15 Results for "

(+)-Cloprostenol

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "(+)-Cloprostenol" in MCE Product Catalog:

Art. -Nr.: HY-108415
CAS. Nr.: 55028-72-3
Reinheit:  99.52%
Synonyms: ICI 80996 sodium salt
Forschungsgebiete:  

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 .
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Art. -Nr.: HY-121314
CAS. Nr.: 40665-92-7
Forschungsgebiete:  

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 .
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Art. -Nr.: HY-107381
CAS. Nr.: 54276-21-0
Reinheit:  99.28%
Synonyms: D-Cloprostenol
Forschungsgebiete:  

Endocrinology

(+)-Cloprostenol is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.
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Art. -Nr.: HY-107381A
CAS. Nr.: 62561-03-9
Synonyms: D-Cloprostenol sodium
Forschungsgebiete:  

Endocrinology

(+)-Cloprostenol sodium is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.
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Art. -Nr.: HY-100571
CAS. Nr.: 157283-66-4
Forschungsgebiete:  

Endocrinology

Cloprostenol isopropyl ester, a prostaglandin F2α analogs, is the intermediate of (+)-Cloprostenol (HY-107381). Cloprostenol isopropyl ester is a FP receptor agonist with a Ki value of 28 nM .
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Art. -Nr.: HY-107381R
CAS. Nr.: 54276-21-0
Synonyms: D-Cloprostenol (Standard)
Forschungsgebiete:  

Endocrinology

(+)-Cloprostenol (Standard) is the analytical standard of (+)-Cloprostenol. This product is intended for research and analytical applications. (+)-Cloprostenol is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.
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Art. -Nr.: HY-134009
CAS. Nr.: 56687-85-5
Target:  

Drug Derivative

Forschungsgebiete:  

Others

(+)-Cloprostenol methyl ester is a 11,13-Dienone analog of cloprostenol (HY-107381) .
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Art. -Nr.: HY-120982
CAS. Nr.: 54276-22-1
Forschungsgebiete:  

Endocrinology

Cloprostenol is a synthetic prostaglandin F2α (PGF2α) analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude as an FP receptor ligand when compared to 15(R)-cloprostenol. However, the specific activity of this isomer has not been well studied.
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Art. -Nr.: HY-120955
CAS. Nr.: 57968-81-7
Forschungsgebiete:  

Others

Cloprostol, a synthetic derivative of prostaglandin F2α, is used as an ossified in veterinary medicine and the research of reproductive disorders in cattle, pigs and horses. (+)-5-trans Cloprostenol is a secondary impurity produced during the synthesis of (+) -cloprostenol .
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Art. -Nr.: HY-100571A
Target:  

Drug Isomer

Forschungsgebiete:  

Metabolic Disease

(+)-5-trans Cloprostenol isopropyl ester is a more lipid-soluble form of (+)-5-trans cloprostenol (HY-120955), which is a synthetic derivative of prostaglandin F2α .
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Art. -Nr.: HY-108415R
CAS. Nr.: 55028-72-3
Synonyms: ICI 80996 sodium salt (Standard)
Forschungsgebiete:  

Endocrinology

Cloprostenol sodium salt (Standard) is the analytical standard of Cloprostenol sodium salt. This product is intended for research and analytical applications. Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent , and is a PGF2α receptor agonist .
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Art. -Nr.: HY-181441
Target:  

Drug Derivative

Forschungsgebiete:  

Others

(+)-Cloprostenol methyl amide is a derivative analog of the carboxylic acid terminus of (+)-Cloprostenol (HY-107381).
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Art. -Nr.: HY-176009
Target:  

Drug Derivative

Forschungsgebiete:  

Others

15-Keto cloprostenol isopropyl ester is a potential impurity in cloprostenol isopropyl ester preparations .
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Art. -Nr.: HY-116679
CAS. Nr.: 221246-34-0
Synonyms: 17-Trifluoromethylphenyl trinor PGF2α
Forschungsgebiete:  

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.
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Art. -Nr.: HY-176075
Forschungsgebiete:  

Others

16-(3-Fluorophenoxy) tetranor prostaglandin F2α methyl is a Prostaglandin F2a analog and a derivative of cloprostenol.
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