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(Q104969401)
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English
Methyl 2-(hexopyranosyloxy)-4-(2-oxoethyl)-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylate
group of isomers
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Statements
instance of
group of stereoisomers
0 references
subclass of
secoiridoid monoterpenoid
0 references
glycoside
0 references
mass
388.136946968
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₇H₂₄O₁₀
0 references
canonical SMILES
O=CCC1C(=COC(OC2OC(CO)C(O)C(O)C2O)C1C=C)C(=O)OC
0 references
found in taxon
Polygala fallax
1 reference
stated in
Xanthone O-glycosides from Polygala tenuifolia.
Carapichea affinis
2 references
stated in
Is a metabolic enzyme complex involved in the efficient and accurate control of Ipecac alkaloid biosynthesis in Psychotria ipecacuanha?
stated in
Chemical Constituents of Psychotria nemorosa Gardner and Antinociceptive Activity
Carapichea klugii
2 references
stated in
Is a metabolic enzyme complex involved in the efficient and accurate control of Ipecac alkaloid biosynthesis in Psychotria ipecacuanha?
stated in
Chemical Constituents of Psychotria nemorosa Gardner and Antinociceptive Activity
Lonicera japonica
2 references
stated in
Structures of iridoids from lonicera morrowii A. Gray II
stated in
Influence of sulfur fumigation on the chemical constituents and antioxidant activity of buds of Lonicera japonica
Strychnos spinosa
1 reference
stated in
Alkaloids and iridoids from Strychnos nux-vomica fruits
Alangium lamarckii
1 reference
stated in
Protoberberine Alkaloids and Cancer Chemopreventive Properties of Compounds from Alangium salviifolium
Catharanthus roseus
1 reference
stated in
Characterization of a second secologanin synthase isoform producing both secologanin and secoxyloganin allows enhanced de novo assembly of a Catharanthus roseus transcriptome.
Carapichea ipecacuanha
1 reference
stated in
Chemical Constituents of Psychotria nemorosa Gardner and Antinociceptive Activity
Lonicera morrowii
1 reference
stated in
Secoiridoid glycosides from the flower buds of Lonicera japonica
Hydrangea macrophylla
1 reference
stated in
Studies on Monoterpene Glucosides and Related Natural Products Part 51. Absolute Structures of Hydrangenosides A, B, C, D, E, F, and G. Novel Type Secoiridoid Glucosides from TwoHydrangea Plants
Sinoadina racemosa
1 reference
stated in
Flavonoid glycosides from Adina racemosa and their inhibitory activities on eukaryotic protein synthesis
Identifiers
InChI
InChI=1S/C17H24O10/c1-3-8-9(4-5-18)10(15(23)24-2)7-25-16(8)27-17-14(22)13(21)12(20)11(6-19)26-17/h3,5,7-9,11-14,16-17,19-22H,1,4,6H2,2H3
0 references
InChIKey
CSKKDSFETGLMSB-UHFFFAOYSA-N
0 references
PubChem CID
369002
1 reference
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
UniChem compound ID
24671048
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-RIKEN-PR308944
1 reference
InChIKey
CSKKDSFETGLMSB-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN-PR310691
1 reference
InChIKey
CSKKDSFETGLMSB-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
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