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: 9747)
Tschesche R, Wiemann W
Steroid saponins with more than one sugar chain. XI. Desgluco- avenacosides A and B, biologically active nuatigenin glycosides
Chemische Berichte 110 (1977)
2416-2423
Journal NLM ID: 0372723Publisher: Verlag Chemie
The publication contains the following compound(s):
- Compound ID: 23720
|
a-L-Rhap-(1-4)-+
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = nuatigenin = SMILES C[C@H]1[C@H]2[C@@H](O[C@]13CC[C@@](C)({26}CO)O3)C[C@@H]4[C@]2(C)CC[C@H]5[C@H]4CC=C6[C@]5(C)CC{3}[C@H](O)C6 |
Show graphically |
Structure type: oligomer
Trivial name: 26-desgluco-avenacoside-B, avenacoside, avenacin avenacoside
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
8546, CBank-STR:11238
- Compound ID: 23721
|
a-L-Rhap-(1-4)-+
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = nuatigenin = SMILES C[C@H]1[C@H]2[C@@H](O[C@]13CC[C@@](C)({26}CO)O3)C[C@@H]4[C@]2(C)CC[C@H]5[C@H]4CC=C6[C@]5(C)CC{3}[C@H](O)C6 |
Show graphically |
Structure type: oligomer
Trivial name: 26-desgluco-avenacoside-A, avenacoside, desgluco-avenacoside, avenacin avenacoside
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
8547, CBank-STR:7279
Expand this publication
Collapse this publication
2. (Article ID: 11368)
Lásztity R, Hidevégi M, Bata Á
Saponins in food
Food Reviews International 14(4) (1998)
371-390
Five new ether-soluble resin glycosides were isolated from whole plants of Ipomoea stalonifera. Their structures have been determined on the basis of chemical and spectral data. Similar to the resin glycosides previously isolated, all of them are monomers of a jalapinolic acid tetra- or penta-glycoside in which the sugar moiety is partially acylated by organic acids and also combined with the carboxy group-of the aglycone to form a macrocyclic ester structure.
structural elucidation, triterpenoid saponins, glycine-max merrill, pisum-sativum-l, group-a saponin, soyasapogenol-a, soybean seed, chemical-constituents, sapogenol
Journal NLM ID: 8604138Publisher: New York, NY: Marcel Dekker
Institutions: Department of Biochemistry and Food Technology Technical University of Budapest, Budapest, Hungary, Department of Animal Hygiene University of Veterinary Sciences Budapest, István, Hungary
The publication contains the following compound(s):
- Compound ID: 28806
|
Subst-(2-22)-+
|
/Variants 0/-b-D-GlcpA-(1-3)-SoyasapogenolB
/Variants 0/ is:
a-L-Arap-(1-2)-
OR (exclusively)
a-D-Galp-(1-2)-
Subst = 2,3-dihydro-2,5-dihydroxy-6-methyl-4H-pyran-4-one = SMILES O=C1C{2}C(O)C/C={5}C1/O |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28859
|
b-D-Xylp2Ac3Ac4Ac-(1-4)-a-L-Arap-(1-22)-+
|
/Variants 0/-b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-SoyasapogenolA
/Variants 0/ is:
b-D-Glcp-(1-2)-
OR (exclusively)
a-L-Arap-(1-2)- |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28860
|
b-D-Glcp2Ac3Ac4Ac6Ac-(1-4)-a-L-Arap-(1-22)-+
|
/Variants 0/-b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-SoyasapogenolA
/Variants 0/ is:
b-D-Glcp-(1-2)-
OR (exclusively)
a-L-Rhap-(1-2)- |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28861
|
b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-+
|
b-D-Glcp2Ac3Ac4Ac6(%)Ac-(1-4)-a-L-Arap-(1-22)-SoyasapogenolA |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28862
|
a-L-Arap-(1-2)-b-D-GlcpA-(1-3)-+
|
b-D-Glcp2Ac3Ac4Ac6(%)Ac-(1-4)-a-L-Arap-(1-22)-SoyasapogenolA |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28863
|
Subst-(2-22)-+
|
b-D-Glcp-(1-2)-/Variants 0/-b-D-GlcpA-(1-3)-SoyasapogenolB
/Variants 0/ is:
a-L-Arap-(1-2)-
OR (exclusively)
a-D-Galp-(1-2)-
Subst = 2,3-dihydro-2,5-dihydroxy-6-methyl-4H-pyran-4-one = SMILES O=C1C{2}C(O)C/C={5}C1/O |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28864
|
Subst-(2-22)-+
|
a-L-Rhap-(1-2)-/Variants 0/-b-D-GlcpA-(1-3)-SoyasapogenolB
/Variants 0/ is:
b-D-Galp-(1-2)-
OR (exclusively)
a-L-Arap-(1-2)-
Subst = 2,3-dihydro-2,5-dihydroxy-6-methyl-4H-pyran-4-one = SMILES O=C1C{2}C(O)C/C={5}C1/O |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28865
|
Subst2-(2-22)-+
|
a-L-Rhap-(1-2)-a-D-Galp-(1-2)-b-D-GlcpA-(1-3)-Subst1
Subst1 = olean-12-en-28-al-3β,22β,24-triol = SMILES C[C@]5(C)C{22}C(O)C4(C=O)CC[C@]3(C)/C(=C\CC2[C@@]1(C)CC{3}[C@H](O)[C@](C)({24}CO)C1CC[C@]23C)C4C5;
Subst2 = 2,3-dihydro-2,5-dihydroxy-6-methyl-4H-pyran-4-one = SMILES O=C1C{2}C(O)C/C={5}C1/O |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 28867
|
b-D-Glcp-(1-27)-+
|
a-L-Rhap-(1-2)-+ |
| |
?%b-D-Glcp-(1-3)-b-D-Glcp-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = 22,25-epoxyfurost-5-en-27-ol = SMILES C[C@H]5C4C(CC3C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@@]34C)C[C@]56CCC(C)({27}CO)C6 |
Show graphically |
Structure type: oligomer
Trivial name: avenacosid B, avenacosid A
Compound class: triterpenoid glycoside
- Compound ID: 28866
|
b-D-Xyl-(1-3)-+
|
b-D-Glcp-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = morolic acid = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC[C@]4([H])C5=CC(C)(C)CC[C@@]({28}C(O)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H] |
Show graphically |
Structure type: oligomer
Compound class: triterpenoid 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