SCHEMBL11100676

SCHEMBL11100676

Nc1c(N=Nc2ccc(S(=O)(=O)CCOS(=O)(=O)[O-])cc2)c(S(=O)(=O)[O-])cc2cc(S(=O)(=O)[O-])cc(O)c12.[Na+].[Na+].[Na+]

nearest known ligand 0.82

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 3/20 0.82
▸ MEN1 O00255 1/20 0.47
▸ POLB P06746 1/20 0.47
▸ GRK2 P25098 1/20 0.47
▸ KMT2A Q03164 1/20 0.47
▸ PLEC Q15149 1/20 0.47
▸ APP P05067 1/20 0.44
▸ PTPN1 P18031 3/20 0.43
▸ USP2 O75604 1/20 0.43
▸ ATM Q13315 1/20 0.43
▸ L3MBTL1 Q9Y468 1/20 0.43
▸ ENPP2 Q13822 4/20 0.43
▸ APEX1 P27695 2/20 0.43
▸ DUSP5 Q16690 1/20 0.39
▸ ALDH1A1 P00352 1/20 0.38
▸ CYP3A4 P08684 1/20 0.38
▸ ALOX15 P16050 1/20 0.38
▸ ALOX12 P18054 1/20 0.38
▸ MAPK1 P28482 1/20 0.38
▸ RECQL P46063 1/20 0.38

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
SCHEMBL29833902 0.91 THRB (1.00) THRBMEN1POLBGRK2KMT2A
SCHEMBL2304009 0.91 THRB (1.00) THRBMEN1POLBGRK2KMT2A
SCHEMBL109532 0.91 THRB (1.00) THRBMEN1POLBGRK2KMT2A
SCHEMBL2304007 0.85 THRB (0.89) THRBMEN1POLBGRK2KMT2A
SCHEMBL2304038 0.85 THRB (0.89) THRBMEN1POLBGRK2KMT2A
SCHEMBL13069904 0.83 THRB (0.62) THRBMEN1KMT2AENPP2MAPK1
SCHEMBL7977352 0.83 THRB (0.62) THRBMEN1KMT2AENPP2MAPK1
SCHEMBL29425680 0.80 ENPP2 (0.61) THRBMEN1POLBGRK2KMT2A
SCHEMBL15153906 0.80 ENPP2 (0.61) THRBMEN1POLBGRK2KMT2A
SCHEMBL11129981 0.78 THRB (0.78) THRBMEN1POLBGRK2KMT2A

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
US-4464297-A Fiber reactive bisazo dye having both a vinylsulfone type reactive group and an ortho-nitrophenyl group SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1984-08-07 — — US disclosed
EP-0071035-A1 Reactive mono-functional bisazo blue-black dye SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1983-02-09 — — EP disclosed
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