2-chloro-6-[(2R)-2-hydroxy-3-{[2-methyl-1-(naphthalen-2-yl)propan-2-yl]amino}propoxy]benzonitrile

• ChemBase编号: 73115
• 分子式: C24H25ClN2O2
• 平均质量: 408.9205
• 单一同位素质量: 408.16045573
• SMILES: c1(cccc(c1C#N)OC[C@@H](CNC(Cc1ccc2c(c1)cccc2)(C)C)O)Cl
• Canonical SMILES: N#Cc1c(cccc1Cl)OC[C@@H](CNC(Cc1ccc2c(c1)cccc2)(C)C)O
• InChI: InChI=1S/C24H25ClN2O2/c1-24(2,13-17-10-11-18-6-3-4-7-19(18)12-17)27-15-20(28)16-29-23-9-5-8-22(25)21(23)14-26/h3-12,20,27-28H,13,15-16H2,1-2H3/t20-/m1/s1
• InChIKey: PZUJQWHTIRWCID-HXUWFJFHSA-N

名称和登记号

名称

• IUPAC标准名: 2-chloro-6-[(2R)-2-hydroxy-3-{[2-methyl-1-(naphthalen-2-yl)propan-2-yl]amino}propoxy]benzonitrile
• IUPAC传统名: 2-chloro-6-[(2R)-2-hydroxy-3-{[2-methyl-1-(naphthalen-2-yl)propan-2-yl]amino}propoxy]benzonitrile
• 别名: NPS2143; NPS-2143

登记号

• CAS号: 284035-33-2
• PubChem SID: 162038035
• PubChem CID: 6918446

理论计算性质

• Acid pKa: 14.087248
• 质子受体: 4
• 质子供体: 2
• LogD (pH = 5.5): 1.8088325
• LogD (pH = 7.4): 2.9092243
• Log P: 4.9807396
• 摩尔折射率: 116.6093 cm^3
• 极化性: 46.79733 Å^3
• 极化表面积: 65.28 Å^2
• 可自由旋转的化学键: 8
• 里宾斯基五规则: true

分子性质

安全信息

• 保存条件: -20°C

药理学性质

• 作用靶点: Calcium channel

产品相关信息

• 成盐信息: Free Base

详细说明

Selleck Chemicals - S2633

Biological Activity

• Description: NPS 2143 is a novel potent and selective antagonist of Ca(2+) receptor with IC50 of 43 nM in HEK 293 cells.
• Targets: Ca(2+) receptor
• IC50: 43 nM ^[1]
• In Vitro: NPS 2143 blocks increases in cytoplasmic Ca^2+ concentrations with IC50 of 43 nM elicited by activating the Ca^2+ receptor in HEK 293 cells expressing the human Ca^2+ receptor. ^[1] NPS 2143 stimulates parathyroid hormone (PTH) secretion from bovine parathyroid cells with EC50 of 41 nM. Moreover, NPS 214 also blocks the inhibitory effects of calcimimetic NPS R-467 on PTH secretion from bovine parathyroid cells and the inhibitory effects of extracellular Ca2+ on isoproterenol-stimulated increases in cyclic AMP formation. ^[1] In HEK-293 cells transiently expressing hCaSRs, NPS 2143 significantly suppresses the kokumi taste by effectively inhibiting the activity of both GSH (data not shown) and γ-Glu-Val-Gly. ^[3] A recent study shows that NPS 2143 treatment suppresses low molecular weight fractions of azuki hydrolysate-induced cholecystokinin (CCK) secretion in CaSR-transfected HEK 293 cells. ^[4]
• In Vivo: In rats, NPS 2143 results in a rapid 4- to 5-fold increase in plasma PTH levels and also a transient increase in plasma Ca^2+ levels. ^[1] In normotensive rats, NPS 2143 administration (1 mg/kg) by i.v. markedly increases mean arterial blood pressure (MAP) in the presence of parathyroid glands. ^[2]

Protocol

• Protocol: Kinase Assay ^[1]
• Assays for Assessing Potency and Selectivity of Compounds on Ca2+ Receptor: This clonal cell line, referred to as HEK 293 4.0-7 cells, are used in a high-throughput screening format to detect agonists and allosteric activators of the Ca^2+ receptor. Changes in the concentration of cytoplasmic Ca^2+([Ca2+]i) provide a quantitative and functional assessment of Ca^2+receptor activity in these cells and the results using this assay parallel those obtained using a homologous expression system of bovine parathyroid cells. On-line continuous measurements of fluorescence in fluo-3- or fura-2-loaded HEK 293 4.0-7 cells are obtained using a custom-built spectrofluorimeter or a fluorescence imaging plate reader instrument. NPS 2143 is incubated with cells for 1 minute before increasing the concentration of extracellular Ca^2+ from 1.0 mM to 1.75 mM. NPS 2143 is tested individually at a concentration of 100 μg/ml (20 μM–80 μM) and those causing more than a 40% inhibition of the control response are considered to be biologically active. To determine the potencies (IC50) of NPS 2143 with biological activity, concentration-response curves are obtained and then, as an initial assessment of selectivity, the effects of NPS 2143 on [Ca^2+]i evoked by other G protein-coupled receptors are examined at a concentration several times their IC50. Wild-type HEK 293 cells (and HEK 293 4.0-7 cells) express receptors for thrombin, bradykinin, and ATP, which couple to the mobilization of intracellular Ca^2+. These responses can be studied to quickly assess any nonselective action of compounds on G protein-coupled receptors. Additional assays for selectivity include HEK 293 cells engineered to express receptors most homologous in sequence and topology to the Ca2+ receptor. These include native or chimeric receptors for various metabotropic glutamate and γ-aminobutyric acid type B receptors (GABABRs). Chimeric receptors are created using partial sequences of metabotropic glutamate receptors and Ca^2+ receptors, engineered to couple to activation of phospholipase C and release of intracellular Ca^2+ in HEK 293 cells. NPS 2143 lacking pan-activity are then subjected to structural modifications and their potencies and selectivities monitored using these HEK 293 4.0-7 cell assays in an iterative process.
• Protocol: Animal Study ^[1]
• Animal Models: Chronic indwelling catheters are implanted in the inferior vena cava and in the abdominal aorta of male Sprague-Dawley rats.
• Formulation: NPS 2143 is dissolved in 20% aqueous solution of 2-hydroxypropyl-β-cyclodextrin.
• Doses: ≤0.1 μmol/kg · min
• Administration: Administered via i.v.

References

• References: [1] Nemeth EF, et al. J Pharmacol Exp Ther. 2001, 299(1), 323-331.
• References: [2] Rybczynska A, et al. J Endocrinol. 2006, 191(1), 189-195.
• References: [3] Ohsu T, et al. J Biol Chem. 2010, 285(2), 1016-1022.
• References: [4] Nakajima S, et al. Mol Nutr Food Res. 2012, 56(5), 753-760.

参考文献

• Nemeth EF, et al. J Pharmacol Exp Ther. 2001, 299(1), 323-331.
• Rybczynska A, et al. J Endocrinol. 2006, 191(1), 189-195.
• Ohsu T, et al. J Biol Chem. 2010, 285(2), 1016-1022.
• Nakajima S, et al. Mol Nutr Food Res. 2012, 56(5), 753-760.