Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Elisabethatriene"'
Autor:
Amber C. Kohl, Russell G. Kerr
Publikováno v:
Marine Drugs, Vol 1, Iss 1, Pp 54-65 (2003)
Abstract: Putative precursors in pseudopterosin biosynthesis, the hydrocarbons isoelisabethatriene (10) and erogorgiaene (11), have been identified from an extract of Pseudopterogorgia elisabethae collected in the Florida Keys. Biosynthetic experimen
Externí odkaz:
https://doaj.org/article/04b22d74b23f4e9ab8e4f5bd45a1485e
Autor:
Russell G. Kerr, Amber C. Kohl
Publikováno v:
Marine Drugs, Vol 1, Iss 1, Pp 54-65 (2003)
Marine Drugs
Marine Drugs; Volume 1; Issue 1; Pages: 54-65
Marine Drugs
Marine Drugs; Volume 1; Issue 1; Pages: 54-65
Putative precursors in pseudopterosin biosynthesis, the hydrocarbons isoelisabethatriene (10) and erogorgiaene (11), have been identified from an extract of Pseudopterogorgia elisabethae collected in the Florida Keys. Biosynthetic experiments designe
Autor:
Oscar Osorno, Noriyuki Hara, Hebelin Correa, Yoshinori Fujimoto, Teigo Asai, Carmenza Duque, Mónica Puyana, Andrea Arias, Leonardo Castellanos
Publikováno v:
Tetrahedron. 62:4205-4213
Chemical investigations of the MeOH–CH 2 Cl 2 extract of Pseudopterogorgia elisabethae specimens collected in the islands of San Andres and Providencia, Colombian Caribbean, yielded four new diterpenes ( 1 , 3 , 5 , 7 ) along with seco-pseudopteros
Autor:
Thomas Brück, Russell G. Kerr
Publikováno v:
Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology. 143:269-278
The Bahamian octocoral Pseudopterogorgia elisabethae is the source of pseudopterosins, diterpene glycosides with potent anti-inflammatory activity. The first committed step in pseudopterosin biosynthesis comprises the cyclisation of the universal dit
Publikováno v:
ChemInform. 43
Publikováno v:
Chemicalpharmaceutical bulletin. 60(5)
In the past, we have questioned the accuracy of the stereochemistry of elisabethatriene, a putative biosynthetic intermediate of pseudopterosins, in light of the configuration of elisabethatrienol isolated from Pseudopterogorgia elisabethae, which wa
Publikováno v:
Journal of industrial microbiologybiotechnology. 33(7)
The pseudopterosins are a family of diterpene glycosides isolated from the gorgonian coral Pseudopterogorgia elisabethae. These metabolites exhibit potent anti-inflammatory activity, and this review describes our efforts to elucidate their biosynthet
Autor:
Russell G. Kerr, Amber C. Kohl
Publikováno v:
Archives of biochemistry and biophysics. 424(1)
The pseudopterosins are diterpene glycosides isolated from the marine gorgonian, Pseudopterogorgia elisabethae, which exhibit anti-inflammatory and analgesic activity greater than the industry standard, indomethacin. Previously, we isolated the pseud
Publikováno v:
Chemistrybiology. 10(11)
Investigations are reported that identify the biosynthetic source and origins of the pseudopterosins, pharmacologically important diterpene glycosides, in the gorgonian coral Pseudopterogorgia elisabethae . We report here the isolation of physiologic
Publikováno v:
ChemInform. 34
Analysis of the terpene metabolites of Pseudopterogorgia elisabethae collected from the Florida Keys has resulted in the identification of a novel hydroxyquinone, elisabethadione (1), as well as new pseudopterosins and seco-pseudopterosins. Anti-infl