SCHEMBL1015129

SCHEMBL1015129

Cc1ccc(-c2ccc(F)cc2)cc1NC(=O)C(=O)Nc1ccc(Cl)cc1C(=O)[O-].[Na+]

nearest known ligand 0.46

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 19)

geneUniProtsupporting neighboursconfidence
PPARG known ✓ P37231 3/20 0.41
THRB known ✓ P10828 1/20 0.40
MAPT P10636 2/20 0.42
TDP1 Q9NUW8 1/20 0.42
PPARA Q07869 2/20 0.41
KMT2A Q03164 2/20 0.41
TP53 P04637 2/20 0.41
LMNA P02545 1/20 0.41
HTT P42858 1/20 0.41
RXFP1 Q9HBX9 1/20 0.41
NOX1 Q9Y5S8 1/20 0.40
SERPINE1 P05121 2/20 0.40
GAA P10253 2/20 0.39
POLB P06746 1/20 0.39
FABP4 P15090 1/20 0.39
CNR1 P21554 1/20 0.39
TAS1R3 Q7RTX0 1/20 0.39
TAS1R1 Q7RTX1 1/20 0.39
TAS1R2 Q8TE23 1/20 0.39

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
SCHEMBL1016283 0.88 KDM4E (0.52) MAPTTDP1PPARGPPARARXFP1
SCHEMBL1015128 0.87 KDM4E (0.51) MAPTTDP1PPARGPPARARXFP1
SCHEMBL1015774 0.86 ALDH1A1 (0.43) MAPTTDP1KMT2ATP53LMNA
SCHEMBL1016254 0.79 ALDH1A1 (0.43) MAPTTP53LMNARXFP1THRB
SCHEMBL1015626 0.76 RXFP1 (0.53) MAPTTDP1TP53LMNARXFP1
SCHEMBL1015634 0.75 ALDH1A1 (0.53) MAPTTDP1KMT2ATP53LMNA
SCHEMBL417503 0.75 MAPT (0.64) MAPTTDP1KMT2ALMNARXFP1
SCHEMBL1018976 0.75 PTPN1 (0.52) MAPTKMT2ATP53LMNAHTT
SCHEMBL1015137 0.73 KLK7 (0.46) MAPTKMT2ALMNAGAACNR1
SCHEMBL1015947 0.72 CNR1 (0.51) MAPTPPARGPPARALMNASERPINE1

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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2990057-B1 PAI-1 INHIBITOR FOR USE IN ENHANCING THE ANTITUMOR EFFECT OF AN ANTITUMOR AGENT IN A PATIENT RENASCIENCE CO LTD (JP) 2019-03-20 EP disclosed
EP-2990057-A1 NOVEL USE FOR PAI-1 INHIBITOR Renascience Co., Ltd. (JP) 2016-03-02 EP disclosed
EP-2272822-A1 INHIBITOR OF PLASMINOGEN ACTIVATOR INHIBITOR-1 Renascience CO., LTD. (JP) 2011-01-12 EP disclosed