Glutethimide

CHEMBL1102 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
217.3 g/mol
LogP
1.9
Phase
4

A sedative-hypnotic medication that was formerly prescribed to treat insomnia by depressing the central nervous system, but has largely been withdrawn from clinical use due to its high potential for abuse, dependence, and dangerous overdose. It shares many of the risks associated with barbiturates and has been replaced by safer sleep medications. Illicitly, it has been abused in combination with codeine.

Khối lượng phân tử

217,2600 g/mol

LogP

1,90

TPSA

46,20 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Cơ chế tác dụng

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Cấu trúc 2D

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SMILES

CCC1(c2ccccc2)CCC(=O)NC1=O

InChI

InChI=1S/C13H15NO2/c1-2-13(10-6-4-3-5-7-10)9-8-11(15)14-12(13)16/h3-7H,2,8-9H2,1H3,(H,14,15,16)

Molecular Formula

C13H15NO2

HBD / HBA

1 / 2

Liên kết có thể quay

2

Nguyên tử nặng

16

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

A sedative-hypnotic medication that was formerly prescribed to treat insomnia by depressing the central nervous system, but has largely been withdrawn from clinical use due to its high potential for abuse, dependence, and dangerous overdose. It shares many of the risks associated with barbiturates and has been replaced by safer sleep medications. Illicitly, it has been abused in combination with codeine.

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Yes, Glutethimide 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). CHEMBL1102. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3487. Chemical information database.

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

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.