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119813-87-5

119813-87-5 Structure

119813-87-5 Structure
IdentificationBack Directory
[Name]

5,8,8a,9,10,11,12,12a,13,13a-decahydro-3-methoxy-12-(methylsulfonyl)-6H-isoquino(2,1-g)(1,6)naphthyridine
[CAS]

119813-87-5
[Synonyms]

5,8,8a,9,10,11,12,12a,13,13a-decahydro-3-methoxy-12-(methylsulfonyl)-6H-isoquino(2,1-g)(1,6)naphthyridine
6H-Isoquino[2,1-g][1,6]naphthyridine, 5,8,8a,9,10,11,12,12a,13,13a-decahydro-3-methoxy-12-(methylsulfonyl)-, (8aR,12aS,13aS)-rel-
[Molecular Formula]

C18H26N2O3S
[MOL File]

119813-87-5.mol
[Molecular Weight]

350.48
Chemical PropertiesBack Directory
[Boiling point ]

507.5±60.0 °C(Predicted)
[density ]

1.29±0.1 g/cm3(Predicted)
[pka]

7.70±0.20(Predicted)
Hazard InformationBack Directory
[Description]

RS 15385-197 is a potent and selective alpha 2-adrenoceptor antagonist.
[Uses]

rel-Delequamine (rel-RS-15385-197) is an orally active, brain-penetrant, potent and selective M2-adrenoceptor antagonist and α2-adrenoceptor antagonist. rel-Delequamine has a pKi of 9.45 for α2-adrenoceptors in the rat cortex. rel-Delequamine augments K+-evoked release of noradrenaline with an EC50 of 1 nM[1].
[References]

[1] Brown CM, et al. The pharmacology of RS-15385-197, a potent and selective alpha 2-adrenoceptor antagonist. Br J Pharmacol. 1993 Feb;108(2):516-25. DOI:10.1111/j.1476-5381.1993.tb12834.x
[2] Redfern WS, et al. Modulation of central noradrenergic function by RS-15385-197. Br J Pharmacol. 1993 Feb;108(2):526-33. DOI:10.1111/j.1476-5381.1993.tb12835.x
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