Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
14
pubmed:dateCreated
2001-7-18
pubmed:abstractText
A series of nicotinamide N-oxides was synthesized and shown to be novel, potent, and selective antagonists of the CXCR2 receptor. Furthermore, these compounds showed significant functional activity against GRO-alpha-driven human neutrophil chemotaxis. Compounds of this class may be useful for the treatment of inflammatory, auto-immune, and allergic disorders.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0960-894X
pubmed:author
pubmed:issnType
Print
pubmed:day
23
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1951-4
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:11459668-Autoimmune Diseases, pubmed-meshheading:11459668-Binding Sites, pubmed-meshheading:11459668-Chemokine CXCL1, pubmed-meshheading:11459668-Chemokines, CXC, pubmed-meshheading:11459668-Chemotactic Factors, pubmed-meshheading:11459668-Chemotaxis, pubmed-meshheading:11459668-Growth Substances, pubmed-meshheading:11459668-Humans, pubmed-meshheading:11459668-Hypersensitivity, pubmed-meshheading:11459668-Inflammation, pubmed-meshheading:11459668-Inhibitory Concentration 50, pubmed-meshheading:11459668-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:11459668-Interleukin-8, pubmed-meshheading:11459668-Neutrophils, pubmed-meshheading:11459668-Niacinamide, pubmed-meshheading:11459668-Protein Binding, pubmed-meshheading:11459668-Receptors, Interleukin-8B, pubmed-meshheading:11459668-Structure-Activity Relationship
pubmed:year
2001
pubmed:articleTitle
Nicotinamide N-oxides as CXCR2 antagonists.
pubmed:affiliation
Department of Chemistry, Celltech R&D, Inc., 1631 220th Street SE, 98021, Bothell, WA, USA. neil.cutshall@celltechgroup.com
pubmed:publicationType
Journal Article