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ChemicalBook--->CAS DataBase List--->35121-78-9

35121-78-9

35121-78-9 Structure

35121-78-9 Structure
IdentificationBack Directory
[Name]

Epoprostenol
[CAS]

35121-78-9
[Synonyms]

PGX
PGl2
U 53217
U-53217A
Vasocyclin
Cyclo-Prostin
ProstaglandinI
Prostaglandin X
Prostaglandin l2
PGX(prostaglandin)
Epoprostenol USP/EP/BP
Prostacyclin (Epoprostenol)
5Z13E-15S-69-ALPHA-EPOXY-11-ALPHA
6(9)-Oxy-11,15-dihydroxyprosta-5,13-dienoic acid
(5Z,9α,11α,13E,15S)-6,9-Epoxy-11,15-dihydroxyprosta-5,13-dien-1-oicacid
(5z,13e)-(15s)-6,9-alpha-epoxy-11-alpha,15-dihydroxyprosta-5,13-dienoate
5-[7-hydroxy-8-(3-hydroxyoct-1-enyl)-4-oxabicyclo[3.3.0]oct-3-ylidene]pentanoic acid
[Molecular Formula]

C20H31O5.Na
[MOL File]

35121-78-9.mol
[Molecular Weight]

374.45
Chemical PropertiesBack Directory
[Boiling point ]

530.2±50.0 °C(Predicted)
[density ]

1.221
[pka]

4.70±0.10(Predicted)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Potassium tert-butoxide
Hazard InformationBack Directory
[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
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