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1.
(
Organism ID:
14803)
Acanthopanax
koreanum
(
NCBI TaxID 96667
,
species name lookup
)
Later renamed to:
Eleutherococcus koreanus
Taxonomic group:
plant
Phylum:
Streptophyta
The following compound(s) are assigned to this organism:
Compound ID:
27496
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst Subst = lup-20(29)-en-3α-ol-23,28-dioic acid = SMILES C[C@@]1({23}C(O)=O){3}[C@H](O)CC[C@]2(C)[C@@]3([H])CC[C@]4([H])[C@@]5([H])[C@H](C(C)=C)CC[C@@]({28}C(O)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H]
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Structure type:
oligomer ; 979.4878 [M+Na]+
C48H76O19
Trivial name:
acankoreoside A
Compound class:
triterpenoid glycoside
Reference(s) to other database(s):
CCSD:
8972
, CBank-STR:21885
Chemical and Pharmaceutical Bulletin
1998, "Two new lupane-triterpene glycosides from leaves of Acanthopanax koreanum"
CSDB ID 120833
(all data & tools)
Compound ID:
27497
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst Subst = lup-20(29)-en-3α,11α,23-triol-28-oic acid = SMILES C[C@@]1({23}CO){3}[C@H](O)CC[C@]2(C)[C@@]3([H]){11}[C@H](O)C[C@]4([H])[C@@]5([H])[C@H](C(C)=C)CC[C@@]({28}C(O)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H]
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Structure type:
oligomer ; 957 [M-H]-
C48H78O19
Trivial name:
acankoreoside B
Compound class:
triterpenoid glycoside
Reference(s) to other database(s):
CCSD:
8999
, CBank-STR:21886
Chemical and Pharmaceutical Bulletin
1998, "Two new lupane-triterpene glycosides from leaves of Acanthopanax koreanum"
CSDB ID 120834
(all data & tools)
Compound ID:
29777
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst Subst = 3α,11α-dihydroxy-lup-20(29)-en-28-oic acid = SMILES C=C(C)[C@@H]4CC[C@]5({28}C(=O)O)CC[C@]3(C)C(C{11}[C@@H](O)C2[C@@]1(C)CC{3}[C@@H](O)[C@](C)(C)C1CC[C@]23C)C45
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Structure type:
oligomer ; 965.5073 [M+Na]+
C48H78O18
Compound class:
triterpenoid glycoside
Phytochemistry
1998, "A lupane-triterpene glycoside from leaves of two Acanthopanax"
CSDB ID 63519
(all data & tools)
Compound ID:
31066
b-D-Glcp-(1-3)-+ | a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst Subst = 3α,11α-dihydroxylup-20(29)-en-28-oic acid = SMILES C=C(C)[C@@H]1CC[C@]2({28}C(=O)O)CC[C@]3(C)[C@H](C{11}[C@@H](O)[C@@H]4[C@@]5(C)CC{3}[C@@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
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Structure type:
oligomer ; 1103 [M-H]-
C54H88O23
Trivial name:
acankoreoside C
Compound class:
saponin glycoside
Phytochemistry
1999, "Lupane-triterpene glycosides from leaves of Acanthopanax koreanum"
CSDB ID 64148
(all data & tools)
Compound ID:
31067
b-D-Glcp-(1-3)-Subst Subst = 3α,11α-dihydroxylup-20(29)-en-28-oic acid = SMILES C=C(C)[C@@H]1CC[C@]2({28}C(=O)O)CC[C@]3(C)[C@H](C{11}[C@@H](O)[C@@H]4[C@@]5(C)CC{3}[C@@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
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Structure type:
monomer ; 633 [M-H]-
C36H57O9
Compound class:
saponin glycoside
Phytochemistry
1999, "Lupane-triterpene glycosides from leaves of Acanthopanax koreanum"
CSDB ID 64149
(all data & tools)
Compound ID:
31068
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Subst Subst = 3α,11α-dihydroxylup-23-al-20(29)-en-28-oic acid = SMILES C=C(C)[C@@H]1CC[C@]2({28}C(=O)O)CC[C@]3(C)[C@H](C{11}[C@@H](O)[C@@H]4[C@@]5(C)CC{3}[C@@H](O)[C@@](C)(C=O)[C@@H]5CC[C@]43C)[C@@H]12
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Structure type:
oligomer ; 955 [M-H]-
C48H75O19
Trivial name:
acankoreoside D
Compound class:
saponin glycoside
Phytochemistry
1999, "Lupane-triterpene glycosides from leaves of Acanthopanax koreanum"
CSDB ID 64150
(all data & tools)
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