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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:180907 - 2-hydroxyputrescine
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ChEBI Ontology
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ChEBI Name
2-hydroxyputrescine
ChEBI ID
CHEBI:180907
Definition
An alkane-α,ω-diamine that is putrescine substituted by a hydroxy group at position 2.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Anne Morgat
Supplier Information
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Molfile
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Molfile
Formula
C4H12N2O
Net Charge
0
Average Mass
104.153
Monoisotopic Mass
104.09496
InChI
InChI=1S/C4H12N2O/c5-2-1-4(7)3-6/h4,7H,1-3,5-6H2
InChIKey
HXMVNCMPQGPRLN-UHFFFAOYSA-N
SMILES
NCCC(O)CN
Metabolite of Species
Details
Rattus norvegicus
(NCBI:txid10116)
Found in brain
(BTO:0000142)
. See:
PubMed
Rhizobacter bergeniae
(NCBI:txid1395940)
of strain PLGR-1 See:
PubMed
Pelistega suis
(NCBI:txid1631957)
See:
PubMed
Caenimonas
sp.
HX-9-20
(NCBI:txid2596921)
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
)
Biological Role
(s):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
Application
(s):
anticonvulsant
A drug used to prevent seizures or reduce their severity.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
2-hydroxyputrescine (
CHEBI:180907
)
has functional parent
putrescine (
CHEBI:17148
)
2-hydroxyputrescine (
CHEBI:180907
)
has role
anticonvulsant (
CHEBI:35623
)
2-hydroxyputrescine (
CHEBI:180907
)
has role
bacterial metabolite (
CHEBI:76969
)
2-hydroxyputrescine (
CHEBI:180907
)
is a
alkane-α,ω-diamine (
CHEBI:35411
)
2-hydroxyputrescine (
CHEBI:180907
)
is a
secondary alcohol (
CHEBI:35681
)
2-hydroxyputrescine (
CHEBI:180907
)
is conjugate base of
2-hydroxyputrescine(2+) (
CHEBI:180908
)
Incoming
2-hydroxyputrescine(2+) (
CHEBI:180908
)
is conjugate acid of
2-hydroxyputrescine (
CHEBI:180907
)
IUPAC Name
1,4-diaminobutan-2-ol
Synonym
Source
1,4-diamino-2-butanol
ChemIDplus
Manual Xref
Database
144344
ChemSpider
View more database links
Registry Number
Type
Source
539-59-3
CAS Registry Number
ChemIDplus
Citations
Types
Sources
14308471
PubMed citation
Europe PMC
1805240
PubMed citation
Europe PMC
25389149
PubMed citation
Europe PMC
26449759
PubMed citation
Europe PMC
3335858
PubMed citation
Europe PMC
3392545
PubMed citation
Europe PMC
4698227
PubMed citation
Europe PMC
5513251
PubMed citation
Europe PMC
5804734
PubMed citation
Europe PMC
Last Modified
26 November 2021