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ChEBI
> Main
CHEBI:87142 -
N
-myristoylglycine
Main
ChEBI Ontology
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ChEBI Name
N
-myristoylglycine
ChEBI ID
CHEBI:87142
ChEBI ASCII Name
N-myristoylglycine
Definition
An
N
-acylglycine in which the acyl group is specified as myristoyl (tetradecanoyl).
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C16H31NO3
Net Charge
0
Average Mass
285.42220
Monoisotopic Mass
285.23039
InChI
InChI=1S/C16H31NO3/c1-
2-
3-
4-
5-
6-
7-
8-
9-
10-
11-
12-
13-
15(18)
17-
14-
16(19)
20/h2-
14H2,1H3,(H,17,18)
(H,19,20)
InChIKey
DYUGTPXLDJQBRB-UHFFFAOYSA-N
SMILES
CCCCCCCCCCCCCC(=O)NCC(O)=O
Metabolite of Species
Details
Homo sapiens
(NCBI:txid9606)
Found in blood serum
(BTO:0000133)
. See:
PubMed
Homo sapiens
(NCBI:txid9606)
Found in urine
(BTO:0001419)
. 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):
human urinary metabolite
Any metabolite (endogenous or exogenous) found in human urine samples.
human blood serum metabolite
Any metabolite (endogenous or exogenous) found in human blood serum samples.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-myristoylglycine (
CHEBI:87142
)
has functional parent
tetradecanoic acid (
CHEBI:28875
)
N
-myristoylglycine (
CHEBI:87142
)
has role
human blood serum metabolite (
CHEBI:85234
)
N
-myristoylglycine (
CHEBI:87142
)
has role
human urinary metabolite (
CHEBI:84087
)
N
-myristoylglycine (
CHEBI:87142
)
is a
N
-acylglycine (
CHEBI:16180
)
N
-myristoylglycine (
CHEBI:87142
)
is a
fatty amide (
CHEBI:29348
)
N
-myristoylglycine (
CHEBI:87142
)
is conjugate acid of
N
-myristoylglycinate (
CHEBI:86500
)
Incoming
N
-myristoylglycinate (
CHEBI:86500
)
is conjugate base of
N
-myristoylglycine (
CHEBI:87142
)
N
-tetradecanoylglycyl group (
CHEBI:133050
)
is substituent group from
N
-myristoylglycine (
CHEBI:87142
)
IUPAC Name
N
-tetradecanoylglycine
Synonyms
Sources
Myristoylglycine
HMDB
tetradecanoylglycine
ChEBI
Manual Xref
Database
HMDB0013250
HMDB
View more database links
Registry Numbers
Types
Sources
14246-55-0
CAS Registry Number
ChemIDplus
14246-55-0
CAS Registry Number
NIST Chemistry WebBook
1794967
Reaxys Registry Number
Reaxys
Citations
Types
Sources
23111557
PubMed citation
Europe PMC
3140788
PubMed citation
Europe PMC
8660675
PubMed citation
Europe PMC
Last Modified
10 February 2021