SCHEMBL3718103

SCHEMBL3718103

Cc1[n-]c(COP(=O)(O)O)c(-c2ccc(Oc3ccc(OC(F)(F)F)cc3)cc2)c(=O)c1Cl.Cc1[n-]c(COP(=O)(O)O)c(-c2ccc(Oc3ccc(OC(F)(F)F)cc3)cc2)c(=O)c1Cl.[Na+].[Na+]

nearest known ligand 0.42

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 13)

geneUniProtsupporting neighboursconfidence
PTGER4 P35408 1/20 0.33
S1PR1 P21453 3/20 0.32
S1PR3 Q99500 2/20 0.32
S1PR4 O95977 1/20 0.32
S1PR5 Q9H228 1/20 0.32
TRPV1 Q8NER1 1/20 0.32
AR P10275 1/20 0.32
GRM2 Q14416 1/20 0.31
SLC2A1 P11166 1/20 0.31
PTGDR2 Q9Y5Y4 1/20 0.31
GALR1 P47211 1/20 0.31
NPBWR1 P48145 1/20 0.31
MCHR1 Q99705 1/20 0.31

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
SCHEMBL3716510 1.00 PTGER4 (0.33) PTGER4S1PR1S1PR3S1PR4S1PR5
Potassium Ion SCHEMBL3713067 0.98 PTGER4 (0.33) PTGER4S1PR1S1PR3S1PR4S1PR5
SCHEMBL3711185 0.79 SLC2A1 (0.38) PTGER4S1PR1S1PR3S1PR4S1PR5
SCHEMBL3716508 0.78 SLC2A1 (0.38) PTGER4S1PR1S1PR3S1PR4S1PR5
SCHEMBL3713064 0.78 SLC2A1 (0.38) PTGER4S1PR1S1PR3S1PR4S1PR5
SCHEMBL3718102 0.78 SLC2A1 (0.38) PTGER4S1PR1S1PR3S1PR4S1PR5
Tromethamine SCHEMBL3709545 0.74 S1PR1 (0.42) S1PR1S1PR3
SCHEMBL13259632 0.73 AR (0.36) PTGER4S1PR1S1PR3ARMCHR1
SCHEMBL4472453 0.68 SLC2A1 (0.58) SLC2A1NPBWR1MCHR1
SCHEMBL3110262 0.68 SLC2A1 (0.43) PTGER4SLC2A1

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-2010094738-A1 PHOSPHATE ESTER OF A 4-PYRIDONE DERIVATIVE AND ITS USE IN THE CHEMOTHERAPY OF PARASITIC INFECTIONS GLAXO GROUP LIMITED (GB) 2010-08-26 WO disclosed