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...

A calcineurin antifungal strategy with analogs of FK506

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2465-2471

2017

Volltextzugriff (PDF)

Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1467-1470

2005

Volltextzugriff (PDF)

A new family of H3 receptor antagonists based on the natural product Conessine

Bioorganic & medicinal chemistry letters, 2008-02, Vol.18 (4), p.1490-1494

2008

Volltextzugriff (PDF)

Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1063-1066

2002

Volltextzugriff (PDF)

Discovery and Structure−Activity Relationship of 3-Methoxy-N-(3-(1-methyl-1H-pyrazol-5-yl)-4-(2-morpholinoethoxy)phenyl)benzamide (APD791): A Highly Selective 5-Hydroxytryptamine2A Receptor Inverse Agonist for the Treatment of Arterial Thrombosis

Journal of medicinal chemistry, 2010-06, Vol.53 (11), p.4412-4421

2010

Volltextzugriff (PDF)

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT2A inverse-agonists and their application as antiplatelet agents

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (18), p.5486-5489

2009

Volltextzugriff (PDF)

Synthesis of a tetramethyl analog of teleocidin

Journal of organic chemistry, 1991-07, Vol.56 (15), p.4706-4713

1991

Volltextzugriff (PDF)

Alkaloid synthesis via intramolecular ene reactions. 1. Application to (.+-.)-crinane

Journal of the American Chemical Society, 1981-06, Vol.103 (11), p.3173-3177

1981

Volltextzugriff (PDF)

Discovery of 1-[3-(4-Bromo-2-methyl-2 H -pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine 2A Inverse Agonists for the Treatment of Insomnia

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.1923-1936

2010

Volltextzugriff (PDF)

Discovery and SAR of new benzazepines as potent and selective 5-HT 2C receptor agonists for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1467-1470

2005

Volltextzugriff (PDF)

Mono-N-alkylation of anthranilamides via quinazolinones. An efficient synthesis of G5598, a benzodiazepine dione gpIIbIIIa antagonist

Tetrahedron letters, 1994-04, Vol.35 (14), p.2113-2116

1994

Volltextzugriff (PDF)

A new family of H 3 receptor antagonists based on the natural product Conessine

Bioorganic & medicinal chemistry letters, 2008-02, Vol.18 (4), p.1490-1494

2008

Volltextzugriff (PDF)

Discovery of 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine2A Inverse Agonists for the Treatment of Insomnia

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.1923-1936

2010

Volltextzugriff (PDF)

Resource ReviewsMastering the Instructional Design Process: A Systematic Approach, (2nd Ed.), by RothwellWilliam J.KazanasH. C.San Francisco, CA: Jossey-Bass, 1998. 425 pages, hard cover

Academy of Management learning & education, 2002-12, Vol.1 (2), p.220-221

Webb, Robert R.

2002

Volltextzugriff (PDF)

Synthesis of 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]butane and 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]-2-butene, novel heterobifunctional crosslinking reagents

Bioconjugate chemistry, 1990-03, Vol.1 (2), p.96-99

1990

Volltextzugriff (PDF)

Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidine

Journal of organic chemistry, 1982-03, Vol.47 (7), p.1302-1309

1982

Volltextzugriff (PDF)

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT sub(2A) inverse-agonists and their application as antiplatelet agents

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (18), p.5486-5489

2009

Volltextzugriff (PDF)

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT 2A inverse-agonists and their application as antiplatelet agents

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (18), p.5486-5489

2009

Volltextzugriff (PDF)

Lewis acid catalyzed cyclocondensations of formaldehyde with activated dienes. A direct route to pyranosidal pentoses

Journal of organic chemistry, 1984-06, Vol.49 (11), p.1955-1958

1984

Volltextzugriff (PDF)

From Peptide to Non-Peptide. 2. The de Novo Design of Potent, Non-peptidal Inhibitors of Platelet Aggregation Based on a Benzodiazepinedione Scaffold

Journal of the American Chemical Society, 1994-06, Vol.116 (12), p.5077-5083

1994

Volltextzugriff (PDF)

A new family of H sub(3) receptor antagonists based on the natural product Conessine

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1490-1494

2008

Volltextzugriff (PDF)

1 – 25 von 1.728

Suche als RSS-Feed

Aktive Filter

PublikationsformBücher

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.538)
Mit Volltextzugriff
(1.371)

Publikationsform

Sprache

Englisch
(1.724)
Deutsch
(1)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(1.225)
Life Sciences & Biomedicine
(926)
Humans
(664)
Female
(378)
Male
(355)
Biological And Medical Sciences
(350)
Physical Sciences
(264)
Medical Sciences
(252)
Animals
(245)
Middle Aged
(186)
Adult
(185)
Aged
(151)
Cardiovascular System & Cardiology
(127)
Fundamental And Applied Biological Sciences. Psychology
(110)
Cardiac & Cardiovascular Systems
(105)
General & Internal Medicine
(93)
Biochemistry & Molecular Biology
(89)
Social Sciences
(88)
Adolescent
(87)
Chemistry
(85)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

A calcineurin antifungal strategy with analogs of FK506

Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity

A new family of H3 receptor antagonists based on the natural product Conessine

Discovery and Structure−Activity Relationship of (1R)-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT2C Receptor Agonist for the Treatment of Obesity

Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1

Discovery and Structure−Activity Relationship of 3-Methoxy-N-(3-(1-methyl-1H-pyrazol-5-yl)-4-(2-morpholinoethoxy)phenyl)benzamide (APD791): A Highly Selective 5-Hydroxytryptamine2A Receptor Inverse Agonist for the Treatment of Arterial Thrombosis

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT2A inverse-agonists and their application as antiplatelet agents

Synthesis of a tetramethyl analog of teleocidin

Alkaloid synthesis via intramolecular ene reactions. 1. Application to (.+-.)-crinane

Discovery of 1-[3-(4-Bromo-2-methyl-2 H -pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine 2A Inverse Agonists for the Treatment of Insomnia

Discovery and SAR of new benzazepines as potent and selective 5-HT 2C receptor agonists for the treatment of obesity

Mono-N-alkylation of anthranilamides via quinazolinones. An efficient synthesis of G5598, a benzodiazepine dione gpIIbIIIa antagonist

A new family of H 3 receptor antagonists based on the natural product Conessine

Discovery of 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine2A Inverse Agonists for the Treatment of Insomnia

Discovery and Structure−Activity Relationship of 3-Methoxy- N -(3-(1-methyl-1 H -pyrazol-5-yl)-4-(2-morpholinoethoxy)phenyl)benzamide (APD791): A Highly Selective 5-Hydroxytryptamine 2A Receptor Inverse Agonist for the Treatment of Arterial Thrombosis

Resource ReviewsMastering the Instructional Design Process: A Systematic Approach, (2nd Ed.), by RothwellWilliam J.KazanasH. C.San Francisco, CA: Jossey-Bass, 1998. 425 pages, hard cover

Synthesis of 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]butane and 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]-2-butene, novel heterobifunctional crosslinking reagents

Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidine

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT sub(2A) inverse-agonists and their application as antiplatelet agents

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT 2A inverse-agonists and their application as antiplatelet agents

Lewis acid catalyzed cyclocondensations of formaldehyde with activated dienes. A direct route to pyranosidal pentoses

From Peptide to Non-Peptide. 2. The de Novo Design of Potent, Non-peptidal Inhibitors of Platelet Aggregation Based on a Benzodiazepinedione Scaffold

Discovery and Structure-Activity Relationship of (1R)-8-Chloro-2,3,4,5-tetrahydro-l-methyl-1H-3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT2C Receptor Agonist for the Treatment of Obesity

Discovery and Structure−Activity Relationship of (1 R )-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1 H -3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT 2C Receptor Agonist for the Treatment of Obesity

A new family of H sub(3) receptor antagonists based on the natural product Conessine

Aktive Filter

Suchergebnisse filtern