InChI=1S/C29H42O10/c1-15-22(32)23(33)24(34)25(38-15)39-17-3-8-27(14-30)19-4-7-26(2)18(16-11-21(31)37-13-16)6-10-29(26,36)20(19)5-9-28(27,35)12-17/h11,14-15,17-20,22-25,32-36H,3-10,12-13H2,1-2H3/t15-,17-,18+,19-,20+,22-,23+,24+,25-,26+,27-,28-,29-/m0/s1 |
HULMNSIAKWANQO-JQKSAQOKSA-N |
[H][C@@]1(CC[C@]2(O)[C@]3([H])CC[C@]4(O)C[C@H](CC[C@]4(C=O)[C@@]3([H])CC[C@]12C)O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)C1=CC(=O)OC1 |
|
Convallaria majalis
(NCBI:txid32189)
|
Found in
aerial part
(BTO:0001658).
See:
PubMed
|
Convallaria majalis
(NCBI:txid32189)
|
Found in
rhizome
(BTO:0001181).
See:
PubMed
|
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
|
|
vasodilator agent
A drug used to cause dilation of the blood vessels.
|
|
3β-(6-deoxy-α-L-mannopyranosyloxy)-5,14-dihydroxy-19-oxo-5β-card-20(22)-enolide
|
3β-(α-L-rhamnopyranosyloxy)-5,14-dihydroxy-19-oxo-5β-card-20(22)-enolide
|
(3β,5β)-3-((6-deoxy-α-L-mannopyranosyl)oxy)-5,14-dihydroxy-19-oxo-card-20(22)-enolide
|
ChEBI
|
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-13-methyl-17-(5-oxo-2,5-dihydrofuran-3-yl)-3-((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)hexadecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde
|
ChEBI
|
3β-((6-deoxy-α-L-mannopyranosyl)oxy)-5,14-dihydroxy-19-oxo-5β-card-20(22)-enolide
|
ChEBI
|
5β,14β-Dihydroxy-19-oxo-3β[(α-L-rhamnopyranosyl)oxy]card-20,22-enolide
|
ChEBI
|
convallaton
|
ChEBI
|
Convallatoxin
|
KEGG COMPOUND
|
convallatoxoside
|
ChEBI
|
Convallotoxin
|
ChemIDplus
|
corglycon
|
ChEBI
|
Corglycone
|
ChemIDplus
|
korglykon
|
ChEBI
|
Strophanthidin 3-O-alpha-L-rhamnoside
|
KEGG COMPOUND
|
Strophanthidin, 3-(6-deoxy-alpha-L-mannopyranoside)
|
ChemIDplus
|
101532
|
Reaxys Registry Number
|
Reaxys
|
101532
|
Beilstein Registry Number
|
Beilstein
|
508-75-8
|
CAS Registry Number
|
KEGG COMPOUND
|
508-75-8
|
CAS Registry Number
|
ChemIDplus
|