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Cited by 26 publications
(23 citation statements)
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References 247 publications
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“…119-1238C, [a] D þ10, C 37 H 58 O 12 , FAB-MS m/z 756 [M þ þNa þ K], responded positively to Liebermann-Burchardt [10], xanthydrol [10], Keller-Killiani [10], and Feigl tests [2], indicating it to be a steroidal glycoside of 2,6-dideoxy and normal hexose(s). The presence of two anomeric protons and carbons at d 5.…”
Section: Resultsmentioning
confidence: 99%
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“…119-1238C, [a] D þ10, C 37 H 58 O 12 , FAB-MS m/z 756 [M þ þNa þ K], responded positively to Liebermann-Burchardt [10], xanthydrol [10], Keller-Killiani [10], and Feigl tests [2], indicating it to be a steroidal glycoside of 2,6-dideoxy and normal hexose(s). The presence of two anomeric protons and carbons at d 5.…”
Section: Resultsmentioning
confidence: 99%
“…An important mass ion fragment that arose by rearrangement involving migration of the acetyl group of S2 at C-3 to C-1 of the same sugar, after the radical ion fission of C1ZC2 bond [2], resulting in the cleavage of the terminal sugar appeared at m/z 553. This fragment further confirmed that the esterified D-canarose is the terminal sugar.…”
Section: Resultsmentioning
confidence: 99%
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“…Previous chemical investigation on this genus led to the isolation of members of structural diversity metabolites, involving cembranes [1,2], eunicellane diterpenes [3 -12], sesquiterpenes [13], steroids and glycolipids [14 -17]. Pregnane-type steroids are a class of natural products mainly occurring in soft corals, and various plant species mostly belonging to the Asclepiadaceae family [19]. Zheng et al have isolated two anti-tumour active pregnane glycosides from Cladiella krempfi [16] and two pregnenones from Cladiella sp.…”
Section: Introductionmentioning
confidence: 99%