2013
DOI: 10.1055/s-0033-1350648
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Diterpenes and Phenylpropanoids from Clerodendrum splendens

Abstract: Four new clerodane diterpenes (1-4) and one new phenylpropanoid (5) have been isolated from Clerodendrum splendens aerial parts, together with nine known compounds. Their structures were determined by spectroscopic and spectrometric analysis and chemical methods. The absolute configuration of the 15,16-diol moiety in 4 was determined by Snatzke's method. Antiproliferative activity of diterpenes in HeLa cells was also evaluated. The IC50 values were 98 ± 11 µM for 3 and 101 ± 8 µM for 1, respectively.

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Cited by 4 publications
(4 citation statements)
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“…Its high-molecular-weight subfraction induced nitrous oxide and cytokine, TNF, granulocyte macrophage-colony stimulating factor, peripheral blood mononuclear cells, and monocytes with other wide-ranging agonist activities that considerably reduced disease severity ( 117 , 118 ). Four clerodane diterpenes and phenyl propanoids from aerial parts showed antiproliferative activity ( 119 ).…”
Section: Medicinal Plants Exhibiting Immunomodulation Activitymentioning
confidence: 99%
“…Its high-molecular-weight subfraction induced nitrous oxide and cytokine, TNF, granulocyte macrophage-colony stimulating factor, peripheral blood mononuclear cells, and monocytes with other wide-ranging agonist activities that considerably reduced disease severity ( 117 , 118 ). Four clerodane diterpenes and phenyl propanoids from aerial parts showed antiproliferative activity ( 119 ).…”
Section: Medicinal Plants Exhibiting Immunomodulation Activitymentioning
confidence: 99%
“…Scientific research on this species allowed to isolate and identify four new clerodane diterpenoids, namely 2α-acetoxy-3β-(2′,3′-diacetoxy-2′-methyl)-butanoyloxy-14-hydro-15-hydroxyclerodin (74) , 3β,15-dihydroxy-14-hydro-clerodin (75) , 2α,15-dihydroxy-3β-(2′-hydroxy-2′-methyl-3′-acetoxy)-butanoyloxy-6α,18-diacetoxy-4α,17-epoxy-clerodan-11,16-lactone (76) and 3β,14S,15-trihydroxy-6α,18-diacetoxy-4α,17-epoxy-clerodan-11,16-lactone (77) [ 91 ]. The extraction method used for the phytochemical analyses of this plant species is shown in Table 10 .…”
Section: A Review Of Diterpenoid Compounds Isolated From Cl...mentioning
confidence: 99%
“…The results indicate that 2α-acetoxy-3β-(2′,3′-diacetoxy-2′-methyl)-butanoyloxy-14-hydro-15-hydroxyclerodin (74) and 2α,15-dihydroxy-3β-(2′-hydroxy-2′-methyl-3′-acetoxy)-butanoyloxy-6α,18-diacetoxy-4α,17-epoxy-clerodan-11,16-lactone (76) exhibit cell growth inhibition activity. In addition, the IC 50 values for the two compounds, viz., (76) and (74) , were found to be 101 μM and 98 μM, respectively, after 72 h incubation [ 91 ].…”
Section: A Review Of Diterpenoid Compounds Isolated From Cl...mentioning
confidence: 99%
“…The diterpenes from Callicarpa longissima (Liu et al , ), Clerodendrum splendens (Faiella et al , ), Fagonia mollis (Sallam et al , ), Icacina trichantha (Zhao et al , ), Hedychium longipetalum (Zhao et al , ), Micromonospora sp. (Mullowney et al , ), Cespitularia taeniata (Wang et al , ), Caesalpinia spinosa (He et al , ), Nephthea columnaris (Hsiao et al , ), Bursera microphylla (Messina et al , ), Teucrium viscidum (Gao et al , ), Euphorbia ebracteolata (Yuan et al , ), Euphorbia aellenii (Yazdiniapour et al , ), Perenniporia subacida (Wen et al , ), Abies fargesii (Wu et al , ) and Premna tomentosa (Rekha et al , ) were also evident to exert cytotoxic effects on a number of human cancer cell lines.…”
Section: Diterpenic Anticancer Traitsmentioning
confidence: 99%