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...

In Vitro and In Vivo Activities of Novel, Semisynthetic Thiopeptide Inhibitors of Bacterial Elongation Factor Tu

Antimicrobial Agents and Chemotherapy, 2011-11, Vol.55 (11), p.5277-5283

2011

Volltextzugriff (PDF)

Organotitanium compounds in organic synthesis

Pure and applied chemistry, 1996-01, Vol.68 (3), p.667-670

1996

Volltextzugriff (PDF)

ACE2 X-Ray Structures Reveal a Large Hinge-bending Motion Important for Inhibitor Binding and Catalysis

Journal of molecular biology, 2004-04, Vol.279 (17), p.17996-18007

2004

Volltextzugriff (PDF)

Total synthesis of cycloisodityrosine, RA-VII, deoxybouvardin, and N29-desmethyl-RA-VII: Identification of the pharmacophore and reversal of the subunit functional roles

Journal of the American Chemical Society, 1993-05, Vol.115 (9), p.3420-3430

1993

Volltextzugriff (PDF)

Cyclic imides as potent and selective alpha-1A adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 2001-07, Vol.11 (14), p.1959-1962

2001

Volltextzugriff (PDF)

Ocular iontophoresis of EGP-437 (dexamethasone phosphate) in dry eye patients: results of a randomized clinical trial

Clinical ophthalmology (Auckland, N.Z.), 2011-01, Vol.5 (default), p.633-643

2011

Volltextzugriff (PDF)

Selective alpha-1a adrenergic receptor antagonists. Effects of pharmacophore regio- and stereochemistry on potency and selectivity

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (18), p.2495-2500

1998

Volltextzugriff (PDF)

Substrate-Based Design of the First Class of Angiotensin-Converting Enzyme-Related Carboxypeptidase (ACE2) Inhibitors

Journal of the American Chemical Society, 2002-10, Vol.124 (40), p.11852-11853

2002

Volltextzugriff (PDF)

Phenylacetamides as selective alpha-1A adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1621-1624

2000

Volltextzugriff (PDF)

Identification of 2-{2-[2-(5-Bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl}-4,5-dihydro-1H-imidazole (ML00253764), a Small Molecule Melanocortin 4 Receptor Antagonist That Effectively Reduces Tumor-Induced Weight Loss in a Mouse Model

Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1602-1604

2004

Volltextzugriff (PDF)

Impairment of immunocompetent mouse spleen cell functions by infection with coxsackievirus B3

The Journal of infectious diseases, 1982-12, Vol.146 (6), p.797-805

1982

Volltextzugriff (PDF)

Synthesis and biological evaluation of imidazole-based small molecule antagonists of the melanocortin 4 receptor (MC4-R)

Bioorganic & medicinal chemistry letters, 2004-07, Vol.14 (14), p.3721-3725

2004

Volltextzugriff (PDF)

Identification and structure–activity relationships of a new series of Melanocortin-4 receptor antagonists

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (8), p.2302-2305

2006

Volltextzugriff (PDF)

Identification of ortho-amino benzamides and nicotinamides as MCHr1 antagonists

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (19), p.4174-4179

2005

Volltextzugriff (PDF)

Selective α-1A adrenergic receptor antagonists. effects of pharmacophore regio- and stereochemistry on potency and selectivity

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (18), p.2495-2500

1998

Volltextzugriff (PDF)

Determination of the relative and absolute stereochemistry of a potent and alpha1A-selective adrenoceptor antagonist

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (24), p.2705-2707

2000

Volltextzugriff (PDF)

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 2. Approaches to eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4778-4793

1999

Volltextzugriff (PDF)

Phenylacetamides as selective α-1A adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1621-1624

2000

Volltextzugriff (PDF)

Expedient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2(1 H)-ones

Tetrahedron letters, 1998-12, Vol.39 (51), p.9315-9318

1998

Volltextzugriff (PDF)

Design, synthesis and evaluation of bouvardin, deoxybouvardin and RA-I-XIV pharmacophore analogs

Bioorganic & medicinal chemistry, 1994-02, Vol.2 (2), p.85-100

1994

Volltextzugriff (PDF)

A claisen rearrangement strategy for the three-atom ring expansion of cyclic ketones. A total synthesis of (±) precapnelladiene

Tetrahedron letters, 1990, Vol.31 (47), p.6799-6802

1990

Volltextzugriff (PDF)

Synthesis of 8-membered ring lactones from dioxolenones

Journal of the Chemical Society. Chemical communications, 1990 (11), p.836-837

1990

Volltextzugriff (PDF)

4-Amino-2-[4-[1-(benzyloxycarbonyl)-2(S)- [[(1,1-dimethylethyl)amino]carbonyl]-piperazinyl]-6, 7-dimethoxyquinazoline (L-765,314): a potent and selective alpha1b adrenergic receptor antagonist

Journal of medicinal chemistry, 1998-04, Vol.41 (8), p.1205-1208

1998

Volltextzugriff (PDF)

Complestatin to chloropeptin I via a quantitative acid catalyzed rearrangement. Absolute stereochemical determination of complestatin

Tetrahedron letters, 1998-04, Vol.39 (16), p.2247-2248

1998

Volltextzugriff (PDF)

4-Amino-2-[4-[1-(benzyloxycarbonyl)-2(S)-[[(1,1-dimethylethyl)amino]carbonyl]-pi perazinyl]-6,7-dimethoxyquinazoline (L-765,314) : A potent and selective α1b adrenergic receptor antagonist

Journal of medicinal chemistry, 1998, Vol.41 (8), p.1205-1208

1998

Volltextzugriff (PDF)

1 – 25 von 941

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(723)
Mit Volltextzugriff
(795)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(538)
Physical Sciences
(285)
Technology
(193)
Physics
(191)
Life Sciences & Biomedicine
(190)
Humans
(172)
Physics, Applied
(117)
Male
(106)
Female
(95)
Materials Science
(76)
Animals
(67)
Biological And Medical Sciences
(65)
Physics, Condensed Matter
(65)
Materials Science, Multidisciplinary
(61)
Medical Sciences
(55)
Exact Sciences And Technology
(52)
Middle Aged
(51)
Adult
(50)
Engineering
(44)
Imaging Science & Photographic Technology
(44)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(5)
... seit 90 Tagen
(12)

Menü

Weitere Dienste

Einstellungen

In Vitro and In Vivo Activities of Novel, Semisynthetic Thiopeptide Inhibitors of Bacterial Elongation Factor Tu

Organotitanium compounds in organic synthesis

ACE2 X-Ray Structures Reveal a Large Hinge-bending Motion Important for Inhibitor Binding and Catalysis

Total synthesis of cycloisodityrosine, RA-VII, deoxybouvardin, and N29-desmethyl-RA-VII: Identification of the pharmacophore and reversal of the subunit functional roles

Cyclic imides as potent and selective alpha-1A adrenergic receptor antagonists

Ocular iontophoresis of EGP-437 (dexamethasone phosphate) in dry eye patients: results of a randomized clinical trial

Selective alpha-1a adrenergic receptor antagonists. Effects of pharmacophore regio- and stereochemistry on potency and selectivity

Substrate-Based Design of the First Class of Angiotensin-Converting Enzyme-Related Carboxypeptidase (ACE2) Inhibitors

Phenylacetamides as selective alpha-1A adrenergic receptor antagonists

Identification of 2-{2-[2-(5-Bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl}-4,5-dihydro-1H-imidazole (ML00253764), a Small Molecule Melanocortin 4 Receptor Antagonist That Effectively Reduces Tumor-Induced Weight Loss in a Mouse Model

Impairment of immunocompetent mouse spleen cell functions by infection with coxsackievirus B3

Synthesis and biological evaluation of imidazole-based small molecule antagonists of the melanocortin 4 receptor (MC4-R)

Identification and structure–activity relationships of a new series of Melanocortin-4 receptor antagonists

Identification of ortho-amino benzamides and nicotinamides as MCHr1 antagonists

Selective α-1A adrenergic receptor antagonists. effects of pharmacophore regio- and stereochemistry on potency and selectivity

Determination of the relative and absolute stereochemistry of a potent and alpha1A-selective adrenoceptor antagonist

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 2. Approaches to eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety

Phenylacetamides as selective α-1A adrenergic receptor antagonists

Expedient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2(1 H)-ones

Design, synthesis and evaluation of bouvardin, deoxybouvardin and RA-I-XIV pharmacophore analogs

A claisen rearrangement strategy for the three-atom ring expansion of cyclic ketones. A total synthesis of (±) precapnelladiene

Synthesis of 8-membered ring lactones from dioxolenones

4-Amino-2-[4-[1-(benzyloxycarbonyl)-2(S)- [[(1,1-dimethylethyl)amino]carbonyl]-piperazinyl]-6, 7-dimethoxyquinazoline (L-765,314): a potent and selective alpha1b adrenergic receptor antagonist

Complestatin to chloropeptin I via a quantitative acid catalyzed rearrangement. Absolute stereochemical determination of complestatin

4-Amino-2-[4-[1-(benzyloxycarbonyl)-2(S)-[[(1,1-dimethylethyl)amino]carbonyl]-pi perazinyl]-6,7-dimethoxyquinazoline (L-765,314) : A potent and selective α1b adrenergic receptor antagonist

Suchergebnisse filtern