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Compound Detail

CHEMBL1201010

FLUDROCORTISONE ACETATE
💊 Approved Drug
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💊 Approved Drug
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

Basic Information

ChEMBL ID CHEMBL1201010
Name FLUDROCORTISONE ACETATE
Phase Approved
Structure Type MOL
InChI Key SYWHXTATXSMDSB-GSLJADNHSA-N
Therapeutic ✓ Yes
Active Moiety CHEMBL1201388

Known Names

Astonin Florinef Fludrocortisona Fludrocortisone 21-acetate Fludrocortisone acetate Fludrocortisoni acetas Fludrocortone Fluorocortisol acetate NSC-15186 Panotile Scherofluron
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
20
Publications
11
Known Names
15
Indications
1
Mechanisms

Molecular Properties

422.5
MW (Da)
2.44
ALogP
6
HBA
2
HBD
100.9
PSA (Ų)
0.68
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
First Approval 1955
Availability Prescription
Chirality Single Enantiomer

Routes of Administration

Oral

Flags

Prodrug
USAN Stem -cort-

Extended Properties

Molecular Formula C23H31FO6
MW 422.49
Aromatic Rings 0
Heavy Atoms 30
NP-Likeness 1.90

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Mineralocorticoid receptor agonist AGONIST Mineralocorticoid receptor

Indications

Addison Disease Addison Disease Adrenogenital Syndrome Prostatic Neoplasms Prostatic Neoplasms Severe Acute Respiratory Syndrome Severe Acute Respiratory Syndrome Shock, Septic Adrenal Hyperplasia, Congenital Melanoma Ovarian Hyperstimulation Syndrome Parkinson Disease Subarachnoid Hemorrhage Depressive Disorder Hearing Loss, Sensorineural

ATC Classification

H02AA02
fludrocortisone
Level 1: SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS
Level 2: CORTICOSTEROIDS FOR SYSTEMIC USE

Activity Summary

IC50 1 meas. best 7.7
Ki 1 meas. best 8.03

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Glucocorticoid receptor
CHEMBL2034
Ki 8.03 8.03 9.3 1
Glucocorticoid receptor
CHEMBL2034
IC50 7.7 7.7 20.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL3885881 Rattus norvegicus 273
- 10.6019/CHEMBL4689842 HEK-293T 10
- 10.6019/CHEMBL4689842 U2OS 8
- 10.6019/CHEMBL4689842 Fibroblast 6
- 10.6019/CHEMBL4495565 SARS-CoV-2 4
37468498 10.1038/s41467-023-40064-9 Nuclear receptor subfamily 1 group I member 2 3
37468498 10.1038/s41467-023-40064-9 Beta-1 adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 Alpha-1A adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 Beta-2 adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2A 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2B 2
37468498 10.1038/s41467-023-40064-9 Gamma-aminobutyric acid receptor subunit alpha-1 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 1A 2
- 10.6019/CHEMBL4808148 Histone deacetylase 6 2
- 10.6019/CHEMBL4495564 Replicase polyprotein 1ab 2
37468498 10.1038/s41467-023-40064-9 Alpha-2A adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 Androgen receptor 2
37468498 10.1038/s41467-023-40064-9 Muscarinic acetylcholine receptor M2 2
37468498 10.1038/s41467-023-40064-9 Cannabinoid receptor 1 2
20843939 10.1124/dmd.110.035113 Hepatotoxicity 1

Data from ChEMBL 36 via Core Engine