SCHEMBL9437697

SCHEMBL9437697

CCCCCCCCC=CCCCCCCCC(=O)NCCOC(=O)C(CC(=O)[O-])S(=O)(=O)O.CCCCCCCCC=CCCCCCCCC(=O)NCCOC(=O)C(CC(=O)[O-])S(=O)(=O)O.[Na+].[Na+]

nearest known ligand 0.54

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 15)

geneUniProtsupporting neighboursconfidence
EPHX2 P34913 4/20 0.54
LPAR1 Q92633 2/20 0.53
LPAR2 Q9HBW0 2/20 0.53
ENPP2 Q13822 1/20 0.53
SLC6A5 Q9Y345 2/20 0.51
CNR1 P21554 4/20 0.49
ALDH1A1 P00352 2/20 0.48
HPGD P15428 2/20 0.48
TRPV1 Q8NER1 1/20 0.48
MEN1 O00255 1/20 0.48
MAPT P10636 1/20 0.48
ALOX12 P18054 1/20 0.48
BLM P54132 1/20 0.48
KMT2A Q03164 1/20 0.48
TDP1 Q9NUW8 1/20 0.48

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
SCHEMBL28701810 0.93 EPHX2 (0.44) EPHX2LPAR1LPAR2ENPP2ALDH1A1
SCHEMBL3697476 0.93 EPHX2 (0.44) EPHX2LPAR1LPAR2ENPP2ALDH1A1
SCHEMBL27943740 0.93 EPHX2 (0.44) EPHX2LPAR1LPAR2ENPP2ALDH1A1
SCHEMBL29392097 0.93 LPAR1 (0.52) EPHX2LPAR1LPAR2ENPP2SLC6A5
SCHEMBL29391868 0.87 LPAR1 (0.48) EPHX2LPAR1LPAR2ENPP2SLC6A5
Disodium Lauramido Mea SCHEMBL3697471 0.85 FAAH (0.43) EPHX2LPAR1LPAR2ENPP2ALDH1A1
SCHEMBL23064683 0.85 FABP3 (0.48) EPHX2SLC6A5
SCHEMBL4261598 0.85 FABP3 (0.48) EPHX2SLC6A5
SCHEMBL4261589 0.85 FABP3 (0.48) EPHX2SLC6A5
SCHEMBL28761180 0.85 FABP3 (0.48) EPHX2SLC6A5

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
US-5336446-A Mixture of anionic surfactant salts and N-substituted betaines GOODMAN ROBERT M (US) 1994-08-09 US disclosed