2013
DOI: 10.3390/molecules18021720
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Sinapyl Alcohol Derivatives from the Lipo-soluble Part of Dichrocephala benthamii C. B. Clarke

Abstract: Four new sinapyl alcohol derivatives dichrocephols A–D (compounds 1–4) were isolated from the lipo-soluble part of the whole herb of Dichrocephala benthamii C. B. Clarke, together with the known compound syringenin isovalerate (5). Their structures were elucidated on the basis of spectroscopic analysis. Their absolute configurations were established by the method of alkaline hydrohysis. Compounds 1–3 showed moderate cytotoxity against HeLa cells, with IC50 values of 14.8 μM, 51.6 μM and 81.6 μM, respectively. … Show more

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Cited by 9 publications
(7 citation statements)
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“…Compound 24 was tentatively identified as ethyl rosmarinate. The mass spectrum of 26 exhibited base peak at m/z 207, corresponding to dihydrosinapoyl moiety, which was formed by cleavage of the ester bond that resulted in loss of glucose (180 Da) (Tian et al, 2013;El-Sayed et al, 2017). Compound 26 was tentatively assigned as dihydrosinapic acid-O-glucoside.…”
Section: Compounds Detected By Rphplc-esi-ms/ms Analyses Of Stem Ethamentioning
confidence: 99%
“…Compound 24 was tentatively identified as ethyl rosmarinate. The mass spectrum of 26 exhibited base peak at m/z 207, corresponding to dihydrosinapoyl moiety, which was formed by cleavage of the ester bond that resulted in loss of glucose (180 Da) (Tian et al, 2013;El-Sayed et al, 2017). Compound 26 was tentatively assigned as dihydrosinapic acid-O-glucoside.…”
Section: Compounds Detected By Rphplc-esi-ms/ms Analyses Of Stem Ethamentioning
confidence: 99%
“…1 and S1) including nine new chemical entities for bioactive assay. In this Letter, we describe the isolation and structural determination of tripolinolate A (1) from T. vulgare, the synthesis of tripolinolate A and its analogs (13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31), and the activity of compounds (1-31) in suppressing the proliferation of glioma and colorectal cancer cells.…”
Section: Introductionmentioning
confidence: 99%
“…They are 4,9-diacetyl-coniferol (13), 21 4-acetyl-9-propionyl-coniferol (14), 4-propionyl-9-acetyl-coniferol (15), 4,9-dipropionyl-coniferol (16), 21 4-acetyl-9-isobutyryl-coniferol (17), 4-isobutyryl-9-acetylconiferol (18), 22 4-acetyl-9-butyryl-coniferol (19), 4-butyryl-9-acetyl-coniferol (20), 4-acetyl-9-(2S-methylbutyryl)-coniferol (21), 4,9-diisobutyryl-coniferol (22), 22 4,9-dibutyryl-coniferol (23), 21 4-butyryl-9-isovaleryl-coniferol (24), 4-isovaleryl-9-butyryl-coniferol (25), 4,9-di(2S-methylbutyryl)-coniferol (26), 4,9-diisovaleryl-coniferol (27), 23 4,9-divaleryl-coniferol (28), 21 4,9-dihexanoyl-coniferol (29), 21 4,9-diheptanoyl-coniferol (30), 21 and 4,9-dioctanoyl-coniferol (31). 21 Compounds 14,15,17,[19][20][21], and 24-26 are nine new compounds. The 1 H, 13 C NMR, and HRESIMS data of these new compounds were summarized in Tables 1 and S1.…”
Section: Introductionmentioning
confidence: 99%
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“…Compound 7, oil, characterized as dichrocephol B [16]. Compound 8, oil, identified as dichrocephol C [16]. Compounds 1-5 were isolated from Dichrocephala genus for the first time.…”
mentioning
confidence: 99%