Yue-Wei Guo and co-workers at the Chinese Academy of Sciences have reported in Organic Letters on the isolation of some diterpenoids.

Posted by naturalproductman on December 29, 2012
Yue-Wei Guo and co-workers at the Chinese Academy of Sciences have reported in Organic Letters on the isolation of some diterpenoids.

Posted in Diterpenoids, Protein Targets, protein tyrosine phosphatase 1B (PTP1B) | Leave a Comment »
Posted by naturalproductman on November 6, 2012
Posted in Cascade Reactions, Cycloaddition, Diels-Alder, Diterpenoids, Methodology, Named Reactions, Pericyclic reactions, Total Synthesis | Leave a Comment »
Posted by naturalproductman on February 10, 2012
Shoei-Sheng Lee and co-workers from National Taiwan University have reported in JNP on the isolation of some hypoglycemic compounds.

Posted in Diabetes Type 1, Diseases, Diterpenoids | Leave a Comment »
Posted by naturalproductman on December 30, 2011
Yang Ye and co-workers at the Shanghai Institute of Materia Medica have reported in Organic Letters on the isolation of bicunningines, dimeric diterpenoids.

Posted in Dimer, Diterpenoids | Leave a Comment »
Posted by naturalproductman on December 19, 2011
Han-Dong Sun and co-workers at the Kunming Institute of Botany have reported in Organic Letters on the isolation of neolaxiflorin A.

Posted in Diterpenoids | Leave a Comment »
Posted by naturalproductman on December 19, 2011
Marc Litaudon and co-workers at CNRS have reported in Organic Letters on a chlorinated diterpenoid orthoester.

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Posted by naturalproductman on March 17, 2011
Koichi Takeya and co-workers from Tokyo University of Pharmacy and Life Sciences have reported in Tetrahedron Letters on the structure of salvileucalin C isolated from a plant called Salvia leucantha.
Posted in Diterpenoids, Neoclerodane | Leave a Comment »
Posted by naturalproductman on December 9, 2010
Orazio Taglialatela-Scafati and co-workers at Universita di Napoli have published in Organic Letters on the isolation of some diterpenoids including a novel spirocycle, spirocurcasone, however, this new spirocyclic compound did not seem to have any biological activity. A related structure, curcasone C, had an IC50 value of 0.08 micrograms/mL against the L5178Y (mouse lymphoma) cell line.

Posted in Diterpenoids | Leave a Comment »