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SB 204741

SIGMA/S0693 - >98% (HPLC)

Synonym: N-(1-Methyl-1H-5-indolyl)-N′-(3-methyl-5-isothiazolyl)urea

CAS Number: 152239-46-8
Empirical Formula (Hill Notation): C14H14N4OS
Molecular Weight: 286.35
MDL Number: MFCD00923644
Linear Formula: C14H14N4OS
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-S0693-10MG 10 mg
$236.00
1/EA
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45-S0693-50MG 50 mg
$946.00
1/EA
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assay >98% (HPLC)
color off-white to tan
form solid
InChI 1S/C14H14N4OS/c1-9-7-13(20-17-9)16-14(19)15-11-3-4-12-10(8-11)5-6-18(12)2/h3-8H,1-2H3,(H2,15,16,19)
InChI key USFUFHFQWXDVMH-UHFFFAOYSA-N
originator GlaxoSmithKline
Quality Level 100 
SMILES string Cc1cc(NC(=O)Nc2ccc3n(C)ccc3c2)sn1
solubility DMSO: soluble >20 mg/mL
storage temp. 2-8°C
Application: SB 204741 has been used as a 5-hydroxytryptamine receptor 2B (Htr2B) antagonist:
• to inhibit Htr2b signaling to test its effect on hepatic stellate cell (HSC) activation in three-month-old adult zebrafish
• to test its effect on the inhibition of fluoxetine effects in depressive-like behavioral studies in mice
• to test its effect in reducing scratching behavior evoked by sertraline in mice

Biochem/physiol Actions: 5-HT2B serotonin receptor antagonist.
Biochem/physiol Actions: SB 204741 reduces the synaptic facilitation induced by the low dose of buprenorphine in spinal C-fiber synapses.
Features and Benefits: This compound was developed by GlaxoSmithKline . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
Legal Information: Sold for research purposes under agreement from Glaxo­Smith­Kline
Packaging: 10, 50 mg in glass bottle
Purity >98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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