2016
DOI: 10.1016/j.fitote.2016.01.015
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Cycloartane and oleanane-type glycosides from Astragalus pennatulus

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Cited by 13 publications
(9 citation statements)
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“…In the low-field of 13 C NMR spectrum, in addition to oxymethine resonances, a tertiary alcohol carbon at δ 73.4 and a carbonyl carbon at δ 217.4 were also noticed (Table 2). The presence of a double bond as ketone group suggested that the skeleton had pentacyclic nature including the characteristic cyclopropane ring.…”
Section: Resultsmentioning
confidence: 99%
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“…In the low-field of 13 C NMR spectrum, in addition to oxymethine resonances, a tertiary alcohol carbon at δ 73.4 and a carbonyl carbon at δ 217.4 were also noticed (Table 2). The presence of a double bond as ketone group suggested that the skeleton had pentacyclic nature including the characteristic cyclopropane ring.…”
Section: Resultsmentioning
confidence: 99%
“…A detailed analysis of 1 H and 13 C NMR data, and comparison with those of cycloartane-type aglycones derived from Astragalus genus proposed that compound 1 was closely related with cyclocanthogenin [3β,6α,16β,24(S)-25-pentahydroxycycloartane] [27] (Tables 1 and 2). Complete NMR assignments of 1 were accomplished by HSQC and COSY experiments, whereas to reveal the complete skeleton via connecting the partial structures, the HMBC spectrum was evaluated (Fig.…”
Section: Resultsmentioning
confidence: 99%
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