Clerodane Diterpenoids with Anti-hyperglycemic Activity from Tinospora crispa [PDF]
Four new clerodane diterpenoids, tinosporols A–C (2–4) and tinosporoside A (5), together with six known analogues were isolated from the vines of Tinospora crispa. Their structures were established by extensive spectroscopic analysis.
Yuan Gao +7 more
doaj +4 more sources
Laeviganoids A–T, ent-Clerodane-Type Diterpenoids from Croton laevigatus
Laeviganoids A–T (1–20), 20 new ent-clerodane-type diterpenoids featuring a 2-furanone (1–3) or a furan (4–20) ring, as well as six analogues (21–26), were isolated from the roots of Croton laevigatus.
Yang Dai (36730) +7 more
core +10 more sources
-Clerodane Diterpenoids from [PDF]
Nine neo -clerodane diterpenoids, scutaltisins B-G, scupolin I, scutecolumnin C and 11- epi -scutecolumnin C have been isolated from the acetone extract of the aerial parts of Scutellaria altissima. Scutaltisins B-G are new compounds, whereas scupolin I,
Petko I. Bozov, Josep Coll
doaj +4 more sources
-Clerodane Diterpenoids from var. [PDF]
Six new naturally occurring ajugarin-like neo -clerodane diterpenoids, ajugaflorins A-F, along with six known compounds [the parent ajugarin I, ajugalides B and C, ajugamarin F4, ajugamacrin E, and ajugatakasin B] were isolated from A.
Amaya Castro +3 more
doaj +2 more sources
-Clerodane Diterpenoids from [PDF]
Four neo -clerodane diterpenoids, neoajugapyrin A, scutegalerins A and B and scutecolumnin C have been isolated from the acetone extract of the aerial parts of Scutellaria galericulata .
Petko I. Bozov +2 more
doaj +4 more sources
Ent–Clerodane Diterpenoid Inhibitors of Glucose-6-phosphatase from Croton guatemalensis Lotsy [PDF]
The Croton genus includes a diverse group of plants with remarkable potential in natural products research, particularly due to their bioactive compounds with hypoglycemic and phytochemical significance.
Sonia Marlen Escandón-Rivera +4 more
doaj +2 more sources
Novel neo-clerodane diterpenoids from Teucrium quadrifarium and their anti-ferroptosis effect [PDF]
Teucrifarides A–D (1–4), four previously unreported neo-clerodane-type diterpenoids, combined with sixteen known analogs (5–20), were purified from Teucrium quadrifarium.
Huan Wang +7 more
doaj +2 more sources
Clerodane diterpenoids with anti-inflammatory activity from the tuberous root of Paratinospora sagittata (Oliv.) Wei Wang [PDF]
Seven novel clerodane diterpenoids, designated tinotanoids I–O (1−7), were isolated from the tuberous roots of Paratinospora sagittata (Oliv.) Wei Wang [syn.: Tinospora sagittata var. yunnanensis (S.Y.Hu) H.S.Lo; Menispermaceae].
Hailin Li +3 more
doaj +2 more sources
The Antiproliferative Activity and NO Inhibition of Neo-Clerodane Diterpenoids from Salvia guevarae in RAW 264.7 Macrophages [PDF]
In this study, nine neo-clerodane-type diterpenoids (1–9) were isolated from the dichloromethane extract of Salvia guevarae Bedolla & Zamudio leaves. Compounds 1–6 were new natural products, and 7–9 were acetone artifacts.
Juan Pablo Torres-Médicis +7 more
doaj +2 more sources
CYP76BK1 orthologs catalyze furan and lactone ring formation in clerodane diterpenoids across the mint family. [PDF]
SUMMARY The Lamiaceae (mint family) is the largest known source of furanoclerodanes, a subset of clerodane diterpenoids with broad bioactivities including insect antifeedant properties. The Ajugoideae subfamily, in particular, accumulates significant numbers of structurally related furanoclerodanes.
Schlecht NJ +5 more
europepmc +2 more sources

