Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:16436 - CDP-choline
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
CDP-choline
ChEBI ID
CHEBI:16436
Definition
A member of the class of phosphocholines that is the chloine ester of CDP. It is an intermediate obtained in the biosynthetic pathway of structural phospholipids in cell membranes.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:41440, CHEBI:13268, CHEBI:3268, CHEBI:20867
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
more structures >>
Molfile
expand
Wikipedia
License
Read full article at Wikipedia
Formula
C14H26N4O11P2
Net Charge
0
Average Mass
488.32412
Monoisotopic Mass
488.10733
InChI
InChI=1S/C14H26N4O11P2/c1-
18(2,3)
6-
7-
26-
30(22,23)
29-
31(24,25)
27-
8-
9-
11(19)
12(20)
13(28-
9)
17-
5-
4-
10(15)
16-
14(17)
21/h4-
5,9,11-
13,19-
20H,6-
8H2,1-
3H3,(H3-
,15,16,21,22,23,24,25)
/t9-
,11-
,12-
,13-
/m1/s1
InChIKey
RZZPDXZPRHQOCG-OJAKKHQRSA-N
SMILES
C[N+](C)(C)CCOP([O-])(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(N)nc1=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net 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
)
Biological Role
(s):
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
Application
(s):
psychotropic drug
A loosely defined grouping of drugs that have effects on psychological function.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
CDP-choline (
CHEBI:16436
)
has functional parent
CDP (
CHEBI:17239
)
CDP-choline (
CHEBI:16436
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
CDP-choline (
CHEBI:16436
)
has role
human metabolite (
CHEBI:77746
)
CDP-choline (
CHEBI:16436
)
has role
mouse metabolite (
CHEBI:75771
)
CDP-choline (
CHEBI:16436
)
has role
neuroprotective agent (
CHEBI:63726
)
CDP-choline (
CHEBI:16436
)
has role
psychotropic drug (
CHEBI:35471
)
CDP-choline (
CHEBI:16436
)
is a
nucleotide-(amino alcohol)s (
CHEBI:25604
)
CDP-choline (
CHEBI:16436
)
is a
phosphocholines (
CHEBI:36700
)
CDP-choline (
CHEBI:16436
)
is conjugate base of
CDP-choline(1+) (
CHEBI:49086
)
Incoming
CDP-choline(1+) (
CHEBI:49086
)
is conjugate acid of
CDP-choline (
CHEBI:16436
)
IUPAC Name
5'-
O
-[hydroxy({[2-(trimethylammonio)ethoxy]phosphinato}oxy)phosphoryl]cytidine
INNs
Sources
citicolina
ChemIDplus
citicolinum
ChemIDplus
Synonyms
Sources
[2-CYTIDYLATE-O'-PHOSPHONYLOXYL]-ETHYL-TRIMETHYL-AMMONIUM
PDBeChem
CDP-colina
ChemIDplus
Citicoline
KEGG COMPOUND
citidin difosfato de colina
ChemIDplus
cyticholine
ChEBI
Cytidindiphosphocholin
ChemIDplus
cytidine 5'-(choline diphosphate)
ChemIDplus
cytidine 5'-(cholinyl pyrophosphate)
ChemIDplus
Cytidine 5'-diphosphocholine
KEGG COMPOUND
cytidine 5'-diphosphoric choline
ChemIDplus
Manual Xrefs
Databases
664
DrugCentral
C00007231
KNApSAcK
C00307
KEGG COMPOUND
CDC
PDBeChem
Citicoline
Wikipedia
D00057
KEGG DRUG
DB04290
DrugBank
HMDB0001413
HMDB
View more database links
Registry Numbers
Types
Sources
4170138
Reaxys Registry Number
Reaxys
987-78-0
CAS Registry Number
ChemIDplus
Citations
Types
Sources
10701532
PubMed citation
Europe PMC
10796523
PubMed citation
Europe PMC
8709678
PubMed citation
Europe PMC
Last Modified
22 February 2017