Calhex 231
Synonym(s):4-Chloro-N-[(1S,2S)-2-[[(1R)-1-(1-naphthalenyl)ethyl]amino]cyclohexyl]-benzamide hydrochloride
- CAS NO.:652973-93-8
- Empirical Formula: C25H27ClN2O
- Molecular Weight: 406.95
- MDL number: MFCD18252543
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-04-24 14:58:55
What is Calhex 231?
Chemical properties
White Solid
The Uses of Calhex 231
Calhex 231 hydrochloride has been used:
- as a calcium-sensing receptor (CaSR) antagonist: to test its impact on hearing in rats
- to test its effect on blood pressure levels spontaneous hypertensive rats (SHRs)
- to test its effect on acoustic response bias in zebrafish
- in Caco-2 cells to test its effect on, overexpression of fibroblast growth factor-23 (FGF-23 )
The Uses of Calhex 231
A new calcium sensing receptor ligand demonstrating potent calcilytic activity.
What are the applications of Application
Calhex 231 is an inhibitor of the CaSR via negative allosteric modulation
Biological Activity
calhex 231 hydrochloride is a novel potent negative allosteric modulator of ca2+-sensing receptor (casr) with an ic50 value of 0.39 μm to the increase in [3h]inositol phosphates induced by transiently expressed human wild-type casr in hek293 cells [1].the casr belongs to g-protein-coupled receptor (gpcr) class 3. casr is activated by charged molecules including spermidine, spermine, β-amyloid peptides, and several antibiotics. casr is also activated by mg2+ and ca2+ present in the extracellular fluids [1].in hek293 cells transiently expressing human wt casr, increasing the concentration of extracellular ca2+ from 0.3 to 10 mm resulted in a 10-fold increase in [3h]ip accumulation, while no significant increase in [3h]ip accumulation was detected in cells transiently transfected with an empty control plasmid. the analysis of the dose-response curve resulted in an ec50 value of 3.4 ± 0.1 mm for ca2+. preincubation with calhex 231 concentration-dependently inhibited the ip response to 10 mm ca2+ in hek293 cells expressing the human wt casr. the analysis of the dose-response curve resulted in an ic50 value of 0.39 ± 0.08 μm for calhex 231 [1].calhex 231 produced significant myocyte depolarizations in segments of mesenteric arteries from both zucker diabetic fatty (zdf) and zucker lean (zl) rats. in the continuing presence of calhex 231, hyperpolarizations to the calcium-sensing receptor (car) activator calindol were significantly reduced [2].
Biochem/physiol Actions
Calhex 231 is a negative allosteric modulator of the calcium sensing receptor CaSR. Calhex 231 blocks calcium-induced accumulation of inositol phosphate with an IC50 of 0.36 μM.
References
[1]. petrel c, kessler a, maslah f, et al. modeling and mutagenesis of the binding site of calhex 231, a novel negative allosteric modulator of the extracellular ca2+-sensing receptor. journal of biological chemistry, 2003, 278(49): 49487-49494.
[2]. weston ah, absi m, harno e, et al. the expression and function of ca2+-sensing receptors in rat mesenteric artery; comparative studies using a model of type ii diabetes. british journal of pharmacology, 2008, 154(3): 652-662.
Properties of Calhex 231
| Melting point: | 53-55°C |
| storage temp. | -20°C Freezer |
| solubility | DMSO: soluble15mg/mL, clear |
| form | powder |
| color | white to beige |
| CAS DataBase Reference | 652973-93-8 |
Safety information for Calhex 231
Computed Descriptors for Calhex 231
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