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J Nat Prod ; 67(3): 441-4, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15043426

ABSTRACT

Cyclonellin (1), a new cyclic octapeptide, was isolated from an aqueous extract of the marine sponge Axinella carteri. Its structure was elucidated by interpretation of NMR spectral data of the intact compound and N-terminal Edman sequencing of linear peptide fragments obtained by partial hydrolysis of 1. The absolute configurations of the constituent amino acids were determined by acid hydrolysis, derivitization with FDAA, and LC-MS analyses.


Subject(s)
Peptides, Cyclic/isolation & purification , Porifera/chemistry , Animals , Drug Screening Assays, Antitumor , Humans , Micronesia , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Pacific Ocean , Peptides, Cyclic/chemistry , Peptides, Cyclic/pharmacology , Tumor Cells, Cultured
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