Structure via PubChem · Public domain (PubChem)
albaconazole
Sign in to saveAlbaconazole (development code UR-9825) is an experimental triazole antifungal. It has potential broad-spectrum activity. The drug blocks a number of CYP450 liver enzymes.
Chemical data
- Formula
- C20H16ClF2N5O2
- Molecular weight
- 431.8 g/mol
- IUPAC name
- 7-chloro-3-[(2R,3R)-3-(2,4-difluorophenyl)-3-hydroxy-4-(1,2,4-triazol-1-yl)butan-2-yl]quinazolin-4-one
- SMILES
- C[C@H]([C@](CN1C=NC=N1)(C2=C(C=C(C=C2)F)F)O)N3C=NC4=C(C3=O)C=CC(=C4)Cl
- InChIKey
- UHIXWHUVLCAJQL-MPBGBICISA-N
- XLogP
- 2.5
- Polar surface area
- 83.6 Ų
- H-bond donors
- 1
- H-bond acceptors
- 7
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
- Indications
- vulvovaginitis, tinea pedis, tinea unguium
via ChEMBL · EBI
Research
49 papers- Albaconazole Polymeric Nanocapsules for Treating Trypanosoma cruzi Infections.Pathogens (Basel, Switzerland) · 2025
- Novel triazole antifungal drugs: focus on isavuconazole, ravuconazole and albaconazole.Current opinion in investigational drugs (London, England : 2000) · 2010
- Emerging azole antifungals.Expert opinion on emerging drugs · 2005
- Newer antifungal agents.Expert review of anti-infective therapy · 2011
- Activity of the new triazole derivative albaconazole against Trypanosoma (Schizotrypanum) cruzi in dog hosts.Antimicrobial agents and chemotherapy · 2004
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 431.096
Show 4 more facts
- chemical formula
- C₂₀H₁₆ClF₂N₅O₂
- isomeric SMILES
- C[C@H]([C@](CN1C=NC=N1)(C2=C(C=C(C=C2)F)F)O)N3C=NC4=C(C3=O)C=CC(=C4)Cl
- canonical SMILES
- CC(C(CN1C=NC=N1)(C2=C(C=C(C=C2)F)F)O)N3C=NC4=C(C3=O)C=CC(=C4)Cl
- subject has role
- antifungal
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Albaconazole (development code UR-9825) is an experimental triazole antifungal. It has potential broad-spectrum activity. The drug blocks a number of CYP450 liver enzymes.
It has also been studied as an antiprotozoal agent.
Excerpted from Wikipedia’s “albaconazole” article, available under the CC BY-SA 4.0 licence.
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