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pgf2

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Aldose Reductase (1) Angiotensin Receptor (1) Apoptosis (8) Autophagy (8) Biochemical Assay Reagents (5) Drug Derivative (13) Drug Intermediate (1) Drug Isomer (2) Drug Metabolite (5) Endogenous Metabolite (29) ERK (1) Isotope-Labeled Compounds (12) Leukotriene Receptor (3) p38 MAPK (1) PGE synthase (1) Progesterone Receptor (1) Prostaglandin Receptor (77) Reference Standards (7)
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125

Inhibitors & Agonists

Fluorescent Dyes

Natural
Products

Isotope-Labeled Compounds

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-12956

Dinoprost 5+ Cited Publications Prostaglandin F2α; pgf2α	Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis	Endocrinology
Dinoprost (Prostaglandin F2α) is an orally active, potent *prostaglandin F (PGF) receptor (FP receptor)* agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

HY-108415

Cloprostenol sodium salt ICI 80996 sodium salt	Prostaglandin Receptor	Endocrinology
Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent , and is a PGF2α receptor agonist ^[2].

HY-12956A

Dinoprost tromethamine salt 5+ Cited Publications Prostaglandin F2α tromethamine salt; pgf2α THAM; Prostaglandin F2α THAM	Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis	Endocrinology
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) is an orally active, potent *prostaglandin F (PGF) receptor (FP receptor)* agonist. Dinoprost tromethamine salt is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost tromethamine salt plays a key role in the onset and progression of labour ^[2].

HY-12956S

Dinoprost-d4 Prostaglandin F2a-d₄; pgf2α-d₄	Isotope-Labeled Compounds Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis	Endocrinology
Dinoprost-d₄ is the deuterium labeled Dinoprost. Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

HY-121314

Cloprostenol	Prostaglandin Receptor	Metabolic Disease
Cloprostenol is a prostaglandin F-2α (PGF2α (HY-12956)) analogue. Cloprostenol induces luteolysis in marmoset monkeys. Cloprostenol can be used for the research of open-cervix pyometra ^[2].

HY-101438

Darbufelone CI-1004	Prostaglandin Receptor Leukotriene Receptor	Inflammation/Immunology Endocrinology
Darbufelone is a dual inhibitor of cellular *PGF_2α* and LTB₄ production. Darbufelone potently inhibits *PGHS-2* (IC₅₀= 0.19 μM) but is much less potent with PGHS-1 (IC₅₀=20 μM).

HY-128428

Carboprost 15(S)-15-Methyl Prostaglandin F2α; 15-Methyl-pgf2α	Prostaglandin Receptor	Endocrinology
Carboprost (15(S)-15-Methyl Prostaglandin F2α) is a metabolically stable synthetic analog of prostaglandin F2α. Carboprost stimulates uterine contractions and induces abortion. Carboprost is used for postpartum hemorrhage due to uterine atony and for the termination of pregnancy in the second trimester ^[2].

HY-107381

(+)-Cloprostenol D-Cloprostenol	Prostaglandin Receptor	Endocrinology
(+)-Cloprostenol is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.

HY-113209

8-Isoprostaglandin F2α 8-iso-pgf2α	Endogenous Metabolite	Others
8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-129953

9α,11β-Prostaglandin F2α 9α,11β-pgf2α	Endogenous Metabolite	Inflammation/Immunology
9α,11β-Prostaglandin F₂α (9α,11β-PGF2α) is an endogenous metabolite present in urine, which can be used for asthma research ^[2].

HY-112284

Ebopiprant 2 Publications Verification OBE022	Prostaglandin Receptor	Endocrinology
Ebopiprant (OBE022) is an oral and selective prostaglandin F_2α (PGF_2α) receptor antagonist, with K_is of 1 nM, 26 nM for human and rat FP receptors, respectively.

HY-125774

Bimatoprost acid 17-Phenyl trinor pgf2α	Prostaglandin Receptor	Others
Bimatoprost acid (17-Phenyl trinor PGF2α), the acid hydrolysis product of Bimatoprost (HY-B0191), is a potent agonist of prostaglandin FP receptor .

HY-113208

13,14-Dihydro-15-keto Prostaglandin F2α 13,14-Dihydro-15-keto-pgf2α	Endogenous Metabolite	Others
13,14-Dihydro-15-keto Prostaglandin F2α (13,14-Dihydro-15-keto-PGF2α) is an endogenous metabolite present in Blood that can be used for the research of Pregnancy ^[2].

HY-116161A

*17-Phenyl trinor PGF2α isopropyl ester*	Prostaglandin Receptor	Metabolic Disease
17-Phenyl trinor PGF₂α isopropyl ester is a FP receptor agonist and intraocular pressure-lowering agent. 17-Phenyl trinor PGF₂α isopropyl ester induces iris sphincter contraction, reduces intraocular pressure and pupil diameter, causes no ocular irritation, and only leads to mild conjunctival hyperemia. 17-Phenyl trinor PGF₂α isopropyl ester is applicable to relevant research on glaucoma ^[2].

HY-125150

AL-3138 11-Deoxy-16-fluoro pgf2α	Prostaglandin Receptor Endogenous Metabolite	Endocrinology
AL-3138 (11-Deoxy-16-fluoro PGF2α) is a prostaglandin F2 alpha (PGF2alpha) analogue that antagonises FP prostaglandin receptor-mediated inositol phosphate production .

HY-125774S

Bimatoprost acid-d4 17-Phenyl trinor pgf2α-d₄	Isotope-Labeled Compounds	Others
Bimatoprost acid-d₄ (17-Phenyl trinor PGF2α-d₄) is the deuterium labeled Bimatoprost acid .

HY-178792

TGI-15	Prostaglandin Receptor	Inflammation/Immunology Endocrinology
TGI-15 is a highly selective prostaglandin F receptor antagonist. TGI-15 inhibits downstream signaling pathways by blocking the binding of PGF2 α to FP receptors. TGI-15 can be used for research on fibrotic and inflammatory conditions .

HY-113209S

8-Isoprostaglandin F2α-d4 8-iso-pgf2α-d₄	Isotope-Labeled Compounds	Metabolic Disease
8-Iso-PGF2a-d₄ (8-iso Prostaglandin F2α-d₄) is an active compound. 8-Iso-PGF2a-d₄ can be used the internal standard .

HY-118816

11β-Prostaglandin F2α 11-epi pgf2α-EA; 11β-pgf2α-EA; 11β-Prostamide F2α	Drug Metabolite	Metabolic Disease
11β-Prostaglandin F2α ethanolamide (11β-PGF2α-EA) is the theoretical hepatic metabolite of PGD2-EA, produced during COX-2 metabolism of the endogenous cannabinoid AEA which is found in brain, liver, and other mammalian tissues.1 AEA can be used directly by COX-2 and specific PG synthase to produce ethanolamide congeners of the classical PGs. PGD2-EA is formed in activated RAW 264.7 cells treated with AEA.

HY-111478

Tiaprost Iliren	Prostaglandin Receptor	Metabolic Disease Endocrinology
Tiaprost is a prostaglandin F_2α (PGF_2α) analogue.

HY-107381A

(+)-Cloprostenol sodium D-Cloprostenol sodium	Prostaglandin Receptor	Endocrinology
(+)-Cloprostenol sodium is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.

HY-129953A

5-trans Prostaglandin F2α 5-trans pgf2α	Endogenous Metabolite	Cardiovascular Disease
5-trans Prostaglandin F2α is an endogenous metabolite present in Blood that can be used for the research of Myocardial Infarction ^[2].

HY-101438A

Darbufelone mesylate CI-1004 mesylate	Prostaglandin Receptor Leukotriene Receptor	Inflammation/Immunology Endocrinology
Darbufelone mesylate (CI-1004 mesylate) is a dual inhibitor of cellular *PGF_2α* and LTB₄ production. Darbufelone potently inhibits *PGHS-2* (IC₅₀ = 0.19 μM) but is much less potent with PGHS-1 (IC₅₀= 20 μM).

HY-129953F

Prostaglandin F2α-biotin pgf2α-biotin	Biochemical Assay Reagents Prostaglandin Receptor	Others
Prostaglandin F2α-biotin (PGF2α-biotin) is a biotinylated form of Prostaglandin F2α (HY-12956). Prostaglandin F2α-biotin can be used in the study of the mechanism of action of prostaglandins. In addition, Prostaglandin F2α-biotin can be detected in the ethanolic extract of Hawm Gra Dang Ngah rice .

HY-114867

(15R)-Bimatoprost 15(R)-17-phenyl trinor pgf2α ethyl amide	Prostaglandin Receptor	Endocrinology
(15R)-Bimatoprost (15(R)-17-phenyl trinor PGF2α ethyl amide) is a prostaglandin analog used to study glaucoma and ocular hypertension. (15R)-Bimatoprost is an isomer of Bimatoprost with an inverted (β) hydroxyl group on C-15 .

HY-116161

Bimatoprost isopropyl ester	Drug Intermediate	Cardiovascular Disease Others
15(R)-17-phenyl trinor Prostaglandin F2α isopropyl ester (15(R)-17-phenyl trinor PGF2α isopropyl ester) is the latanoprost-related isomer containing both a double bond at 13,14 and an inverted (β) hydroxyl group at C-15. Similar to 15(S)-latanoprost, 15(R)-17-phenyl trinor PGF2α isopropyl ester is a potential impurity in most commercial preparations of the latanoprost bulk drug product. The IC₅₀ values for the free acid forms of 15(S)-17-phenyl trinor PGF2α and 15(R)-17-phenyl trinor PGF2α were determined to be 0.71 nM and 30 nM, respectively, in a FP receptor binding assay using the cat iris sphincter muscle.1 A 3 μg dose of 15(R)-17-phenyl trinor PGF2α caused a 1.9 mmHg reduction of IOP in normotensive cynomolgus monkeys.

HY-132277

15-Keto Bimatoprost	Prostaglandin Receptor	Endocrinology
15-Keto Bimatoprost is a prostaglandin F2α (PGF2α) analog that can be used for the research of ocular hypotensive .

HY-172574

8-iso-17-Phenyl trinor prostaglandin F2α 8-iso-17-Phenyl trinor pgf2α	Drug Isomer Drug Derivative	Neurological Disease
8-Iso-17-phenyl trinor prostaglandin F2α (8-Iso-17-phenyl trinor PGF2), the C-8 epimer of Bimatoprost (HY-B0191), is a PGF_2α (HY-12956) analog. Bimatoprost can be used in the research of glaucoma and high intraocular pressure.

HY-106037

PGF2α-isopropyl ester	Prostaglandin Receptor	Others
PGF2α-isopropyl ester is a Prostaglandin F2α (HY-12956) derivative, which is active in lowering the intraocular pressure (IOP) through increased uveoscleral outflow of aqueous humor. PGF2α-isopropyl ester causes side effects of conjunctival hyperemia and ocular irritation .

HY-137547

*20-Hydroxy-PGF2α*	Prostaglandin Receptor	Metabolic Disease
20-hydroxy Prostaglandin F2α (20-hydroxy PGF2α) is the ω-oxidation product of PGF2α. Cultured type II alveolar cells from pregnant rabbits metabolize exogenous PGF2α via microsomal cytochrome P450 ω-oxidation, producing 20-hydroxy PGF2α and its 15-hydroxy PGDH metabolites. Cells from male rabbits exhibit only the 15-hydroxy PGDH pathway.

HY-125396

11-Deoxyprostaglandin F2β 11-Deoxy-pgf2β	Endogenous Metabolite	Others
11-Deoxyprostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β (HY-12956B). PGF2β is a metabolite produced by cyclooxygenase metabolism of arachidonic acid. PGF2β induces dose-dependent release of hexose containing mucin ^[2] .

HY-137544

16-Phenyl tetranor Prostaglandin F2α 16-Phenyl tetranor pgf2α	Prostaglandin Receptor Drug Metabolite	Metabolic Disease
16-phenyl tetranor Prostaglandin F2α (16-phenyl tetranor PGF2α) is a metabolically stable analog of PGF2α. The affinity of 16-phenyl tetranor PGF2α at the FP receptor of ovine luteal cells is poor (8.7%) compared to PGF2α.

HY-136627

PGF2α analogue-1	Prostaglandin Receptor	Endocrinology
PGF2α analogue-1 is an analog of Dinoprost (HY-12956) containing an acetylenic fluorobenzene substituent in the lower side chain.

HY-116549

Prostaglandin F2α alcohol pgf2α alcohol	Prostaglandin Receptor	Inflammation/Immunology
Prostaglandin F2α alcohol (PGF2α alcohol) is an analog of PGF2α. Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist .

HY-W746888

17-Phenyl trinor prostaglandin F2α diethyl amide 17-p-pgf2α-NEt2; 17-Phenyl trinor pgf2α diethyl amide	Prostaglandin Receptor	Cardiovascular Disease
17-Phenyl trinor prostaglandin F2α diethyl amide (17-phenyl trinor PGF2α diethyl amide) is a *PGF_2α* analog with hypotensive efficacy .

HY-137412

PGF2α 1,15-lactone Prostaglandin F2α 1,15-lactone	Drug Derivative	Endocrinology
PGF2α 1,15-lactone (Prostaglandin F2α 1,15-lactone) is a lipid-soluble internal ester of PGF2α. PGF2α 1,15-lactone decreases menstrual cycle lengths in non-pregnant rhesus monkeys. PGF2α 1,15-lactone terminates early pregnancy in the monkey .

HY-139063

16-Phenoxy tetranor prostaglandin F2α 16-Phenoxy tetranor pgf2α	Prostaglandin Receptor Endogenous Metabolite	Metabolic Disease
16-phenoxy tetranor Prostaglandin F2α (16-phenoxy tetranor PGF2α) is a metabolically stable analog of PGF2α. It binds to the FP receptor on ovine luteal cells with much greater affinity (440%) than PGF2α.

HY-114841

ONO 207 13,14-Dihydrodinoprost; 13,14-dihydro pgf2α	Prostaglandin Receptor	Endocrinology
13,14-dihydro Prostaglandin F2α (13,14-dihydro PGF2α) is the analog of PGF2α which has no unsaturation in the lower side chain. It causes luteolysis in hamsters with a potency five times higher than PGF2α. The ED50 value for 13,14-dihydro PGF2α as a luteolytic agent in hamsters is 1.5 μg/100 g.

HY-114850

5-trans Prostaglandin F2β 5-trans-pgf2β	Prostaglandin Receptor	Endocrinology
5-trans Prostaglandin F2β (5-trans-PGF2β) is the 9β-hydroxy isomer of 5-trans PGF2α .

HY-116051

16,16-Dimethylprostaglandin F2α 16,16-Dimethyl-pgf2α	Prostaglandin Receptor	Cardiovascular Disease
16,16-Dimethylprostaglandin F2α (16,16-Dimethyl-PGF2α) is a potent analog of PGF2α (HY-12956), which exhibits similar binding potency as PGF2α does. 16,16-Dimethylprostaglandin F2α serves as a bronchoconstrictor ^[2].

HY-118648

Prostaglandin F2α methyl ester pgf2α methyl ester; Dinoprost methyl	Prostaglandin Receptor	Others
Prostaglandin F2α methyl ester (PGF2α methyl ester; Dinoprost methyl) is a PGF_2α analog with more lipid solubility. Prostaglandin F2α methyl ester exhibits efficacy in maintaining the ocular hypotensive .

HY-116051A

16,16-Dimethylprostaglandin F2β 16,16-Dimethyl-pgf2β	Prostaglandin Receptor	Cardiovascular Disease
16,16-Dimethylprostaglandin F2β (16,16-Dimethyl-PGF2β) is an analog of PGF2β (HY-12956B), which is an irratant, but prevents the aspecifically induced bronchospasm .

HY-W399193

PGF2α 1,9-lactone Prostaglandin F2α 1,9-lactone	Prostaglandin Receptor	Metabolic Disease
PGF2α 1,9-lactone (Prostaglandin F2α 1,9-lactone) is a prostaglandin lactone. PGF2α 1,9-lactone shows resistant to hydrolysis by plasma esterases .

HY-137504

20-ethyl Prostaglandin F2α ICI 74205; 20-ethyl pgf2α	Prostaglandin Receptor Drug Metabolite	Metabolic Disease
20-ethyl Prostaglandin F2α (ICI 74205; 20-ethyl PGF2α) is an analog of *PGF2α* and an arachidonic acid (HY-109590) metabolite.

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.

HY-128550

Carboprost methyl Methyl carboprost; 15(S)-15-Methyl pgf2α methyl ester; U-36384	Prostaglandin Receptor	Endocrinology
15(S)-15-methyl Prostaglandin F2α methyl ester (15(S)-15-methyl PGF2α methyl ester) is a derivative of 15(S)-15-methyl PGF2α with increased membrane permeability. Hydrolysis of the methyl ester in vivo releases the biologically active 15(S)-15-methyl PGF2α, which is a potent uterine stimulant and abortifacient.

HY-158571

17-Phenoxy trinor prostaglandin F2α 17-Phenoxy trinor pgf2α	Prostaglandin Receptor	Metabolic Disease Inflammation/Immunology
17-Phenoxy trinor prostaglandin F_2α is a PGF_2α analog .

HY-138244

8-iso Prostaglandin F2β 8-iso pgf2β	Biochemical Assay Reagents	Inflammation/Immunology
8-iso Prostaglandin F2β (8-iso PGF2β) is a biomarker for assessing oxidative stress, and its content in serum can indirectly reflect the level of oxidative stress .

HY-N7857

19(R)-Hydroxy-prostaglandin F2α 19(R)-Hydroxy pgf2α	Drug Metabolite	Metabolic Disease
19(R)-Hydroxy-prostaglandin F2α (19(R)-hydroxy PGF2α) is an ω-1 hydroxylase metabolite of PGF2α found in human semen. The concentration of 19(R)-Hydroxy-PGFs compounds (F2α and F1α together) in fresh human semen is about 20 μg/mL. 19(R)-Hydroxy-prostaglandin F2α exhibits no activity at the FP receptor of the cat iris sphincter muscle at concentrations up to 1 μM.

HY-158595

15(R),19(R)-Hydroxy prostaglandin F2α 15(R),19(R)-Hydroxy pgf2α	Drug Derivative	Others
15(R),19(R)-Hydroxy prostaglandin F2α (15(R),19(R)-Hydroxy PGF2α) is an analog of 19(R)-Hydroxy-prostaglandin F2α. 19(R)-Hydroxy-prostaglandin F2α (HY-N7857) is an ω-1 hydroxylase metabolite of PGF2α found in human semen .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-12956

Dinoprost 5+ Cited Publications Prostaglandin F2α; pgf2α	Classification of Application Fields Ketones, Aldehydes, Acids Endogenous metabolite Disease Research Fields Endocrinology Source Classification	Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis
Dinoprost (Prostaglandin F2α) is an orally active, potent *prostaglandin F (PGF) receptor (FP receptor)* agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

HY-12956A

Dinoprost tromethamine salt 5+ Cited Publications Prostaglandin F2α tromethamine salt; pgf2α THAM; Prostaglandin F2α THAM	Classification of Application Fields Ketones, Aldehydes, Acids Endogenous metabolite Disease Research Fields Endocrinology Source Classification	Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) is an orally active, potent *prostaglandin F (PGF) receptor (FP receptor)* agonist. Dinoprost tromethamine salt is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost tromethamine salt plays a key role in the onset and progression of labour ^[2].

HY-113209

8-Isoprostaglandin F2α 8-iso-pgf2α	Structural Classification Classification of Application Fields Ketones, Aldehydes, Acids Other Diseases Endogenous metabolite Disease Research Fields Source Classification	Endogenous Metabolite
8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-129953

9α,11β-Prostaglandin F2α 9α,11β-pgf2α	Structural Classification Classification of Application Fields Ketones, Aldehydes, Acids Endogenous metabolite Inflammation/Immunology Disease Research Fields Source Classification	Endogenous Metabolite
9α,11β-Prostaglandin F₂α (9α,11β-PGF2α) is an endogenous metabolite present in urine, which can be used for asthma research ^[2].

HY-113208

13,14-Dihydro-15-keto Prostaglandin F2α 13,14-Dihydro-15-keto-pgf2α	Classification of Application Fields Ketones, Aldehydes, Acids Other Diseases Endogenous metabolite Disease Research Fields Source Classification	Endogenous Metabolite
13,14-Dihydro-15-keto Prostaglandin F2α (13,14-Dihydro-15-keto-PGF2α) is an endogenous metabolite present in Blood that can be used for the research of Pregnancy ^[2].

HY-125150

AL-3138 11-Deoxy-16-fluoro pgf2α	Natural Products Classification of Application Fields Endogenous metabolite Disease Research Fields Endocrinology Source Classification	Prostaglandin Receptor Endogenous Metabolite
AL-3138 (11-Deoxy-16-fluoro PGF2α) is a prostaglandin F2 alpha (PGF2alpha) analogue that antagonises FP prostaglandin receptor-mediated inositol phosphate production .

HY-125396

11-Deoxyprostaglandin F2β 11-Deoxy-pgf2β	Classification of Application Fields Ketones, Aldehydes, Acids Other Diseases Endogenous metabolite Disease Research Fields Source Classification	Endogenous Metabolite
11-Deoxyprostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β (HY-12956B). PGF2β is a metabolite produced by cyclooxygenase metabolism of arachidonic acid. PGF2β induces dose-dependent release of hexose containing mucin ^[2] .

HY-113246

15-keto-Prostaglandin F2a 15-keto-pgf2α	Classification of Application Fields Ketones, Aldehydes, Acids Endogenous metabolite Disease Research Fields Endocrinology Source Classification	Prostaglandin Receptor Endogenous Metabolite
15-keto-Prostaglandin F2α (15-keto-PGF2α) is a metabolite of Prostaglandin F2α. Prostaglandin F2α. Prostaglandin F2α is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist and plays a key role in the onset and progression of labour .

HY-N12119

ent-Prostaglandin F2α	Ketones, Aldehydes, Acids Endogenous metabolite Source Classification	Endogenous Metabolite
ent-Prostaglandin F2α is the opposite enantiomer of PGF2α. ent-Prostaglandin F2α can be found in urine .

HY-12956B

(5R)-Dinoprost Prostaglandin F2β; pgf2β	Classification of Application Fields Ketones, Aldehydes, Acids Other Diseases Endogenous metabolite Disease Research Fields Source Classification	Endogenous Metabolite
(5R)-Dinoprost is a metabolite produced by cyclooxygenase metabolism of arachidonic acid. (5R)-Dinoprost (Prostaglandin F2β) induces dose-dependent release of hexose containing mucin ^[2].

HY-12956R

Dinoprost (Standard) Prostaglandin F2α (Standard); pgf2α (Standard)	Structural Classification Ketones, Aldehydes, Acids Endogenous metabolite Source Classification	Reference Standards Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis
Dinoprost (Standard) is the analytical standard of Dinoprost. This product is intended for research and analytical applications. Dinoprost (Prostaglandin F2α) is an orally active, potent *prostaglandin F (PGF) receptor (FP receptor)* agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

HY-113209R

8-Isoprostaglandin F2α (Standard) 8-iso-pgf2α (Standard)	Structural Classification Ketones, Aldehydes, Acids Endogenous metabolite Source Classification	Reference Standards Endogenous Metabolite
8-Isoprostaglandin F2α (Standard) is the analytical standard of 8-Isoprostaglandin F2α. This product is intended for research and analytical applications. 8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-12956AR

Dinoprost tromethamine salt (Standard) Prostaglandin F2α tromethamine salt (Standard); pgf2α THAM (Standard); Prostaglandin F2α THAM (Standard)	Structural Classification Ketones, Aldehydes, Acids Endogenous metabolite Source Classification	Reference Standards Prostaglandin Receptor Endogenous Metabolite Autophagy Apoptosis
Dinoprost (tromethamine salt) (Standard) is the analytical standard of Dinoprost (tromethamine salt). This product is intended for research and analytical applications. Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost tromethamine salt is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost tromethamine salt plays a key role in the onset and progression of labour ^[2].

Cat. No.	Product Name	Chemical Structure

HY-12956S

Dinoprost-d4
Dinoprost-d₄ is the deuterium labeled Dinoprost. Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

HY-125774S

Bimatoprost acid-d4
Bimatoprost acid-d₄ (17-Phenyl trinor PGF2α-d₄) is the deuterium labeled Bimatoprost acid .

HY-113209S

8-Isoprostaglandin F2α-d4
8-Iso-PGF2a-d₄ (8-iso Prostaglandin F2α-d₄) is an active compound. 8-Iso-PGF2a-d₄ can be used the internal standard .

HY-113459S1

13,14-Dihydro-15-keto Prostaglandin F2α-d4
13,14-Dihydro-15-keto Prostaglandin F2α-d4 (13,14-Dihydro-15-keto-PGF2α-d4) is a deuterated labeled 13,14-Dihydro-15-keto Prostaglandin F2α (HY-113208). 13,14-Dihydro-15-keto Prostaglandin F2α-d4 is an endogenous metabolite present in Blood that can be used for the research of Pregnancy ^[2].

HY-132277S

15-Keto Bimatoprost-d5
15-Keto Bimatoprost-d₅ is the deuterium labeled 15-Keto Bimatoprost. 15-Keto Bimatoprost is a prostaglandin F2α (PGF2α) analog that can be used for the research of ocular hypotensive ^[2].

HY-129397S

2,3-Dinor-11β-prostaglandin F2α-d9
2,3-Dinor-11β-prostaglandin F2α-d₉ is the deuterium labeled 2,3-Dinor-11β-prostaglandin F2α .

HY-113209S1

8-Isoprostaglandin F2α-d9

8-iso Prostaglandin F2α-d₉ is the deuterium labeled 8-Isoprostaglandin F2α. 8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-113208AS1

11β-13,14-Dihydro-15-keto Prostaglandin F2α-d4
11β-13,14-Dihydro-15-keto Prostaglandin F2α-d₄ is is the deuterium labeled 11β-13,14-dihydro-15-keto Prostaglandin F2α.

HY-12956S1

Dinoprost-d9
Dinoprost-d₉ is the deuterium labeled Dinoprost. Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

HY-113209S2

8-Isoprostaglandin F2α-13C5

8-Isoprostaglandin F2α- ¹³C₅ is ¹³C labeled 8-Isoprostaglandin F2α (HY-113209). 8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-129953S1

9α,11β-Prostaglandin F2α-d9
9α,11β-Prostaglandin F2α-d₉ is the deuterium labeled 9α,11β-Prostaglandin F2α .

HY-129953S

9α,11β-Prostaglandin F2α-d4
9α,11β-Prostaglandin F2α-d4 is a deuterated labeled 9α,11β-Prostaglandin F2α . 9α,11β-Prostaglandin F2α is an endogenous metabolite present in Urine that can be used for the research of Asthma ^[2] .

HY-12956S2

Dinoprost-13C5
Dinoprost- ¹³C₅ is ¹³C labeled Dinoprost (HY-12956). Dinoprost (Prostaglandin F2α) is an orally active, potent *prostaglandin F (PGF) receptor (FP receptor)* agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour ^[2].

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