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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
16 Results for "
luteolytic
" in MedChemExpress (MCE) Product Catalog:
Products (16)
16 Results for "luteolytic" in MCE Product Catalog:
10
10 Publications Verification
Synonyms: Prostaglandin F2α; PGF2α
10
10 Publications Verification
Synonyms: Prostaglandin F2α tromethamine salt; PGF2α THAM; Prostaglandin F2α THAM
Synonyms: ICI 80996 sodium salt
Target:
Research Areas:
Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent , and is a PGF2α receptor agonist .
Cat. No.: HY-12956S
CAS No.: 34210-11-2
Synonyms: Prostaglandin F2a-d4; PGF2α-d4
Cat. No.: HY-118624
CAS No.: 73275-76-0
Target:
Research Areas:
Fluprostenol methyl ester is an F-series prostaglandin analog which has been approved for many years as a luteolytic in veterinary animals .
Cat. No.: HY-113909
CAS No.: 101913-98-8
Synonyms: Prostaglandin F2α (methoxyamine); PGF2α (methoxyamine)
Research Areas:
Dinoprost methoxyamine is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost methoxyamine is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost methoxyamine plays a key role in the onset and progression of labour .
Cat. No.: HY-12956S2
Synonyms: Prostaglandin F2α-13C5; PGF2α-13C5
Cat. No.: HY-12956AR
CAS No.: 38562-01-5
Synonyms: Prostaglandin F2α tromethamine salt (Standard); PGF2α THAM (Standard); Prostaglandin F2α THAM (Standard)
Cat. No.: HY-123420
CAS No.: 64675-08-7
Synonyms: Dinordrin I
Target:
Research Areas:
Dinordrin (Dinordrin I) is a steroid with a luteolytic effect. Dinordrin can cause depression of both plasma estrogen and progesterone levels .
Cat. No.: HY-108415R
CAS No.: 55028-72-3
Synonyms: ICI 80996 sodium salt (Standard)
Research Areas:
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 .
Cat. No.: HY-136494
CAS No.: 40666-16-8
Synonyms: ICI 81008
Target:
Research Areas:
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 .
Cat. No.: HY-12956S1
Synonyms: Prostaglandin F2a-d9; PGF2α-d9
Cat. No.: HY-114841
CAS No.: 27376-74-5
Synonyms: 13,14-Dihydrodinoprost; 13,14-dihydro PGF2α
Target:
Research Areas:
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.
Cat. No.: HY-116679
CAS No.: 221246-34-0
Synonyms: 17-Trifluoromethylphenyl trinor PGF2α
Target:
Research Areas:
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.
Cat. No.: HY-106074
CAS No.: 88980-20-5
Synonyms: MDL 646
Target:
Research Areas:
Mexiprostil (MDL 646) is an orally active gastric protectant, being a synthetic analogue of Prostaglandin E1 (HY-B0131). Mexiprostil exhibits significant inhibition of gastric acid secretion caused by Histamine (HY-B1204) and Bethanechol (HY-B0406) in rats, dogs, and cats. Mexiprostil can also inhibit the increase in gastric acid secretion caused by Pentagastrin (HY-A0261) in cats, while it does not have this effect in dogs and rats. Mexiprostil does not cause pregnancy termination. Mexiprostil can be used for research on gastric ulcers .
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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
