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Drug ReportsDoxribtimine
Doxribtimine
Doxribtimine is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
644 clinical trials
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Down syndromeD004314EFO_0001064Q90————11
Digeorge syndromeD004062—D82.1————11
AneuploidyD000782——————11
SyndromeD013577——————11
Klinefelter syndromeD007713EFO_1001006Q98.0————11
Trisomy 18 syndromeD000073842—Q91.3————11
Trisomy 13 syndromeD000073839—Q91.7————11
Turner syndromeD014424Orphanet_881Q96————11
Chromosome deletionD002872——————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameDoxribtimine
INNdoxribtimine
Description
1-(2-Deoxypentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione is a pyrimidine 2'-deoxyribonucleoside.
Classification
Small molecule
Drug class—
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Structure (InChI/SMILES or Protein Sequence)
Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O
Identifiers
PDB—
CAS-ID50-89-5
RxCUI—
ChEMBL IDCHEMBL52609
ChEBI ID17748
PubChem CID1134
DrugBankDB04485
UNII IDVC2W18DGKR (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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105 adverse events reported
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