Results 11 to 20 of about 10,911 (198)

Clerodane diterpenes from leaves of Casearia sylvestris Swartz [PDF]

open access: yesQuímica Nova, 2007
Ethanolic extracts of the leaves of Casearia sylvestris yielded a novel clerodane diterpene, 15-hydroxy-3-cleroden-2-one, together with the known diterpenes (-)-hardwickiic acid, reported for the first time from this species, and casearins B and G ...
André G. dos Santos   +4 more
doaj   +7 more sources

Two New Clerodane Diterpenes from Tinospora sagittata [PDF]

open access: yesMolecules, 2016
Two new clerodane-type diterpenes, tinosporins C (1) and tinosporins D (2) were isolated from the stems of Tinospora sagittata (Oliv.), together with three known ones, columbin (3), tinophylloloside (4), and tinospinoside D (5).
Guanhua Li   +3 more
doaj   +4 more sources

13C-NMR Data of Diterpenes Isolated from Aristolochia Species

open access: yesMolecules, 2009
The genus Aristolochia,an important source of physiologically active compounds that belong to different chemical classes, is the subject of research in numerous pharmacological and chemical studies.
Antônio Flávio de Carvalho Alcântara   +3 more
doaj   +2 more sources

Cytotoxic clerodane diterpenes from Glossocarya calcicola

open access: yesPhytochemistry, 2005
Three clerodane diterpenes were isolated and identified from leaf extract of Glossocarya calcicola. Compound has been characterised as (rel)-10betaH-trans-12xi-(2-methylbut-2(E)-enoyl)-1beta-(isobutanoyl)-6alpha,13xi-dihydroxyclerodan-4(20),8(18)-dien-7,15-dione-15,16-oxide, to which we have assigned the trivial name calcicolin-A.
Rasikari, Heidi L   +7 more
openaire   +4 more sources

Clerodane Diterpenes from the Marine Sponge Raspailia bouryesnaultae Collected in South Brazil

open access: yesMarine Drugs, 2019
The marine sponge Raspailia bouryesnaultae, collected in South Brazil, was selected for detailed investigation considering the results of a screening that pointed to an in vitro antiproliferative effect against non-small cells of human lung cancer (A549)
Cintia Lhullier   +7 more
doaj   +2 more sources

Bioactive Clerodane Diterpenes from Roots of [PDF]

open access: yesNatural Product Communications, 2010
Two new clerodane diterpenes were isolated from roots of Carex distachya Desf., a perennial plant widely distributed in the coastal area of the Mediterranean basin.
Antonio Fiorentino   +5 more
doaj   +4 more sources

Three New Clerodane Diterpenes from Polyalthia longifolia var. pendula

open access: yesMolecules, 2014
Three new clerodane diterpenes, (4→2)-abeo-cleroda-2,13E-dien-2,14-dioic acid (1), (4→2)-abeo-2,13-diformyl-cleroda-2,13E-dien-14-oic acid (2), and 16(R&S)- methoxycleroda-4(18),13-dien-15,16-olide (3), were isolated from the unripe fruit of ...
Tung-Ho Wu   +11 more
doaj   +2 more sources

Neo-clerodane diterpenes from Clerodendron inerme

open access: yesPhytochemistry, 1993
Abstract Structures of insect growth inhibitive and antifeedant neo-clerodane diterpenes, clerodendrin B and C, isolated from the leaves of Clerodendron inerme, were established mainly by NMR spectral analysis.
L. Jagan Mohan Rao   +2 more
openaire   +2 more sources

Epoxy Clerodane Diterpene Attenuates the Differentiated Adipocyte Hypertrophy and Enhances Mitochondrial Metabolism. [PDF]

open access: yesChemistryOpen
Epoxy Clerodane Diterpene (ECD) significantly reduces adipocyte hypertrophy and lipid accumulation in human mesenchymal stem cell (hMSC)‐derived adipocytes. ECD improves mitochondrial membrane potential (ΔΨm), increases thermogenic regulators (UCP‐1, PPARγC1α), decreases adipogenic markers (C/EBPα, PPARγ), and reduces inflammatory mediators (TNF‐α, NF ...
AlSedairy SA   +4 more
europepmc   +2 more sources

Clerodane diterpenes from the leaves of Laetia procera

open access: yesPhytochemistry, 1996
Four novel clerodane diterpenes have been isolated from the leaves of Laetia procera. They were characterized by extensive use of HMBC spectroscopy as a mixture of rel-18(S),19(R)-diacetoxy-18,19-epoxy-2(R),7(S),16-trihydroxy-6(S)-myristoyloxy-5(R),8(R),9(S),10(R)-cleroda-3,12,14-triene and rel-18(S),19(R)-diacetoxy-18,19-epoxy-2(R),7(S),16-trihydroxy ...
Gibbons, Simon   +2 more
openaire   +3 more sources

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