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Dibotermin Alfa

CHEMBL2109171 Phase 4 Approved Protein
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
— g/mol
LogP
—
Phase
4

A recombinant human bone morphogenetic protein-2 (rhBMP-2) used to promote bone formation and healing. It is used in spinal fusion surgery and bone repair procedures.

Therapeutic Areas

Hypertension Osteoporosis

Mechanism of Action

As a recombinant protein, it replicates the function of the naturally occurring human protein, supplementing or replacing deficient endogenous production to restore normal physiological activity.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

As a recombinant protein, it replicates the function of the naturally occurring human protein, supplementing or replacing deficient endogenous production to restore normal physiological activity.

HBD / HBA

- / -

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.

Frequently Asked Questions

A recombinant human bone morphogenetic protein-2 (rhBMP-2) used to promote bone formation and healing. It is used in spinal fusion surgery and bone repair procedures.

As a recombinant protein, it replicates the function of the naturally occurring human protein, supplementing or replacing deficient endogenous production to restore normal physiological activity.

Yes, Dibotermin Alfa is an approved drug. It has reached clinical phase 4. It is classified as a Protein.

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2109171. Open-access bioactivity database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-02-27.

Medical Disclaimer

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.