Serdexmethylphenidate

CHEMBL4301162 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
499.5 g/mol
LogP
2.2
Phase
4

Serdexmethylphenidate is a prodrug of d-methylphenidate designed to provide an extended-duration, abuse-deterrent formulation for the treatment of attention deficit hyperactivity disorder (ADHD). The prodrug is cleaved by gut enzymes to release d-methylphenidate, which inhibits dopamine and norepinephrine reuptake transporters in the prefrontal cortex and striatum, enhancing executive function and attention. The prodrug design confers reduced abuse potential because parenteral administration does not provide rapid dopamine surge.

น้ำหนักโมเลกุล

499.5000 g/mol

LogP

2.20

TPSA

149.00 Ų

Lipinski RO5

ผ่าน

กลไกการออกฤทธิ์

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

กลไก

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

โครงสร้าง 2 มิติ

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SMILES

COC(=O)[C@H](c1ccccc1)[C@H]1CCCCN1C(=O)OC[n+]1cccc(C(=O)N[C@@H](CO)C(=O)O)c1

InChI

InChI=1S/C25H29N3O8/c1-35-24(33)21(17-8-3-2-4-9-17)20-11-5-6-13-28(20)25(34)36-16-27-12-7-10-18(14-27)22(30)26-19(15-29)23(31)32/h2-4,7-10,12,14,19-21,29H,5-6,11,13,15-16H2,1H3,(H-,26,30,31,32)/p+1/t19-,20+,21+/m0/s1

Molecular Formula

C25H29N3O8

HBD / HBA

2 / 8

พันธะที่หมุนได้

10

อะตอมหนัก

36

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.

คำถามที่พบบ่อย

Serdexmethylphenidate is a prodrug of d-methylphenidate designed to provide an extended-duration, abuse-deterrent formulation for the treatment of attention deficit hyperactivity disorder (ADHD). The prodrug is cleaved by gut enzymes to release d-methylphenidate, which inhibits dopamine and norepinephrine reuptake transporters in the prefrontal cortex and striatum, enhancing executive function and attention. The prodrug design confers reduced abuse potential because parenteral administration does not provide rapid dopamine surge.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Serdexmethylphenidate 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). CHEMBL4301162. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 134823895. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.