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ChEBI
> Main
CHEBI:15727 - carnosine
Main
ChEBI Ontology
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ChEBI Name
carnosine
ChEBI ID
CHEBI:15727
Definition
A dipeptide that is the
N
-(β-alanyl) derivative of
L
-histidine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:3428, CHEBI:13948, CHEBI:23040
Supplier Information
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Molfile
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Wikipedia
License
Read full article at Wikipedia
Formula
C9H14N4O3
Net Charge
0
Average Mass
226.236
Monoisotopic Mass
226.10659
InChI
InChI=1S/C9H14N4O3/c10-
2-
1-
8(14)
13-
7(9(15)
16)
3-
6-
4-
11-
5-
12-
6/h4-
5,7H,1-
3,10H2,(H,11,12)
(H,13,14)
(H,15,16)
/t7-
/m0/s1
InChIKey
CQOVPNPJLQNMDC-ZETCQYMHSA-N
SMILES
NCCC(=O)N[C@@H](CC1=CNC=N1)C(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Daphnia magna
(NCBI:txid35525)
See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Chemical Role
(s):
antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
Application
(s):
anticonvulsant
A drug used to prevent seizures or reduce their severity.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
carnosine (
CHEBI:15727
)
has role
Daphnia magna
metabolite (
CHEBI:83056
)
carnosine (
CHEBI:15727
)
has role
anticonvulsant (
CHEBI:35623
)
carnosine (
CHEBI:15727
)
has role
antineoplastic agent (
CHEBI:35610
)
carnosine (
CHEBI:15727
)
has role
antioxidant (
CHEBI:22586
)
carnosine (
CHEBI:15727
)
has role
geroprotector (
CHEBI:176497
)
carnosine (
CHEBI:15727
)
has role
human metabolite (
CHEBI:77746
)
carnosine (
CHEBI:15727
)
has role
mouse metabolite (
CHEBI:75771
)
carnosine (
CHEBI:15727
)
has role
neuroprotective agent (
CHEBI:63726
)
carnosine (
CHEBI:15727
)
is a
dipeptide (
CHEBI:46761
)
carnosine (
CHEBI:15727
)
is conjugate acid of
carnosinate (
CHEBI:66874
)
carnosine (
CHEBI:15727
)
is tautomer of
carnosine zwitterion (
CHEBI:57485
)
Incoming
N
-acetylcarnosine (
CHEBI:67249
)
has functional parent
carnosine (
CHEBI:15727
)
carnosinate (
CHEBI:66874
)
is conjugate base of
carnosine (
CHEBI:15727
)
carnosine zwitterion (
CHEBI:57485
)
is tautomer of
carnosine (
CHEBI:15727
)
IUPAC Name
N
α
-(β-alanyl)-
L
-histidine
Synonyms
Sources
(2
S
)-2-(3-aminopropanamido)-3-(1
H
-imidazol-4-yl)propanoic acid
IUPAC
beta-alanyl-L-histidine
ChEBI
β-alanyl-
L
-histidine
IUPAC
Carnosine
KEGG COMPOUND
ignotine
ChemIDplus
L
-carnosine
ChemIDplus
N
-(3-aminopropanoyl)-
L
-histidine
ChEBI
N-2-M
ChemIDplus
N
-β-alanyl-
L
-histidine
HMDB
Nalpha-(beta-alanyl)-L-histidine
KEGG COMPOUND
Brand Names
Sources
Karnozin
ChemIDplus
Karnozzn
ChemIDplus
Manual Xrefs
Databases
388363
ChemSpider
8V0
PDBeChem
C00052222
KNApSAcK
C00386
KEGG COMPOUND
Carnosine
Wikipedia
DB11695
DrugBank
HMDB0000033
HMDB
View more database links
Registry Numbers
Types
Sources
305-84-0
CAS Registry Number
KEGG COMPOUND
305-84-0
CAS Registry Number
ChemIDplus
87671
Reaxys Registry Number
Reaxys
Citations
Types
Sources
10841274
PubMed citation
Europe PMC
10951105
PubMed citation
Europe PMC
10951108
PubMed citation
Europe PMC
11470131
PubMed citation
Europe PMC
11707898
PubMed citation
Europe PMC
11911459
PubMed citation
Europe PMC
11976203
PubMed citation
Europe PMC
12139778
PubMed citation
Europe PMC
15853927
PubMed citation
Europe PMC
15878720
PubMed citation
Europe PMC
15941308
PubMed citation
Europe PMC
16162015
PubMed citation
Europe PMC
16181134
PubMed citation
Europe PMC
16287364
PubMed citation
Europe PMC
16406688
PubMed citation
Europe PMC
16804013
PubMed citation
Europe PMC
17031479
PubMed citation
Europe PMC
1735411
PubMed citation
Europe PMC
17443912
PubMed citation
Europe PMC
18019400
PubMed citation
Europe PMC
18076890
PubMed citation
Europe PMC
18773880
PubMed citation
Europe PMC
19309105
PubMed citation
Europe PMC
20017611
PubMed citation
Europe PMC
20681748
PubMed citation
Europe PMC
24398899
PubMed citation
Europe PMC
2674258
PubMed citation
Europe PMC
29463897
PubMed citation
Europe PMC
31951767
PubMed citation
Europe PMC
33586561
PubMed citation
Europe PMC
33704575
PubMed citation
Europe PMC
34067694
PubMed citation
Europe PMC
8689392
PubMed citation
Europe PMC
9029640
PubMed citation
Europe PMC
9928418
PubMed citation
Europe PMC
Last Modified
23 September 2021