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ChEBI
> Main
CHEBI:27747 -
L
-homoarginine
Main
ChEBI Ontology
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Models
ChEBI Name
L
-homoarginine
ChEBI ID
CHEBI:27747
ChEBI ASCII Name
L-homoarginine
Definition
An
L
-lysine derivative that is the
L
-enantiomer of homoarginine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:43266, CHEBI:5749, CHEBI:24605
Supplier Information
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Formula
C7H16N4O2
Net Charge
0
Average Mass
188.22750
Monoisotopic Mass
188.12733
InChI
InChI=1S/C7H16N4O2/c8-5(6(12)13)3-1-2-4-11-7(9)10/h5H,1-4,8H2,(H,12,13)(H4,9,10,11)/t5-/m0/s1
InChIKey
QUOGESRFPZDMMT-YFKPBYRVSA-N
SMILES
N[C@@H](CCCCNC(N)=N)C(O)=O
Metabolite of Species
Details
Rattus norvegicus
(NCBI:txid10116)
See:
PubMed
Lathyrus cicera
(NCBI:txid3856)
See:
PubMed
Lathyrus sativus
(NCBI:txid3860)
See:
PubMed
Trypanosoma brucei brucei
(NCBI:txid5702)
of strain WT427 See:
MetaboLights Study
Trypanosoma brucei brucei
(NCBI:txid5702)
of strain WT427 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):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
EC 3.1.3.1 (alkaline phosphatase) inhibitor
An EC 3.1.3.* (phosphoric monoester hydrolase) inhibitor that interferes with the action of alkaline phosphatase (EC 3.1.3.1).
xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound.
rat metabolite
Any mammalian metabolite produced during a metabolic reaction in rat (
Rattus norvegicus
).
Application
(s):
biomarker
A substance used as an indicator of a biological state.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
L
-homoarginine (
CHEBI:27747
)
has role
biomarker (
CHEBI:59163
)
L
-homoarginine (
CHEBI:27747
)
has role
EC 3.1.3.1 (alkaline phosphatase) inhibitor (
CHEBI:63332
)
L
-homoarginine (
CHEBI:27747
)
has role
human metabolite (
CHEBI:77746
)
L
-homoarginine (
CHEBI:27747
)
has role
rat metabolite (
CHEBI:86264
)
L
-homoarginine (
CHEBI:27747
)
has role
xenobiotic metabolite (
CHEBI:76206
)
L
-homoarginine (
CHEBI:27747
)
is a
L
-lysine derivative (
CHEBI:25095
)
L
-homoarginine (
CHEBI:27747
)
is a
homoarginine (
CHEBI:24606
)
L
-homoarginine (
CHEBI:27747
)
is a
non-proteinogenic
L
-α-amino acid (
CHEBI:83822
)
L
-homoarginine (
CHEBI:27747
)
is conjugate base of
L
-homoarginine(1+) (
CHEBI:143006
)
Incoming
L
-homoarginine(1+) (
CHEBI:143006
)
is conjugate acid of
L
-homoarginine (
CHEBI:27747
)
IUPAC Name
N
6
-carbamimidoyl-
L
-lysine
Synonyms
Sources
Homo-L-arginine
HMDB
Homoarginine
KEGG COMPOUND
L
-
N
6
-amidinolysine
ChemIDplus
N6-(Aminoiminomethyl)-L-lysine
HMDB
N6-amidino-L-Lysine
HMDB
N6-amidino-Lysine
HMDB
Manual Xrefs
Databases
C00001364
KNApSAcK
C01924
KEGG COMPOUND
DB03974
DrugBank
HMDB0000670
HMDB
HRG
PDBeChem
View more database links
Registry Numbers
Types
Sources
156-86-5
CAS Registry Number
KEGG COMPOUND
156-86-5
CAS Registry Number
ChemIDplus
1726127
Reaxys Registry Number
Reaxys
Citations
Types
Sources
12768501
PubMed citation
Europe PMC
18802314
PubMed citation
Europe PMC
21737361
PubMed citation
Europe PMC
25153574
PubMed citation
Europe PMC
25474016
PubMed citation
Europe PMC
25618752
PubMed citation
Europe PMC
25647833
PubMed citation
Europe PMC
25746168
PubMed citation
Europe PMC
25792110
PubMed citation
Europe PMC
25820767
PubMed citation
Europe PMC
25828044
PubMed citation
Europe PMC
25832546
PubMed citation
Europe PMC
25894888
PubMed citation
Europe PMC
25957527
PubMed citation
Europe PMC
26031828
PubMed citation
Europe PMC
26055922
PubMed citation
Europe PMC
26077714
PubMed citation
Europe PMC
26210755
PubMed citation
Europe PMC
26562034
PubMed citation
Europe PMC
26573540
PubMed citation
Europe PMC
26676627
PubMed citation
Europe PMC
6174211
PubMed citation
Europe PMC
6186121
PubMed citation
Europe PMC
6191705
PubMed citation
Europe PMC
7518015
PubMed citation
Europe PMC
Last Modified
14 February 2019