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InChI=1S/CH4O/c1-2/h2H,1H3
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CHEBI:131580 - 6-azathymidine
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ChEBI Ontology
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ChEBI Name
6-azathymidine
ChEBI ID
CHEBI:131580
Definition
A
N
-glycosyl-1,2,4-triazine that is the 6-aza analogue of thymidine.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C9H13N3O5
Net Charge
0
Average Mass
243.217
Monoisotopic Mass
243.08552
InChI
InChI=1S/C9H13N3O5/c1-
4-
8(15)
10-
9(16)
12(11-
4)
7-
2-
5(14)
6(3-
13)
17-
7/h5-
7,13-
14H,2-
3H2,1H3,(H,10,15,16)
/t5-
,6+,7+/m0/s1
InChIKey
LXHOFEUVCQUXRZ-RRKCRQDMSA-N
SMILES
[C@@H]1(N2C(NC(=O)C(=N2)C)=O)O[C@H](CO)[C@H](C1)O
Metabolite of Species
Details
Mycoplasma genitalium
(NCBI:txid2097)
See:
PubMed
Roles Classification
Biological Role
(s):
Mycoplasma genitalium metabolite
Any bacterial metabolite produced during a metabolic reaction in
Mycoplasma genitalium
.
antiviral agent
A substance that destroys or inhibits replication of viruses.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
6-azathymidine (
CHEBI:131580
)
has functional parent
6-azathymine (
CHEBI:102328
)
6-azathymidine (
CHEBI:131580
)
has role
Mycoplasma genitalium
metabolite (
CHEBI:131604
)
6-azathymidine (
CHEBI:131580
)
has role
antiviral agent (
CHEBI:22587
)
6-azathymidine (
CHEBI:131580
)
is a
N
-glycosyl-1,2,4-triazine (
CHEBI:48018
)
6-azathymidine (
CHEBI:131580
)
is a
nucleoside analogue (
CHEBI:60783
)
IUPAC Name
2-
(2-
deoxy-
β-
D
-
erythro
-
pentofuranosyl)-
6-
methyl-
1,2,4-
triazine-
3,5(2
H
,4
H
)-
dione
Synonyms
Sources
2'-deoxy-6-azathymidine
ChEBI
2'-deoxy-6-azathymine
ChEBI
2-(2'-Deoxy-D-ribofuranosyl)-6-methyl-as-triazine-3,5(2H,4H)-dione
ChemIDplus
2-(2-Deoxy-beta-D-erythro-pentofuranosyl)-6-methyl-1,2,4-triazine-3,5(2H,4H)-dione
ChemIDplus
6-aza-2'-deoxythymidine
ChEBI
6-aza-2'-deoxythymine
ChEBI
Azathymidine
ChemIDplus
Registry Numbers
Types
Sources
13410-30-5
CAS Registry Number
ChemIDplus
30380
Reaxys Registry Number
Reaxys
30380
Beilstein Registry Number
ChemIDplus
Citations
Types
Sources
13299319
PubMed citation
Europe PMC
13315367
PubMed citation
Europe PMC
14421504
PubMed citation
Europe PMC
14435160
PubMed citation
Europe PMC
4291096
PubMed citation
Europe PMC
Last Modified
04 April 2016