product summary
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company name :
Tocris Bioscience
product type :
chemical
product name :
SB 206553 hydrochloride
catalog :
1661/10
quantity :
10 mg (also 50 mg)
price :
299 USD
more info or order :
citations: 9
Reference
Li Y, Lucas Osma A, Black S, Bandet M, Stephens M, Vavrek R, et al. Pericytes impair capillary blood flow and motor function after chronic spinal cord injury. Nat Med. 2017;23:733-741 pubmed publisher
Kuo H, Lai Y, Wu J, Lee K, Chu C, Chen I, et al. A xanthine-derivative K(+)-channel opener protects against serotonin-induced cardiomyocyte hypertrophy via the modulation of protein kinases. Int J Biol Sci. 2013;10:64-72 pubmed publisher
Li Y, Li L, Stephens M, Zenner D, Murray K, Winship I, et al. Synthesis, transport, and metabolism of serotonin formed from exogenously applied 5-HTP after spinal cord injury in rats. J Neurophysiol. 2014;111:145-63 pubmed publisher
Bigford G, Chaudhry N, Keane R, Holohean A. 5-Hydroxytryptamine 5HT2C receptors form a protein complex with N-methyl-D-aspartate GluN2A subunits and activate phosphorylation of Src protein to modulate motoneuronal depolarization. J Biol Chem. 2012;287:11049-59 pubmed publisher
Delaney C, Gien J, Grover T, Roe G, Abman S. Pulmonary vascular effects of serotonin and selective serotonin reuptake inhibitors in the late-gestation ovine fetus. Am J Physiol Lung Cell Mol Physiol. 2011;301:L937-44 pubmed publisher
Fouad K, Rank M, Vavrek R, Murray K, Sanelli L, Bennett D. Locomotion after spinal cord injury depends on constitutive activity in serotonin receptors. J Neurophysiol. 2010;104:2975-84 pubmed publisher
Murray K, Nakae A, Stephens M, Rank M, D Amico J, Harvey P, et al. Recovery of motoneuron and locomotor function after spinal cord injury depends on constitutive activity in 5-HT2C receptors. Nat Med. 2010;16:694-700 pubmed publisher
Canal C, Olaghere da Silva U, Gresch P, Watt E, Sanders Bush E, Airey D. The serotonin 2C receptor potently modulates the head-twitch response in mice induced by a phenethylamine hallucinogen. Psychopharmacology (Berl). 2010;209:163-74 pubmed publisher
Hampson L, Mackin P, Agius L. Stimulation of glycogen synthesis and inactivation of phosphorylase in hepatocytes by serotonergic mechanisms, and counter-regulation by atypical antipsychotic drugs. Diabetologia. 2007;50:1743-51 pubmed
product information
brand :
Tocris, a Bio-Techne brand
catalog number base :
1661
SKU :
1661/10
product name :
SB 206553 hydrochloride
description :
Potent and selective 5-HT2B and 5-HT2C antagonist; orally active
target :
5-HT2C Receptor Antagonists
unit size :
10 mg (also 50 mg)
category :
Small Molecules
purity :
99%
storage :
Desiccate at RT
observed molecular weight :
328.8
url print :
?utm_source=biocompare&utm_medium=referral&utm_campaign=product&utm_term=smallmolecules
details of functionality :
SB 206553 hydrochloride is a potent and selective 5-HT2B/5-HT2C receptor antagonist (rat 5-HT2B pA2 = 8.89, human 5-HT2C pKi = 7.92). Displays 80-fold selectivity over all other 5-HT receptor subtypes and a variety of other receptors (pKi 6). Centrally active following oral administration in vivo .
product keywords :
Potent selective 5-HT2C/5-HT2B antagonists Serotonin 5-HT2B Receptors 5-HT2C SB206553 hydrochloride GlaxoSmithKline GSK 5-HT2C Receptors 5-HT2B Receptors 1661,
extended description :
Potent and selective 5-HT2B and 5-HT2C antagonist; orally active
chemical name text :
3,5-Dihydro-5-methyl-N-3-pyridinylbenzo[1,2-b:4,5-b ]dipyrrole-1(2H)-carboxamide hydrochloride
formula :
C17H16N4O.HCl
formula text :
C17H16N4O.HCl
cas num :
1197334-04-5
USD :
296
USD 2025 :
299 USD
product details :
Potent and selective 5-HT2B and 5-HT2C antagonist; orally active
more info or order :
company information
Tocris Bioscience
The Watkins Building
Atlantic Road
Avonmouth, Bristol
BS11 9QD
info@bio-techne.com
https://www.tocris.com
800-343-7475
headquarters: UK