SCHEMBL7738539

SCHEMBL7738539

CC(C)(C)c1cc([O-])cc(C(C)(C)C)c1.[Na+]

nearest known ligand 0.50

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
GABRA1 known ✓ P14867 1/20 0.50
GABRB2 known ✓ P47870 1/20 0.50
POLB P06746 1/20 0.40
GAA P10253 2/20 0.37
MAPT P10636 2/20 0.37
KDM4E B2RXH2 1/20 0.37
HTR1D P28221 2/20 0.34
RXRA P19793 5/20 0.34
RXRB P28702 5/20 0.34
RXRG P48443 3/20 0.34
ALDH1A1 P00352 3/20 0.33
HPGD P15428 1/20 0.33
ALOX15 P16050 1/20 0.33
HSD17B10 Q99714 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
TSHR P16473 1/20 0.33
CYP2C19 P33261 1/20 0.32
LMNA P02545 1/20 0.32
TYR P14679 1/20 0.32
HTR1B P28222 1/20 0.31

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 SCHEMBL7743976 0.94 GABRA1 (0.50) GABRA1GABRB2POLBGAAMAPT
SCHEMBL5702852 0.94 GABRA1 (0.50) GABRA1GABRB2POLBGAAMAPT
Lithium Ion SCHEMBL7743757 0.94 GABRA1 (0.50) GABRA1GABRB2POLBGAAMAPT
Hydrochloric Acid SCHEMBL6040026 0.92 GABRA1 (0.48) GABRA1GABRB2POLBGAAMAPT
SCHEMBL4366299 0.87 GABRA1 (0.44) GABRA1GABRB2POLBGAAMAPT
SCHEMBL93161 0.80 GABRA1 (0.69) GABRA1GABRB2POLBGAAMAPT
SCHEMBL10394690 0.77 GABRA1 (0.65) GABRA1GABRB2POLBGAAMAPT
SCHEMBL10415675 0.77 GABRA1 (0.65) GABRA1GABRB2POLBGAAMAPT
Trifluoromethanesulfonic Acid SCHEMBL7086757 0.76 GPR3 (0.38) GABRA1GABRB2ALDH1A1
Trifluoromethanesulfonic Acid SCHEMBL7089707 0.75 GABRA1 (0.39) GABRA1GABRB2RXRARXRBRXRG

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-6429273-B1 ANIONIC POLYMERIZATION OF STYRENE USING MAGNESIUM AND ALKALI METAL-BASED INITIATORS; CONTROLLED MOLECULAR WEIGHT DISTRIBUTION; CONTROLLABLE RATE PREVENTS RUNAWAY REACTION; EXCELLENT MOLDING CHARACTERISTICS ASAHI KASEI KABUSHIKI KAISHA (JP) 2002-08-06 US disclosed