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> Main
CHEBI:102525 -
N
6
-carbamoylmethyladenine
Main
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ChEBI Name
N
6
-carbamoylmethyladenine
ChEBI ID
CHEBI:102525
ChEBI ASCII Name
N(6)-carbamoylmethyladenine
Definition
A nucleobase analogue that is adenine in which one of the exocyclic amino hydrogens is replaced by a carbamoylmethyl group.
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This entity has been manually annotated by the ChEBI Team.
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Formula
C7H8N6O
Net Charge
0
Average Mass
192.178
Monoisotopic Mass
192.07596
InChI
InChI=1S/C7H8N6O/c8-4(14)1-9-6-5-7(11-2-10-5)13-3-12-6/h2-3H,1H2,(H2,8,14)(H2,9,10,11,12,13)
InChIKey
WIFHSKZDPZUSLN-UHFFFAOYSA-N
SMILES
C=12C(=NC=NC1NCC(=O)N)NC=N2
Metabolite of Species
Details
Mycoplasma genitalium
(NCBI:txid2097)
See:
PubMed
Roles Classification
Biological Role
(s):
Mycoplasma genitalium metabolite
Any bacterial metabolite produced during a metabolic reaction in
Mycoplasma genitalium
.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
has functional parent
adenine (
CHEBI:16708
)
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
has role
Mycoplasma genitalium
metabolite (
CHEBI:131604
)
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
is a
6-aminopurines (
CHEBI:20706
)
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
is a
amino acid amide (
CHEBI:22475
)
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
is a
glycine derivative (
CHEBI:24373
)
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
is a
monocarboxylic acid amide (
CHEBI:29347
)
N
6
-carbamoylmethyladenine (
CHEBI:102525
)
is a
nucleobase analogue (
CHEBI:67142
)
IUPAC Name
N
2
-1
H
-purin-6-ylglycinamide
Synonym
Source
2-(9
H
-purin-6-ylamino)acetamide
ChEBI
Citation
Type
Source
22817898
PubMed citation
Europe PMC
Last Modified
05 April 2016