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Drug ReportsIdraparinux sodium
Idraparinux sodium
Idraparinux sodium is an oligosaccharide 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
7 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
ThrombosisD01392744
Venous thrombosisD020246HP_0004936I82.4044
Pulmonary embolismD011655HP_0002204I2633
EmbolismD00461733
Atrial fibrillationD001281EFO_0000275I48.022
ThromboembolismD013923HP_000190711
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameIdraparinux sodium
INNidraparinux sodium
Description
Idraparinux sodium is an oligosaccharide pharmaceutical. It is currently being investigated in clinical studies.
Classification
Oligosaccharide
Drug classantihrombotic indirect selective synthetic factor Xa inhibitors
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Structure (InChI/SMILES or Protein Sequence)
CO[C@H]1O[C@H](COS(=O)(=O)[O-])[C@@H](O[C@H]2O[C@@H](C(=O)[O-])[C@@H](O[C@H]3O[C@H](COS(=O)(=O)[O-])[C@@H](O[C@@H]4O[C@H](C(=O)[O-])[C@@H](O[C@H]5O[C@H](COS(=O)(=O)[O-])[C@@H](OC)[C@H](OC)[C@H]5OC)[C@H](OC)[C@H]4OC)[C@H](OS(=O)(=O)[O-])[C@H]3OS(=O)(=O)[O-])[C@H](OC)[C@H]2OC)[C@H](OS(=O)(=O)[O-])[C@H]1OS(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL1908371
ChEBI ID
PubChem CID
DrugBank
UNII IDH84IXP29FN (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 14 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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