Triterpenoid Saponins from <i>Rubus ellipticus</i> var. <i>obcordatus</i>

Li, Wei; Fu, Hongwei; Bai, Hong; Sasaki, Tatsunori; Kato, Hiroyoshi; Koike, Kazuo

doi:10.1021/np900237a

Cited by 69 publications

(39 citation statements)

References 21 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…We evaluated the isolated compounds for their inhibitory activity against α -glucosidase since some compounds are known α -glucosidase inhibitors [15]. The results are shown in Table 3, with acarbose used as a positive control.…”

Section: Resultsmentioning

confidence: 99%

α-Glucosidase Inhibitory Constituents from Acanthopanax senticosus Harm Leaves

et al. 2012

View full text Add to dashboard Cite

A new triterpene glycoside, 3-O-[(α-L-rhamnopyranosyl)(1→2)]-[β-D-glucuronopyranosyl-6-O-methyl ester]-olean-12-ene-28-olic acid (1) and a new indole alkaloid, 5-methoxy-2-oxoindolin-3-acetic acid methyl ester (5) were isolated from the leaves of Acanthopanax senticosus Harms along with six known compounds. The structures of the new compounds were determined by means of 2D-NMR experiments and chemical methods. All the isolated compounds were evaluated for their glycosidase inhibition activities and compound 6 showed significant α-glucosidase inhibition activity.

show abstract

Section: Resultsmentioning

confidence: 99%

α-Glucosidase Inhibitory Constituents from Acanthopanax senticosus Harm Leaves

et al. 2012

View full text Add to dashboard Cite

show abstract

“…A C C E P T E D ACCEPTED MANUSCRIPT 11 were mainly isolated from Rosaceous plants [35][36][37]. From this type of compounds, In another approach, we focused on the activity of compounds that were chemically altered in C-28 side chain with ester group of ring A modified structures.…”

Section: Structure−activity Relationship Studiesmentioning

confidence: 99%

Pentacyclic triterpene derivatives possessing polyhydroxyl ring A inhibit Gram-positive bacteria growth by regulating metabolism and virulence genes expression

Huang

Luo

et al. 2015

European Journal of Medicinal Chemistry

View full text Add to dashboard Cite

“…Furthermore, the absolute configuration of these sugars was determinate by GC analysis, according to a method previously reported with some modification. 6 Briefly, solution of were also observed. Thus, the glucose unit should be located at C-29 through an ether linkage to C-1′.…”

Section: Methodsmentioning

confidence: 99%

Three New Oleanane-Type Triterpene Saponins from Gladiolus gandavensis

Tai¹,

Cai²,

Yang³

et al. 2010

Bulletin of the Korean Chemical Society

View full text Add to dashboard Cite

Three new oleanane-type triterpene saponins (1, 2 and 3) were isolated from aerial parts of Gladiolus gandavensis, along with two known compounds (4 and 5). Their structures were elucidated as 29 (2), and 2β,3β,29-trihydroxyolean-12-en-28-oic acid 28 (3), by spectroscopic methods, and by comparison with known analogues. These oleanane-type triterpene saponins glycosidated at C-29 were not obtained frequently.

show abstract

Triterpenoid Saponins from Rubus ellipticus var. obcordatus

Cited by 69 publications

References 21 publications

α-Glucosidase Inhibitory Constituents from Acanthopanax senticosus Harm Leaves

α-Glucosidase Inhibitory Constituents from Acanthopanax senticosus Harm Leaves

Pentacyclic triterpene derivatives possessing polyhydroxyl ring A inhibit Gram-positive bacteria growth by regulating metabolism and virulence genes expression

Three New Oleanane-Type Triterpene Saponins from Gladiolus gandavensis

Contact Info

Product

Resources

About