ChemicalBook--->CAS DataBase List--->1962928-26-2

1962928-26-2

1962928-26-2 Structure

1962928-26-2 Structure
IdentificationBack Directory
[Name]

BGC 20-1531 (hydrochloride)
[CAS]

1962928-26-2
[Synonyms]

AP 1531
BGC20-1531 (PGN-1531
AP-1531 hydrochloride
GTPL3380 hydrochloride
BGC 20-1531 (hydrochloride)
BGC201531 hydrochloride(1186532615 free base),BGC 20 1531 hydrochloride(1186532 61 5 free base)
4-[[4-(5-Methoxy-2-pyridinyl)phenoxy]methyl]-5-methyl-N-[(2-methylphenyl)sulfonyl]-2-furancarboxamide hydrochloride
[Molecular Formula]

C26H25ClN2O6S
[MDL Number]

MFCD30182277
[MOL File]

1962928-26-2.mol
[Molecular Weight]

529
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 1 mg/ml; DMSO: 1 mg/ml
[form ]

A crystalline solid
Hazard InformationBack Directory
[Description]

BGC 20-1531 is a potent and selective antagonist of the prostaglandin E2 (PGE2; ) receptor subtype 4 (EP4) with Ki values of 11.7, >10,000, and >10,000 nM for EP4, EP2, and EP3, respectively. It is selective for EP4, exhibiting <50% inhibition at 47 ion channels, cell-surface transporters, enzymes, and nuclear receptors at a concentration of 10 μM. BGC 20-1531 antagonizes PGE2-induced cAMP accumulation in a dose-dependent manner in HEK293 EBNA cells that stably express human EP4 receptors. It also reverses PGE2-induced vasorelaxation (Kb = 15.85 nM) in human middle cerebral and middle meningeal arterial rings. BGC 20-1531 prevents PGE2-induced increases in carotid blood flow and decreases in carotid resistance with an ID50 value of 5 mg/kg in dogs.
[Uses]

BGC 20-1531 Hydrochloride, is a potent and selective EP4 antagonist, exhibiting <50% inhibition at 47 ion channels, cell-surface transporters, enzymes, and nuclear receptors at a concentration of 10 μM. It also Inhibits PGE2-induced vasodilation of middle cerebral and meningeal arterieshuman middle cerebral and middle meningeal arterial rings.
[storage]

Desiccate at RT
Spectrum DetailBack Directory
[Spectrum Detail]

BGC 20-1531 (hydrochloride)(1962928-26-2)1HNMR
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