Beraprost

Beraprost
Clinical data
AHFS/Drugs.com International Drug Names
Routes of
administration
Oral
ATC code B01AC19 (WHO)
Legal status
Legal status
  • ?
Pharmacokinetic data
Bioavailability 50–70%
Metabolism Unknown
Biological half-life 35–40 minutes
Excretion ?
Identifiers
CAS Number 88430-50-6 YesY 88475-69-8
PubChem (CID) 6917951
IUPHAR/BPS 1967
ChemSpider 5293169 YesY
UNII 35E3NJJ4O6 YesY
ChEMBL CHEMBL1207745 N
Chemical and physical data
Formula C24H30O5
Molar mass 398.492 g/mol
3D model (Jmol) Interactive image
 NYesY (what is this?)  (verify)

Beraprost is a pharmaceutical drug used in several Asian countries, including Japan and South Korea, as a vasodilator and antiplatelet agent.[1] It is classified as a prostacyclin analog.[1][2]

It has been studied for the treatment of pulmonary hypertension and for use in avoiding reperfusion injury.

Clinical pharmacology

As an analog of prostacyclin PGI2, beraprost affects vasodilation, which in turn lowers blood pressure. Beraprost also inhibits platelet aggregation, though the role this phenomenon may play in relation to pulmonary hypertension has yet to be determined.

Dosage and administration

Beraprost is administered orally as a pill available in strength of 20 mcg. Dose ranges from 60 to 180 mcg in divided doses after meals.

References

  1. 1 2 "Beraprost". drugs.com.
  2. Melian EB, Goa KL (2002). "Beraprost: a review of its pharmacology and therapeutic efficacy in the treatment of peripheral arterial disease and pulmonary arterial hypertension". Drugs. 62 (1): 107–33. doi:10.2165/00003495-200262010-00005.


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