2013
DOI: 10.1016/j.phytochem.2013.01.008
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Rearranged abietane diterpenoids from the roots of Clerodendrum trichotomum and their cytotoxicities against human tumor cells

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Cited by 43 publications
(39 citation statements)
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“…All the proton signals were assigned to the corresponding carbons through direct 1 H and 13 C correlations in the HSQC spectrum. The overall 1 H and 13 C NMR spectroscopic data confirmed that 1 was an oxygenated diterpenoid possessing a fused butenolide unit [21][22]. The partial structures were deduced by 1 H\ \ 1 H COSY spectrum and the whole structure was connected on the long-ranged correlations observed in the HMBC spectrum (Fig.…”
Section: Resultsmentioning
confidence: 68%
“…All the proton signals were assigned to the corresponding carbons through direct 1 H and 13 C correlations in the HSQC spectrum. The overall 1 H and 13 C NMR spectroscopic data confirmed that 1 was an oxygenated diterpenoid possessing a fused butenolide unit [21][22]. The partial structures were deduced by 1 H\ \ 1 H COSY spectrum and the whole structure was connected on the long-ranged correlations observed in the HMBC spectrum (Fig.…”
Section: Resultsmentioning
confidence: 68%
“…Additionally, the 1 The HSQC spectrum displayed all of the proton signals assigned to the corresponding carbons through direct 1 H and 13 C correlations. The overall 1 H and 13 C NMR spectroscopic data confirmed that 1 is an oxynitride diterpene possessing a fused butenolide unit [9,10], and its entire structure was connected, as confirmed using HSQC, HMBC, and 1 H-1 H-COSY spectra ( Figure 2 showed that the hydroxyl group was β-oriented at C-20, and the methyl group at C-14 and the ethoxy group at C-12 were all α-oriented. The same carbon skeleton with the trans/anti/trans system of three six-membered rings A, B, and C, and the oriented proton at C-8 was β-axial and the oriented protons at C-5/C-9 was α-axial, which are well established on all cassane diterpenes isolated so far from the genus Caesalpinia [3,8,11].…”
Section: Structure Elucidation Of Compounds 1-2mentioning
confidence: 69%
“…Lima senyawa yang berhasil diidentifikasi dalam tanaman genus ini yaitu apigenin 7-glucoside, hispidulin, scutellarein-7-O-beta-D-glucuronate, acteoside dan verbascoside menunjukan interaksi dengan protein kanker melalui simulasi penambatan molekul dan berpotensi menimbulkan efek terapi (Gogoi et al 2017 Wang, Zhu, et al 2013;Wang, Xiong, et al 2013;Xu et al 2013 memiliki aktivitas antikanker dari tanaman genus Clerodendrum adalah pheophorbide-related compounds (purpurin 7 dimethyl ester, pheophorbide a, methyl (10S)-hydroxypheophorbide a) (Cheng et al 2001); asam lemak (asam oleat, asam oktadekanoat, asam n-heksadekanoat, dan 6-metil-2-heptanon) (Erukainure et al 2016); asam oleanolik dan clerodinin A (Sannigrahi et al 2012); abitane diterpenoid (trichotomone, trichotomone D, trichotomone F, uncinatone, mandarone E, teuvincenone E, dan trichotomone H) (Wang, Xiong, et al 2013;Wang, Zhu, et al 2013) dan dua senyawa steroid (Xu et al 2013). Mekanisme antikanker beberapa tanaman genus Clerodendrum melalui aktivitas fotositoksisitas (Nakamura et al 1996;Choi et al 2014;Cheng et al 2001), apoptosis, antiproliferatif dan anti-migrasi (Sun et al 2013;Chacko et al 2015).…”
Section: Aktivitasunclassified
“…Dengan menggunakan CellTiter Glo TM luminescent cell viability assay, nilai IC50 tujuh senyawa abitane diterpenoid pada sel kanker tersebut antara 0,83 -50,99 μM (Wang, Zhu, et al 2013;Wang, Xiong, et al 2013). Dua senyawa steroid yang diisolasi daun C. trichotomum menunjukan aktivitas sitotoksik pada sel HeLa dengan nilai IC50 35,67 dan 28,92 μg/ml menggunakan metode MTT (Xu et al 2013) …”
Section: Clerodendrum Trichotomumunclassified