Bifonazole

Bifonazole

SCHEMBL394764

c1ccc(-c2ccc([C@@H](c3ccccc3)n3ccnc3)cc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ERG11hmg1

The experimentally established mechanism targets of Bifonazole. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP17A1 P05093 10/20 1.00
MEN1 O00255 1/20 1.00
NR1I2 O75469 1/20 1.00
USP2 O75604 1/20 1.00
ABCB11 O95342 1/20 1.00
ALDH1A1 P00352 1/20 1.00
PLA2G1B P04054 1/20 1.00
TP53 P04637 1/20 1.00
PGR P06401 1/20 1.00
HSP90AA1 P07900 1/20 1.00
CYP3A4 P08684 1/20 1.00
MAPT P10636 1/20 1.00
IDO1 P14902 1/20 1.00
HPGD P15428 1/20 1.00
MAOA P21397 1/20 1.00
CNR1 P21554 1/20 1.00
HTR2A P28223 1/20 1.00
MAPK1 P28482 1/20 1.00
ADRA1A P35348 1/20 1.00
OPRK1 P41145 1/20 1.00

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Bifonazole SCHEMBL1551534 1.00 CYP17A1 (1.00) CYP17A1MEN1NR1I2USP2ABCB11
Bifonazole SCHEMBL36803 1.00 CYP17A1 (1.00) CYP17A1MEN1NR1I2USP2ABCB11
Bifonazole SCHEMBL1606037 1.00 CYP17A1 (1.00) CYP17A1MEN1NR1I2USP2ABCB11
Bifonazole SCHEMBL7598897 1.00 CYP17A1 (1.00) CYP17A1MEN1NR1I2USP2ABCB11
SCHEMBL11349905 0.98 CYP17A1 (1.00) CYP17A1MEN1NR1I2USP2ABCB11
SCHEMBL25873391 0.92 CYP17A1 (0.85) CYP17A1MEN1NR1I2USP2ABCB11
SCHEMBL738495 0.91 CYP19A1 (1.00) CYP17A1MEN1NR1I2USP2ABCB11
SCHEMBL24177881 0.91 CYP17A1 (0.82) CYP17A1MEN1NR1I2USP2ABCB11
SCHEMBL11362753 0.91 CYP17A1 (0.85) CYP17A1MEN1NR1I2USP2ABCB11
SCHEMBL11353276 0.91 CYP19A1 (0.91) CYP17A1MEN1NR1I2USP2ABCB11

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 2433 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3946279-B1 STRUCTURED ENCAPSULATED SILICON-CONTAINING PARTICLES SISAF LTD (GB) 2025-07-23 EP claimed
US-12280032-B2 Methods and compositions for increasing the potency of antifungal agents PACIFIC NORTHWEST RESEARCH INSTITUTE (US) 2025-04-22 US claimed
WO-2025076059-A1 ROCAGLATE DERIVATIVES AND USES THEREOF TRUSTEES OF BOSTON UNIVERSITY (US) 2025-04-10 WO claimed
US-20250099557-A1 ANTIBIOTIC PHARMACEUTICAL COMPOSITION CAPABLE OF SUBCUTANEOUS ADMINISTRATION SHANGHAI BAO PHARMACEUTICALS CO., LTD. (CN) 2025-03-27 US claimed
WO-2024264012-A1 BIOAVAILABILITY ENHANCING IONIC LIQUID FORMULATIONS INCLUDING ANTHELMINITIC BENZIMIDAZOLE COMPOUNDS AND USES THEREOF ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2024-12-26 WO claimed
WO-2024264013-A1 BIOAVAILABILITY ENHANCING IONIC LIQUID FORMULATIONS AND USES THEREOF ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2024-12-26 WO claimed
WO-2024233677-A2 ANTIFUNGAL COMPOUNDS AND USES THEREOF DUKE UNIVERSITY (US) 2024-11-14 WO claimed
EP-4374848-A1 ANTIBIOTIC PHARMACEUTICAL COMPOSITION CAPABLE OF SUBCUTANEOUS ADMINISTRATION Shanghai Bao Pharmaceuticals Co., Ltd. (CN) 2024-05-29 EP claimed
WO-2024095296-A1 SOLVENT FREE SOLID ORAL COMPOSITION OF BCS CLASS IV DRUGS REDASANI VIJAYENDRAKUMAR VIRENDRAKUMAR (IN) 2024-05-10 WO claimed
US-11725227-B2 Devices and methods for examining drug effects on microorganisms ESSENLIX CORPORATION (US) 2023-08-15 US claimed
WO-2004082655-A1 MEDICATED SKIN CLEANSING PRODUCTS COMPRISING AN ANTIMYCOTIC AGENT AGIS INDUSTRIES (1983) LTD. (IL) 2004-09-30 WO claimed
US-20040131628-A1 Nucleic acids for the treatment of disorders associated with microorganisms BRATZLER ROBERT L (US) 2004-07-08 US claimed
US-20030198659-A1 Fibrous pest control CORNELL RESEARCH FOUNDATION, INC. 2003-10-23 US claimed
WO-2003061554-A2 COMPOSITION CONTAINING MOUTAN ROOT BARK EXTRACT AS ACTIVE INGREDIENT MICRO SCIENCE TECH CO., LTD (KR) 2003-07-31 WO claimed
EP-0827553-B1 COMBINATIONS OF ACTIVE SUBSTANCES BAYER AG (DE) 2002-11-27 EP claimed
EP-1073470-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2001-02-07 EP claimed
WO-2000048636-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2000-08-24 WO claimed
EP-0827553-A1 COMBINATIONS OF ACTIVE SUBSTANCES BAYER AG (DE) 1998-03-11 EP claimed
WO-1996036739-A1 COMBINATIONS OF ACTIVE SUBSTANCES BAYER AKTIENGESELLSCHAFT (DE) 1996-11-21 WO claimed
EP-0310122-B1 ANTIFUNGAL COMPOSITION KAKEN PHARMACEUTICAL CO., LTD. (JP) 1991-07-24 EP claimed