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Velusetrag hydrochloride

Chemical Structure : Velusetrag hydrochloride

CAS No.: 866933-51-9

Velusetrag hydrochloride (TD-5108 hydrochloride)

Catalog No.: PC-62095Not For Human Use, Lab Use Only.

Velusetrag (TD-5108) is a potent, selective and oral 5-HT4 receptor agonist with pKi of 7.7, shows >500-fold selectivity over other 5-HT receptors.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    Velusetrag (TD-5108) hydrochloride is a potent, selective and oral 5-HT4 receptor agonist with pKi of 7.7, shows >500-fold selectivity over other 5-HT receptors.
    Velusetrag (TD-5108) displays >25-fold selectivity over other biogenic amine receptors, and no effect on hERG channels.
    Velusetrag (TD-5108) increases the contractility of the canine antrum, duodenum and jejunum with higher potency than tegaserod, demonstrates robust in vivo activity in the guinea pig, rat and dog gastrointestinal tracts.

    Physicochemical Properties

    M.Wt 541.104
    Formula C25H37ClN4O5S
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20 °C 12 Months; 4°C 6 Months
    In Solvent
    -80 °C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    N-((1R,3R,5S)-8-((R)-2-hydroxy-3-(N-methylmethylsulfonamido)propyl)-8-azabicyclo[3.2.1]octan-3-yl)-1-isopropyl-2-oxo-1,2-dihydroquinoline-3-carboxamide hydrochloride

    References

    1. Beattie DT, et al. Naunyn Schmiedebergs Arch Pharmacol. 2008 Jul;378(1):139-47.

    2. Smith JA, et al. Naunyn Schmiedebergs Arch Pharmacol. 2008 Jul;378(1):125-37.

    3. Manini ML, et al. Neurogastroenterol Motil. 2010 Jan;22(1):42-9, e7-8.

    4. Long DD, et al. Bioorg Med Chem Lett. 2012 Oct 1;22(19):6048-52.

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