SCHEMBL5528852

SCHEMBL5528852

Oc1ccc(Oc2ccc(Oc3ccccc3)cc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 6/20 1.00
NR1H2 P55055 1/20 1.00
BAX Q07812 1/20 1.00
MEN1 O00255 1/20 0.78
KMT2A Q03164 1/20 0.78
ESR1 P03372 1/20 0.78
ESR2 Q92731 1/20 0.78
TSHR P16473 1/20 0.67
MAOA P21397 1/20 0.56
CA1 P00915 2/20 0.56
CA2 P00918 2/20 0.56
LMNA P02545 1/20 0.54
CYP1A2 P05177 1/20 0.54
PTGS1 P23219 1/20 0.54
SLC6A2 P23975 1/20 0.54
CYP2C19 P33261 1/20 0.54
PTGS2 P35354 1/20 0.54
SLC6A3 Q01959 1/20 0.54
HIF1A Q16665 1/20 0.54
HDAC6 Q9UBN7 1/20 0.54

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
SCHEMBL74847 1.00 LTA4H (1.00) LTA4HNR1H2BAXMEN1KMT2A
SCHEMBL5376734 1.00 LTA4H (1.00) LTA4HNR1H2BAXMEN1KMT2A
Phenol SCHEMBL5380064 0.97 LTA4H (0.95) LTA4HNR1H2BAXMEN1KMT2A
Phenol SCHEMBL636047 0.97 LTA4H (0.95) LTA4HNR1H2BAXMEN1KMT2A
SCHEMBL27714320 0.97 LTA4H (0.95) LTA4HNR1H2BAXMEN1KMT2A
Diphenylether SCHEMBL1246776 0.97 LTA4H (0.94) LTA4HNR1H2BAXMEN1KMT2A
Phenol SCHEMBL15732394 0.94 LTA4H (0.90) LTA4HNR1H2BAXMEN1KMT2A
SCHEMBL5374943 0.93 LTA4H (0.86) LTA4HNR1H2BAXMEN1KMT2A
SCHEMBL16280741 0.93 LTA4H (0.86) LTA4HNR1H2BAXMEN1KMT2A
Diphenylether SCHEMBL11315604 0.92 LTA4H (0.84) LTA4HNR1H2BAXMEN1KMT2A

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5219477-A Containing organometallic salts and inorganic metal borates; fromo reactinmetal hydroxide with phenols or aromatic carboxylic acid THE DOW CHEMICAL COMPANY (US) 1993-06-15 US claimed
EP-1400548-B1 Novel aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR CORP (JP) 2007-07-11 EP disclosed
US-7163988-B2 Aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR CORPORATION (JP) 2007-01-16 US disclosed
EP-1400548-A1 Novel aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR Corporation (JP) 2004-03-24 EP disclosed
US-20040044166-A1 Novel aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR CORPORATION (JP) 2004-03-04 US disclosed
US-5219477-A Containing organometallic salts and inorganic metal borates; fromo reactinmetal hydroxide with phenols or aromatic carboxylic acid THE DOW CHEMICAL COMPANY (US) 1993-06-15 US disclosed