SCHEMBL5123243

SCHEMBL5123243

O=S([O-])c1sccc1-c1ccc(OC(F)(F)F)cc1.[Na+]

nearest known ligand 0.38

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 17)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 3/20 0.33
PTGS1 known ✓ P23219 1/20 0.33
CASP3 P42574 1/20 0.36
KIF11 P52732 1/20 0.35
GALR1 P47211 1/20 0.35
ERCC5 P28715 1/20 0.34
FEN1 P39748 1/20 0.34
NOTUM Q6P988 1/20 0.34
AURKA O14965 1/20 0.33
TPX2 Q9ULW0 1/20 0.33
MAPK8 P45983 1/20 0.33
EPHX2 P34913 1/20 0.33
IDO1 P14902 1/20 0.33
NPC1 O15118 1/20 0.33
RAB9A P51151 1/20 0.33
NISCH Q9Y2I1 1/20 0.33
PIM1 P11309 1/20 0.32

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
SCHEMBL14033481 0.84 EPHX2 (0.37) CASP3KIF11ERCC5FEN1NOTUM
SCHEMBL5123239 0.83 CASP3 (0.36) CASP3KIF11ERCC5FEN1NOTUM
SCHEMBL5052822 0.72 CASP3 (0.41) CASP3KIF11IDO1NPC1RAB9A
SCHEMBL14605699 0.72 KIF11 (0.41) CASP3KIF11GALR1ERCC5FEN1
SCHEMBL5051726 0.71 POLQ (0.38) KIF11ERCC5FEN1PTGS2AURKA
SCHEMBL5134292 0.71 KIF11 (0.45) KIF11ERCC5FEN1PTGS2MAPK8
SCHEMBL1584402 0.71 EPHX2 (0.43) KIF11GALR1NOTUMAURKATPX2
SCHEMBL5055342 0.70 KIF11 (0.42) CASP3KIF11NOTUMPTGS2AURKA
Lithium Ion SCHEMBL3254006 0.67 ERCC5 (0.49) KIF11GALR1ERCC5FEN1NOTUM
SCHEMBL5134293 0.66 KIF11 (0.45) CASP3KIF11ERCC5FEN1PTGS2

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-20080249137-A1 PPAR active compounds PLEXXIKON INC 2008-10-09 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080249137-A1 PPAR active compounds PPARG, PPARA, PPARD PTGS2 557/4885PTGS1 323/4885CASP3 1482/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.