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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:15570 -
D
-alanine
Main
ChEBI Ontology
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ChEBI Name
D
-alanine
ChEBI ID
CHEBI:15570
ChEBI ASCII Name
D-alanine
Definition
The
D
-enantiomer of alanine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:10840, CHEBI:41848, CHEBI:41756, CHEBI:41877, CHEBI:41798, CHEBI:4087, CHEBI:20893, CHEBI:12899
Supplier Information
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Molfile
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Formula
C3H7NO2
Net Charge
0
Average Mass
89.09322
Monoisotopic Mass
89.04768
InChI
InChI=1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m1/s1
InChIKey
QNAYBMKLOCPYGJ-UWTATZPHSA-N
SMILES
C[C@@H](N)C(O)=O
Metabolite of Species
Details
Escherichia coli
(NCBI:txid562)
See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
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):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
EC 4.3.1.15 (diaminopropionate ammonia-lyase) inhibitor
An EC 4.3.1.* (ammonia-lyase) inhibitor that interferes with the action of diaminopropionate ammonia-lyase (EC 4.3.1.15).
fundamental metabolite
Any metabolite produced by all living cells.
(via
alanine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-alanine (
CHEBI:15570
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
D
-alanine (
CHEBI:15570
)
has role
EC 4.3.1.15 (diaminopropionate ammonia-lyase) inhibitor (
CHEBI:77881
)
D
-alanine (
CHEBI:15570
)
has role
human metabolite (
CHEBI:77746
)
D
-alanine (
CHEBI:15570
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-alanine (
CHEBI:15570
)
is a
alanine (
CHEBI:16449
)
D
-alanine (
CHEBI:15570
)
is conjugate acid of
D
-alaninate (
CHEBI:32435
)
D
-alanine (
CHEBI:15570
)
is conjugate base of
D
-alaninium (
CHEBI:32436
)
D
-alanine (
CHEBI:15570
)
is enantiomer of
L
-alanine (
CHEBI:16977
)
D
-alanine (
CHEBI:15570
)
is tautomer of
D
-alanine zwitterion (
CHEBI:57416
)
Incoming
β-(2-thienyl)-
D
-alanine (
CHEBI:77819
)
has functional parent
D
-alanine (
CHEBI:15570
)
D
-alanine derivative (
CHEBI:83944
)
has functional parent
D
-alanine (
CHEBI:15570
)
D
-lupinic acid (
CHEBI:30886
)
has functional parent
D
-alanine (
CHEBI:15570
)
fusarithioamide A (
CHEBI:141359
)
has functional parent
D
-alanine (
CHEBI:15570
)
metalaxyl-M (
CHEBI:60607
)
has functional parent
D
-alanine (
CHEBI:15570
)
pradimicin A (
CHEBI:8349
)
has functional parent
D
-alanine (
CHEBI:15570
)
pradimicin B (
CHEBI:8350
)
has functional parent
D
-alanine (
CHEBI:15570
)
pradimicin C (
CHEBI:8351
)
has functional parent
D
-alanine (
CHEBI:15570
)
D
-alaninium (
CHEBI:32436
)
is conjugate acid of
D
-alanine (
CHEBI:15570
)
D
-alaninate (
CHEBI:32435
)
is conjugate base of
D
-alanine (
CHEBI:15570
)
L
-alanine (
CHEBI:16977
)
is enantiomer of
D
-alanine (
CHEBI:15570
)
D
-alanine residue (
CHEBI:29949
)
is substituent group from
D
-alanine (
CHEBI:15570
)
D
-alanino group (
CHEBI:32438
)
is substituent group from
D
-alanine (
CHEBI:15570
)
D
-alanyl group (
CHEBI:32437
)
is substituent group from
D
-alanine (
CHEBI:15570
)
D
-alanine zwitterion (
CHEBI:57416
)
is tautomer of
D
-alanine (
CHEBI:15570
)
IUPAC Name
D
-alanine
Synonyms
Sources
(2
R
)-2-aminopropanoic acid
IUPAC
(
R
)-2-aminopropanoic acid
ChEBI
(
R
)-alanine
NIST Chemistry WebBook
D-2-Aminopropionic acid
KEGG COMPOUND
D-Ala
KEGG COMPOUND
D
-Alanin
ChEBI
D-Alanine
KEGG COMPOUND
D
-α-alanine
NIST Chemistry WebBook
D
-α-aminopropionic acid
ChEBI
DAL
PDBeChem
Manual Xrefs
Databases
C00019654
KNApSAcK
C00133
KEGG COMPOUND
D-ALANINE
MetaCyc
DAL
PDBeChem
DB01786
DrugBank
ECMDB01310
ECMDB
HMDB0001310
HMDB
YMDB00993
YMDB
View more database links
Registry Numbers
Types
Sources
1720249
Beilstein Registry Number
Beilstein
1720249
Reaxys Registry Number
Reaxys
338-69-2
CAS Registry Number
KEGG COMPOUND
338-69-2
CAS Registry Number
ChemIDplus
338-69-2
CAS Registry Number
NIST Chemistry WebBook
82157
Gmelin Registry Number
Gmelin
Citations
Types
Sources
10977898
PubMed citation
Europe PMC
1450921
PubMed citation
Europe PMC
22005737
PubMed citation
Europe PMC
22075031
PubMed citation
Europe PMC
22123251
PubMed citation
Europe PMC
22313760
PubMed citation
Europe PMC
3275662
PubMed citation
Europe PMC
Last Modified
15 August 2018