Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2006-11-20
pubmed:abstractText
The synthesis of a series of novel docetaxel analogues possessing a peptide side chain at the C2 position as well as peptide macrocyclic taxoids is described. These compounds were designed to mimic a region of the alpha-tubulin loop equivalent to the paclitaxel binding pocket of beta-tubulin. Fifteen new peptide taxoids were obtained and evaluated as inhibitors of microtubule disassembly as well as cell proliferation. The relationships between these new taxoids and the tau protein motif interacting with microtubules are discussed.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0968-0896
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
563-74
pubmed:meshHeading
pubmed-meshheading:17064914-Antineoplastic Agents, pubmed-meshheading:17064914-Binding Sites, pubmed-meshheading:17064914-Cell Line, Tumor, pubmed-meshheading:17064914-Cell Proliferation, pubmed-meshheading:17064914-Computational Biology, pubmed-meshheading:17064914-Crystallography, X-Ray, pubmed-meshheading:17064914-Drug Screening Assays, Antitumor, pubmed-meshheading:17064914-Humans, pubmed-meshheading:17064914-Macrocyclic Compounds, pubmed-meshheading:17064914-Models, Molecular, pubmed-meshheading:17064914-Molecular Conformation, pubmed-meshheading:17064914-Peptides, pubmed-meshheading:17064914-Protein Structure, Secondary, pubmed-meshheading:17064914-Sensitivity and Specificity, pubmed-meshheading:17064914-Stereoisomerism, pubmed-meshheading:17064914-Structure-Activity Relationship, pubmed-meshheading:17064914-Taxoids
pubmed:year
2007
pubmed:articleTitle
Novel C2-C3' N-peptide linked macrocyclic taxoids. Part 2: synthesis and biological activities of docetaxel analogues with a peptide side chain at C2 and their macrocyclic derivatives.
pubmed:affiliation
Institut de Chimie des Substances Naturelles, CNRS, 1 avenue de la Terrasse, 91198 Gif-sur-Yvette Cedex, France.
pubmed:publicationType
Journal Article