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ChEBI
> Main
CHEBI:85360 -
L
-dihydroanticapsin
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ChEBI Name
L
-dihydroanticapsin
ChEBI ID
CHEBI:85360
ChEBI ASCII Name
L-dihydroanticapsin
Definition
An
L
-alanine derivative in which one of the methyl hydrogens of
L
-alanine is replaced by a 5-hydroxy-7-oxabicyclo[4.1.0]heptan-2-yl group.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C9H15NO4
Net Charge
0
Average Mass
201.21970
Monoisotopic Mass
201.10011
InChI
InChI=1S/C9H15NO4/c10-
5(9(12)
13)
3-
4-
1-
2-
6(11)
8-
7(4)
14-
8/h4-
8,11H,1-
3,10H2,(H,12,13)
/t4-
,5-
,6+,7+,8-
/m0/s1
InChIKey
YMLXTGCTHGQQKS-TXXZRHAASA-N
SMILES
N[C@@H](C[C@@H]1CC[C@@H](O)[C@@H]2O[C@H]12)C(O)=O
Metabolite of Species
Details
Bacillus subtilis
(NCBI:txid1423)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
L
-dihydroanticapsin (
CHEBI:85360
)
has role
bacterial metabolite (
CHEBI:76969
)
L
-dihydroanticapsin (
CHEBI:85360
)
is a
L
-alanine derivative (
CHEBI:83943
)
L
-dihydroanticapsin (
CHEBI:85360
)
is a
epoxide (
CHEBI:32955
)
L
-dihydroanticapsin (
CHEBI:85360
)
is a
non-proteinogenic
L
-α-amino acid (
CHEBI:83822
)
L
-dihydroanticapsin (
CHEBI:85360
)
is a
oxabicycloalkane (
CHEBI:46733
)
L
-dihydroanticapsin (
CHEBI:85360
)
is a
secondary alcohol (
CHEBI:35681
)
L
-dihydroanticapsin (
CHEBI:85360
)
is tautomer of
L
-dihydroanticapsin zwitterion (
CHEBI:84358
)
Incoming
L
-dihydroanticapsin zwitterion (
CHEBI:84358
)
is tautomer of
L
-dihydroanticapsin (
CHEBI:85360
)
IUPAC Name
3-
[(1
R
,2
S
,5
R
,6
S
)-
5-
hydroxy-
7-
oxabicyclo[4.1.0]heptan-
2-
yl]-
L
-
alanine
Manual Xref
Database
CPD-17531
MetaCyc
View more database links
Registry Number
Type
Source
27406393
Reaxys Registry Number
Reaxys
Citation
Type
Source
23317005
PubMed citation
Europe PMC
Last Modified
31 March 2015