Found 2 publications.
Displayed publications from 1 to 2
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 10431)
Miyakoshi M, Ida Y, Isoda S, Shoji J
3-EPI-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Phytochemistry 33 (1993)
891-895
Three novel 3-epi-oleanene type triterpene oligo-glycosyl esters, spinosides D1–D3, were isolated from the leaves of Acanthopanax spinosus. The structures were established to be 28-O-α-l-rhamnopyranosyl(1→4)-β-d-glucopyranosyl(1→6)-β-d-glucopyranosyl esters of 3-epi-serratagenic acid, 3α-hydroxy-23-oxoolean-12-ene-28,29-dioic acid and 3α,23-dihydroxy-olean-12-ene-28,29-dioic acid.
araliaceae, triterpenoid saponin, Acanthopanax spinosus, 3-epi-serratagenic acid, 3α, 23-dihydroxy-olean-12-ene-28, 29-dioic acid, 3α-hydroxy-23-oxoolean-12-ene-28, 3-epi-hederagenin
Publication DOI: 10.1016/0031-9422(93)85298-6Journal NLM ID: 0151434Publisher: Elsevier
Institutions: School of Pharmaceutical Sciences, Showa University, Tokyo, Japan
Methods: 13C NMR, 1H NMR, gel filtration, IR, FAB-MS, reduction, PCD oxidation
The publication contains the following compound(s):
Expand this publication
Collapse this publication
2. (Article ID: 11078)
Miyakoshi M, Isoda S, Sato H, Hirai Y, Shoji J, Ida Y
3α-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Phytochemistry 46(7) (1997)
1255-1259
Four novel 3 α-hydroxy-oleanane type triterpene oligoglycosyl esters, spinoside C2, C3, C6 and C7, were isolated from the leaves of Acanthopanax spinosus. The structures were established to be 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranosyl esters of 3α,30-dihydroxy-23-oxo-olean-12-en-28-oic acid, 3α,20α-dihydroxy-30-nor-olean-12-en-28-oic acid, 3α,20α-dihydroxy-23-oxo-30-nor-olean-12-en-28-oic acid and 3α,20α, 23-trihydroxy-30-nor-olean-12-en-28-oic acid.
araliaceae, triterpenoid saponin, Acanthopanax spinosus, 3α, triterpene glycosyl ester, 20α-dihydroxy-30-nor-olean-12-en-28-oic acid, 20α-dihydroxy-23-oxo-30-nor-olean-12-en-28-oic acid, 20α, 23-trihydroxy-30-nor-olean-12-en-28-oic acid, 3a, 30-dihydroxy-23-oxo-olean-12-en-28-oic acid, spinogenin, spinoside
Publication DOI: 10.1016/S0031-9422(97)80022-2Journal NLM ID: 0151434Publisher: Elsevier
Institutions: School of Pharmaceutical Sciences, Showa University, Hatanodai 1-5-8, Shinagawa-ku, Tokyo 142, Japan
Methods: 13C NMR, 1H NMR, NMR-2D, IR, FAB-MS, TLC, acid hydrolysis, GC, HPLC, extraction, reduction
The publication contains the following compound(s):
- Compound ID: 27597
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst
Subst = 23-oxo-olean-12-en-3α,30-diol-28-oic acid = SMILES O{3}[C@@H]1CC[C@]2(C([C@]1(C)C=O)CC[C@@]3(C2CC=C4[C@]3(CC[C@@]5(C4C[C@@]({30}CO)(CC5)C){28}C(O)=O)C)C)C |
Show graphically |
Structure type: oligomer
; 955 [M-H]-
C48H76O19
Trivial name: spinoside C2
Compound class: saponin glycoside
- Compound ID: 27598
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst
Subst = 30-norolean-12-en-3α,20α-diol-28-oic acid = SMILES CC1(C){3}[C@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])C{20}[C@](C)(O)CC[C@@]({28}C(O)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H] |
Show graphically |
Structure type: oligomer
; 927 [M-H]-
C47H76O18
Trivial name: spinoside C3
Compound class: saponin glycoside
- Compound ID: 27599
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst
Subst = 30-norolean-12-en-3α,20α,23-triol-28-oic acid = SMILES C[C@@]1({23}CO){3}[C@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])C{20}[C@](C)(O)CC[C@@]({28}C(O)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H] |
Show graphically |
Structure type: oligomer
; 943 [M-H]-
C47H76O19
Trivial name: spinoside C6
Compound class: saponin glycoside
- Compound ID: 27600
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst
Subst = 23-oxo-30-norolean-12-en-3α,20α-diol-28-oic acid = SMILES C[C@@]1(C=O){3}[C@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])C{20}[C@](C)(O)CC[C@@]({28}C(O)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H] |
Show graphically |
Structure type: oligomer
; 943 [M-H]-
C47H76O19
Trivial name: spinoside C7
Compound class: saponin glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec