Prostanoid Receptor
Prostanoid receptors are activated by the endogenous ligands prostaglandin (PG) D2, PGE2, PGF2α , PGH2, prostacyclin (PGI2) and thromboxane A2. Cyclooxygenase (COX) converts arachidonic acid to PGH2, from which the other prostaglandins are synthesized.
Products for Prostanoid Receptor
- Cat.No. Product Name Information/Activity
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BCC7068
BMY 45778
Non-prostanoid prostacyclin IP receptor partial agonist
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BCC7315
(±)-Cloprostenol sodium salt
Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent, and is a PGF2α receptor agonist.
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BCC7843
16,16-Dimethyl Prostaglandin E2
16,16-Dimethyl prostaglandin E2 (16,16-dimethyl PGE2) is an orally active vertebrate Hematopoietic stem cells (HSCs) homeostasis critical regulator. 16,16-Dimethyl prostaglandin E2 can act through EP2/EP4 and has an interaction with the Wnt pathway.
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BCC7534
Epoprostenol
Epoprostenol sodium (Prostaglandin I2 (sodium salt)), the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH). Epoprostenol sodium is used in pulmonary hypertension and transplantation as a potent inhibitor of platelet aggregation.
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BCC7247
Iloprost
Iloprost (ZK 36374) is a synthetic analogue of prostacyclin PGI2.
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BCC5240
Misoprostol
59122-46-2
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BCC7316
Prostaglandin E2
Prostaglandin E2 is a hormone-like substance that participate in a wide range of body functions such as the contraction and relaxation of smooth muscle, the dilation and constriction of blood vessels, control of blood pressure, and modulation of inflammation.
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BCC7889
Prostaglandin F2α
Dinoprost tromethamine salt is a naturally occurring prostaglandin used in medicine to induce labor and as an abortifacient.
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BCC7661
NS 304
Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor).
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BCC7547
Sulprostone
60325-46-4
