SCHEMBL7033474

SCHEMBL7033474

CC(C)(Oc1ccccc1)C(=O)[O-].[Na+]

nearest known ligand 0.47

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 20)

geneUniProtsupporting neighboursconfidence
PPARG known ✓ P37231 9/20 0.46
CA2 known ✓ P00918 1/20 0.40
CA4 known ✓ P22748 1/20 0.40
PPARA Q07869 9/20 0.47
MEN1 O00255 3/20 0.47
KMT2A Q03164 3/20 0.47
CYP2C19 P33261 2/20 0.47
MAPT P10636 2/20 0.47
CYP1A2 P05177 1/20 0.47
CYP3A4 P08684 1/20 0.47
CYP2D6 P10635 1/20 0.47
PPARD Q03181 2/20 0.43
CYP2C9 P11712 1/20 0.43
KDM4E B2RXH2 2/20 0.41
ALDH1A1 P00352 1/20 0.41
POLB P06746 1/20 0.41
TSHR P16473 1/20 0.41
FABP2 P12104 1/20 0.41
SLC22A12 Q96S37 1/20 0.41
PTPN7 P35236 1/20 0.40

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
Potassium Ion SCHEMBL11787600 0.96 PPARA (0.47) PPARAMEN1KMT2ACYP2C19MAPT
Glycinebetaine SCHEMBL7022972 0.86 PPARG (0.41) PPARAMEN1KMT2ACYP2C19MAPT
Choline SCHEMBL7022303 0.82 PPARA (0.43) PPARAMEN1KMT2ACYP2C19MAPT
SCHEMBL247466 0.81 PPARA (0.68) PPARAMEN1KMT2ACYP2C19MAPT
SCHEMBL27597867 0.81 PPARA (0.41) PPARAMEN1KMT2ACYP2C19MAPT
Clofibric Acid SCHEMBL11639907 0.81 PPARA (0.68) PPARAMEN1KMT2ACYP2C19MAPT
SCHEMBL7288524 0.80 KCNN4 (0.52) PPARAMEN1KMT2ACYP2C19MAPT
Hydrochloric Acid SCHEMBL8889149 0.79 PPARA (0.66) PPARAMEN1KMT2ACYP2C19MAPT
SCHEMBL13072375 0.79 PPARA (0.50) PPARAMEN1KMT2ACYP2C19MAPT
SCHEMBL7032523 0.79 PPARA (0.66) PPARAMEN1KMT2ACYP2C19MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0997453-B1 Phenoxyisobutyric acid ammonium salts and pharmaceutical formulations containing them FATRO SPA (IT) 2003-02-05 EP disclosed
EP-0997453-A1 Phenoxyisobutyric acid ammonium salts and pharmaceutical formulations containing them FATRO S.p.A. (IT) 2000-05-03 EP disclosed