“…The absence of correlation between H–C(13) and H–C(16), as shown by COSY ( Fig. ), indicated that D ‐ring adopt boat conformation and the 16‐MeO was installed in β ‐confirguration . In the NOESY spectrum, the cross‐peak between 16‐MeO and H–C(13) further confirmed the configuration of 16‐MeO.…”
Section: Resultsmentioning
confidence: 81%
“…Ten known compounds, methyllycaconitine ( 6 ), shawurensine ( 7 ), delavaine A ( 8 ), delavaine B ( 9 ), delsemine A ( 10 ), delsemine B ( 11 ), tianshanisine ( 12 ), delcorine ( 13 ), 6‐deoxydelpheline ( 14 ) and blacknidine ( 15 ), were identified by comparison of their spectroscopic data with the literature data.…”
Five new diterpenoid alkaloids, tianshanitines A-E (1 - 5), along with ten known compounds (6 - 15), were isolated from the EtOH extracts of the whole plant of Delphinium tianshanicum W.T.Wang. Their structures were determined based on extensive spectroscopic analyses, including 1D- and 2D-NMR, HR-ESI-MS, and the structure of tianshanitine C (3) was confirmed by X-ray diffraction analysis. Tianshanitine A (1) is the first example of natural diterpenoid alkaloid containing a benzoyl group at C(1) position. Tianshanitine B (2) is a rare natural diterpenoid alkaloid bearing a OH group at C(16) position. Compounds 1 - 5, 6, 8, 10, 12 and 14 were evaluated for cytotoxicity against HCT116, MCF-7 and HepG2 human cancer cell lines.
“…The absence of correlation between H–C(13) and H–C(16), as shown by COSY ( Fig. ), indicated that D ‐ring adopt boat conformation and the 16‐MeO was installed in β ‐confirguration . In the NOESY spectrum, the cross‐peak between 16‐MeO and H–C(13) further confirmed the configuration of 16‐MeO.…”
Section: Resultsmentioning
confidence: 81%
“…Ten known compounds, methyllycaconitine ( 6 ), shawurensine ( 7 ), delavaine A ( 8 ), delavaine B ( 9 ), delsemine A ( 10 ), delsemine B ( 11 ), tianshanisine ( 12 ), delcorine ( 13 ), 6‐deoxydelpheline ( 14 ) and blacknidine ( 15 ), were identified by comparison of their spectroscopic data with the literature data.…”
Five new diterpenoid alkaloids, tianshanitines A-E (1 - 5), along with ten known compounds (6 - 15), were isolated from the EtOH extracts of the whole plant of Delphinium tianshanicum W.T.Wang. Their structures were determined based on extensive spectroscopic analyses, including 1D- and 2D-NMR, HR-ESI-MS, and the structure of tianshanitine C (3) was confirmed by X-ray diffraction analysis. Tianshanitine A (1) is the first example of natural diterpenoid alkaloid containing a benzoyl group at C(1) position. Tianshanitine B (2) is a rare natural diterpenoid alkaloid bearing a OH group at C(16) position. Compounds 1 - 5, 6, 8, 10, 12 and 14 were evaluated for cytotoxicity against HCT116, MCF-7 and HepG2 human cancer cell lines.
“…[33][34][35][36][37] Budelphine (36) from D. buschianum possesses a rare 1,2-epoxy group. 36 There are 12 alkaloids (39)(40)(41)(42)(43)(44)(45)(46)(47)(48)(49)(50) with an N-CHO formamide group formed from a C-21 aldehyde. 4,[38][39][40][41][42][43][44][45] Among these compounds, alkaloids 41-45 are DAs that have no oxygen-containing group at C-16.…”
Multiple chemical constituents, mainly diterpenoid alkaloids, from Delphinium showed great research significance for their novel structures and broad bioactivities.
“…As regards its constituents, a number of alkaloids have been isolated from the roots and the aerial parts [2]. Moreover, acylated kaempferol glycosides in the flowers of D. formosum are reported [3].…”
Section: Introductionmentioning
confidence: 99%
“…As part of our continuing investigation on the chemical constituents in the Ranunculaceous plants [4][5][6], we report one new chromone glycoside (1) isolated from D. hybridum cv. ''Belladonna Casablanca,'' together with six known flavonol glycosides (2)(3)(4)(5)(6)(7).…”
One new chromone and six known flavonol glycosides were isolated from the stems and leaves of Delphinium hybridum cv. ''Belladonna Casablanca'' (Ranunculaceae). The new chromone glycoside was elucidated as 2-methyl-chromone-5,7-diol 7-O-a-L-rhamnopyranosyl-(1 fi 6)-b-D-glucopyranoside (1). The six known flavonol glycosides were designated as compounds 2-5, being kaempferol-type glycosides, and compounds 6 and 7, being quercetin-type glycosides. The structures of these glycosides were determined by two-dimensional nuclear magnetic resonance (2D NMR) spectroscopic analysis and chemical evidence.
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