SCHEMBL1804430

SCHEMBL1804430

O=C1c2ccccc2C(=O)C(S(=O)(=O)[O-])C1S(=O)(=O)[O-].[Na+].[Na+]

nearest known ligand 0.48

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
THRB known ✓ P10828 1/20 0.40
PPARG known ✓ P37231 1/20 0.40
MEN1 O00255 6/20 0.44
KMT2A Q03164 6/20 0.44
S100A4 P26447 3/20 0.44
POLB P06746 2/20 0.44
PTPN1 P18031 1/20 0.42
CDC25B P30305 1/20 0.42
MAPT P10636 4/20 0.41
LMNA P02545 2/20 0.41
MAPK1 P28482 2/20 0.41
TP53 P04637 2/20 0.41
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
HTR2B P41595 1/20 0.41
NPC1 O15118 3/20 0.40
RAB9A P51151 3/20 0.40
KDM4E B2RXH2 2/20 0.40
HTT P42858 2/20 0.40
SMN1; SMN2 Q16637 2/20 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
SCHEMBL1804432 0.73 MEN1 (0.44) MEN1KMT2AS100A4POLBCDC25B
SCHEMBL31589614 0.72 S100A4 (0.50) MEN1KMT2AS100A4POLBPTPN1
Anthraquinone SCHEMBL5082838 0.72 MEN1 (0.71) MEN1KMT2AS100A4POLBPTPN1
SCHEMBL7561441 0.71 SLC25A5 (0.40) MEN1KMT2AS100A4POLBCDC25B
SCHEMBL31493507 0.69 S100A4 (0.37) MEN1KMT2AS100A4POLBPTPN1
SCHEMBL677629 0.67 MEN1 (0.55) MEN1KMT2AS100A4POLBCDC25B
SCHEMBL15245116 0.67 MEN1 (0.55) MEN1KMT2AS100A4POLBCDC25B
Sulfuric Acid SCHEMBL989868 0.67 S100A4 (0.48) MEN1KMT2AS100A4POLBPTPN1
Sulfuric Acid SCHEMBL30989355 0.67 S100A4 (0.48) MEN1KMT2AS100A4POLBPTPN1
Naphthoquinone SCHEMBL5157257 0.67 IDO1 (0.70) MEN1KMT2AS100A4POLBPTPN1

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-2011055142-A2 1,4-QUINONES AND THEIR SULFUR ANALOGUES USEFUL AS LIGANDS OF N-ACETYLTRANSFERASES ISIS INNOVATION LIMITED (GB) 2011-05-12 WO disclosed