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ChEBI
> Main
CHEBI:132793 - albiflorin
Main
ChEBI Ontology
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ChEBI Name
albiflorin
ChEBI ID
CHEBI:132793
Definition
A monoterpene glycoside with formula C
23
H
28
O
11
, originally isolated from the roots of
Paeonia lactiflora
.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
qingping liu
Supplier Information
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Formula
C23H28O11
Net Charge
0
Average Mass
480.463
Monoisotopic Mass
480.16316
InChI
InChI=1S/C23H28O11/c1-
21-
8-
13(25)
12-
7-
23(21,33-
19-
17(28)
16(27)
15(26)
14(9-
24)
32-
19)
22(12,20(30)
34-
21)
10-
31-
18(29)
11-
5-
3-
2-
4-
6-
11/h2-
6,12-
17,19,24-
28H,7-
10H2,1H3/t12-
,13+,14+,15+,16-
,17+,19-
,21-
,22-
,23-
/m0/s1
InChIKey
QQUHMASGPODSIW-ICECTASOSA-N
SMILES
O1[C@@]
2([C@]
3(O[C@@H]
4O[C@@H]
([C@@H]
(O)
[C@H]
(O)
[C@H]
4O)
CO)
[C@@]
([C@@]
(C3)
([C@H]
(O)
C2)
[H]
)
(C1=O)
COC(=O)
C5=CC=CC=C5)
C
Metabolite of Species
Details
Paeonia lactiflora
(NCBI:txid35924)
Found in root
(BTO:0001188)
. See:
PubMed
Roles Classification
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application
(s):
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
albiflorin (
CHEBI:132793
)
has role
neuroprotective agent (
CHEBI:63726
)
albiflorin (
CHEBI:132793
)
has role
plant metabolite (
CHEBI:76924
)
albiflorin (
CHEBI:132793
)
is a
β-
D
-glucoside (
CHEBI:22798
)
albiflorin (
CHEBI:132793
)
is a
γ-lactone (
CHEBI:37581
)
albiflorin (
CHEBI:132793
)
is a
benzoate ester (
CHEBI:36054
)
albiflorin (
CHEBI:132793
)
is a
bridged compound (
CHEBI:35990
)
albiflorin (
CHEBI:132793
)
is a
monoterpene glycoside (
CHEBI:72293
)
albiflorin (
CHEBI:132793
)
is a
secondary alcohol (
CHEBI:35681
)
Incoming
6'-
O
-galloylalbiflorin (
CHEBI:132816
)
has functional parent
albiflorin (
CHEBI:132793
)
IUPAC Name
[(1
R
,3
R
,4
R
,6
S
,9
S
)-
1-
(β-
D
-
glucopyranosyloxy)-
4-
hydroxy-
6-
methyl-
8-
oxo-
7-
oxatricyclo[4.3.0.0
3,9
]nonan-
9-
yl]methyl benzoate
Manual Xrefs
Databases
C00033623
KNApSAcK
C17457
KEGG COMPOUND
View more database links
Registry Numbers
Types
Sources
18602070
Reaxys Registry Number
Reaxys
39011-90-0
CAS Registry Number
ChemIDplus
Citations
Types
Sources
22674837
PubMed citation
Europe PMC
22782934
PubMed citation
Europe PMC
23695964
PubMed citation
Europe PMC
23707745
PubMed citation
Europe PMC
24422408
PubMed citation
Europe PMC
24646307
PubMed citation
Europe PMC
24907546
PubMed citation
Europe PMC
25042570
PubMed citation
Europe PMC
25423839
PubMed citation
Europe PMC
25507561
PubMed citation
Europe PMC
25938872
PubMed citation
Europe PMC
26058364
PubMed citation
Europe PMC
26080568
PubMed citation
Europe PMC
26089940
PubMed citation
Europe PMC
26475043
PubMed citation
Europe PMC
26719283
PubMed citation
Europe PMC
27038516
PubMed citation
Europe PMC
27070118
PubMed citation
Europe PMC
27313650
PubMed citation
Europe PMC
27376264
PubMed citation
Europe PMC
27429639
PubMed citation
Europe PMC
27608949
PubMed citation
Europe PMC
27633302
PubMed citation
Europe PMC
27646789
PubMed citation
Europe PMC
27975815
PubMed citation
Europe PMC
27993636
PubMed citation
Europe PMC
Last Modified
20 January 2017