterations in receptor binding properties of muscarinic agonists

Life sciences (1973), 1995, Vol.56 (11), p.923-929

1995

Volltextzugriff (PDF)

Molecular modeling studies of the m1 and m2 muscarinic receptors leading to the design of selective m1 agonists

Life sciences (1973), 1993, Vol.52 (5), p.561-561

1993

Volltextzugriff (PDF)

The doubly hindered 7,11-dicis, 7,9,11-tricis, 7,11,13-tricis and all-cis isomers of retinonitrile and retinal

Tetrahedron, 1990, Vol.46 (11), p.3769-3780

1990

Volltextzugriff (PDF)

The shape of a three-dimensional binding site of rhodopsin based on molecular modeling analyses of isomeric and other visual pigment analogues: bioorganic studies of visual pigments. XI

Journal of the American Chemical Society, 1988, Vol.110 (26), p.8617-8623

1988

Volltextzugriff (PDF)

1 – 25 von 118

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(110)
Mit Volltextzugriff
(105)

Publikationsform

Sprache

Englisch
(118)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists: binding to a common chemokine receptor motif within the helical bundle

D3R Grand Challenge 3: blind prediction of protein–ligand poses and affinity rankings

Sequence Analyses of G-Protein-Coupled Receptors: Similarities to Rhodopsin

Substrate-dependent inhibition or stimulation of HIV RNase H activity by non-nucleoside reverse transcriptase inhibitors (NNRTIs)

Identification of Residues in the Monocyte Chemotactic Protein-1 That Contact the MCP-1 Receptor, CCR2

Rational design of 6-methylsulfonylindoles as selective cyclooxygenase-2 inhibitors

Lactams as EP4 Prostanoid Receptor Agonists. 3. Discovery of N-Ethylbenzoic Acid 2-Pyrrolidinones as Subtype Selective Agents

Possible Role of the 11-cis-Retinyl Conformation in Controlling the Dual Decay Processes of Excited Rhodopsin

Synthesis and Sar of bulky 1-azabicyclo[2.2.1]-3-one oximes as muscarinic receptor subtype selective agonists

Design of Annulated Pyrazoles As Inhibitors of HIV-1 Reverse Transcriptase

Sequence Analyses of G-Protein-Coupled Receptors: Similarities to Rhodopsin

CI-1017, a functionally M1-selective muscarinic agonist: design, synthesis, and preclinical pharmacology

(±)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-methyl-5-aryl-2-penten-4-ynyl) oximes: Potent muscarinic agonists

A rationale for the design and synthesis of m1 selective muscarinic agonists

Crystal Structure of Phenylmethanesulfonyl Fluoride-Treated Human Chymase at 1.9 Å

Z-(±)-1-azabicyclo[2.2.1]heptan-3-one, O-(3-aryl-2-propynyl) oximes as potential m1-subtype selective muscarinic agonists

Substitution of Lysine-181 to Aspartic Acid in the Third Transmembrane Region of the Endothelin (ET) Type B Receptor Selectively Reduces Its High-Affinity Binding with ET-3 Peptide

Isomers, visual pigment, and bacteriorhodopsin analogs of 3,7,13-trimethyl-10-isopropyl-2,4,6,8,10-tetradecapentaenal and 3,7,11-trimethyl-10-isopropyl-2,4,6,8,10-dodecapentaenal (two ring open retinal analogs)

Design and Synthesis of m1-Selective Muscarinic Agonists: (R)-(−)-(Z)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-(3‘-Methoxyphenyl)-2-propynyl)- oxime Maleate (CI-1017), a Functionally m1-Selective Muscarinic Agonist

Azulenic retinoids: novel nonbenzenoid aromatic retinoids with anticancer activity

Replacement of lysine-181 by aspartic acid in the third transmembrane region of endothelin type B receptor reduces its affinity to endothelin peptides and sarafotoxin 6c without affecting G protein coupling

Mutations of aspartate 103 in the Hm2 receptor and alterations in receptor binding properties of muscarinic agonists

Molecular modeling studies of the m1 and m2 muscarinic receptors leading to the design of selective m1 agonists

The doubly hindered 7,11-dicis, 7,9,11-tricis, 7,11,13-tricis and all-cis isomers of retinonitrile and retinal

The shape of a three-dimensional binding site of rhodopsin based on molecular modeling analyses of isomeric and other visual pigment analogues: bioorganic studies of visual pigments. XI

Suchergebnisse filtern