Cinacalcet Hydrochloride

CHEMBL1200776 Phase 4 승인됨 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
393.9 g/mol
LogP
Phase
4

The hydrochloride salt form of cinacalcet is the standard oral preparation used in patients with chronic kidney disease on dialysis to control secondary hyperparathyroidism. It should be taken with food to maximize absorption. Nausea and vomiting are common initial side effects that often improve with dose titration.

분자량

393.9000 g/mol

TPSA

12.00 Ų

치료 영역

작용 기전

Mimics or modulates parathyroid hormone activity to stimulate osteoblast-mediated bone formation, increasing bone mineral density and reducing fracture risk.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

기전

Mimics or modulates parathyroid hormone activity to stimulate osteoblast-mediated bone formation, increasing bone mineral density and reducing fracture risk.

2D 구조

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SMILES

C[C@@H](NCCCc1cccc(C(F)(F)F)c1)c1cccc2ccccc12.Cl

InChI

InChI=1S/C22H22F3N.ClH/c1-16(20-13-5-10-18-9-2-3-12-21(18)20)26-14-6-8-17-7-4-11-19(15-17)22(23,24)25;/h2-5,7,9-13,15-16,26H,6,8,14H2,1H3;1H/t16-;/m1./s1

Molecular Formula

C22H23ClF3N

HBD / HBA

2 / 4

회전 가능 결합

6

무거운 원자

27

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

자주 묻는 질문

The hydrochloride salt form of cinacalcet is the standard oral preparation used in patients with chronic kidney disease on dialysis to control secondary hyperparathyroidism. It should be taken with food to maximize absorption. Nausea and vomiting are common initial side effects that often improve with dose titration.

Mimics or modulates parathyroid hormone activity to stimulate osteoblast-mediated bone formation, increasing bone mineral density and reducing fracture risk.

Yes, Cinacalcet Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200776. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 156418. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

의학적 면책조항

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.