0 citations
Dereplication of Phorbol Bioactives: Lyngbya majuscula and Croton cuneatus
Journal of Natural Products1990Vol. 53(4), pp. 867–874
Citations Over Time
Abstract
Lyngbya majuscula and Croton cuneatus were used as prototypes for the dereplication of phorbol ester receptor binding activity using a combination of hplc-uv and online phorbol dibutyrate (PDBu) receptor binding and batch fractionation over either Si gel or diolbonded Si gel. Debromoaplysiatoxin was responsible for the bioactivity of Lyngbya, whereas a complex of potent phorbol esters was detected in C. cuneatus.
Related Papers
- → Synthesis of Marine Diterpene Isocyanide (−)-Kalihinol Y and Diterpene Isothiocyanate (−)-10-Epi-kalihinol I(2012)17 cited
- → An unexpected Lewis acid-mediated structural conversion of a Euphorbia Diterpene: From a Lathyrane skeleton to diterpene pseudo-alkaloids(2020)11 cited
- → Structures of croverin (X-ray analysis) and dihydrocroverin, two new diterpene lactones from Croton verreauxii Baill.(1980)10 cited
- → An ingenane diterpene from belizian Mabea excelsa(1990)7 cited
- → Poilaneic acid, a cembranoid diterpene from Croton poilanei(1981)18 cited