ChemicalBook--->CAS DataBase List--->149007-54-5

149007-54-5

149007-54-5 Structure

149007-54-5 Structure
IdentificationBack Directory
[Name]

(S)-WAY 100135 dihydrochloride
[CAS]

149007-54-5
[Synonyms]

(S)-WAY-100135 hydrochloride
WAY 100135 dihydrochloride, (S)-
[Molecular Formula]

C24H33N3O2.2HCl
[MDL Number]

MFCD00923003
[MOL File]

149007-54-5.mol
[Molecular Weight]

432.01
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

<46.85mg/ml in DMSO;insoluble in H2O;insoluble in H2O
[form ]

solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]


GHS09
[Signal word ]

Warning
[Hazard statements ]

H400
[Precautionary statements ]

P273-P391-P501
Hazard InformationBack Directory
[Uses]

(S)-WAY 100135 Dihydrochloride is a selective 5-?HT1A receptor antagonist.
[Biological Activity]

(s)-way 100135 dihydrochloride is a potent and selective antagonist of 5-ht1a receptor with ic50 value of 15 nm.the 5-ht1a receptor is a g protein-coupled receptor for endogenous neurotransmitter serotonin (5-ht) and mediates inhibitory neurotransmission.(s)-way 100135 dihydrochloride is a potent and selective somatodendritic and postsynaptic 5-ht1a receptors antagonist. (+/-)-way100135 inhibited 5-ht1a receptor in the rat hippocampal with ic50 value of 34 nm [1].in the murine elevated plus-maze test, (s)-way 100135 (10 mg/kg) exhibited anxiolytic-like effects [2]. in free feeding rats, way-100135 (3 mg/kg) significantly inhibited hyperphagia and the increased incidence of feeding induced by 8-oh-dpat (0.1 mg/kg), which was mediated by somatodendritic 5-ht1a autoreceptor [3]. in rats, (s)-way 100135 (0.2, 1, 5 ug/ul) inhibited the impairment of choice accuracy induced by intrahippocampal scopolamine (3.75 ug/ul) in a dose-dependent way. however, (s)-way 100135 didn’t influence the acquisition of spatial learning [4]. in rats, way-100135 (10.0 mg/kg) inhibited the decrease of 5-ht release induced by buspirone, a 5-ht1a receptor partial agonist [5].
[storage]

Store at -20°C
[References]

[1]. fletcher a, bill dj, bill sj, et al. way100135: a novel, selective antagonist at presynaptic and postsynaptic 5-ht1a receptors. eur j pharmacol, 1993, 237(2-3): 283-291.
[2]. rodgers rj, cole jc. anxiolytic-like effect of (s)-way 100135, a 5-ht1a receptor antagonist, in the murine elevated plus-maze test. eur j pharmacol, 1994, 261(3): 321-325.
[3]. hartley je, fletcher a. the effects of way-100135 and 8-hydroxy-2-(di-n-propylamino)tetralin on feeding in the rat. eur j pharmacol, 1994, 252(3): 329-332.
[4]. carli m, luschi r, samanin r. (s)-way 100135, a 5-ht1a receptor antagonist, prevents the impairment of spatial learning caused by intrahippocampal scopolamine. eur j pharmacol, 1995, 283(1-3): 133-139.
[5]. routledge c, gurling j, ashworth-preece ma, et al. differential effects of way-100135 on the decrease in 5-hydroxytryptamine release induced by buspirone and nan-190. eur j pharmacol, 1995, 276(3): 281-284.
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