SCHEMBL15516624

SCHEMBL15516624

FC(F)(F)Oc1ccc([B-](c2ccc(OC(F)(F)F)cc2)(c2ccc(OC(F)(F)F)cc2)c2ccc(OC(F)(F)F)cc2)cc1.[Na+]

nearest known ligand 0.44

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. 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
SCN5A known ✓ Q14524 4/20 0.39
SCN1A known ✓ P35498 1/20 0.38
SCN2A known ✓ Q99250 1/20 0.38
MAPT P10636 3/20 0.44
EPHX2 P34913 1/20 0.44
GPR3 P46089 1/20 0.41
L3MBTL1 Q9Y468 2/20 0.39
KDM4E B2RXH2 1/20 0.39
POLB P06746 1/20 0.39
KIF11 P52732 1/20 0.38
PDE2A O00408 1/20 0.38
NISCH Q9Y2I1 1/20 0.38
GALR1 P47211 1/20 0.38
ALDH1A1 P00352 2/20 0.37
TSHR P16473 2/20 0.37
MAOB P27338 1/20 0.37
AOC3 Q16853 1/20 0.37
MEN1 O00255 1/20 0.37
TP53 P04637 1/20 0.37
CYP3A4 P08684 1/20 0.37

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
SCHEMBL254957 0.82 MAPT (0.56) MAPTEPHX2GPR3L3MBTL1KDM4E
SCHEMBL28780452 0.74 EPHX2 (0.50) MAPTEPHX2GPR3SCN5AL3MBTL1
SCHEMBL19977307 0.73 SLC6A2 (0.37) MAPTKDM4EKIF11TSHRMEN1
SCHEMBL3336949 0.73 GPR3 (0.47) MAPTEPHX2GPR3L3MBTL1KDM4E
SCHEMBL13863723 0.72 MAPT (0.48) MAPTEPHX2GPR3L3MBTL1KDM4E
SCHEMBL255560 0.72 GPR3 (0.52) MAPTEPHX2GPR3L3MBTL1KDM4E
SCHEMBL306823 0.71 KIF11 (0.50) SCN5AKIF11NISCHSCN1ASCN2A
SCHEMBL18293362 0.71 KIF11 (0.50) SCN5AKIF11NISCHSCN1ASCN2A
SCHEMBL15372299 0.70 MAPT (0.47) MAPTEPHX2GPR3SCN5AL3MBTL1
SCHEMBL513525 0.70 MAPT (0.52) MAPTEPHX2GPR3L3MBTL1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014033967-A1 PHOTO ACID GENERATOR AND ITS SYNTHETIC METHOD RHODIA OPERATIONS (FR) 2014-03-06 WO disclosed