141 Results for "

F2α

" in MedChemExpress (MCE) Product Catalog:
Products (141)

141 Results for "F2α" in MCE Product Catalog:

10
10 Publications Verification
Cat. No.: HY-12956
CAS No.: 551-11-1
Purity:  99.63%
Synonyms: Prostaglandin F2α; PGF2α
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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10
10 Publications Verification
Cat. No.: HY-12956A
CAS No.: 38562-01-5
Purity:  ≥98.0%
Synonyms: Prostaglandin F2α tromethamine salt; PGF2α THAM; Prostaglandin F2α THAM
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].
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5
5 Cited Publications
Cat. No.: HY-B0577
CAS No.: 130209-82-4
Synonyms: PHXA41
Research Areas:  

Cardiovascular Disease Others

Latanoprost (PHXA41) is a prostaglandin F2α analogue and can be used for glaucoma research. Latanoprost can effectively pass through cornea and be hydrolyzed by esterase to latanoprost acid. latanoprost acid is an F-prostaglandin (FP) receptor agonist, and can effectively reduce intraocular pressure (IOP) by increasing the outflow of aqueous humor through uvea .
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2
2 Cited Publications
Cat. No.: HY-112284
CAS No.: 2005486-31-5
Purity:  98.65%
Synonyms: OBE022
Research Areas:  

Endocrinology

Ebopiprant (OBE022) is an oral and selective prostaglandin F (PGF) receptor antagonist, with Kis of 1 nM, 26 nM for human and rat FP receptors, respectively.
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1
1 Cited Publications
Cat. No.: HY-113756A
CAS No.: 41639-83-2
Purity:  99.62%
Latanoprost acid, an analog of prostaglandin (PG) F2α, is an selective prostanoid receptor (FP) agonist that specifically activates the FP-PG receptor . Latanoprost acid inhibits RANKL-induced osteoclastgenesis and function by inhibiting ERK, AKT, JNK, and p38 cascade, following by the c-fos/NFATc1 pathway. Latanoprost acid is a medication which works to lower pressure inside the eyes [2].
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Cat. No.: HY-128428
CAS No.: 35700-23-3
Purity:  ≥98.0%
Synonyms: 15(S)-15-Methyl Prostaglandin F2α; 15-Methyl-PGF2α
Research Areas:  

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].
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Cat. No.: HY-113209
CAS No.: 27415-26-5
Purity:  ≥99.0%
Synonyms: 8-iso-PGF2α
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.
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Cat. No.: HY-118388
CAS No.: 612532-48-6
Research Areas:  

Endocrinology

AS604872 is an orally active, potent and selective prostaglandin F2α receptor (FP) antagonist with a Ki of 35 nM in humans, 158 nM in rats and 323 nM in mice. AS604872 inhibits contractions and delays labour .
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Cat. No.: HY-121314
CAS No.: 40665-92-7
Research Areas:  

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].
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Cat. No.: HY-129953
CAS No.: 38432-87-0
Synonyms: 9α,11β-PGF2α
9α,11β-Prostaglandin F2α (9α,11β-PGF2α) is an endogenous metabolite present in urine, which can be used for asthma research [2].
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Cat. No.: HY-107381
CAS No.: 54276-21-0
Purity:  99.28%
Synonyms: D-Cloprostenol
Research Areas:  

Endocrinology

(+)-Cloprostenol is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.
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Cat. No.: HY-130660
CAS No.: 353787-70-9
Synonyms: Prostamide F2α
Research Areas:  

Endocrinology

Prostaglandin F2α ethanolamide (Prostamide F2α) is an ethanolamide-like G protein-coupled receptor. Prostaglandin F2α is also a luteinizing hormone in sheep and may be a nociceptive mediator in the spinal cord [2] .
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Cat. No.: HY-113208
CAS No.: 27376-76-7
Purity:  ≥99.0%
Synonyms: 13,14-Dihydro-15-keto-PGF2α
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].
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Cat. No.: HY-114810
CAS No.: 1135226-99-1
Research Areas:  

Endocrinology

Prostaglandin F2α serinol amide is a serinolamide G protein-coupled receptor that increases calcium levels in human non-small cell lung cancer cells. Prostaglandin F2α is also a luteinizing hormone in sheep and may be a nociceptive mediator in the spinal cord [2] .
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Cat. No.: HY-129953A
CAS No.: 36150-01-3
Synonyms: 5-trans PGF2α
Target:  

Endogenous Metabolite

Research Areas:  

Cardiovascular Disease

5-trans Prostaglandin F2α is an endogenous metabolite present in Blood that can be used for the research of Myocardial Infarction [2].
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Cat. No.: HY-118816
CAS No.: 714966-38-8
Synonyms: 11-epi PGF2α-EA; 11β-PGF2α-EA; 11β-Prostamide F2α
Target:  

Drug Metabolite

Research Areas:  

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.
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Cat. No.: HY-137119
CAS No.: 179094-11-2
Purity:  ≥99.0%
Synonyms: 5-iso Prostaglandin F2α-VI
Research Areas:  

Others

(±)5-iPF2α-VI (5-iso Prostaglandin F2α-VI) is the racemate of 5-iPF2α-VI. 5-iPF2α-VI is a regioisomeric isoprostane formed from arachidonic acid (AA) and is a biomarker of oxidative stress .
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Cat. No.: HY-118520
CAS No.: 51638-90-5
Research Areas:  

Endocrinology

16-Phenoxy tetranor Prostaglandin F2α methyl ester is a metabolically stable form of Prostaglandin F2α that can binds to FP receptor. 16-Phenoxy tetranor Prostaglandin F2α methyl ester serves as prodrug that can be hydrolyzed to generate bioactive free acid .
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Cat. No.: HY-113209A
CAS No.: 214748-66-0
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

Ent-8-Iso-15(S)-prostaglandin F2α is an isomer of 8-Isoprostaglandin F2α, with a better inhibiting activity in the whole blood platelet aggregation inhibition assay .
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Cat. No.: HY-149588
CAS No.: 195503-20-9
Research Areas:  

Endocrinology

17-Trifluoromethylphenyl trinor prostaglandin F2α methyl ester is an analog of PGF2α .
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