ChemicalBook--->CAS DataBase List--->160521-72-2

160521-72-2

160521-72-2 Structure

160521-72-2 Structure
IdentificationBack Directory
[Name]

BW 723C86
[CAS]

160521-72-2
[Synonyms]

BW 723C8
BW 723C86
BW723C86HCl
Zinc02379519
BW 723C86 hydrochlor
BW-723C86 (BW 723C86
BW 723C86 HYDROCHLORIDE
A-Methyl-5-(2-Thienylmethox
BW 723C86 \ 5-HT2B SEROTONIN RECEPTOR AG ONIST
a-methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanaminehydrochloride
α-methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanaminehydrochloride
1-(5-(Thiophen-2-ylmethoxy)-1H-indol-3-yl)propan-2-amine hydrochloride
α-Methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanamine Monohydrochloride
a-Methyl-5-(2-thienylmethoxy)-1H-indole-3-ethanamine Monohydrochloride
ALPHA-METHYL-5-(2-THIENYLMETHOXY)-1H-INDOLE-3-ETHANAMINE HYDROCHLORIDE
ALPHA-METHYL-5-(2-THIENYLMETHOXY)-1H-INDOLE-3-ETHANAMINE, MONOHYDROCHLORIDE
Α-METHYL-5-(2-THIENYLMETHOXY)-1H-INDOLE-3-,ETHANAMINEMONOHYDROCHLORIDE(BW723C86)
[Molecular Formula]

C16H19ClN2OS
[MDL Number]

MFCD01321066
[MOL File]

160521-72-2.mol
[Molecular Weight]

322.85
Chemical PropertiesBack Directory
[storage temp. ]

Desiccate at +4°C
[solubility ]

DMSO: >10 mg/mL
[form ]

solid
[color ]

white
[Water Solubility ]

H2O: 1mg/mL, clear
Safety DataBack Directory
[WGK Germany ]

3
[RTECS ]

NL8504715
Hazard InformationBack Directory
[Uses]

BW 723C86 is a selective 5-HT2B receptor agonist. It is used in the treatment of certain CNS disorders, in particular epilepsy, migraine and feeding disorders.
[Biological Activity]

Selective 5-HT 2B receptor agonist.
[Biochem/physiol Actions]

5-HT2B serotonin receptor agonist.
[in vivo]

BW-723C86 (1-20 mg/kg, s.c., 30 min pre-test (grooming)) causes hyperphagia and decreased grooming in rats, with increasing the time spent in feeding behaviour[2].
BW-723C86 (10-30 mg/kg, i.p. 30 min pre-test) shows anxiolytic effects in rats via 5-HT2B receptor[3].
BW-723C86 (3-10 mg/kg, s.c. 30 min pretest) exerts an appreciable anxiolytic-like profile in rats, with increasing total social interaction[4].
BW-723C86 (5 mg/kg, p.o., 20 or 30 min before the liquid meal) inhibits liquid meal-induced gastric accommodation in normal Hartley guinea pigs[5].

Animal Model:Male Sprague Dawley (CD) rats (220–250 g) for vogel conflict test[3]
Dosage:0.3, 1, 3, 10, 30 mg/kg
Administration:Intraperitoneal injection (i.p.), 30 min pre-test
Result:Increased the number of punishments accepted in the rat Vogel conflict test over 3 min.
Had no significant effect on either the amount of time spent drinking or the latency to drink.
Did not affect apparent shock sensitivity.
[IC 50]

5-HT2B Receptor
[storage]

Store at -20°C
[References]

[1]. kennett ga, bright f, trail b, et al. effects of the 5-ht2b receptor agonist, bw 723c86, on three rat models of anxiety. br j pharmacol, 1996, 117(7): 1443-1448.
[2]. dergacheva o, wang x, kamendi h, et al. 5ht2 receptor activation facilitates p2x receptor mediated excitatory neurotransmission to cardiac vagal neurons in the nucleus ambiguus. neuropharmacology, 2008, 54(7): 1095-1102.
[3]. kennett ga, trail b, bright f. anxiolytic-like actions of bw 723c86 in the rat vogel conflict test are 5-ht2b receptor mediated. neuropharmacology, 1998, 37(12): 1603-1610.
[4]. urtikova n, berson n, van steenwinckel j, et al. antinociceptive effect of peripheral serotonin 5-ht2b receptor activation on neuropathic pain. pain, 2012, 153(6): 1320-1331.
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