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...

1-2-(2,2,2-Trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (10), p.3125-3128

2010

Volltextzugriff (PDF)

1,2,3,4-Tetrahydroisoquinolinyl sulfamic acids as phosphatase PTP1B inhibitors

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (6), p.1574-1578

2006

Volltextzugriff (PDF)

1,2,4-Triazole d-ribose derivatives: Design, synthesis and antitumoral evaluation

European journal of medicinal chemistry, 2012, Vol.47 (1), p.104-110

2012

Volltextzugriff (PDF)

1,2,4-Triazolo[3,4- a]pyridine as a novel, constrained template for fibrinogen receptor (GPIIb/IIIa) antagonists

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (19), p.2619-2622

2001

Volltextzugriff (PDF)

1,2,5,6-tetrahydropyridine oxime ethers incorporating electron withdrawing groups are potent and selective muscarinic agonists

Bioorganic & medicinal chemistry letters, 1994-02, Vol.4 (4), p.557-562

1994

Volltextzugriff (PDF)

1-(2-Ethoxyethyl)-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (10), p.3120-3124

2010

Volltextzugriff (PDF)

1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (16), p.1867-1870

2000

Volltextzugriff (PDF)

1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (16), p.1863-1866

2000

Volltextzugriff (PDF)

1-(2-Naphthyl)-1H-pyrazole-5-carboxylamides as potent factor xa inhibitors. Part 2: A survey of P4 motifs

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (5), p.1221-1227

2004

Volltextzugriff (PDF)

1-(2-Naphthyl)-1H-pyrazole-5-carboxylamides as potent factor xa inhibitors. Part 3: Design, synthesis and sar of orally bioavailable benzamidine-P4 inhibitors

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (5), p.1229-1234

2004

Volltextzugriff (PDF)

1,25-Dihydroxyvitamin D3 induces splenocyte apoptosis and enhances BALB/c mice sensitivity to toxoplasmosis

The Journal of steroid biochemistry and molecular biology, 2005-07, Vol.96 (2), p.179-185

2005

Volltextzugriff (PDF)

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2741-2745

2001

Volltextzugriff (PDF)

1,3-dioxane-4,6-dione-5-carboxamide-based inhibitors of human group IIa phospholipase A2 : X-ray structure of the complex and interfacial selection of inhibitors from a structural library

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1097-1102

1999

Volltextzugriff (PDF)

1,4-Benzodiazepin-2-one derived neurokinin-1 receptor antagonists

Bioorganic & medicinal chemistry letters, 1997-08, Vol.7 (15), p.2037-2042

1997

Volltextzugriff (PDF)

1,4-Benzodiazepine-2,5-diones as small molecule antagonists of the HDM2–p53 interaction: discovery and SAR

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (3), p.765-770

2005

Volltextzugriff (PDF)

1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

Bioorganic & medicinal chemistry letters, 1997-12, Vol.7 (24), p.3153-3158

1997

Volltextzugriff (PDF)

1,4-substituted indoles: a potent and selective class of angiotensin II receptor antagonists

Bioorganic & medicinal chemistry letters, 1994-01, Vol.4 (1), p.145-150

1994

Volltextzugriff (PDF)

1.5-5 Years of uninterrupted cis-diamminedichloroplatinum II chemotherapy for metastatic cervical cancer

Gynecologic oncology, 1987-05, Vol.27 (1), p.24-33

1987

Volltextzugriff (PDF)

1,5-Bis(4-amidinophenoxy) pentane (pentamidine) is a potent inhibitor of [3H]idazoxan binding to imidazoline I2 binding sites

European journal of pharmacology, 1998-07, Vol.353 (1), p.97-103

1998

Volltextzugriff (PDF)

A 1.5-Mb Contig within the Cat Eye Syndrome Critical Region at Human Chromosome 22q11.2

Genomics (San Diego, Calif.), 1999-04, Vol.57 (2), p.306-309

1999

Volltextzugriff (PDF)

A 1.5-Megabase Physical Map Encompassing the Multiple Endocrine Neoplasia Type-1 (MEN1) Locus on Chromosome 11q13

Genomics (San Diego, Calif.), 1996-12, Vol.38 (2), p.166-173

1996

Volltextzugriff (PDF)

1,5-Substituted nipecotic amides: Selective PDE8 inhibitors displaying diastereomer-dependent microsomal stability

Bioorganic & medicinal chemistry letters, 2011-05, Vol.21 (10), p.3095-3098

2011

Volltextzugriff (PDF)

1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitors

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3217-3220

2004

Volltextzugriff (PDF)

1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor

European journal of pharmacology, 1989-02, Vol.161 (2), p.281-282

1989

Volltextzugriff (PDF)

1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK3

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (8), p.2230-2234

2009

Volltextzugriff (PDF)

1 – 25 von 33.600

Suche als RSS-Feed

Aktive Filter

KollektionElsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)

ThemaMedical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32.207)
Mit Volltextzugriff
(33.328)

Publikationsform

Artikel
(33.213)
Tagungsberichte
(387)

Sprache

Englisch
(33.600)
Französisch
(3)

Erscheinungsjahr

n.n

Thema

Biological And Medical Sciences
(33.598)
Science & Technology
(28.063)
Life Sciences & Biomedicine
(27.830)
Humans
(21.821)
Male
(16.061)
Female
(15.225)
Adult
(9.279)
Middle Aged
(9.104)
Pharmacology. Drug Treatments
(8.795)
Animals
(8.190)
Aged
(6.335)
Pharmacology & Pharmacy
(4.810)
Neurosciences & Neurology
(3.774)
Rats
(3.702)
Adolescent
(3.625)
Psychology. Psychoanalysis. Psychiatry
(3.308)
Cardiovascular System & Cardiology
(3.174)
Neurosciences
(3.004)
Cardiac & Cardiovascular Systems
(3.001)

14 weitere anzeigen...

Weniger anzeigen...

Kollektion

Ingenta
(32.178)
Elsevier ScienceDirect Journals Complete
(31.770)
MEDLINE
(28.913)
WK Lippincott Williams & Wilkins–Connect here FIRST to enable access
(11.630)
NUS Single-Journal Subscriptions
(6.806)
IngentaConnect Journals
(3.453)
EZB Electronic Journals Library
(2.338)
BSC - Ebsco (Business Source Ultimate)
(1.212)
EBSCO - Psychology & Behavioral Sciences Collection
(1.212)
Applied Social Sciences Index & Abstracts (ASSIA)
(848)
Oxford Journals
(550)
Oxford Journals 2020 Medicine
(550)
Wiley Online Library
(355)
Sociological Abstracts
(277)
Wiley Online Library
(209)
SpringerLink Series
(186)
ERIC
(114)
SAGE Journals Online
(47)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(15)

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

1-2-(2,2,2-Trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

1,2,3,4-Tetrahydroisoquinolinyl sulfamic acids as phosphatase PTP1B inhibitors

1,2,4-Triazole d-ribose derivatives: Design, synthesis and antitumoral evaluation

1,2,4-Triazolo[3,4- a]pyridine as a novel, constrained template for fibrinogen receptor (GPIIb/IIIa) antagonists

1,2,5,6-tetrahydropyridine oxime ethers incorporating electron withdrawing groups are potent and selective muscarinic agonists

1-(2-Ethoxyethyl)-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists

1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents

1-(2-Naphthyl)-1H-pyrazole-5-carboxylamides as potent factor xa inhibitors. Part 2: A survey of P4 motifs

1-(2-Naphthyl)-1H-pyrazole-5-carboxylamides as potent factor xa inhibitors. Part 3: Design, synthesis and sar of orally bioavailable benzamidine-P4 inhibitors

1,25-Dihydroxyvitamin D3 induces splenocyte apoptosis and enhances BALB/c mice sensitivity to toxoplasmosis

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity

1,3-dioxane-4,6-dione-5-carboxamide-based inhibitors of human group IIa phospholipase A2 : X-ray structure of the complex and interfacial selection of inhibitors from a structural library

1,4-Benzodiazepin-2-one derived neurokinin-1 receptor antagonists

1,4-Benzodiazepine-2,5-diones as small molecule antagonists of the HDM2–p53 interaction: discovery and SAR

1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

1,4-substituted indoles: a potent and selective class of angiotensin II receptor antagonists

1.5-5 Years of uninterrupted cis-diamminedichloroplatinum II chemotherapy for metastatic cervical cancer

1,5-Bis(4-amidinophenoxy) pentane (pentamidine) is a potent inhibitor of [3H]idazoxan binding to imidazoline I2 binding sites

A 1.5-Mb Contig within the Cat Eye Syndrome Critical Region at Human Chromosome 22q11.2

A 1.5-Megabase Physical Map Encompassing the Multiple Endocrine Neoplasia Type-1 (MEN1) Locus on Chromosome 11q13

1,5-Substituted nipecotic amides: Selective PDE8 inhibitors displaying diastereomer-dependent microsomal stability

1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitors

1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor

1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK3

Aktive Filter

Suchergebnisse filtern