ostenol — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
TN1120	Osthenol		MAO , Monoamine Oxidase
	Osthenol is a natural product, and is selective, reversible, and competitive human monoamine oxidase-A (hMAO-A) inhibitor (Ki=0.26 µM).It shows antitumor-promoting activity, it also has antifungal and antibacterial activ...		MAO , Monoamine Oxidase
T21224	(+)-Fluprostenol	Fluprostenol, (+)-,Travoprost acid,AL-5848	Prostaglandin Receptor
	(+)-Fluprostenol (AL-5848), an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).		Prostaglandin Receptor
TN7070	Ergostenol	delta8(14)-Ergostenol,alpha-Ergostenol,Ergost-8(14)-en-3beta-ol	Others
	Ergostenol (Ergost-8(14)-en-3beta-ol) is a biological precursor and a provitamin of vitamin D2.		Others
T5847	Cloprostenol sodium salt	ICI 80996 sodium salt,DL-Cloprostenol sodium,Cloprostenol sodium	Prostaglandin Receptor
	Cloprostenol sodium salt (ICI 80996 sodium salt) is a more water solute, crystalline form of cloprostenol than the free acid, is a synthetic analog of prostaglandin F2α.		Prostaglandin Receptor
T35321	Zymostenol	delta(8)-Cholestenol,5a-Cholest-8-en-3b-ol,Δ8-Cholesterol	Endogenous Metabolite , ROR
	Zymostenol (5a-Cholest-8-en-3b-ol) is a RORγ agonist with an EC50 of 1 μM.Zymostenol is a late stage precursor of cholesterol biosynthesis.		Endogenous Metabolite , ROR
T38115	Fluprostenol serinol amide
	2-arachidonyl glycerol (2-AG) exhibits cannabinoid (CB) agonist activity at the CB1 receptor, is an important endogenous monoglyceride species, and is thus considered to be the natural ligand for the CB1 receptor. 2-AG c...
T15238	Epoprostenol sodium	Prostaglandin I2 sodium salt,Prostacyclin sodium salt,Flolan	Others
	Epoprostenol sodium is a potent inhibitor of platelet aggregation used in pulmonary hypertension and transplantation.		Others
T37813	Fluprostenol methyl ester
	Fluprostenol is an F-series prostaglandin analog which has been approved for many years as a luteolytic in veterinary animals. The isopropyl ester of fluprostenol (travoprost) is an effective ocular hypotensive drug. CAY...
T13461	(+)-Cloprostenol	D-Cloprostenol	Others
	(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic.		Others
T20778	Epoprostenol	U 53217,U 53,217,U-53,217
	Epoprostenol, a prostaglandin, is a powerful vasodilator. It inhibits platelet aggregation.
T13503	31-Norlanostenol		Others
	31-Norlanostenol is a triterpene isolated from the latex of Euphorbia officinarum. It can act as an efficient insect growth regulator on S. frugiperda and Tenebrio molitor.		Others
T37929	14-dehydro Zymostenol
	14-dehydro Zymostenol is a precursor to cholesterol .1It increases the percentage of myelin basic protein-positive (MBP+) oligodendrocytes formed from oligodendrocyte precursor cells when used at concentrations of 5.8 an...
T32977	Luprostenol
	Luprostenol is a bioactive chemical.
T20592	Cloprostenol	Estrofan,Oestrophan
	Cloprostenol is a synthetic analogue of prostaglandin.
T37231	(+)-Cloprostenol methyl ester
	(+)-Cloprostenol is a synthetic analog of prostaglandin F2α (PGF2α). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters. It is 200 times and 100 times more potent than PGF2α in terminating pr...
T29245	(+)-Cloprostenol sodium	D-Cloprostenol,D-Cloprostenol sodium salt
	(+) - cloprostenol sodium is a kind of water-soluble prostaglandin F2 α ( PGF2 α) Analogues. It is an FP receptor agonist and a potent luteinizing agent in rats and hamsters.
T37230	(+)-5-trans Cloprostenol
	Cloprostenol is a synthetic derivative of prostaglandin F2α that is used in veterinary medicine as a luteolytic agent for the induction of estrus and in the treatment of reproductive disorders in cattle, swine, and horse...
T29246	Cloprostenol isopropyl ester	(+)-16-m-chlorophenoxy tetranor Prostaglandin F2α isopropyl ester,(+)-Cloprostenol isopropyl ester
	Cloprostenol isopropyl ester is a PGF2α agonist and a similar synthetic prostaglandin F2α (PGF2α), which can induce luteal dissolution in mares during the luteal phase without causing clinical side effects or stress resp...