SCHEMBL101880

SCHEMBL101880

c1ccc(P(c2ccccc2)c2ccccc2Oc2ccccc2P(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.50

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
ESR1 P03372 2/20 0.39
ESR2 Q92731 2/20 0.39
DRD1 P21728 2/20 0.39
KDM4E B2RXH2 1/20 0.35
GAA P10253 1/20 0.35
LTA4H P09960 1/20 0.32
TSHR P16473 1/20 0.32
TOP1 P11387 1/20 0.31
CA1 P00915 2/20 0.31
CA2 P00918 2/20 0.31
CA7 P43166 2/20 0.31
CA9 Q16790 2/20 0.31
CA12 O43570 1/20 0.31
CA4 P22748 1/20 0.31
CA14 Q9ULX7 1/20 0.31
HTT P42858 1/20 0.31

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
SCHEMBL31153795 0.98 CYP3A4 (0.48) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL2142709 0.98 CYP3A4 (0.48) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL29375055 0.98 CYP3A4 (0.48) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL31059892 0.98 CYP3A4 (0.48) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL17674561 0.98 CYP3A4 (0.48) CYP3A4TDP1ESR1ESR2DRD1
Bromide SCHEMBL4290668 0.96 CYP3A4 (0.46) CYP3A4TDP1ESR1ESR2DRD1
Hydrochloric Acid SCHEMBL2126739 0.96 CYP3A4 (0.46) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL30015097 0.92 CYP3A4 (0.42) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL31435873 0.92 CYP3A4 (0.42) CYP3A4TDP1ESR1ESR2DRD1
SCHEMBL2126742 0.92 CYP3A4 (0.42) CYP3A4TDP1ESR1ESR2DRD1

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 5512 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12637412-B2 Preparation of aromatic carboxyamides by a palladium-catalyzed carbonylation reaction BASF SE (DE) 2026-05-26 US claimed
CN-120463615-B Asymmetric azobenzene compound, synthetic method and application 湘潭大学 2026-05-19 CN claimed
CN-122036825-A C2-quaternary carbon amino sugar and preparation method and application thereof 常州大学 2026-05-15 CN claimed
WO-2026086030-A1 METHOD FOR CONSTRUCTING CHIRALITY OF PYRAN RING IN ORFORGLIPRON BY MEANS OF ENZYMATIC CATALYSIS 成都安迈博生物医药有限公司 2026-04-30 WO claimed
EP-4731703-A1 LINEAR POLYAMINES HAVING A LONG CARBON CHAIN, METHOD FOR PRODUCING SAME, AND USES THEREOF Commissariat à l'Energie Atomique et aux Energies Alternatives (FR) 2026-04-29 EP claimed
EP-4725945-A1 PREPARATION METHOD FOR FORMAMIDE COMPOUNDS Shanghai Senhui Medicine Co., Ltd. (CN) 2026-04-15 EP claimed
EP-4713315-A1 PROCESS FOR THE PREPARATION OF DEUCRAVACITINIB, AND CRYSTALLINE FORMS THEREOF Alivus Life Sciences Limited (IN) 2026-03-25 EP claimed
US-12577236-B2 Processes for preparation of Tezacaftor LAURUS LABS LIMITED (IN) 2026-03-17 US claimed
US-20260062361-A1 PROCESS FOR THE PREPARATION OF BIO-BASED OLEFINS FROM PRIMARY ALCOHOL BASF SE (DE) 2026-03-05 US claimed
US-20250388564-A1 METHODS OF MANUFACTURING PYRIDAZINONE COMPOUNDS EDGEWISE THERAPEUTICS INC (US) 2025-12-25 US claimed
WO-2005075462-A1 COUPLING REACTIONS USEFUL IN THE PREPARATION OF (1H-TETRAZOL-5-YL)-BIPHENYL DERIVATIVES NOVARTIS AG (CH) 2005-08-18 WO claimed
EP-1244608-A4 ALLYL ALCOHOL HYDROFORMYLATION ARCO CHEM TECH (US) 2005-08-03 EP claimed
CN-1196664-C hydroformylation of allyl alcohol ARCO CHEM TECH (US) 2005-04-13 CN claimed
WO-2004101496-A1 METHOD OF FORMING A CARBON-HETEROATOM BOND RHODIA CHIMIE (FR) 2004-11-25 WO claimed
JP-2003519203-A 2003-06-17 JP claimed
CN-1394197-A hydroformylation of allyl alcohol ARCO CHEM TECH (US) 2003-01-29 CN claimed
EP-1244608-A1 ALLYL ALCOHOL HYDROFORMYLATION ARCO Chemical Technology, L.P. (US) 2002-10-02 EP claimed
WO-2001049643-A1 ALLYL ALCOHOL HYDROFORMYLATION ARCO CHEMICAL TECHNOLOGY, L.P. (US) 2001-07-12 WO claimed
US-6225509-B1 REDUCING THE FORMATION OF SATURATED C3 (PROPYL-) COMPOUNDS BY MAINTAINING THE CONCENTRATION OF CARBON MONOXIDE IN THE LIQUID PHASE DURING HYDROFORMYLATION OF ALLYL ALCOHOL USING A RHODIUM COMPLEX CATALYST AND BIDENDATE DIPHOSPHINE LIGAND ARCO CHEMICAL TECHNOLOGY, L.P. 2001-05-01 US claimed
US-6107521-A Process for the preparation of secondary amines CELGRO (US) 2000-08-22 US claimed