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Fluprostenol

" in MedChemExpress (MCE) Product Catalog:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B0584
    Travoprost
    2 Publications Verification

    Fluprostenol isopropyl ester; AL6221; Flu-Ipr

    		 Prostaglandin Receptor Endocrinology
    Travoprost (Fluprostenol isopropyl ester), an isopropyl ester proagent, is a high affinity, selective FP prostaglandin full receptor agonist. Travoprost has the ocular hypotensive efficacy and has the potential for glaucoma and ocular hypertension .
    Travoprost
  • HY-108560
    (+)-Fluprostenol

    		Prostaglandin Receptor Others
    (+)-Fluprostenol is a potent agonist of PTGER2. (+)-Fluprostenol decreases the expression of Oviductal glycoprotein 1 (OVGP1) .
    (+)-Fluprostenol
  • HY-136494
    Fluprostenol

    ICI 81008

    		 Endogenous Metabolite Endocrinology
    Fluprostenol (ICI 81008) is a synthetic prostaglandin F2α (PGF2α) derivative. Fluprostenol, as a luteolytic agent, can cause luteal degeneration and regulate reproductive cycle. Fluprostenol can be used in the study of infertility in animals and the control of the reproductive cycle of domestic animals .
    Fluprostenol
  • HY-126911
    11-keto Fluprostenol

    Fluprostenol Prostaglandin D2

    		 Prostaglandin Receptor Endocrinology
    11-keto Fluprostenol is an analog of prostaglandin D2 (PGD2) with structural modifications intended to give it a prolonged half-life and greater potency. Fluprostenol is a well-studied, potent analog of PGF2α and acts primarily through the FP receptor. Oxidation at C-11 of fluprostenol yields 11-keto fluprostenol. 11-keto Fluprostenol exhibits moderate binding to the CRTH2/DP2 receptor compared to PGD2 and essentially no activity at the DP1 receptor.
    11-keto Fluprostenol
  • HY-118624
    Fluprostenol methyl ester

    		Prostaglandin Receptor Endocrinology
    Fluprostenol methyl ester is an F-series prostaglandin analog which has been approved for many years as a luteolytic in veterinary animals .
    Fluprostenol methyl ester
  • HY-120892
    Fluprostenol serinol amide

    Flu-SA

    		 Others Others
    Fluprostenol serinol amide (Flu-SA) is used for proteomics research.
    Fluprostenol serinol amide
  • HY-137043
    9-Keto Travoprost

    Fluprostenol Prostaglandin E2

    		 Prostaglandin Receptor Endocrinology
    9-Keto Travoprost is a derivative of Fluprostenol (HY-108560). 9-Keto Travoprost is an EP receptor agonist. 9-Keto Travoprost can be used in endocrine-related research .
    9-Keto Travoprost
  • HY-B0584R
    Travoprost (Standard)

    Fluprostenol isopropyl ester(Standard); AL6221(Standard); Flu-Ipr (Standard)

    		 Prostaglandin Receptor Endocrinology
    Travoprost (Standard) is the analytical standard of Travoprost. This product is intended for research and analytical applications. Travoprost (Fluprostenol isopropyl ester), an isopropyl ester proagent, is a high affinity, selective FP prostaglandin full receptor agonist. Travoprost has the ocular hypotensive efficacy and has the potential for glaucoma and ocular hypertension .
    Travoprost (Standard)
  • HY-108560R
    (+)-Fluprostenol (Standard)

    		Prostaglandin Receptor Others
    (+)-Fluprostenol (Standard) is the analytical standard of (+)-Fluprostenol. This product is intended for research and analytical applications. (+)-Fluprostenol is a potent agonist of PTGER2. (+)-Fluprostenol decreases the expression of Oviductal glycoprotein 1 (OVGP1) .
    (+)-Fluprostenol (Standard)
  • HY-108560A
    15(S)-Fluprostenol

    		Prostaglandin Receptor Others
    15(S)-Fluprostenol is the isomer of (+)-Fluprostenol (HY-108560). (+)-Fluprostenol is a potent agonist of PTGER2. (+)-Fluprostenol decreases the expression of Oviductal glycoprotein 1 (OVGP1) .
    15(S)-Fluprostenol
  • HY-124209
    9-keto Fluprostenol

    		Prostaglandin Receptor Endocrinology
    9-keto Fluprostenol is an analog of prostaglandin E2 (PGE2) with structural modifications intended to give it a prolonged half-life and greater potency. Fluprostenol is a well-studied, potent analog of PGF2α and acts primarily through the FP receptor. Oxidation at C-9 of fluprostenol yields 9-keto fluprostenol. It is anticipated that this analog will have strong affinity for EP receptors and act as a PGE2 agonist.
    9-keto Fluprostenol
  • HY-116617
    15-Keto Travoprost

    15-Keto Fluprostenol isopropyl ester

    		 Drug Metabolite Others
    15-Keto Travoprost (15-Keto Fluprostenol isopropyl ester) is a metabolite of Travoprost (HY-B0584). 15-Keto Travoprost shows stimulatory effect on the growth and thickening of the eyelashes .
    15-Keto Travoprost
  • HY-158550
    13(R),14(R)-epoxy Fluprostenol isopropyl ester

    13(R),14(R)-epoxy Travoprost

    		 Others Inflammation/Immunology
    13(R),14(R)-epoxy Fluprostenol isopropyl ester is a Prostaglandin derivative .
    13(R),14(R)-epoxy Fluprostenol isopropyl ester
  • HY-114385
    13,14-epoxy Travoprost

    13,14-epoxy Fluprostenol isopropyl ester

    		 Others Others
    13,14-epoxy Travoprost (13,14-epoxy Fluprostenol isopropyl ester) is a mixture of diastereomeric epoxides generated during production of Travoprost (HY-B0584). Travoprost is a selective agonist for prostaglandin F receptor, which exhibits an ocular hypotensive efficacy .
    13,14-epoxy Travoprost
  • HY-B0584A
    5,6-trans-Travoprost

    5,6-trans-Fluprostenol isopropyl ester; 5,6-trans-AL6221; 5,6-trans-Flu-Ipr

    		 Others Endocrinology
    5,6-trans-Travoprost is the isomer of Travoprost (HY-B0584), and can be used as an experimental control. Travoprost (Fluprostenol isopropyl ester), an isopropyl ester proagent, is a high affinity, selective FP prostaglandin full receptor agonist. Travoprost has the ocular hypotensive efficacy and has the potential for glaucoma and ocular hypertension .
    5,6-trans-Travoprost
  • HY-116679
    17-trifluoromethylphenyl trinor Prostaglandin F2α

    17-Trifluoromethylphenyl trinor PGF2α

    		 Prostaglandin Receptor Endocrinology
    A number of 17-phenyl trinor prostaglandin F2α (17-phenyl trinor PGF2α) derivatives have been approved for glaucoma. Of these, the unsubstituted or meta-substituted aromatic derivatives are the most potent FP receptor agonists.4 17-trifluoromethylphenyl trinor PGF2α bears an aromatic ring which is reminiscent of the trifluoromethyl-phenoxy ring of travoprost ((+)-fluprostenol isopropyl ester). As an ocular hypotensive agent, it would be expected that 17-trifluoromethylphenyl trinor PGF2α would act very much like the free acid of travoprost. 17-phenyl trinor PGF2α is a potent luteolytic, with a potency equal to or greater than fluprostenol and cloprostenol.
    17-trifluoromethylphenyl trinor Prostaglandin F2α
  • HY-118190
    AL 8810 methyl ester

    		Prostaglandin Receptor Endocrinology
    AL 8810 methyl ester is a prostaglandin F(2α) analog and a prostaglandin F(2α) receptor agonist. Can competitively antagonize the effects of the FP receptor agonist Fluprostenol (HY-108560). AL 8810 methyl ester has no significant potency against TP, DP, EP(2), EP(4) receptor subtypes in cell lines .
    AL 8810 methyl ester

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