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...

Analogues of 2'-hydroxychalcone with modified C4-substituents as the inhibitors against human acetylcholinesterase

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.130-137

2021

Volltextzugriff (PDF)

Synthesis, Biological Evaluation and Molecular Modelling of 2'-Hydroxychalcones as Acetylcholinesterase Inhibitors

Molecules (Basel, Switzerland), 2016-07, Vol.21 (7), p.955

2016

Volltextzugriff (PDF)

An efficient one-pot synthesis of flavones

Tetrahedron letters, 2011-06, Vol.52 (24), p.3120-3123

2011

Volltextzugriff (PDF)

Flavonoids with M1 muscarinic acetylcholine receptor binding activity

Molecules (Basel, Switzerland), 2014-06, Vol.19 (7), p.8933-8948

2014

Volltextzugriff (PDF)

Accurate determinations of the extent to which the SE2' reactions of allyl-, allenyl- and propargylsilanes are stereospecifically anti

Organic & biomolecular chemistry, 2004-03, Vol.2 (5), p.749-769

2004

Volltextzugriff (PDF)

Rational Discovery of Dengue Type 2 Non-Competitive Inhibitors

Chemical biology & drug design, 2013-07, Vol.82 (1), p.1-11

2013

Volltextzugriff (PDF)

Synthesis of (±)-kuwanon V and (±)-dorsterone methyl ethers via Diels–Alder reaction

Tetrahedron letters, 2011-04, Vol.52 (15), p.1797-1799

2011

Volltextzugriff (PDF)

Synthesis, characterization, X-ray crystallography, acetyl cholinesterase inhibition and antioxidant activities of some novel ketone derivatives of gallic hydrazide-derived Schiff bases

Molecules (Basel, Switzerland), 2012-02, Vol.17 (3), p.2408-2427

2012

Volltextzugriff (PDF)

Correction: Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists

MedChemComm, 2018-03, Vol.9 (3), p.593-594

2018

Volltextzugriff (PDF)

Synthesis, characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel Schiff bases derived from 1-(2-ketoiminoethyl)piperazines

Molecules (Basel, Switzerland), 2011-11, Vol.16 (11), p.9316-9330

2011

Volltextzugriff (PDF)

Phosphodiesterase-5 inhibitors and their analogues as adulterants of herbal and food products: analysis of the Malaysian market, 2014-16

Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 2017-07, Vol.34 (7), p.1101-1109

2017

Volltextzugriff (PDF)

2-Aryl-3-(arylideneamino)-1,2-dihydroquinazoline-4(3 H )-ones as inhibitors of cholinesterases and self-induced β-amyloid (Aβ) aggregation: biological evaluations and mechanistic insights from molecular dynamics simulations

RSC advances, 2018-01, Vol.8 (14), p.7818-7831

2018

Volltextzugriff (PDF)

In vitro functional evaluation of isolaureline, dicentrine and glaucine enantiomers at 5‐HT2 and α1 receptors

Chemical biology & drug design, 2019-02, Vol.93 (2), p.132-138

2019

Volltextzugriff (PDF)

In vitro functional evaluation of isolaureline, dicentrine and glaucine enantiomers at 5-HT 2 and α 1 receptors

Chemical biology & drug design, 2019-02, Vol.93 (2), p.132-138

2019

Volltextzugriff (PDF)

An efficient synthesis of (±)-panduratin A and (±)-isopanduratin A, inhibitors of dengue-2 viral activity

Tetrahedron letters, 2010-01, Vol.51 (3), p.495-498

2010

Volltextzugriff (PDF)

Correction: Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT 2 and α 1 receptor antagonists

MedChemComm, 2018-03, Vol.9 (3), p.593-594

2018

Volltextzugriff (PDF)

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT 2 and α 1 receptor antagonists

MedChemComm, 2018-03, Vol.9 (3), p.576-582

2018

Volltextzugriff (PDF)

Structure-Based Identification of Aporphines with Selective 5-HT2A Receptor-Binding Activity

Chemical biology & drug design, 2013-02, Vol.81 (2), p.250-256

2013

Volltextzugriff (PDF)

Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1

Tetrahedron letters, 2015-09, Vol.56 (36), p.5082-5085

2015

Volltextzugriff (PDF)

Homology modeling of the human 5-HT1A, 5-HT2A, D1, and D2 receptors: model refinement with molecular dynamics simulations and docking evaluation

Journal of molecular modeling, 2012-08, Vol.18 (8), p.3639-3655

2012

Volltextzugriff (PDF)

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists

MedChemComm, 2018, Vol.9 (3), p.576-582

2018

Volltextzugriff (PDF)

Toward activated homology models of the human M1 muscarinic acetylcholine receptor

Journal of molecular graphics & modelling, 2014-04, Vol.49, p.91-98

2014

Volltextzugriff (PDF)

2-Aryl-3-(arylideneamino)-1,2-dihydroquinazoline-4(3H)-ones as inhibitors of cholinesterases and self-induced β-amyloid (Aβ) aggregation: biological evaluations and mechanistic insights from molecular dynamics simulationsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ra11872d

2018-02

Volltextzugriff (PDF)

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonistsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7md00629b

2018-03

Volltextzugriff (PDF)

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7md00629b

MedChemComm, 2018-02, Vol.9 (3), p.576-582

2018

Volltextzugriff (PDF)

1 – 25 von 69

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(62)
Mit Volltextzugriff
(64)

Publikationsform

Artikel
(66)
Reviews
(2)
Berichte
(1)

Sprache

Englisch
(68)

Erscheinungsjahr

n.n

Thema

Science & Technology
(40)
Life Sciences & Biomedicine
(24)
Physical Sciences
(21)
Chemistry
(19)
Humans
(19)
Biochemistry & Molecular Biology
(10)
Chemistry, Organic
(10)
Animals
(7)
Binding Sites
(7)
Molecular Structure
(6)
Organic Chemistry
(6)
Alzheimer's Disease
(5)
Chemistry, Multidisciplinary
(5)
Exact Sciences And Technology
(5)
Male
(5)
Models, Molecular
(5)
Oncology
(5)
Astronomy & Astrophysics
(4)
Biological And Medical Sciences
(4)
Cholinesterase Inhibitors - Chemical Synthesis
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Analogues of 2'-hydroxychalcone with modified C4-substituents as the inhibitors against human acetylcholinesterase

Synthesis, Biological Evaluation and Molecular Modelling of 2'-Hydroxychalcones as Acetylcholinesterase Inhibitors

An efficient one-pot synthesis of flavones

Flavonoids with M1 muscarinic acetylcholine receptor binding activity

Accurate determinations of the extent to which the SE2' reactions of allyl-, allenyl- and propargylsilanes are stereospecifically anti

Rational Discovery of Dengue Type 2 Non-Competitive Inhibitors

Synthesis of (±)-kuwanon V and (±)-dorsterone methyl ethers via Diels–Alder reaction

Synthesis, characterization, X-ray crystallography, acetyl cholinesterase inhibition and antioxidant activities of some novel ketone derivatives of gallic hydrazide-derived Schiff bases

Correction: Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists

Synthesis, characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel Schiff bases derived from 1-(2-ketoiminoethyl)piperazines

Phosphodiesterase-5 inhibitors and their analogues as adulterants of herbal and food products: analysis of the Malaysian market, 2014-16

2-Aryl-3-(arylideneamino)-1,2-dihydroquinazoline-4(3 H )-ones as inhibitors of cholinesterases and self-induced β-amyloid (Aβ) aggregation: biological evaluations and mechanistic insights from molecular dynamics simulations

In vitro functional evaluation of isolaureline, dicentrine and glaucine enantiomers at 5‐HT2 and α1 receptors

In vitro functional evaluation of isolaureline, dicentrine and glaucine enantiomers at 5-HT 2 and α 1 receptors

An efficient synthesis of (±)-panduratin A and (±)-isopanduratin A, inhibitors of dengue-2 viral activity

Correction: Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT 2 and α 1 receptor antagonists

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT 2 and α 1 receptor antagonists

Structure-Based Identification of Aporphines with Selective 5-HT2A Receptor-Binding Activity

Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1

Homology modeling of the human 5-HT1A, 5-HT2A, D1, and D2 receptors: model refinement with molecular dynamics simulations and docking evaluation

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists

Toward activated homology models of the human M1 muscarinic acetylcholine receptor

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonistsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7md00629b

Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7md00629b

Suchergebnisse filtern