UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 161

Sortiert nach

Pterostilbene, a New Agonist for the Peroxisome Proliferator-Activated Receptor α-Isoform, Lowers Plasma Lipoproteins and Cholesterol in Hypercholesterolemic Hamsters

Journal of agricultural and food chemistry, 2005-05, Vol.53 (9), p.3403-3407

2005

Volltextzugriff (PDF)

Effects of synephrine and beta-phenethylamine on human alpha-adrenoceptor subtypes

Planta medica, 2010-07, Vol.76 (10), p.981

2010

Volltextzugriff (PDF)

Pharmacological effects of ephedrine alkaloids on human alpha(1)- and alpha(2)-adrenergic receptor subtypes

The Journal of pharmacology and experimental therapeutics, 2007-07, Vol.322 (1), p.214

2007

Volltextzugriff (PDF)

Activation of peroxisome proliferator-activated receptor isoforms and inhibition of prostaglandin H2 synthases by ibuprofen, naproxen, and indomethacin

Biochemical pharmacology, 2001-12, Vol.62 (12), p.1587-1595

2001

Volltextzugriff (PDF)

Bioassay for the Identification of Natural Product-Based Activators of Peroxisome Proliferator-Activated Receptor-γ (PPARγ): The Marine Sponge Metabolite Psammaplin A Activates PPARγ and Induces Apoptosis in Human Breast Tumor Cells

Journal of natural products (Washington, D.C.), 2006-04, Vol.69 (4), p.547-552

2006

Volltextzugriff (PDF)

Direct effects of ephedrine isomers on human β-adrenergic receptor subtypes

Biochemical pharmacology, 1999-09, Vol.58 (5), p.807-810

1999

Volltextzugriff (PDF)

Medetomidine analogs as selective agonists for the human α2-adrenoceptors

Biochemical pharmacology, 2004, Vol.67 (1), p.87-96

2004

Volltextzugriff (PDF)

2-Amino-4-benzyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridines: Novel Selective β3-Adrenoceptor Agonists

Journal of medicinal chemistry, 1999-06, Vol.42 (12), p.2287-2294

1999

Volltextzugriff (PDF)

Bioisosteric phentolamine analogs as selective human alpha(2)- versus alpha(1)-adrenoceptor ligands

European journal of pharmacology, 2008-08, Vol.590 (1-3), p.53-60

2008

Volltextzugriff (PDF)

Evaluation of β-adrenergic receptor subtypes in the human prostate cancer cell line-LNCaP

Biochemical pharmacology, 2003-05, Vol.65 (9), p.1489-1494

2003

Volltextzugriff (PDF)

Bioisosteric phentolamine analogs as selective human α2-versus α1-adrenoceptor ligands

European journal of pharmacology, 2008-08, Vol.590 (1-3), p.53-60

2008

Volltextzugriff (PDF)

Bioisosteric phentolamine analogs as potent α-adrenergic antagonists

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (21), p.4691-4695

2005

Volltextzugriff (PDF)

1-Benzyl-1,2,3,4-tetrahydroisoquinoline-6,7-diols as novel affinity and photoaffinity probes for β-adrenoceptor subtypes

Bioorganic & medicinal chemistry, 2006-03, Vol.14 (6), p.1684-1697

2006

Volltextzugriff (PDF)

Pseudolaric Acid Analogs as a New Class of Peroxisome Proliferator-Activated Receptor Agonists

Planta medica, 2002-08, Vol.68 (8), p.667-671

2002

Volltextzugriff (PDF)

Synthesis and biological studies of yohimbine derivatives on human α2C-adrenergic receptors

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (11), p.2758-2760

2005

Volltextzugriff (PDF)

Synthesis and in vitro platelet aggregation and TP receptor binding studies on bicyclic 5,8-ethanooctahydroisoquinolines and 5,8-ethanotetrahydroisoquinolines

Bioorganic & medicinal chemistry, 2002-08, Vol.10 (8), p.2779-2793

2002

Volltextzugriff (PDF)

Synthesis and .alpha.-adrenergic activities of 2- and 4-substituted imidazoline and imidazole analogs

Journal of medicinal chemistry, 1992-02, Vol.35 (4), p.750-755

1992

Volltextzugriff (PDF)

Synthesis and Human β-Adrenoceptor Activity of 1-(3,5-Diiodo-4- methoxybenzyl)-1,2,3,4-tetrahydroisoquinolin-6-ol Derivatives in Vitro

Journal of medicinal chemistry, 2000-02, Vol.43 (4), p.591-598

2000

Volltextzugriff (PDF)

A Structure-Activity Relationship Study of Benzylic Modifications of 4-[1-(1-Naphthyl)ethyl]-1H-imidazoles on .alpha.1- and .alpha.2-Adrenergic Receptors

Journal of medicinal chemistry, 1994-07, Vol.37 (15), p.2328-2333

1994

Volltextzugriff (PDF)

Biochemical and functional characterization of 1-benzyl substituted trimetoquinol affinity analogs on rat and human β-adrenoceptors

Biochemical pharmacology, 2000-03, Vol.59 (5), p.517-529

2000

Volltextzugriff (PDF)

Activation of peroxisome proliferator-activated receptor isoforms and inhibition of prostaglandin H2 synthases by ibuprofen, naproxen, and indomethacin11Abbreviations: AA, arachidonic acid; ACO, acyl-CoA oxidase; COX; cyclooxygenase; NSAIDs, nonsteroidal anti-inflammatory drugs; PGHS, prostaglandin endoperoxide H synthase; PPP, platelet-poor plasma; PRP, platelet-rich plasma; PPAR, peroxisome proliferator-activated receptor; PPRE, peroxisome proliferator response element; and CoA coenzyme A

Biochemical pharmacology, 2001-12, Vol.62 (12), p.1587-1595

2001

Volltextzugriff (PDF)

Medetomidine Analogs as α2-Adrenergic Ligands. 3. Synthesis and Biological Evaluation of a New Series of Medetomidine Analogs and Their Potential Binding Interactions with α2-Adrenoceptors Involving a “Methyl Pocket”

Journal of medicinal chemistry, 1997-09, Vol.40 (19), p.3014-3024

1997

Volltextzugriff (PDF)

Activation of peroxisome proliferator-activated receptor isoforms and inhibition of prostaglandin H 2 synthases by ibuprofen, naproxen, and indomethacin

Biochemical pharmacology, 2001-12, Vol.62 (12), p.1587-1595

2001

Volltextzugriff (PDF)

Synthesis and Evaluation of Trimetoquinol Derivatives: Novel Thromboxane A2/Prostaglandin H2 Antagonists with Diminished β-Adrenergic Agonist Activity

Journal of medicinal chemistry, 1997-01, Vol.40 (1), p.85-91

1997

Volltextzugriff (PDF)

Iodinated Analogs of Trimetoquinol as Highly Potent and Selective β2-Adrenoceptor Ligands

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3701-3711

1996

Volltextzugriff (PDF)

1 – 25 von 161

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(151)
Mit Volltextzugriff
(153)

Publikationsform

Artikel
(159)
magazinearticle
(2)

Sprache

Englisch
(161)
Japanisch
(13)

Erscheinungsjahr

n.n

Thema

Science & Technology
(83)
Animals
(82)
Life Sciences & Biomedicine
(79)
Pharmacology & Pharmacy
(63)
Male
(56)
Rats
(54)
Biological And Medical Sciences
(53)
Humans
(53)
Medical Sciences
(48)
Pharmacology. Drug Treatments
(44)
In Vitro Techniques
(36)
Structure-Activity Relationship
(31)
Tretoquinol - Pharmacology
(27)
Chemistry, Medicinal
(25)
Platelet Aggregation - Drug Effects
(24)
Stereoisomerism
(24)
Tretoquinol - Analogs & Derivatives
(20)
Guinea Pigs
(19)
Isoquinolines - Pharmacology
(18)
Cricetinae
(17)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Pterostilbene, a New Agonist for the Peroxisome Proliferator-Activated Receptor α-Isoform, Lowers Plasma Lipoproteins and Cholesterol in Hypercholesterolemic Hamsters

Effects of synephrine and beta-phenethylamine on human alpha-adrenoceptor subtypes

Pharmacological effects of ephedrine alkaloids on human alpha(1)- and alpha(2)-adrenergic receptor subtypes

Activation of peroxisome proliferator-activated receptor isoforms and inhibition of prostaglandin H2 synthases by ibuprofen, naproxen, and indomethacin

Bioassay for the Identification of Natural Product-Based Activators of Peroxisome Proliferator-Activated Receptor-γ (PPARγ): The Marine Sponge Metabolite Psammaplin A Activates PPARγ and Induces Apoptosis in Human Breast Tumor Cells

Direct effects of ephedrine isomers on human β-adrenergic receptor subtypes

Medetomidine analogs as selective agonists for the human α2-adrenoceptors

2-Amino-4-benzyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridines: Novel Selective β3-Adrenoceptor Agonists

Bioisosteric phentolamine analogs as selective human alpha(2)- versus alpha(1)-adrenoceptor ligands

Evaluation of β-adrenergic receptor subtypes in the human prostate cancer cell line-LNCaP

Bioisosteric phentolamine analogs as selective human α2-versus α1-adrenoceptor ligands

Bioisosteric phentolamine analogs as potent α-adrenergic antagonists

1-Benzyl-1,2,3,4-tetrahydroisoquinoline-6,7-diols as novel affinity and photoaffinity probes for β-adrenoceptor subtypes

Pseudolaric Acid Analogs as a New Class of Peroxisome Proliferator-Activated Receptor Agonists

Synthesis and biological studies of yohimbine derivatives on human α2C-adrenergic receptors

Synthesis and in vitro platelet aggregation and TP receptor binding studies on bicyclic 5,8-ethanooctahydroisoquinolines and 5,8-ethanotetrahydroisoquinolines

Synthesis and .alpha.-adrenergic activities of 2- and 4-substituted imidazoline and imidazole analogs

Synthesis and Human β-Adrenoceptor Activity of 1-(3,5-Diiodo-4- methoxybenzyl)-1,2,3,4-tetrahydroisoquinolin-6-ol Derivatives in Vitro

A Structure-Activity Relationship Study of Benzylic Modifications of 4-[1-(1-Naphthyl)ethyl]-1H-imidazoles on .alpha.1- and .alpha.2-Adrenergic Receptors

Biochemical and functional characterization of 1-benzyl substituted trimetoquinol affinity analogs on rat and human β-adrenoceptors

Medetomidine Analogs as α2-Adrenergic Ligands. 3. Synthesis and Biological Evaluation of a New Series of Medetomidine Analogs and Their Potential Binding Interactions with α2-Adrenoceptors Involving a “Methyl Pocket”

Activation of peroxisome proliferator-activated receptor isoforms and inhibition of prostaglandin H 2 synthases by ibuprofen, naproxen, and indomethacin

Synthesis and Evaluation of Trimetoquinol Derivatives: Novel Thromboxane A2/Prostaglandin H2 Antagonists with Diminished β-Adrenergic Agonist Activity

Iodinated Analogs of Trimetoquinol as Highly Potent and Selective β2-Adrenoceptor Ligands

Suchergebnisse filtern