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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:27947 -
D
-histidine
Main
ChEBI Ontology
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ChEBI Name
D
-histidine
ChEBI ID
CHEBI:27947
ChEBI ASCII Name
D-histidine
Definition
An optically active form of histidine having
D
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:42063, CHEBI:4197, CHEBI:21039
Supplier Information
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Formula
C6H9N3O2
Net Charge
0
Average Mass
155.15468
Monoisotopic Mass
155.06948
InChI
InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m1/s1
InChIKey
HNDVDQJCIGZPNO-RXMQYKEDSA-N
SMILES
N[C@H](Cc1c[nH]cn1)C(O)=O
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
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):
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via
histidine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-histidine (
CHEBI:27947
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
D
-histidine (
CHEBI:27947
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-histidine (
CHEBI:27947
)
is a
histidine (
CHEBI:27570
)
D
-histidine (
CHEBI:27947
)
is conjugate acid of
D
-histidinate(1−) (
CHEBI:32523
)
D
-histidine (
CHEBI:27947
)
is conjugate base of
D
-histidinium(1+) (
CHEBI:32526
)
D
-histidine (
CHEBI:27947
)
is enantiomer of
L
-histidine (
CHEBI:15971
)
D
-histidine (
CHEBI:27947
)
is tautomer of
D
-histidine zwitterion (
CHEBI:142967
)
Incoming
D
-histidine derivative (
CHEBI:84077
)
has functional parent
D
-histidine (
CHEBI:27947
)
D
-histidinium(1+) (
CHEBI:32526
)
is conjugate acid of
D
-histidine (
CHEBI:27947
)
D
-histidinate(1−) (
CHEBI:32523
)
is conjugate base of
D
-histidine (
CHEBI:27947
)
L
-histidine (
CHEBI:15971
)
is enantiomer of
D
-histidine (
CHEBI:27947
)
N
π
-
D
-histidino group (
CHEBI:32520
)
is substituent group from
D
-histidine (
CHEBI:27947
)
N
τ
-
D
-histidino group (
CHEBI:32521
)
is substituent group from
D
-histidine (
CHEBI:27947
)
N
2
-
D
-histidino group (
CHEBI:32518
)
is substituent group from
D
-histidine (
CHEBI:27947
)
D
-histidine residue (
CHEBI:29980
)
is substituent group from
D
-histidine (
CHEBI:27947
)
D
-histidyl group (
CHEBI:32522
)
is substituent group from
D
-histidine (
CHEBI:27947
)
D
-histidine zwitterion (
CHEBI:142967
)
is tautomer of
D
-histidine (
CHEBI:27947
)
IUPAC Names
(2
R
)-2-amino-3-(1
H
-imidazol-4-yl)propanoic acid
D
-histidine
Synonyms
Sources
(R)-alpha-Amino-1H-imidazole-4-propionic acid
KEGG COMPOUND
D
-Histidin
ChEBI
D-Histidine
KEGG COMPOUND
D-HISTIDINE
PDBeChem
DHI
PDBeChem
Manual Xrefs
Databases
C06419
KEGG COMPOUND
CPD-12151
MetaCyc
DHI
PDBeChem
YMDB00794
YMDB
View more database links
Registry Numbers
Types
Sources
351-50-8
CAS Registry Number
KEGG COMPOUND
351-50-8
CAS Registry Number
ChemIDplus
83043
Gmelin Registry Number
Gmelin
84089
Reaxys Registry Number
Reaxys
Citations
Types
Sources
15744050
PubMed citation
Europe PMC
24852066
PubMed citation
Europe PMC
80988
PubMed citation
Europe PMC
Last Modified
14 September 2015