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1.
(
Organism ID:
14370)
Acacia
auriculiformis
(
NCBI TaxID 205027
,
species name lookup
)
Taxonomic group:
plant
Phylum:
Streptophyta
The following compound(s) are assigned to this organism:
Compound ID:
25434
b-D-Glcp-(1-6)-+ | a-L-Arap-(1-2)-b-D-Glcp-(1-3)-Subst Subst = 16-epi-acacic acid 21,28-lactone = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)[C@@](O6)([H])C[C@@](C6=O)5{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H]
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Structure type:
oligomer
Trivial name:
acaciaside
Compound class:
saponin glycoside, glycoside
Reference(s) to other database(s):
CCSD:
27983
, CBank-STR:6860
Phytochemistry
1988, "Structure of acaciaside, a triterpenoid trisaccharide from Acacia auriculiformis"
CSDB ID 145560
(all data & tools)
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66666
(all data & tools)
Compound ID:
32250
b-D-Glcp-(1-6)-+ | a-L-Arap-(1-2)-b-D-Glcp-(1-3)-+ | a-L-Rhap-(1-6)-+ | | | b-D-Xylp-(1-2)-b-D-Glcp-(1-28)-Subst | b-D-Glcp-(1-6)-Subst1-(1-21)-+ Subst = acacic acid = SMILES C[C@]12CC{3}[C@H](O)C(C)(C)[C@@H]1CC[C@]3(C)[C@@H]2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}C(O)=O)[C@H]4CC(C)(C){21}[C@@H](O)C5; Subst1 = 6S-menthiafolic acid = SMILES C=C{6}[C@@](C)(O)CC/C=C(C)/{1}C(O)=O
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Structure type:
oligomer
Trivial name:
acaciaside A
Compound class:
glycoside
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66663
(all data & tools)
Compound ID:
32251
a-L-Rhap-(1-6)-+ | b-D-Xylp-(1-2)-b-D-Glcp-(1-28)-+ | b-D-Xylp-(1-2)-b-D-Glcp-(1-6)-Subst1-(1-21)-Subst | b-D-Glcp-(1-6)-+ | | | a-L-Arap-(1-2)-b-D-Glcp-(1-3)-+ Subst = acacic acid = SMILES C[C@]12CC{3}[C@H](O)C(C)(C)[C@@H]1CC[C@]3(C)[C@@H]2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}C(O)=O)[C@H]4CC(C)(C){21}[C@@H](O)C5; Subst1 = 6S-menthiafolic acid = SMILES C=C{6}[C@@](C)(O)CC/C=C(C)/{1}C(O)=O
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Structure type:
oligomer
Trivial name:
acaciaside B
Compound class:
glycoside
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66664
(all data & tools)
Compound ID:
32252
a-L-Rhap-(1-6)-+ | b-D-Xylp-(1-2)-b-D-Glcp-(1-28)-+ | a-L-Rhap-(1-2)-b-D-Glcp-(1-6)-Subst1-(1-21)-Subst | b-D-Glcp-(1-6)-+ | | | a-L-Arap-(1-2)-b-D-Glcp-(1-3)-+ Subst = acacic acid = SMILES C[C@]12CC{3}[C@H](O)C(C)(C)[C@@H]1CC[C@]3(C)[C@@H]2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}C(O)=O)[C@H]4CC(C)(C){21}[C@@H](O)C5; Subst1 = 6S-menthiafolic acid = SMILES C=C{6}[C@@](C)(O)CC/C=C(C)/{1}C(O)=O
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Structure type:
oligomer
Trivial name:
acaciaside C
Compound class:
glycoside
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66665
(all data & tools)
Compound ID:
32253
a-L-Arap-(1-2)-b-D-Glcp-(1-3)-Subst Subst = 16-epi-acacic acid 21,28-lactone = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)[C@@](O6)([H])C[C@@](C6=O)5{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H]
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Structure type:
oligomer
Trivial name:
proacaciaside-I
Compound class:
glycoside
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66667
(all data & tools)
Compound ID:
32254
b-D-Glcp-(1-6)-b-D-Glcp-(1-3)-Subst Subst = 16-epi-acacic acid 21,28-lactone = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)[C@@](O6)([H])C[C@@](C6=O)5{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H]
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Structure type:
oligomer
Trivial name:
proacaciaside-II
Compound class:
glycoside
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66668
(all data & tools)
Compound ID:
32255
a-L-Arap-(1-6)-b-D-GlcpNAc-(1-3)-Subst Subst = 16-epi-acacic acid 21,28-lactone = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)[C@@](O6)([H])C[C@@](C6=O)5{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H]
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Structure type:
oligomer
Trivial name:
acaciamine
Compound class:
glycoside
BOOK: Studies in Natural Products Chemistry (series: Bioactive Natural Products); Eds.: Atta-ur-Rahman; New York: Elsevier
2000, "Chemistry of some natural products of biological interest"
CSDB ID 66669
(all data & tools)
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