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Nat Prod Res ; 29(1): 70-6, 2015.
Article in English | MEDLINE | ID: mdl-25229804

ABSTRACT

A new metabolite 1 has been isolated from the marine soft coral Sarcophyton ehrenbergi along with two known diterpenoids 2 and 3 and cholesterol 4. The structure of 1 was determined by means of detailed spectroscopic analysis and unambiguously confirmed to have the S configuration by the synthesis of both enantiomers using 4-benzyl-2-oxazolidinone auxiliaries. (S)- and (R)-1, 3 and some of the synthetic intermediates were evaluated for cytotoxic activity against human lung cancer (A549), prostate cancer (DU145), cervical cancer (HeLa) and breast cancer (MCF-7) cell lines in an in vitro bioassay.


Subject(s)
Antineoplastic Agents , Diterpenes , Oxazolidinones , Propionates/chemical synthesis , Animals , Anthozoa/chemistry , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/chemistry , Antineoplastic Agents/isolation & purification , Antineoplastic Agents/pharmacology , Breast Neoplasms , Diterpenes/chemical synthesis , Diterpenes/chemistry , Diterpenes/isolation & purification , Diterpenes/pharmacology , Drug Screening Assays, Antitumor , Female , HeLa Cells , Humans , Male , Marine Biology , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Oxazolidinones/chemical synthesis , Oxazolidinones/chemistry , Oxazolidinones/isolation & purification , Oxazolidinones/pharmacology , Propionates/chemistry , Stereoisomerism
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