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ChEBI
> Main
CHEBI:134690 - acromelic acid A
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ChEBI Name
acromelic acid A
ChEBI ID
CHEBI:134690
Definition
A pyrrolidinecarboxylic acid that is siolated from the poisonous mushroom
Clitocybe amoenolens
.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C13H14N2O7
Net Charge
0
Average Mass
310.260
Monoisotopic Mass
310.08010
InChI
InChI=1S/C13H14N2O7/c16-
9(17)
3-
6-
7(4-
14-
10(6)
13(21)
22)
5-
1-
2-
8(12(19)
20)
15-
11(5)
18/h1-
2,6-
7,10,14H,3-
4H2,(H,15,18)
(H,16,17)
(H,19,20)
(H,21,22)
/t6-
,7+,10-
/m0/s1
InChIKey
CWXNEBSQRIECMV-PJKMHFRUSA-N
SMILES
C1(=CC=C(C(N1)=O)[C@@H]2[C@@H]([C@@H](C(O)=O)NC2)CC(=O)O)C(=O)O
Metabolite of Species
Details
Clitocybe amoenolens
(NCBI:txid1144693)
See:
PubMed
Apis cerana
(NCBI:txid7461)
See:
MetaboLights Study
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):
NMDA receptor agonist
An excitatory amino acid agonist which binds to NMDA receptors and triggers a response.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
neurotoxin
A poison that interferes with the functions of the nervous system.
Application
(s):
NMDA receptor agonist
An excitatory amino acid agonist which binds to NMDA receptors and triggers a response.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
acromelic acid A (
CHEBI:134690
)
has functional parent
L
-proline (
CHEBI:17203
)
acromelic acid A (
CHEBI:134690
)
has role
fungal metabolite (
CHEBI:76946
)
acromelic acid A (
CHEBI:134690
)
has role
neurotoxin (
CHEBI:50910
)
acromelic acid A (
CHEBI:134690
)
has role
NMDA receptor agonist (
CHEBI:64571
)
acromelic acid A (
CHEBI:134690
)
is a
pyridone (
CHEBI:38183
)
acromelic acid A (
CHEBI:134690
)
is a
pyrrolidinecarboxylic acid (
CHEBI:46767
)
acromelic acid A (
CHEBI:134690
)
is a
tricarboxylic acid (
CHEBI:27093
)
IUPAC Name
5-
[(3
S
,4
S
,5
S
)-
5-
carboxy-
4-
(carboxymethyl)pyrrolidin-
3-
yl]-
6-
oxo-
1,6-
dihydropyridine-
2-
carboxylic acid
Manual Xrefs
Databases
97186
ChemSpider
C19949
KEGG COMPOUND
View more database links
Registry Numbers
Types
Sources
3628137
Reaxys Registry Number
Reaxys
86630-09-3
CAS Registry Number
ChemIDplus
Citations
Types
Sources
12882485
PubMed citation
Europe PMC
1341901
PubMed citation
Europe PMC
1359719
PubMed citation
Europe PMC
1375859
PubMed citation
Europe PMC
15560485
PubMed citation
Europe PMC
16480870
PubMed citation
Europe PMC
1687368
PubMed citation
Europe PMC
1817797
PubMed citation
Europe PMC
1890926
PubMed citation
Europe PMC
19429136
PubMed citation
Europe PMC
1963751
PubMed citation
Europe PMC
21354794
PubMed citation
Europe PMC
23124023
PubMed citation
Europe PMC
2574623
PubMed citation
Europe PMC
25861935
PubMed citation
Europe PMC
2881596
PubMed citation
Europe PMC
7477968
PubMed citation
Europe PMC
7595634
PubMed citation
Europe PMC
7821331
PubMed citation
Europe PMC
8317271
PubMed citation
Europe PMC
8846097
PubMed citation
Europe PMC
Last Modified
14 August 2017