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> Main
CHEBI:132370 - triptotriterpenic acid A
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ChEBI Name
triptotriterpenic acid A
ChEBI ID
CHEBI:132370
Definition
A pentacyclic triterpenoid with formula C
30
H
48
O
4
, originally isolated from
Tripterygium hypoglaucum
.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
qingping liu
Supplier Information
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Formula
C30H48O4
Net Charge
0
Average Mass
472.701
Monoisotopic Mass
472.35526
InChI
InChI=1S/C30H48O4/c1-
25(2)
20-
10-
13-
30(7)
21(28(20,5)
12-
11-
22(25)
31)
9-
8-
18-
19-
16-
26(3,24(33)
34)
17-
23(32)
27(19,4)
14-
15-
29(18,30)
6/h8,19-
23,31-
32H,9-
17H2,1-
7H3,(H,33,34)
/t19-
,20-
,21+,22-
,23-
,26-
,27+,28-
,29+,30+/m0/s1
InChIKey
JTBGJQZJEYVBJZ-YLXTXNMFSA-N
SMILES
C1[C@H]
(O)
C([C@@]
2(CC[C@@]
3([C@]
(CC=C4[C@]
3(CC[C@@]
5([C@]
4(C[C@@]
(C[C@@H]
5O)
(C(O)
=O)
C)
[H]
)
C)
C)
([C@]
2(C1)
C)
[H]
)
C)
[H]
)
(C)
C
Metabolite of Species
Details
Euonymus laxiflorus
(NCBI:txid1009469)
Found in leaf
(BTO:0000713)
. See:
PubMed
Euonymus laxiflorus
(NCBI:txid1009469)
Found in stem
(BTO:0001300)
. See:
PubMed
Tripterygium hypoglaucum
(NCBI:txid205465)
See:
PubMed
Begonia nantoensis
(NCBI:txid78253)
Found in rhizome
(BTO:0001181)
. See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
triptotriterpenic acid A (
CHEBI:132370
)
has parent hydride
oleanane (
CHEBI:36481
)
triptotriterpenic acid A (
CHEBI:132370
)
has role
plant metabolite (
CHEBI:76924
)
triptotriterpenic acid A (
CHEBI:132370
)
is a
diol (
CHEBI:23824
)
triptotriterpenic acid A (
CHEBI:132370
)
is a
hydroxy monocarboxylic acid (
CHEBI:35868
)
triptotriterpenic acid A (
CHEBI:132370
)
is a
pentacyclic triterpenoid (
CHEBI:25872
)
IUPAC Name
(3β,22α)-3,22-dihydroxyolean-12-en-29-oic acid
Synonyms
Sources
3,22-Dihydroxyolean-12-en-29-oic acid
ChemIDplus
3β,22α-dihydroxyolean-12-en-29-oic acid
ChEBI
Registry Numbers
Types
Sources
100897-87-8
CAS Registry Number
ChemIDplus
5857675
Reaxys Registry Number
Reaxys
Citations
Types
Sources
12713415
PubMed citation
Europe PMC
14993759
PubMed citation
Europe PMC
535601
Chinese Abstracts citation
Europe PMC
Last Modified
24 October 2016