Rezafungin

drug
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Also known as BiafunginCD-101CD101Rezafungin cationRezafungin ionSP-3025

Summary

Rezafungin (CHEMBL3989945) is an approved small molecule; indicated across 2 conditions including fungal infectious disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Indications: 2 conditions
  • Clinical trials: 7
  • Chemistry: 1226.4 Da · C63H85N8O17+

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3989945
NameRezafungin
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID78318119
ChEBICHEBI:229680
Molecular formulaC63H85N8O17+
Molecular weight1226.4
InChIKeyLNFCWEXGZIEGJW-TXSVMFMRSA-O

SMILES: CCCCCOC1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=C(C=C3)C(=O)N[C@H]4C[C@H]([C@H](NC(=O)[C@@H]5[C@H]([C@H](CN5C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]6C[C@H](CN6C(=O)[C@@H](NC4=O)[C@@H](C)O)O)[C@@H]([C@H](C7=CC=C(C=C7)O)O)O)[C@@H](C)O)C)O)OCC[N+](C)(C)C)O

IUPAC name: 2-[[(3S,6S,9S,11R,15S,18S,20R,21R,24S,25S,26S)-6-[(1S,2S)-1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-11,20,25-trihydroxy-3,15-bis[(1R)-1-hydroxyethyl]-26-methyl-2,5,8,14,17,23-hexaoxo-18-[[4-[4-(4-pentoxyphenyl)phenyl]benzoyl]amino]-1,4,7,13,16,22-hexazatricyclo[22.3.0.09,13]heptacosan-21-yl]oxy]ethyl-trimethylazanium

ChEBI definition: A member of the family of echinocandins that inhibits 1,3-β-D-glucan synthase. It is developed by Cidara Therapeutics and approved for the treatment of candidaemia and invasive candidiasis in patients aged ≥ 18 years who have limited or no alternative treatment options.

Also known as: Biafungin, CD-101, CD101, Rezafungin, Rezafungin cation, Rezafungin ion, SP-3025, REZAFUNGIN

Parent form; salt/anhydrous children: CHEMBL3989928

Patent coverage: 536 distinct patent families (1,254 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

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

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

Indications & clinical

Indications

2 indications (0 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
fungal infectious disease1MONDO:0002041MONDO:0002041

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

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
PHASE33
PHASE22
PHASE12

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06774144PHASE3ENROLLING_BY_INVITATIONRezafungin Prophylaxis in Liver Transplant
NCT03667690PHASE3COMPLETEDStudy of Rezafungin Compared to Caspofungin in Subjects With Candidemia and/or Invasive Candidiasis
NCT04368559PHASE3COMPLETEDStudy of Rezafungin Compared to Standard Antimicrobial Regimen for Prevention of Invasive Fungal Diseases in Adults Undergoing Allogeneic Blood and Marrow Transplantation
NCT05835479PHASE2RECRUITINGRezafungin for Treatment of Pneumocystis Pneumonia in HIV Adults
NCT02734862PHASE2COMPLETEDCD101 Compared to Caspofungin Followed by Oral Step Down in Subjects With Candidemia and/or Invasive Candidiasis-Bridging Extension
NCT04117607PHASE1TERMINATEDSafety and Pharmacokinetics of Rezafungin
NCT06329518PHASE1WITHDRAWNRezafungin Pharmacokinetics in Patients on ECMO

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

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

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.