SCHEMBL9250136

SCHEMBL9250136

CC(C)(O)c1ccccc1CC[C@@H](SCC1(CC(=O)[O-])CC1)c1cccc(/C=C/c2ccc3sc(Cl)c(Cl)c3n2)c1.[Na+]

nearest known ligand 0.88

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 10)

geneUniProtsupporting neighboursconfidence
CYSLTR1 known ✓ Q9Y271 19/20 0.88
CYSLTR2 Q9NS75 19/20 0.88
CYP2C8 P10632 1/20 0.75
CYP2C9 P11712 1/20 0.75
FPR1 P21462 1/20 0.75
GPR183 P32249 1/20 0.75
MEN1 O00255 1/20 0.65
RECQL P46063 1/20 0.65
BLM P54132 1/20 0.65
KMT2A Q03164 1/20 0.65

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
SCHEMBL8127534 1.00 CYSLTR2 (0.88) CYSLTR2CYSLTR1CYP2C8CYP2C9FPR1
SCHEMBL8127536 1.00 CYSLTR2 (0.88) CYSLTR2CYSLTR1CYP2C8CYP2C9FPR1
SCHEMBL8126629 0.94 CYSLTR2 (0.77) CYSLTR2CYSLTR1CYP2C8CYP2C9FPR1
SCHEMBL8123270 0.94 CYSLTR2 (0.77) CYSLTR2CYSLTR1CYP2C8CYP2C9FPR1
SCHEMBL8123269 0.94 CYSLTR2 (0.77) CYSLTR2CYSLTR1CYP2C8CYP2C9FPR1
SCHEMBL8126630 0.94 CYSLTR2 (0.77) CYSLTR2CYSLTR1CYP2C8CYP2C9FPR1
SCHEMBL5200473 0.94 CYSLTR2 (1.00) CYSLTR2CYSLTR1CYP2C8MEN1RECQL
SCHEMBL5200470 0.94 CYSLTR2 (1.00) CYSLTR2CYSLTR1CYP2C8MEN1RECQL
SCHEMBL5200477 0.94 CYSLTR2 (1.00) CYSLTR2CYSLTR1CYP2C8MEN1RECQL
SCHEMBL9255522 0.92 CYSLTR2 (0.88) CYSLTR2CYSLTR1MEN1RECQLBLM

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-5472964-A Diaryl 5,6-fused heterocyclic acids as leukotriene antagonists MERCK FROSST CANADA, INC. (CA) 1995-12-05 US disclosed