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324523-20-8

324523-20-8 Structure

324523-20-8 Structure
IdentificationBack Directory
[Name]

2-Chloro-6-[(2R)-3-[[1,1-dimethyl-2-(2-naphthalenyl)ethyl]amino]-2-hydroxypropoxy]benzonitrile hydrochloride
[CAS]

324523-20-8
[Synonyms]

NPS-2143 HCL
NPS-2143 (Mono HCl)
NPS2143;NPS 2143 HCL
SB-262470-A hydrochloride
NPS2143 hydrochloride, >=98%
2-Chloro-6-[(2R)-3-[[1,1-dimethyl-2-(2-naphthalenyl)ethyl]amino]-2-hydroxypropoxy]benzonitrile hydrochloride
2-Chloro-6-[(2R)-3-[[1,1-dimethyl-2-(2-naphthalenyl)ethyl]amino]-2-hydroxypropoxy]-benzonitrile hydrochloride (1:1)
[Molecular Formula]

C24H26Cl2N2O2
[MDL Number]

MFCD16038896
[MOL File]

324523-20-8.mol
[Molecular Weight]

445.38
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: >10mg/mL
[form ]

powder
[color ]

white to beige
[optical activity]

[α]20/D +20 to +24°, c = 1.0 in methanol
Safety DataBack Directory
[Hazard Codes ]

Xn,N
[Risk Statements ]

20/21/22-50/53
[Safety Statements ]

36/37-60-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Calcium-sensing receptor (CaSR) is a G protein-coupled receptor that is involved in calcium homeostasis. Activation of CaSR on parathyroid cells decreases the secretion of parathyroid hormone (PTH), which in turn reduces blood calcium concentration. NPS 2143 is a potent and selective antagonist of CaSR (IC50 = 43 nM) that stimulates PTH secretion from parathyroid cells in vitro (EC50 = 39 nM). It is effective in vivo, causing a sustained increase in plasma PTH in rats when given intravenously. Daily oral administration of NPS 2143 to osteopenic ovariectomized rats results in a dramatic increase in bone turnover, as well as increased circulating PTH levels.
[Uses]

NPS 2143 acts as a potent and selective antagonist for CaSR (Calcium-sensing receptor) which is involved in calcium blood concentration homeostasis.
[Biochem/physiol Actions]

NPS2143 is a phenylalkylamine calcilytic compound, and might be useful in treating autosomal dominant hypocalcemia. It serves as a blocking agent for hERG (human ether-a-go-go-related gene ) channel, CYP2D6 (cytochrome P450 2D6 ) and monoamine transporters.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-6-[(2R)-3-[[1,1-dimethyl-2-(2-naphthalenyl)ethyl]amino]-2-hydroxypropoxy]benzonitrile hydrochloride(324523-20-8)1HNMR
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