> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/dexamethasone-acetate-ece3cebe-986f-4ed0-9012-978d011e1c59
> Record changed: 2026-11-04

# Dexamethasone acetate

Highest phase reached

Approved

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

Drug type

Small molecule

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

First approval year

1973

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

## Development status

**First approval year**

1973

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

**Listing at source**

Listed

**Highest phase reached**

Approved

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

## Names and chemistry

**Drug type**

Small molecule

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

**Drug name**

Dexamethasone acetate

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

**Molecular weight**

434.5

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

**Structure (SMILES)**

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

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

### Brand names (6)

- decadron la
- Decadron-la
- dexamethasone acetate
- Dexamethasone acetate
- neofordex
- Neofordex

### Other names (40)

- BETAMETHASONE ACETATE IMPURITY B \[EP IMPURITY\]
- betamethasone acetate impurity b ep impurity
- decadronal
- DECADRONAL
- dectancyl
- Dectancyl
- dexamethasone 21 acetate
- dexamethasone 21 acetate mi
- Dexamethasone 21-acetate
- DEXAMETHASONE 21-ACETATE \[MI\]
- dexamethasone acetate
- Dexamethasone acetate
- DEXAMETHASONE ACETATE \[EP MONOGRAPH\]
- DEXAMETHASONE ACETATE \[USP MONOGRAPH\]
- DEXAMETHASONE ACETATE \[USP-RS\]
- Dexamethasone acetate \[WHO-DD\]
- DEXAMETHASONE ACETATE \[WHO-IP\]
- dexamethasone acetate anhydrous
- Dexamethasone acetate anhydrous
- dexamethasone acetate ep monograph
- dexamethasone acetate monohydrate
- Dexamethasone acetate monohydrate
- dexamethasone acetate usp monograph
- dexamethasone acetate usp rs
- dexamethasone acetate who dd

And 15 more, listed on the interactive page.

## Identifiers

**CAS registry numbers**

- 1177-87-3

**ChEMBL ID**

CHEMBL1530428

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

**InChIKey**

AKUJBENLRBOFTD-RPRRAYFGSA-N

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1530428)

**PubChem compound IDs**

- 236702

**FDA ingredient codes (UNII)**

- K7V8P532WP

### RxNorm IDs (RxCUI) (2)

- 22690
- 2378841

## Regulatory information

### United States

**Applicant**

MERCK

**Approval date**

6 Sept 1973

**Application number**

NDA016675

### Other regulatory facts

**First in class**

No

**Orphan designation**

No

**Availability**

discontinued

## Approval status

**United States (FDA)**

Approved

## Pharmacology

### Drug classification

#### Administration routes

- Parenteral

### Mechanisms of action

- **Mechanism**  
Glucocorticoid receptor agonist

**Action type**  
Agonist

**Target**  
Glucocorticoid receptor

**Protein identifier**  
P04150

### Open Targets mechanisms

- **Mechanism**  
Glucocorticoid receptor agonist

**Action type**  
Agonist

**Target**  
Glucocorticoid receptor

### DrugCentral mechanisms

- **Action type**  
Agonist

**Gene symbol**  
NR3C1

**Protein identifier**  
P04150

**Organism**  
Homo sapiens

**Target development level**  
Clinical

### Investigated indications (5)

- **Condition**  
Leukemia

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000565

**Subject identifier**  
D007938
- **Condition**  
Lymphoma

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0000574

**Subject identifier**  
D008223
- **Condition**  
Multiple Myeloma

**Highest recorded phase**  
4

**Condition identifier**  
EFO:0001378

**Subject identifier**  
D009101
- **Condition**  
Pancreatitis

**Highest recorded phase**  
2

**Condition identifier**  
EFO:1000652

**Subject identifier**  
D010195
- **Condition**  
Tooth Diseases

**Highest recorded phase**

0.5

**Condition identifier**  
EFO:1001216

**Subject identifier**  
D014076

### Open Targets indications (4)

- **Condition identifier**  
EFO\_0001378

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_1000652

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_1001216
- **Condition identifier**  
MONDO\_0009693

**Highest recorded phase**  
2

### Reported adverse events (30)

- **Event**  
anaphylactic shock

**Reports**  
7

**Reporting signal score**

9.52004
- **Event**  
aphthous ulcer

**Reports**  
6

**Reporting signal score**

15.8134
- **Event**  
arterial thrombosis limb

**Reports**  
3

**Reporting signal score**

12.8005
- **Event**  
cheilitis

**Reports**  
6

**Reporting signal score**

17.1869
- **Event**  
conjunctival irritation

**Reports**  
6

**Reporting signal score**

36.3485
- **Event**  
drug reaction with eosinophilia and systemic symptoms

**Reports**  
17

**Reporting signal score**

32.9663
- **Event**  
eosinophilia

**Reports**  
8

**Reporting signal score**

13.0952
- **Event**  
febrile bone marrow aplasia

**Reports**  
428

**Reporting signal score**

887.334
- **Event**  
febrile neutropenia

**Reports**  
1,923

**Reporting signal score**  
2,236.59
- **Event**  
genital erythema

**Reports**  
6

**Reporting signal score**

33.0206
- **Event**  
hepatic cytolysis

**Reports**  
6

**Reporting signal score**

17.8414
- **Event**  
hypertriglyceridaemia

**Reports**  
5

**Reporting signal score**

10.6017
- **Event**  
hyphaema

**Reports**  
3

**Reporting signal score**

12.1652
- **Event**  
interstitial lung disease

**Reports**  
11

**Reporting signal score**

12.8394
- **Event**  
meningioma

**Reports**  
4

**Reporting signal score**

10.8036
- **Event**  
necrotising ulcerative gingivostomatitis

**Reports**  
5

**Reporting signal score**

32.1315
- **Event**  
neuropathy peripheral

**Reports**  
1,605

**Reporting signal score**  
1,287.82
- **Event**  
neutropenia

**Reports**  
2,480

**Reporting signal score**  
1,836.89
- **Event**  
neutrophil count decreased

**Reports**  
10

**Reporting signal score**

12.2349
- **Event**  
pigmentary glaucoma

**Reports**  
2

**Reporting signal score**

13.682
- **Event**  
plasma cell myeloma

**Reports**  
1,660

**Reporting signal score**  
2,960.49
- **Event**  
platelet count decreased

**Reports**  
14

**Reporting signal score**

10.8644
- **Event**  
polyneuropathy

**Reports**  
8

**Reporting signal score**

16.7452
- **Event**  
pyrexia

**Reports**  
29

**Reporting signal score**

14.9648
- **Event**  
rash erythematous

**Reports**  
12

**Reporting signal score**

19.7153

And 5 more, listed on the interactive page.

### Trial references (8)

- NCT00635154  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00635154)
- NCT01916252  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01916252)
- NCT05052970  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05052970)
- NCT00651261  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00651261)
- NCT01247961  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01247961)
- NCT01421173  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01421173)
- NCT01878708  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01878708)
- NCT02837614  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02837614)

## Chemical properties

**Hydrogen bond acceptors**

6

**Hydrogen bond donors**

2

**Polar surface area**

100.9

**Calculated partition coefficient (ALogP)**

2.47

**Calculated partition coefficient (XLogP)**

2.8

**Prodrug**

No

**Chirality**

Single enantiomer

**Inorganic**

No

**Rule-of-five violations**

0

**Rotatable bonds**

3

**Heavy atoms**

31

**Molecular formula**

C24H31FO6

**Monoisotopic mass**

434.21046687

**Natural product**

No

## Evidence counts

**Recorded assays**

2,086

**Active assays**

63

### Active assay types (4)

- Confirmatory
- Other
- Screening
- Summary

## Pharmacologic actions

- Anti-Inflammatory Agents  
Source: [id.nlm.nih.gov](https://id.nlm.nih.gov/mesh/D000893.html)

## Related records

### Trials (83)

- A Long-Term Safety Study of OZURDEX® in Clinical Practice
- A Phase I Study of Episcleral Dexamethasone for Treatment of Macular Edema
- A Phase III, Non-Inferiority, Randomized, Open-Label, Parallel Group, Multicenter Study To Investigate The Pharmacokinetics, Pharmacodynamics, Safety And Radiological And Clinical Effects Of Subcutaneous Ocrelizumab Versus Intravenous Ocrelizumab In Patients With Multiple Sclerosis
- A Prospective Controlled Treatment Trial for Post-Traumatic Headaches
- A Study Evaluating the Efficacy and Safety of Giredestrant Plus Everolimus Compared With the Physician's Choice of Endocrine Therapy Plus Everolimus in Participants With Estrogen Receptor-Positive, HER2-Negative, Locally Advanced or Metastatic Breast Cancer (evERA Breast Cancer)
- [A Study of MK-5684 in People With Certain Solid Tumors (MK-5684-015/OMAHA-015)](https://trialight.com/data/trial/a-study-of-mk-5684-in-people-with-certain-solid-tumors-mk-461c8734-405e-4e5a-93a0-93cbf569e545.md)
- A Study of Romiplostim N01 as the First-line Treatment for Newly Diagnosed Adult Patients With ITP
- A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulting From Retinal Vein Occlusion
- A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulting From Retinal Vein Occlusion
- A Two Chemoprophylaxis Approaches After Phacoemulsification Surgery
- An Observational Study of OZURDEX® in Diabetic Macular Edema (DME)
- Analgesic Efficacy of Dexamethasone in Different Routes of Administration in Transverse Abdominis Plane Block
- Anosmia and / or Ageusia and Early Corticosteroid Use
- Bioequivalence of Two Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspensions in Otitis Media in Children With Tympanostomy Tubes
- Comparing DCP and DAP for Pemphigus Vulgaris
- Comparing Single Dose and Multiple Dose of Dexamethasone Post TKA
- Comparing Subsartorial Saphenous Nerve Blocks With and Without Dexamethasone for Anterior Cruciate Ligament Reconstruction
- Comparison of Acetaminophen With Aminophylline and Aminophylline With Dexamethasone for Prophylaxis of PDPH in Patients With History of PDPH.
- Comparison of Analgesic Consumption Between Perioperative ıv Dexamethasone and Added to Femoral Block
- Comparison of Dexamethasone Oral Preparations to Assess Taste and Acceptance in Children With Asthma and Croup

### Approved for (1)

- [Plasma cell myeloma](https://trialight.com/data/condition/plasma-cell-myeloma-37186689-2591-5775-9042-2f2bf046a2b5.md)

### In development for (4)

- Acute pancreatitis Phase 2
- [Leukemia](https://trialight.com/data/condition/leukemia-519aefcd-8521-5941-851b-5b77ca925ca5.md) Phase 3
- [Lymphoma](https://trialight.com/data/condition/lymphoma-de4db685-7419-5e0e-b958-4591ffd69d43.md) Phase 1
- Tooth disorder Early phase 1

### Targets (1)

- [NR3C1](https://trialight.com/data/target/nr3c1-98974b8d-fb89-5483-955e-d4a994c71532.md) Glucocorticoid receptor agonist

---

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