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> Main
CHEBI:29022 -
N
-benzyladenine
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ChEBI Name
N
-benzyladenine
ChEBI ID
CHEBI:29022
ChEBI ASCII Name
N-benzyladenine
Definition
A member of the class of 6-aminopurines that is adenine in which one of the hydrogens of the amino group is replaced by a benzyl group.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:42414, CHEBI:2173, CHEBI:21881
Supplier Information
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Wikipedia
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Read full article at Wikipedia
Formula
C12H11N5
Net Charge
0
Average Mass
225.24944
Monoisotopic Mass
225.10145
InChI
InChI=1S/C12H11N5/c1-
2-
4-
9(5-
3-
1)
6-
13-
11-
10-
12(15-
7-
14-
10)
17-
8-
16-
11/h1-
5,7-
8H,6H2,(H2,13,14,15,16,17)
InChIKey
NWBJYWHLCVSVIJ-UHFFFAOYSA-N
SMILES
C(Nc1ncnc2[nH]cnc12)c1ccccc1
Roles Classification
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
cytokinin
A phytohormone that promote cell division, or cytokinesis, in plant roots and shoots.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-benzyladenine (
CHEBI:29022
)
has functional parent
adenine (
CHEBI:16708
)
N
-benzyladenine (
CHEBI:29022
)
has role
cytokinin (
CHEBI:23530
)
N
-benzyladenine (
CHEBI:29022
)
has role
plant metabolite (
CHEBI:76924
)
N
-benzyladenine (
CHEBI:29022
)
is a
6-aminopurines (
CHEBI:20706
)
IUPAC Name
N
-benzyl-9
H
-purin-6-amine
Synonyms
Sources
6-(benzylamino)purine
NIST Chemistry WebBook
6-[(phenylmethyl)amino]-9
H
-purine
NIST Chemistry WebBook
6-BAP
ChemIDplus
6-Benzylaminopurine
KEGG COMPOUND
BAP
ChemIDplus
benzyladenine
ChemIDplus
Cytokinin B
ChemIDplus
N-BENZYL-9H-PURIN-6-AMINE
PDBeChem
N-Benzyladenine
KEGG COMPOUND
N
6
-(benzylamino)purine
ChemIDplus
N6-Benzyladenine
KEGG COMPOUND
Manual Xrefs
Databases
1324
BPDB
6-Benzylaminopurine
Wikipedia
C00000092
KNApSAcK
C11263
KEGG COMPOUND
CPD-4604
MetaCyc
EMU
PDBeChem
HMDB0039238
HMDB
LSM-3396
LINCS
View more database links
Registry Numbers
Types
Sources
1214-39-7
CAS Registry Number
KEGG COMPOUND
1214-39-7
CAS Registry Number
ChemIDplus
1214-39-7
CAS Registry Number
NIST Chemistry WebBook
145502
Gmelin Registry Number
Gmelin
616790
Beilstein Registry Number
Beilstein
616790
Reaxys Registry Number
Reaxys
Citations
Types
Sources
16691305
PubMed citation
Europe PMC
23043692
PubMed citation
Europe PMC
24579378
PubMed citation
Europe PMC
Last Modified
25 February 2016