SCHEMBL443291

SCHEMBL443291

NC(=O)C(c1ccc(O)cc1)c1ccc(O)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.47
KMT2A Q03164 2/20 0.47
ESR1 P03372 8/20 0.44
ESR2 Q92731 7/20 0.44
PDCD1 Q15116 1/20 0.44
CD274 Q9NZQ7 1/20 0.44
TAAR1 Q96RJ0 2/20 0.43
CA2 P00918 2/20 0.43
NFKB1 P19838 2/20 0.43
HIF1A Q16665 2/20 0.43
HTR3A P46098 1/20 0.43
TSHR P16473 1/20 0.43
PEPD P12955 1/20 0.43
SRC P12931 1/20 0.42
ALOX15 P16050 3/20 0.41
KDM4E B2RXH2 2/20 0.41
TDP1 Q9NUW8 2/20 0.41
APEX1 P27695 1/20 0.41
CNR1 P21554 1/20 0.41
CNR2 P34972 1/20 0.41

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
SCHEMBL28038711 0.91 KMT2A (0.54) MEN1KMT2AESR1ESR2TDP1
SCHEMBL5597741 0.82 ESR1 (0.46) MEN1KMT2AESR1ESR2PDCD1
SCHEMBL8365159 0.80 PARP1 (0.43) MEN1KMT2AESR1ESR2TDP1
SCHEMBL5843647 0.79 ESR1 (0.48) MEN1KMT2AESR1ESR2PDCD1
SCHEMBL1354755 0.78 ESR1 (0.42) MEN1KMT2AESR1ESR2PDCD1
SCHEMBL4480606 0.78 HDAC3 (0.57) MEN1KMT2ALMNAALDH1A1
SCHEMBL4877111 0.78 HIF1A (0.48) MEN1KMT2AESR1ESR2PDCD1
SCHEMBL3739983 0.78 HDAC4 (0.57) MEN1KMT2ANFKB1TSHRCNR1
SCHEMBL1354759 0.78 ESR1 (0.42) MEN1KMT2AESR1ESR2PDCD1
SCHEMBL12406374 0.78 ESR1 (0.42) MEN1KMT2AESR1ESR2PDCD1

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

Claimed or disclosed in 191 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7417011-B2 Method and composition for recovering hydrocarbon fluids from a subterranean reservoir NALCO COMPANY (US) 2008-08-26 US claimed
US-20080085844-A1 METHOD AND COMPOSITION FOR RECOVERING HYDROCARBON FLUIDS FROM A SUBTERRANEAN RESERVOIR ECOLAB USA INC. 2008-04-10 US claimed
US-20060189488-A1 Method and composition for recovering hydrocarbon fluids from a subterranean reservoir NORRISEAL-WELLMARK, INC. 2006-08-24 US claimed
WO-2005028589-A1 METHOD AND COMPOSITION FOR RECOVERING HYDROCARBON FLUIDS FROM A SUBTERRANEAN RESERVOIR NALCO ENERGY SERVICES, L.P. (US) 2005-03-31 WO claimed
US-20050065036-A1 Method and composition for recovering hydrocarbon fluids from a subterranean reservoir NALCO ENERGY SERVICES 2005-03-24 US claimed
US-5218075-A Digliceride ethers of amido-dihydric phenols for use in polyepoxide oxygen barriers THE DOW CHEMICAL COMPANY (US) 1993-06-08 US claimed
US-5015778-A Catalytic method to produce hydroxy substituted arylophenones THE DOW CHEMICAL COMPANY (US) 1991-05-14 US claimed
US-11472939-B2 Thermally conductive three-dimensional (3-D) graphene polymer composite materials, methods of making, and uses thereof SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2022-10-18 US disclosed
CN-108219366-B Thermally conductive three-dimensional (3-D) graphene-polymer composite material, preparation method and application thereof 沙特基础工业全球技术公司 2022-04-15 CN disclosed
EP-3555193-B1 THERMALLY CONDUCTIVE THREE-DIMENSIONAL (3-D) GRAPHENEPOLYMER COMPOSITE MATERIALS, METHODS OF MAKING, AND USES THEREOF SABIC GLOBAL TECHNOLOGIES BV (NL) 2022-01-19 EP disclosed
US-11111431-B2 Method for reducing the permeability of a subterranean formation to aqueous-based fluids DOW GLOBAL TECHNOLOGIES LLC (US) 2021-09-07 US disclosed
US-10876032-B2 Method for recovering hydrocarbon fluids from a subterranean reservoir using alpha-glycol containing sulfonated epoxy resin compound DOW GLOBAL TECHNOLOGIES LLC (US) 2020-12-29 US disclosed
US-20200071487-A1 THERMALLY CONDUCTIVE THREE-DIMENSIONAL (3-D) GRAPHENE POLYMER COMPOSITE MATERIALS, METHODS OF MAKING, AND USES THEREOF SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2020-03-05 US disclosed
EP-0506760-A4 CATALYTIC METHOD TO PRODUCE HYDROXY SUBSTITUTED ARYLOPHENONES 1993-03-10 EP disclosed
EP-0506760-A1 CATALYTIC METHOD TO PRODUCE HYDROXY SUBSTITUTED ARYLOPHENONES THE DOW CHEMICAL COMPANY (US) 1992-10-07 EP disclosed
US-5115075-A Copolyethers having a monomer of a dihydric phenol having pendant amido, N-alkylamido and/or hydroxyalkyl groups; containers; films; coatings; packaging of food and drugs THE DOW CHEMICAL COMPANY (US) 1992-05-19 US disclosed
US-5115075-A Copolyethers having a monomer of a dihydric phenol having pendant amido, N-alkylamido and/or hydroxyalkyl groups; containers; films; coatings; packaging of food and drugs THE DOW CHEMICAL COMPANY (US) 1992-05-19 US disclosed
EP-0479445-A2 Hydroxyl functionalized polyetheramines as barrier packaging for oxygen-sensitive materials THE DOW CHEMICAL COMPANY (US) 1992-04-08 EP disclosed
WO-1991009003-A1 CATALYTIC METHOD TO PRODUCE HYDROXY SUBSTITUTED ARYLOPHENONES THE DOW CHEMICAL COMPANY (US) 1991-06-27 WO disclosed
US-5015778-A Catalytic method to produce hydroxy substituted arylophenones THE DOW CHEMICAL COMPANY (US) 1991-05-14 US disclosed