SCHEMBL4796445

SCHEMBL4796445

COc1ccc2nc(S(=O)(=O)N(C)c3ncc(C)c(OC)c3C)n(S(=O)(=O)c3ccc(OCC(=O)[O-])cc3)c2n1.[Na+]

nearest known ligand 0.33

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
PDE10A Q9Y233 5/20 0.33
CYP2C9 P11712 1/20 0.33
PTGDR2 Q9Y5Y4 1/20 0.32
TRPM8 Q7Z2W7 1/20 0.32
KEAP1 Q14145 1/20 0.31
NFE2L2 Q16236 1/20 0.31
MAPT P10636 1/20 0.31
DDAH1 O94760 1/20 0.31
SARM1 Q6SZW1 1/20 0.31
IDO2 Q6ZQW0 1/20 0.31
ENGASE Q8NFI3 1/20 0.31
LMNA P02545 2/20 0.30
MEN1 O00255 1/20 0.30
USP2 O75604 1/20 0.30
ALDH1A1 P00352 1/20 0.30
KMT2A Q03164 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30

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
SCHEMBL4796458 0.83 CYP2C9 (0.36) PDE10ACYP2C9PTGDR2MAPTDDAH1
SCHEMBL3770559 0.79 CYP2C9 (0.37) PDE10ACYP2C9PTGDR2MAPTDDAH1
SCHEMBL4894945 0.76 HPGD (0.34) MAPTDDAH1SARM1IDO2ENGASE
SCHEMBL13008023 0.73 CYP2C9 (0.37) PDE10ACYP2C9PTGDR2MAPTDDAH1
SCHEMBL3771472 0.70 DDAH1 (0.38) CYP2C9MAPTDDAH1SARM1IDO2
SCHEMBL4929481 0.70 HCRTR1 (0.34) PTGDR2LMNAMEN1USP2ALDH1A1
SCHEMBL4925902 0.69 ALDH1A1 (0.35) PTGDR2MAPTLMNAMEN1USP2
SCHEMBL3771197 0.68 CYP2C9 (0.34) CYP2C9DDAH1SARM1IDO2ENGASE
SCHEMBL4847233 0.68
SCHEMBL5763585 0.67 CYP2C9 (0.42) CYP2C9MAPTDDAH1ENGASELMNA

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-2008036201-A1 PRODRUGS OF PROTON PUMP INHIBITORS INCLUDING THE 1H-IMIDAZO[4,5-B] PYRIDINE MOIETY ALEVIUM PHARMACEUTICALS, INC. (US) 2008-03-27 WO disclosed