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ChEBI
> Main
CHEBI:71693 - 9-ribosyl-
trans
-zeatin
Main
ChEBI Ontology
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ChEBI Name
9-ribosyl-
trans
-zeatin
ChEBI ID
CHEBI:71693
ChEBI ASCII Name
9-ribosyl-trans-zeatin
Definition
A 9-ribosylzeatin having
trans
-zeatin as the nucleobase.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula
C15H21N5O5
Net Charge
0
Average Mass
351.35770
Monoisotopic Mass
351.15427
InChI
InChI=1S/C15H21N5O5/c1-
8(4-
21)
2-
3-
16-
13-
10-
14(18-
6-
17-
13)
20(7-
19-
10)
15-
12(24)
11(23)
9(5-
22)
25-
15/h2,6-
7,9,11-
12,15,21-
24H,3-
5H2,1H3,(H,16,17,18)
/b8-
2+/t9-
,11-
,12-
,15-
/m1/s1
InChIKey
GOSWTRUMMSCNCW-HNNGNKQASA-N
SMILES
C\C(CO)=C/CNc1ncnc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Metabolite of Species
Details
Psilotum nudum
(NCBI:txid3240)
See:
PubMed
Cucumis sativus
(NCBI:txid3659)
See:
PubMed
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.
(via
9-ribosylzeatin
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
9-ribosyl-
trans
-zeatin (
CHEBI:71693
)
has functional parent
adenosine (
CHEBI:16335
)
9-ribosyl-
trans
-zeatin (
CHEBI:71693
)
has role
cytokinin (
CHEBI:23530
)
9-ribosyl-
trans
-zeatin (
CHEBI:71693
)
has role
plant metabolite (
CHEBI:76924
)
9-ribosyl-
trans
-zeatin (
CHEBI:71693
)
is a
9-ribosylzeatin (
CHEBI:20838
)
9-ribosyl-
trans
-zeatin (
CHEBI:71693
)
is a
nucleoside analogue (
CHEBI:60783
)
IUPAC Name
N
-[(2
E
)-4-hydroxy-3-methylbut-2-en-1-yl]adenosine
Synonyms
Sources
(E)-N-(4-Hydroxy-3-methyl-2-butenyl)adenosine
ChemIDplus
9-β-
D
-ribofuranosyl-
trans
-zeatin
ChEBI
9-β-
D
-ribosyl-
trans
-zeatin
ChEBI
trans
-zeatin 9-β-
D
-ribofuranoside
ChEBI
trans-Zeatin riboside
KEGG COMPOUND
zeatin riboside
MetaCyc
Manual Xrefs
Databases
C00000096
KNApSAcK
C16431
KEGG COMPOUND
CPD-4208
MetaCyc
HMDB0030388
HMDB
View more database links
Registry Numbers
Types
Sources
6025-53-2
CAS Registry Number
ChemIDplus
630954
Reaxys Registry Number
Reaxys
Citations
Types
Sources
12379786
PubMed citation
Europe PMC
20488581
PubMed citation
Europe PMC
21790030
PubMed citation
Europe PMC
21867755
PubMed citation
Europe PMC
21965753
PubMed citation
Europe PMC
Last Modified
16 April 2015