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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:133094 - cyclo(
L
-Leu-
L
-Pro)
Main
ChEBI Ontology
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ChEBI Name
cyclo(
L
-Leu-
L
-Pro)
ChEBI ID
CHEBI:133094
ChEBI ASCII Name
cyclo(L-Leu-L-Pro)
Definition
A homodetic cyclic peptide composed from leucyl and prolyl residues.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C11H18N2O2
Net Charge
0
Average Mass
210.273
Monoisotopic Mass
210.13683
InChI
InChI=1S/C11H18N2O2/c1-
7(2)
6-
8-
11(15)
13-
5-
3-
4-
9(13)
10(14)
12-
8/h7-
9H,3-
6H2,1-
2H3,(H,12,14)
/t8-
,9-
/m0/s1
InChIKey
SZJNCZMRZAUNQT-IUCAKERBSA-N
SMILES
C1C[C@@]2([H])C(N[C@H](C(N2C1)=O)CC(C)C)=O
Metabolite of Species
Details
Bacillus amyloliquefaciens
(NCBI:txid1390)
See:
PubMed
Achromobacter xylosoxidans
(NCBI:txid85698)
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
)
Biological Role
(s):
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
cyclo(
L
-Leu-
L
-Pro) (
CHEBI:133094
)
has role
bacterial metabolite (
CHEBI:76969
)
cyclo(
L
-Leu-
L
-Pro) (
CHEBI:133094
)
has role
marine metabolite (
CHEBI:76507
)
cyclo(
L
-Leu-
L
-Pro) (
CHEBI:133094
)
is a
dipeptide (
CHEBI:46761
)
cyclo(
L
-Leu-
L
-Pro) (
CHEBI:133094
)
is a
homodetic cyclic peptide (
CHEBI:24613
)
cyclo(
L
-Leu-
L
-Pro) (
CHEBI:133094
)
is a
pyrrolopyrazine (
CHEBI:48337
)
IUPAC Name
(3
S
,8a
S
)-3-(2-methylpropyl)hexahydropyrrolo[1,2-
a
]pyrazine-1,4-dione
Synonyms
Sources
cyclo(
L
-leucyl-
L
-prolyl)
ChEBI
cyclo(
L
-Pro-
L
-Leu)
ChEBI
cyclo(
L
-prolyl-
L
-leucyl)
ChEBI
cyclo(Leu-Pro)
ChEBI
cyclo(Pro-Leu)
ChEBI
Cyclo-L-leu-L-pro
ChemIDplus
Gancidin W
ChemIDplus
L,L-Cyclo(leucylprolyl)
HMDB
L-cyclo(Leu-pro)
HMDB
L-cyclo(Leucyloprolyl)
HMDB
L-Leucyl-L-proline lactam
HMDB
Manual Xref
Database
HMDB0034276
HMDB
View more database links
Registry Numbers
Types
Sources
2873-36-1
CAS Registry Number
ChemIDplus
85716
Reaxys Registry Number
Reaxys
85716
Beilstein Registry Number
ChemIDplus
Citations
Types
Sources
15574949
PubMed citation
Europe PMC
24698790
PubMed citation
Europe PMC
26945590
PubMed citation
Europe PMC
5007250
PubMed citation
Europe PMC
Last Modified
19 August 2016