1989
DOI: 10.1016/0031-9422(89)80211-0
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A pregnane ester oligoglycoside from Oxystelma esculentum

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Cited by 11 publications
(3 citation statements)
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“…Velutinol A has anti-bradykinin and anti-inflammatory activity (Calixto et al, 1988a;1991a,b). The structure of velutinol comprises a novel pregnane skeleton, and steroids of this class are commonly encountered in Apocinaceae Chen et al, 1987) as well as Asclepiadaceae (Bando et al, 1980;Sethi et al, 1988;Trivedi et al, 1989;Zhang et al, 1985) and Meliaceae (Nakanishi et al , 1988). Isolation of velutinol A.…”
Section: Introductionmentioning
confidence: 99%
“…Velutinol A has anti-bradykinin and anti-inflammatory activity (Calixto et al, 1988a;1991a,b). The structure of velutinol comprises a novel pregnane skeleton, and steroids of this class are commonly encountered in Apocinaceae Chen et al, 1987) as well as Asclepiadaceae (Bando et al, 1980;Sethi et al, 1988;Trivedi et al, 1989;Zhang et al, 1985) and Meliaceae (Nakanishi et al , 1988). Isolation of velutinol A.…”
Section: Introductionmentioning
confidence: 99%
“…Column chromatography of the chloroform extract using chloroform: methanol (24:1) as eluent afforded oxysine, a triglycoside of calogenin. [11] A pregnane glycoside Esculentin was also isolated from the roots.…”
Section: General Chemical Analysismentioning
confidence: 99%
“…The configuration of the sugar was determined from the large coupling constant (J = 6 Hz) of the anomeric proton, which suggested the presence of β-oleandropyranoside in 4 Mild acid hydrolysis [19] of 7 (0.05 N H 2 SO 4 in dioxane) afforded a genin identified as calogenin [20] and two sugars identified as D-digitoxose [13] and L-diginose [21] (mp, mmp, TLC, PC, [α] D ). The sugars were further characterized by preparing their known derivatives, D-digitoxono acid phenyl hydrazide [13] for D-digitoxose and L-diginonic acid phenyl hydrazide [21] ] could be interpreted as resulting from the fragment sequence common to 2,6-dideoxy hexoses [22].…”
mentioning
confidence: 99%