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ChEBI
> Main
CHEBI:131825 - 8,5'-cyclo-2'-deoxyadenosine
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ChEBI Ontology
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ChEBI Name
8,5'-cyclo-2'-deoxyadenosine
ChEBI ID
CHEBI:131825
Definition
An organic heterotetracyclic compound obtained by intramolecular formation of a C-C bond between positions 8 and 5' of 2'-deoxyadenosine.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C10H11N5O3
Net Charge
0
Average Mass
249.226
Monoisotopic Mass
249.08619
InChI
InChI=1S/C10H11N5O3/c11-
8-
5-
9(13-
2-
12-
8)
15-
4-
1-
3(16)
7(18-
4)
6(17)
10(15)
14-
5/h2-
4,6-
7,16-
17H,1H2,(H2,11,12,13)
/t3-
,4+,6-
,7-
/m0/s1
InChIKey
MBVGIEDXZGVICG-FXZMZVCPSA-N
SMILES
[C@H]12N3C=4N=CN=C(C4N=C3[C@H]([C@]([C@H](C1)O)(O2)[H])O)N
Metabolite of Species
Details
Mycoplasma genitalium
(NCBI:txid2097)
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):
Mycoplasma genitalium metabolite
Any bacterial metabolite produced during a metabolic reaction in
Mycoplasma genitalium
.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
has functional parent
2'-deoxyadenosine (
CHEBI:17256
)
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
has role
Mycoplasma genitalium
metabolite (
CHEBI:131604
)
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
is a
N
-glycosyl compound (
CHEBI:21731
)
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
is a
aromatic amine (
CHEBI:33860
)
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
is a
bridged compound (
CHEBI:35990
)
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
is a
diol (
CHEBI:23824
)
8,5'-cyclo-2'-deoxyadenosine (
CHEBI:131825
)
is a
organic heterotetracyclic compound (
CHEBI:38163
)
IUPAC Name
(6
R
,7
S
,8
S
,10
R
)-
4-
amino-
7,8,9,10-
tetrahydro-
6
H
-
7,10-
epoxyazepino[1,2-
e
]purine-
6,8-
diol
Synonyms
Sources
2'-Deoxy-8,5'-cycloadenosine
ChemIDplus
8,5'-Cda
ChemIDplus
cyclo-dA
ChEBI
cyclodA
ChEBI
Registry Numbers
Types
Sources
117182-88-4
CAS Registry Number
ChemIDplus
8118367
Reaxys Registry Number
Reaxys
Citations
Types
Sources
22817898
PubMed citation
Europe PMC
23961697
PubMed citation
Europe PMC
24471831
PubMed citation
Europe PMC
25034731
PubMed citation
Europe PMC
25605892
PubMed citation
Europe PMC
26344223
PubMed citation
Europe PMC
Last Modified
21 April 2016