Cinacalcet hydrochloride
Modify Date: 2024-01-01 23:39:43
Cinacalcet hydrochloride structure
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Common Name | Cinacalcet hydrochloride | ||
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| CAS Number | 364782-34-3 | Molecular Weight | 393.873 | |
| Density | N/A | Boiling Point | 440.9ºCat760mmHg | |
| Molecular Formula | C22H23ClF3N | Melting Point | 175-177ºC | |
| MSDS | N/A | Flash Point | 220.5ºC | |
Use of Cinacalcet hydrochlorideCinacalcet hydrochloride is an orally active, allosteric agonist of Ca receptor (CaR), used for cardiovascular disease treatment. |
| Name | cinacalcet hydrochloride |
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| Synonym | More Synonyms |
| Description | Cinacalcet hydrochloride is an orally active, allosteric agonist of Ca receptor (CaR), used for cardiovascular disease treatment. |
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| Related Catalog | |
| In Vivo | Cinacalcet HCl (5 and 10 mg/kg) results in a significant reduction in parathyroid gland weight in 5/6 nephrectomy animals. In sham animals, Cinacalcet HCl has no effect on parathyroid gland cell proliferation or parathyroid weight compared with vehicle treatment. There are no differences in serum phosphorus levels in Cinacalcet HCl (10, 5, or 1 mg/kg) treated 5/6 nephrectomized animals compared with vehicle-treated 5/6 nephrectomized animals. Cinacalcet HCl treatment significantly reduces blood ionized calcium levels in sham animals[1]. Cinacalcet (30 mg/kg/24 h) leads to a marked reduction in circulating parathyroid hormone and a modest reduction in serum Ca. Cinacalcet does not alter UCa when the GHS rats are fed the normal Ca diet but lowers UCa when they are fed the low Ca diet. Cinacalcet does not alter U supersaturation with respect to either CaOx or CaHPO4 on either diet[2]. |
| Animal Admin | To identify apoptosis in parathyroid glands from 5/6 nephrectomized or sham rats treated with vehicle [phosphate-buffered saline (PBS)] or cinacalcet HCl (10 mg/kg), nuclear DNA fragmentation is measured in situ using the Apoptag System. Briefly, parathyroid gland sections from animals treated with vehicle or cinacalcet HCl are digested with 20 μg/mL proteinase K in 0.1 mol/L PBS at room temperature for 15 minutes and incubated with 3% hydrogen peroxide/methanol for 5 minutes to block endogenous peroxidase. Sections are incubated for 1 hour at 37°C with terminal deoxynucleotidyl transferase (TdT) to label exposed 3′-OH DNA ends with digoxigenin-tagged nucleotides. Digoxigenin-labeled DNA is detected by the immunoperoxidase method. Sections are developed with 3,3′-diaminobenzidine (DAB), and the nuclei of apoptotic cells are stained brown. The specificity for apoptosis is verified by negative staining when distilled water is substituted for TdT. |
| References |
| Boiling Point | 440.9ºCat760mmHg |
|---|---|
| Melting Point | 175-177ºC |
| Molecular Formula | C22H23ClF3N |
| Molecular Weight | 393.873 |
| Flash Point | 220.5ºC |
| Exact Mass | 393.147125 |
| PSA | 12.03000 |
| LogP | 7.33490 |
| Storage condition | -20°C Freezer |
| Hazard Codes | C |
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| HS Code | 2921499090 |
| HS Code | 2921499090 |
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| Summary | 2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
| Cinacalcet HCl |
| 1-naphthalenemethanamine, α-methyl-N-[3-[3-(trifluoromethyl)phenyl]propyl]-, (αR)-, hydrochloride |
| N-[(1R)-1-naphthalen-1-ylethyl]-3-[3-(trifluoromethyl)phenyl]propan-1-amine,hydrochloride |
| -Naphthalenemethanamine, α-methyl-N-[3-[3-(trifluoromethyl)phenyl]propyl]-, hydrochloride (1:1), (αR)- |
| 1-Naphthalenemethanamine, α-methyl-N-[3-[3-(trifluoromethyl)phenyl]propyl]-, (αR)-, hydrochloride (1:1) |
| N-[(1R)-1-naphtalén-1-yléthyl]-3-[3-(trifluorométhyl)phényl]propan-1-amine chlorhydrate |
| (R)-N-(1-(naphthalen-1-yl)ethyl)-3-(3-(trifluoromethyl)phenyl)propan-1-amine hydrochloride |
| N-[(1R)-1-Naphthalen-1-ylethyl]-3-[3-(trifluormethyl)phenyl]propan-1-aminhydrochlorid |
| Cinacalcet hydrochloride |
| N-[(1R)-1-(1-Naphthyl)ethyl]-3-[3-(trifluoromethyl)phenyl]-1-propanamine hydrochloride (1:1) |
| N-[(1R)-1-naphthalen-1-ylethyl]-3-[3-(trifluoromethyl)phenyl]propan-1-amine hydrochloride |
| N-[(1R)-1-(1-Naphthyl)ethyl]-3-[3-(trifluoromethyl)phenyl]propan-1-amine hydrochloride (1:1) |
| Mimpara,Sensipar |