Found
1
organism. Displayed organism
1
Expand all organisms
Collapse all organisms
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1.
(
Organism ID:
14177)
Asclepias
curassavica
(
NCBI TaxID 52823
,
species name lookup
)
Taxonomic group:
plant
Phylum:
Streptophyta
The following compound(s) are assigned to this organism:
Compound ID:
24552
b-D-Glcp-(1-3)-b-L-Sugp-(1-3:2-2)-Subst Sug = 2-hydroxy-4,6-dideoxy-b-L-lyxohexapyranose = SMILES O{1}[C@H](O[C@@H](C1)C){2}C({3}[C@H]1O)(O)O; Subst = calotropagenin = SMILES C[C@]12CC[C@H]3[C@H]({14}[C@]1(CC[C@@H]2C4=CC(OC4)=O)O)CC[C@H]5C{3}[C@H]({2}[C@@H](C[C@]35C=O)O)O
Show graphically
Show legend
Show as text
Structure type:
oligomer
Compound class:
saponin glycoside
Reference(s) to other database(s):
CCSD:
1647
, CBank-STR:1050
Chemical and Pharmaceutical Bulletin
1992, "Cardenolide glycosides from the seeds of Asclepias curassavica"
CSDB ID 120044
(all data & tools)
Compound ID:
24553
?%b-D-Glcp-(1-6)-b-D-Glcp-(1-3)-b-L-Sugp-(1-3:2-2)-Subst Sug = 2-hydroxy-4,6-dideoxy-b-L-lyxohexapyranose = SMILES O{1}[C@H](O[C@@H](C1)C){2}C({3}[C@H]1O)(O)O; Subst = 16α-hydroxy-calotropagenin = SMILES C[C@]12CC[C@H]3[C@H]({14}[C@]1(C{16}[C@@H](O)[C@@H]2C4=CC(OC4)=O)O)CC[C@H]5C{3}[C@H]({2}[C@@H](C[C@]35C=O)O)O
Show graphically
Show legend
Show as text
Structure type:
oligomer
Compound class:
saponin glycoside
Reference(s) to other database(s):
CCSD:
1650
, CBank-STR:4189
Chemical and Pharmaceutical Bulletin
1992, "Cardenolide glycosides from the seeds of Asclepias curassavica"
CSDB ID 120045
(all data & tools)
Compound ID:
24554
b-D-6dAllp-(1-4)-{{{-b-D-Glcp-(1-4)-}}}/n=0-1/-b-D-Glcp-(1-3)-Subst Subst = corotoxigenin = SMILES C[C@]12CCC3C({14}[C@]1(CC[C@@H]2C4=CC(OC4)=O)O)CC[C@H]5C{3}[C@H](CC[C@]35C=O)O
Show graphically
Show legend
Show as text
Structure type:
oligomer
Compound class:
saponin glycoside
Chemical and Pharmaceutical Bulletin
1992, "Cardenolide glycosides from the seeds of Asclepias curassavica"
CSDB ID 170044
(all data & tools)
Compound ID:
24555
{{{-b-D-Glcp-(1-4)-}}}/n=1-2/-b-D-6dAllp-(1-3)-Subst Subst = coroglaucigenin = SMILES C[C@]12CCC3C({14}[C@]1(CC[C@@H]2C4=CC(OC4)=O)O)CC[C@H]5C{3}[C@H](CC[C@]35{19}CO)O
Show graphically
Show legend
Show as text
Structure type:
oligomer
Compound class:
saponin glycoside
Chemical and Pharmaceutical Bulletin
1992, "Cardenolide glycosides from the seeds of Asclepias curassavica"
CSDB ID 170045
(all data & tools)
Compound ID:
24556
{{{-b-D-Glcp-(1-4)-}}}/n=0-2/-b-D-6dAllp-(1-3)-Subst Subst = 12β-hydroxy-coroglaucigenin = SMILES C[C@]12{12}[C@H](O)CC3C({14}[C@]1(CC[C@@H]2C4=CC(OC4)=O)O)CC[C@H]5C{3}[C@H](CC[C@]35{19}CO)O
Show graphically
Show legend
Show as text
Structure type:
oligomer
Compound class:
saponin glycoside
Chemical and Pharmaceutical Bulletin
1992, "Cardenolide glycosides from the seeds of Asclepias curassavica"
CSDB ID 170046
(all data & tools)
Compound ID:
31138
b-D-Glcp-(1-3)-Subst Subst = conduritol F = SMILES O{1}[C@H]1/C=C\{4}[C@@H](O){3}[C@H](O){2}[C@H]1O
Show graphically
Show legend
Show as text
Structure type:
monomer
Compound class:
glycoside
Chemical and Pharmaceutical Bulletin
2000, "Conduritol F glucosides and terpenoid glucosides from Cynanchum liukiuense and distribution of conduritol F glucosides in several Asclepiadaceous plants"
CSDB ID 64579
(all data & tools)
Expand this organism
Collapse this organism
Resort organisms by:
publication year
journal name
microorganism
structure type
New query
Export IDs
Home
Help
Total list of
organism IDs
on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent
record IDs
):
Execution: <1 sec
Found 