Fludrocortisone Acetate

CHEMBL1201010 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
422.5 g/mol
LogP
1.7
Phase
4

This acetate salt form of fludrocortisone is a synthetic steroid hormone used to replace the mineralocorticoid function of the adrenal glands in patients with adrenal insufficiency. It helps maintain blood pressure and electrolyte balance by promoting sodium retention in the kidneys.

分子量

422.5000 g/mol

LogP

1.70

TPSA

101.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

Provides an essential mineral element required for numerous enzymatic reactions, structural proteins, and physiological processes. Supplementation addresses deficiency states.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Provides an essential mineral element required for numerous enzymatic reactions, structural proteins, and physiological processes. Supplementation addresses deficiency states.

2D構造

SVG PNG

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SMILES

CC(=O)OCC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C

InChI

InChI=1S/C23H31FO6/c1-13(25)30-12-19(28)22(29)9-7-16-17-5-4-14-10-15(26)6-8-20(14,2)23(17,24)18(27)11-21(16,22)3/h10,16-18,27,29H,4-9,11-12H2,1-3H3/t16-,17-,18-,20-,21-,22-,23-/m0/s1

Molecular Formula

C23H31FO6

HBD / HBA

2 / 7

回転可能結合数

4

重原子数

30

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.

よくある質問

This acetate salt form of fludrocortisone is a synthetic steroid hormone used to replace the mineralocorticoid function of the adrenal glands in patients with adrenal insufficiency. It helps maintain blood pressure and electrolyte balance by promoting sodium retention in the kidneys.

Provides an essential mineral element required for numerous enzymatic reactions, structural proteins, and physiological processes. Supplementation addresses deficiency states.

Yes, Fludrocortisone Acetate 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). CHEMBL1201010. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 225609. Chemical information database.

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

医学的免責事項

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.