SCHEMBL9840142

SCHEMBL9840142

CCCCOCCOCCOCCc1c(C(=O)O)ccc(C(=O)O)c1CCOCCOCCOCCCC.[Na+].c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

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
PTGS2 known ✓ P35354 1/20 0.36
RARB P10826 3/20 0.44
RARA P10276 2/20 0.44
TSHR P16473 6/20 0.39
TDP1 Q9NUW8 2/20 0.39
L3MBTL1 Q9Y468 2/20 0.39
RECQL P46063 2/20 0.39
ALDH1A1 P00352 4/20 0.38
KMT2A Q03164 2/20 0.38
PTK2B Q14289 1/20 0.38
PTPN11 Q06124 2/20 0.38
RARG P13631 1/20 0.38
KDM4E B2RXH2 1/20 0.37
MEN1 O00255 1/20 0.37
CYP3A4 P08684 2/20 0.36
MAPK1 P28482 2/20 0.36
DHODH Q02127 1/20 0.36
HPGD P15428 1/20 0.36
PLK1 P53350 1/20 0.36
GAA P10253 1/20 0.35

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
SCHEMBL17797802 0.88 RARB (0.53) RARBRARATSHRTDP1L3MBTL1
SCHEMBL17797799 0.86 RARB (0.51) RARBRARATSHRTDP1L3MBTL1
SCHEMBL29396469 0.83 RARB (0.49) RARBRARATSHRTDP1L3MBTL1
Phthalic Acid SCHEMBL782536 0.77 TSHR (0.58) RARBRARATSHRTDP1L3MBTL1
SCHEMBL3677297 0.76 RARB (0.46) RARBRARATSHRRARGTP53
SCHEMBL17797914 0.76 ALDH1A1 (0.42) RARBRARATSHRTDP1ALDH1A1
Phthalic Acid SCHEMBL6362073 0.75 TSHR (0.59) RARBRARATSHRTDP1L3MBTL1
SCHEMBL17797929 0.75 RARB (0.44) RARBRARATSHRRECQLRARG
Phthalic Acid SCHEMBL28888377 0.74 TSHR (0.58) RARBRARATSHRTDP1L3MBTL1
SCHEMBL658635 0.74 RARB (0.46) RARBRARATSHRRARGTP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0294472-A4 SECONDARY BATTERY 1991-01-30 EP disclosed
EP-0294472-A1 SECONDARY BATTERY THE DOW CHEMICAL COMPANY (US) 1988-12-14 EP disclosed
WO-1988004834-A1 SECONDARY BATTERY THE DOW CHEMICAL COMPANY (US) 1988-06-30 WO disclosed