Fusidic Acid

drug
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Also known as Acide fusidiqueAcido fusidicoAnhydrous fusidic acidCEM-102Fucidin cavijectFucithalmicFusidateNSC-56192RamycinSQ 16,603SQ-16603TakstaACIDE_FUSIDIQUEC0088555Fucidin LEOFusidic acid

Summary

Fusidic Acid (CHEMBL374975) is an approved small-molecule protein synthesis inhibitor (ATC J01XC01); indicated across 6 conditions including bacterial infectious disease and eye infectious disorder.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J01XC01 (+3 more)
  • Indications: 6 conditions
  • Clinical trials: 9
  • Chemistry: 516.7 Da · C31H48O6

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL374975
NameFusidic Acid
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID3000226
ChEBICHEBI:29013
ATCJ01XC01, S01AA13, D06AX01, D09AA02
Molecular formulaC31H48O6
Molecular weight516.7
InChIKeyIECPWNUMDGFDKC-MZJAQBGESA-N

SMILES: C[C@H]1[C@@H]2CC[C@]3([C@H]([C@]2(CC[C@H]1O)C)[C@@H](C[C@@H]\4[C@@]3(C[C@@H](/C4=C(/CCC=C(C)C)\C(=O)O)OC(=O)C)C)O)C

IUPAC name: (2Z)-2-[(3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7,9,11,12,13,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ylidene]-6-methylhept-5-enoic acid

ChEBI definition: A steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum.

Pharmacological roles (ChEBI): protein synthesis inhibitor, EC 2.7.1.33 (pantothenate kinase) inhibitor.

Other ChEBI roles (chemical / environmental): Escherichia coli metabolite.

Also known as: Acide fusidique, Acido fusidico, Anhydrous fusidic acid, CEM-102, Fucidin caviject, Fucithalmic, Fusidate, Fusidic acid, NSC-56192, Ramycin, SQ 16,603, SQ-16603

Parent form; salt/anhydrous children: CHEMBL1256987

Patent coverage: 13,482 distinct patent families (47,850 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 5 (assay-derived). Sample: Bile salt export pump, ATP-binding cassette sub-family C member 2, Albumin, Broad substrate specificity ATP-binding cassette transporter ABCG2, Bile salt export pump.

Bioactivity

ChEMBL activities: 5 potent at pChembl ≥ 5 of 10 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
O701275.66Ki2200nMCHEMBL_ACT_11002748
Q631205.26Ki5500nMCHEMBL_ACT_11003173
Q631205.12Ki7600nMCHEMBL_ACT_11003248
ABCB115IC5010100nMCHEMBL_ACT_18051762
ABCB115IC5010100nMCHEMBL_ACT_18129084

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

6 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
bacterial infectious disease4MONDO:0005113EFO:0000771
eye infectious disorder4MONDO:0043885EFO:1001888
keloid3MONDO:0005348EFO:0004212
non-small cell lung carcinoma3MONDO:0005233EFO:0003060
skin disorder2MONDO:0005093EFO:0000701

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 9.

Phase distribution

PhaseTrials
PHASE33
Not specified3
PHASE22
PHASE41

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03105505PHASE4UNKNOWNThe Efficacy of Permethrin 5%, Fusidic Acid 1% and Synthomycine 5% for Demodex - Blepharitis
NCT06695143PHASE3NOT_YET_RECRUITINGAntimicrobial Adjuvants to Revert the Imbalance of Skin Microbiota for Improved Outcomes of Complicated Cutaneous Leishmaniasis Treatment in Ethiopia
NCT06911424PHASE3RECRUITINGEfficacy of Fusidic Acid 1% in the Treatment of Bacterial Conjunctivitis
NCT01113125PHASE3UNKNOWNScars After Central Venous Catheters
NCT00948142PHASE2COMPLETEDSafety and Efficacy of CEM-102 Compared to Linezolid in Acute Bacterial Skin Infections
NCT01756924PHASE2TERMINATEDSafety and Efficacy of CEM-102 With Rifampin Compared to Standard Therapy in Patients With Prosthetic Joint Infections or Spacer Infection
NCT01153828Not specifiedCOMPLETEDEU PV for Retapamulin-Prescribing
NCT03052348Not specifiedUNKNOWNEfficacy of Combining Topical Antibiotic/Steroid/Moisturizer Therapy Compared to Active Comparator in Atopic Dermatitis.
NCT03173053Not specifiedTERMINATEDS. Aureus Decolonization in HPN Patients.

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).