Search Results - "Josef, Kurt"
-
1
Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation
Published in Disease models & mechanisms (01-07-2009)“…Examination of embryonic myogenesis of two distinct, but functionally related, skeletal muscle dystrophy mutants (mdx and cav-3(-/-)) establishes for the first…”
Get full text
Journal Article -
2
1,2-Benzothiazine 1,1-Dioxide P2−P3 Peptide Mimetic Aldehyde Calpain I Inhibitors
Published in Journal of medicinal chemistry (11-10-2001)“…A series of peptide mimetic aldehyde inhibitors of calpain I was prepared in which the P2 and P3 amino acids were replaced by substituted…”
Get full text
Journal Article -
3
Poster 78 Novel Bimodal Technology Addresses Vitamin D Malabsorption
Published in PM & R (01-09-2016)Get full text
Journal Article -
4
Synthesis of constrained benzocinnolinone analogues of CEP-26401 (irdabisant) as potent, selective histamine H3 receptor inverse agonists
Published in Bioorganic & medicinal chemistry letters (15-06-2012)“…A novel class of benzocinnolinones analogs of irdabisant were designed and synthesized as histamine H3R antagonists/inverse agonists. Modifications to the…”
Get full text
Journal Article -
5
4-Phenoxypiperidine pyridazin-3-one histamine H3 receptor inverse agonists demonstrating potent and robust wake promoting activity
Published in Bioorganic & medicinal chemistry letters (15-02-2012)“…Structure–activity relationships for a series of phenoxypiperidine pyridazin-3-one H3R antagonists/inverse agonists are disclosed. The search for compounds…”
Get full text
Journal Article -
6
Mixed-Lineage Kinase 1 and Mixed-Lineage Kinase 3 Subtype-Selective Dihydronaphthyl[3,4-a]pyrrolo[3,4-c]carbazole-5-ones: Optimization, Mixed-Lineage Kinase 1 Crystallography, and Oral in Vivo Activity in 1-Methyl-4-phenyltetrahydropyridine Models
Published in Journal of medicinal chemistry (25-09-2008)“…The optimization of the dihydronaphthyl[3,4-a]pyrrolo[3,4-c]carbazole-5-one R2 and R12 positions led to the identification of the first MLK1 and MLK3…”
Get full text
Journal Article -
7
4,5-Dihydropyridazin-3-one derivatives as histamine H3 receptor inverse agonists
Published in Bioorganic & medicinal chemistry letters (01-01-2012)“…H3R structure–activity relationships for a new class of 4,5-dihydropyridazin-3-one H3R antagonists/inverse agonists are disclosed. Modification of the…”
Get full text
Journal Article -
8
Identification of pyridazin-3-one derivatives as potent, selective histamine H3 receptor inverse agonists with robust wake activity
Published in Bioorganic & medicinal chemistry letters (15-09-2011)“…H3R structure–activity relationships on a novel class of pyridazin-3-one H3R antagonists/inverse agonists are disclosed. Modifications of the pyridazinone…”
Get full text
Journal Article -
9
Discovery of (1R,6S)-5-[4-(1-cyclobutyl-piperidin-4-yloxy)-phenyl]-3,4-diaza-bicyclo[4.1.0]hept-4-en-2-one (R,S-4a): Histamine H3 receptor inverse agonist demonstrating potent cognitive enhancing and wake promoting activity
Published in Bioorganic & medicinal chemistry letters (01-03-2014)Get full text
Journal Article -
10
Peptide aptamer microarrays: bridging the bio-detector interface
Published in Faraday discussions (01-01-2011)“…In the near future, personalised medicine and phase-0 trials will require that clinical practitioners move from the "one biomarker per disease" paradigm to the…”
Get more information
Journal Article -
11
Conformationally restrained analogs of pravadoline: nanomolar potent, enantioselective, (aminoalkyl)indole agonists of the cannabinoid receptor
Published in Journal of medicinal chemistry (01-01-1992)“…Pravadoline (1) is an (aminoalkyl)indole analgesic agent which is an inhibitor of cyclooxygenase and, in contrast to other NSAIDs, inhibits neuronally…”
Get full text
Journal Article -
12
Potent peptide α-Ketohydroxamate inhibitors of recombinant human calpain I
Published in Bioorganic & medicinal chemistry letters (08-10-2001)“…A series of potent dipeptide and tripeptide α-ketohydroxamic esters was prepared as inhibitors of recombinant human calpain I. Compound 3c, a Cbz-Leu-Phe…”
Get full text
Journal Article -
13
Does political and social feasibility matter in energy scenarios?
Published in Energy research & social science (01-05-2015)“…Scenarios have become an influential tool in the process of energy system transitions, as they form a basis for, e.g., investment decisions or legislative…”
Get full text
Journal Article -
14
1,3,5-Trialkyl-2,4,6-triiodobenzenes: Novel X-ray Contrast Agents for Gastrointestinal Imaging
Published in Journal of medicinal chemistry (18-05-2000)“…Examination of the gastrointestinal (GI) tract has been performed for decades using barium sulfate. Although this agent has many recognized limitations…”
Get full text
Journal Article -
15
Synthesis and Structure-Activity Relationships of 6-Heterocyclic-Substituted Purines as Inactivation Modifiers of Cardiac Sodium Channels
Published in Journal of medicinal chemistry (01-07-1995)“…Purine-based analogs of SDZ 211-500 (5) were prepared and evaluated as inactivation modifiers of guinea pig or human cardiac sodium (Na) channels expressed in…”
Get full text
Journal Article -
16
Wann kommt die Kostenwende bei der EEG-Umlage? Eine Analyse der Entwicklung und Einflussparameter bis 2030
Published in Zeitschrift für Energiewirtschaft (01-01-2018)“…The apportionment of the German Renewable Energy Sources Act (EEG-Umlage) constitutes a significant portion of the electricity price for domestic and…”
Get full text
Journal Article -
17
SACRED TREES AMONG THE TAMIL PEOPLE OF SOUTH INDIA
Published in Suomen antropologi : Suomen Antropologisen Seuran julkaisu = Antropologi i Finland : Antropologiska sällskapet i Finland (01-03-2015)“…Among the Tamil people of South India the veneration of trees and forests still occupies an important part of their daily life. Once recognized as the abode of…”
Get full text
Journal Article -
18
Discovery of (1R,6S)-5-[4-(1-cyclobutyl-piperidin-4-yloxy)-phenyl]-3,4-diaza-bi c yclo[4.1.0]hept-4-en-2-one (R,S-4a): Histamine H3 receptor inverse agonist demonstrating potent cognitive enhancing and wake promoting activity
Published in Bioorganic & medicinal chemistry letters (01-03-2014)“…A series of fused cyclopropyl-4,5-dihydropyridazin-3-one (3,4-diaza-bicyclo[4.1.0]hept-4-en-2-one) phenoxypiperidine analogs was designed and synthesized,…”
Get full text
Journal Article -
19
1,2-Benzothiazine 1,1-Dioxide P 2 −P 3 Peptide Mimetic Aldehyde Calpain I Inhibitors
Published in Journal of medicinal chemistry (11-10-2001)Get full text
Journal Article -
20
Structure−function studies of an engineered scaffold protein derived from Stefin A. II: Development and applications of the SQT variant
Published in Protein engineering, design and selection (01-09-2011)“…Constrained binding peptides (peptide aptamers) may serve as tools to explore protein conformations and disrupt protein−protein interactions. The quality of…”
Get full text
Journal Article