Epoprostenol
Epoprostenol Basic information
- Product Name:
- Epoprostenol
- Synonyms:
-
- (5z,13e)-(15s)-6,9-alpha-epoxy-11-alpha,15-dihydroxyprosta-5,13-dienoate
- 5Z13E-15S-69-ALPHA-EPOXY-11-ALPHA
- PGX(prostaglandin)
- ProstaglandinI
- 5-[7-hydroxy-8-(3-hydroxyoct-1-enyl)-4-oxabicyclo[3.3.0]oct-3-ylidene]pentanoic acid
- 6(9)-Oxy-11,15-dihydroxyprosta-5,13-dienoic acid
- PGX
- Prostaglandin X
- CAS:
- 35121-78-9
- MF:
- C20H32O5
- MW:
- 352.47
- Product Categories:
-
- API
- Mol File:
- 35121-78-9.mol
Epoprostenol Chemical Properties
- Boiling point:
- 530.2±50.0 °C(Predicted)
- Density
- 1.221
- pka
- 4.70±0.10(Predicted)
Epoprostenol Usage And Synthesis
Originator
Prostacyclin,ZYF Pharm Chemical
Uses
Inhibitor (platelet). [Names previously used: Prostacyclin, PGI2, Prostagland in I2, Prostaglandin X, PGX].
Definition
ChEBI: Prostaglandin I2 is a prostaglandins I. It has a role as a mouse metabolite. It is a conjugate acid of a prostaglandin I2(1-).
Manufacturing Process
Preparation of prostacyclin:
Pig aortas were stripped of adventitia, snap frozen in liquid nitrogen, crushed
into a fine powder, resuspended in 0.05 M Tris buffer (pH 7.5) (1:4, w:v) andhomogenised at high speed in a Polytron (KIMENATIC, LUCERNE,
SWITZERLAND) homogenizer. The homogenate was centrifuged for 15 min
and the resulting supernatant centrifuged again for 5 min. The pellet was
discarded, while the pellet obtained after centrifugation of the supernatant
was resuspended in deionized water and lyophilized. An average yield of 150
mg of aortic microsomal powder (51% protein) per 100 g of aortic tissue was
obtained.
brand name
Flolan (GlaxoSmithKline).
Therapeutic Function
Platelet aggregation inhibitor, Antimetastatic
EpoprostenolSupplier
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