SCHEMBL974086

SCHEMBL974086

O=S(=O)([O-])Oc1cccc2c(OS(=O)(=O)[O-])cccc12.[Na+].[Na+]

nearest known ligand 0.52

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 14)

geneUniProtsupporting neighboursconfidence
ESR2 known ✓ Q92731 2/20 0.46
GAA P10253 3/20 0.46
MEN1 O00255 2/20 0.46
ESR1 P03372 2/20 0.46
KMT2A Q03164 2/20 0.46
SLC6A4 P31645 1/20 0.37
F11 P03951 6/20 0.36
ALDH1A1 P00352 2/20 0.33
SMN1; SMN2 Q16637 2/20 0.33
ELANE P08246 1/20 0.33
CISD1 Q9NZ45 1/20 0.33
NFKB1 P19838 1/20 0.33
PTPN1 P18031 1/20 0.33
DUSP5 Q16690 1/20 0.33

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
SCHEMBL974174 0.91 F11 (0.40) GAAMEN1ESR1KMT2AESR2
SCHEMBL7156677 0.88 ESR1 (0.62) GAAMEN1ESR1KMT2AESR2
SCHEMBL28119137 0.87 KMT2A (0.46) GAAMEN1KMT2AALDH1A1
Methane SCHEMBL27611186 0.86 KMT2A (0.45) GAAMEN1KMT2AALDH1A1
SCHEMBL4094195 0.85 ELANE (0.40) F11ALDH1A1SMN1; SMN2ELANECISD1
SCHEMBL7932480 0.84 MEN1 (0.37) GAAMEN1ESR1KMT2AESR2
SCHEMBL7159703 0.80 GAA (0.50) GAAMEN1ESR1KMT2AESR2
Ether SCHEMBL11474697 0.77 TSHR (0.44) GAAMEN1KMT2ASLC6A4ALDH1A1
SCHEMBL18532780 0.76 ELANE (0.57) GAAMEN1ESR1KMT2AESR2
SCHEMBL10818956 0.76 ESR1 (0.42) GAAMEN1ESR1KMT2AESR2

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
US-7875412-B2 silanetriol sulfonate complexes; for printers, copiers, facsimile machines; improved durability and environmental resistance ORIENT CHEMICAL INDUSTRIES, LTD. (JP) 2011-01-25 US disclosed
EP-1843214-A1 Positive electrified charge control agent and positive electrified toner for developing electrostatic image Orient Chemical Industries, Ltd. (JP) 2007-10-10 EP disclosed
US-20070231726-A1 Positive electrified charge control agent and positive electrified toner for developing electrostatic image ORIENT CHEMICAL INDUSTRIES, LTD. (JP) 2007-10-04 US disclosed