SCHEMBL3674572

SCHEMBL3674572

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(c1ccccc1Cl)c1ccccc1Cl

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNN4 O15554 3/20 0.39
LMNA P02545 3/20 0.36
TSHR P16473 3/20 0.36
CYP19A1 P11511 3/20 0.36
HSD11B1 P28845 1/20 0.33
NR3C1 P04150 2/20 0.32
PDK2 Q15119 4/20 0.31
PDK1 Q15118 3/20 0.31
PDK3 Q15120 3/20 0.31
PDK4 Q16654 3/20 0.31
KCNA3 P22001 2/20 0.31
HTR2A P28223 2/20 0.30
HTR2C P28335 2/20 0.30
OPRK1 P41145 2/20 0.30
KCNH2 Q12809 2/20 0.30
ADRA1A P35348 1/20 0.30
MEN1 O00255 1/20 0.30
SLC22A1 O15245 1/20 0.30
NR1I2 O75469 1/20 0.30
GMNN O75496 1/20 0.30

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
SCHEMBL3675411 1.00 KCNN4 (0.39) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3679610 1.00 KCNN4 (0.39) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3676254 1.00 KCNN4 (0.39) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3673903 1.00 KCNN4 (0.39) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3672759 1.00 KCNN4 (0.39) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3678117 0.98 KCNN4 (0.41) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3675546 0.91 KCNN4 (0.42) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL3671355 0.82 KCNN4 (0.45) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL6521761 0.79 CYP19A1 (0.36) KCNN4LMNATSHRCYP19A1HSD11B1
SCHEMBL6856610 0.79 CYP19A1 (0.36) KCNN4LMNATSHRCYP19A1HSD11B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1329444-B1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR CORP (JP) 2010-05-05 EP disclosed
US-6933068-B2 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA (JP) 2005-08-23 US disclosed
EP-1245554-B1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR CORP (JP) 2005-01-26 EP disclosed
US-6833426-B2 A proton-conductive membrane containing the sulfonic acid group-containing polyarylene (co)polymer JSR CORPORATION (JP) 2004-12-21 US disclosed
US-6794480-B2 POLYARYLENE-BASED COPOLYMER USEFUL AS PROTON-CONDUCTIVE MEMBRANE WHICH CAN BE USED AS ELECTRON FOR PRIMARY BATTERY, ELECTROLYTE FOR SECONDARY BATTERY, HIGH MOLECULAR SOLID ELECTROLYTE FOR FUEL CELL JSR CORPORATION (JP) 2004-09-21 US disclosed
US-20030173547-A1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR CORPORATION (JP) 2003-09-18 US disclosed
EP-1329444-A1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR Corporation (JP) 2003-07-23 EP disclosed
US-20020177656-A1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR CORPORATION (JP) 2002-11-28 US disclosed
US-20020172850-A1 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA, JSR CORPORATION 2002-11-21 US disclosed
EP-1245554-A1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR Corporation (JP) 2002-10-02 EP disclosed