Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
20
pubmed:dateCreated
2006-9-28
pubmed:abstractText
A benzodiazepine-based beta-turn mimetic has been designed, synthesized, and incorporated into angiotensin II. Comparison of the mimetic with beta-turns in crystallized proteins showed that it most closely resembles a type II beta-turn. The compounds exhibited high to moderate binding affinity for the AT2 receptor, and one also displayed high affinity for the AT1 receptor. Molecular modeling showed that the high-affinity compounds could be incorporated into a previously derived model of AT2 receptor ligands.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0022-2623
pubmed:author
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6133-7
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:17004728-Angiotensin II, pubmed-meshheading:17004728-Animals, pubmed-meshheading:17004728-Aorta, Thoracic, pubmed-meshheading:17004728-Benzodiazepines, pubmed-meshheading:17004728-Drug Design, pubmed-meshheading:17004728-Female, pubmed-meshheading:17004728-Ligands, pubmed-meshheading:17004728-Liver, pubmed-meshheading:17004728-Models, Molecular, pubmed-meshheading:17004728-Molecular Mimicry, pubmed-meshheading:17004728-Muscle, Smooth, Vascular, pubmed-meshheading:17004728-Muscle Contraction, pubmed-meshheading:17004728-Peptides, pubmed-meshheading:17004728-Protein Structure, Secondary, pubmed-meshheading:17004728-Rabbits, pubmed-meshheading:17004728-Radioligand Assay, pubmed-meshheading:17004728-Rats, pubmed-meshheading:17004728-Receptor, Angiotensin, Type 1, pubmed-meshheading:17004728-Receptor, Angiotensin, Type 2, pubmed-meshheading:17004728-Swine, pubmed-meshheading:17004728-Uterus
pubmed:year
2006
pubmed:articleTitle
Design, synthesis, and incorporation of a beta-turn mimetic in angiotensin II forming novel pseudopeptides with affinity for AT1 and AT2 receptors.
pubmed:affiliation
Department of Medicinal Chemistry, BMC, Uppsala University, P.O. Box 574, SE-751 23 Uppsala, Sweden.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't