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(Q105341281)
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English
Saussureosides B
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
(3E)-4-(4-hydroxy-2,6,6-trimethyl-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclohex-1-en-1-yl)but-3-en-2-one
1 reference
based on heuristic
inferred from SMILES
4-(4-hydroxy-2,6,6-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclohex-1-en-1-yl)but-3-en-2-one
1 reference
based on heuristic
inferred from SMILES
mass
386.19406792
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
(E)-4-[(3S,4R)-4-hydroxy-2,6,6-trimethyl-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexen-1-yl]but-3-en-2-one
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
chemical formula
C₁₉H₃₀O₈
0 references
canonical SMILES
O=C(C=CC1=C(C)C(OC2OC(CO)C(O)C(O)C2O)C(O)CC1(C)C)C
0 references
isomeric SMILES
CC(=O)/C=C/C1=C(C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)CC1(C)C
0 references
found in taxon
Saussurea medusa
1 reference
stated in
Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa
Sonchus asper
1 reference
stated in
Sesquiterpene lactone glycosides and ionone derivative glycosides from Sonchus asper
Youngia japonica
1 reference
stated in
New guaiane, megastigmane and eudesmane-type sesquiterpenoids and anti-inflammatory constituents from Youngia japonica.
Identifiers
InChI
InChI=1S/C19H30O8/c1-9(21)5-6-11-10(2)17(12(22)7-19(11,3)4)27-18-16(25)15(24)14(23)13(8-20)26-18/h5-6,12-18,20,22-25H,7-8H2,1-4H3/b6-5+/t12-,13+,14+,15-,16+,17+,18-/m0/s1
0 references
InChIKey
XSVHCRJRFKFCSN-MMNBODBLSA-N
0 references
PubChem CID
11567211
1 reference
stated in
PubChem
retrieved
26 December 2021
inferred from
InChIKey
UniChem compound ID
34242529
1 reference
stated in
UniChem
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