Cloprostenol, also known as ICI 80996, is a synthetic analog of prostaglandin F2α (PGF2α). It is 200 times and 100 times more potent than PGF2α in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2α
Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent, and is a PGF2α receptor agonist.
Cloprostenol is a PGF2α receptor agonist.Cloprostenol (0.1 μM) counteracts the adipogenic effects of statil, on both intracellular lipid accumulation and expression of transcripts for proadipogenic factors C/EBPα and PPARγ after treatment for 6 days.
Cloprostenol sodium salt (25 μg) decreases plasma progesterone in pregnant rats.
Related Prodcuts:
Latanoprost Lactol; Latanoprostene bunod; Misoprostol; Carboprost; Tafluprost; Dinoprostone; Dinoprost; Trometamol; Alprostadil; Bimatoprost; (+/-)-Corey lactone diol; Beraprost sodium; Limaprost; D-Cloprostenol sodium; Cloprostenol; D-Cloprostenol isopropyl ester; 5,6-trans-Cloprostenol; (+)-Cloprostenol; 15S-(±)-Cloprostenol