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351490-26-1

351490-26-1 Structure

351490-26-1 Structure
IdentificationBack Directory
[Name]

SB-423557
[CAS]

351490-26-1
[Synonyms]

SB-423557
SB423557,SB 423557
(R)-3-[4-Cyano-3-[2-hydroxy-3-(2-indan-2-yl-1,1-diMethylethylaMino)propoxy]phenyl]propionic acid ethyl ester
(R)-ethyl 3-(4-cyano-3-(3-((1-(2,3-dihydro-1H-inden-2-yl)-2-methylpropan-2-yl)amino)-2-hydroxypropoxy)phenyl)propanoate
Benzenepropanoic acid, 4-cyano-3-[(2R)-3-[[2-(2,3-dihydro-1H-inden-2-yl)-1,1-dimethylethyl]amino]-2-hydroxypropoxy]-, ethyl ester
[Molecular Formula]

C28H36N2O4
[MDL Number]

MFCD22665716
[MOL File]

351490-26-1.mol
[Molecular Weight]

464.6
Chemical PropertiesBack Directory
[Boiling point ]

636.8±55.0 °C(Predicted)
[density ]

1.16±0.1 g/cm3(Predicted)
[pka]

13.83±0.20(Predicted)
Hazard InformationBack Directory
[Uses]

SB-423557 is an orally active calcium-sensing receptor (CaR) antagonist (IC50=520 nM), precursor of SB-423562 (IC50=73 nM). SB-423557 is well tolerated in human and increases plasma concentrations of exogenous parathyroid hormone (PTH) and stimulates bone formation[1].
[in vivo]

SB-423557 (oral administration; 10, 30 or 100 μM/kg; once daily; 12 weeks) elicits transient increases in plasma concentrations of PTH, resulting in increased bone mass and strength in both vertebrae and long bones compared to that of OVX controls[1].

[References]

[1] Kumar S, et al. An orally active calcium-sensing receptor antagonist that transiently increases plasma concentrations of PTH and stimulates bone formation. Bone. 2010 Feb;46(2):534-42. DOI:10.1016/j.bone.2009.09.028
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