Tasimelteon

CHEMBL2103822 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
245.3 g/mol
LogP
2.2
Phase
4

Tasimelteon is a selective melatonin receptor agonist (MT1 and MT2) approved for the treatment of non-24-hour sleep-wake disorder, a circadian rhythm disorder particularly prevalent in totally blind individuals without light perception. It synchronizes the circadian clock by mimicking the endogenous action of melatonin on suprachiasmatic nucleus receptors. It is also being studied for major depressive disorder and other circadian-related conditions.

Khối lượng phân tử

245,3200 g/mol

LogP

2,20

TPSA

38,30 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Cơ chế tác dụng

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Cấu trúc 2D

SVG PNG

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SMILES

CCC(=O)NC[C@@H]1C[C@H]1c1cccc2c1CCO2

InChI

InChI=1S/C15H19NO2/c1-2-15(17)16-9-10-8-13(10)11-4-3-5-14-12(11)6-7-18-14/h3-5,10,13H,2,6-9H2,1H3,(H,16,17)/t10-,13+/m0/s1

Molecular Formula

C15H19NO2

HBD / HBA

1 / 2

Liên kết có thể quay

4

Nguyên tử nặng

18

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.

Câu hỏi thường gặp

Tasimelteon is a selective melatonin receptor agonist (MT1 and MT2) approved for the treatment of non-24-hour sleep-wake disorder, a circadian rhythm disorder particularly prevalent in totally blind individuals without light perception. It synchronizes the circadian clock by mimicking the endogenous action of melatonin on suprachiasmatic nucleus receptors. It is also being studied for major depressive disorder and other circadian-related conditions.

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Yes, Tasimelteon 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). CHEMBL2103822. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 10220503. Chemical information database.

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

Tuyên bố miễn trách y tế

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.