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albaconazole

Structure via PubChem · Public domain (PubChem)

EntityQ4708967· pop 8· linked from 95 articles

albaconazole

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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.

In the Vinony graph

Within Vinony's link graph, albaconazole is referenced by 95 other articles, and connects out to medication, digital object identifier and infection.

It sits within the topics Chloroarenes, Drugs not assigned an ATC code and Drugs with no legal status.

Its subject is documented across 8 Wikipedia language editions.

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

via PubMed

Wikidata facts

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 sections
Contents
  • 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.

Available in 8 languages

via Wikidata sitelinks · CC0

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