SCHEMBL7534353

SCHEMBL7534353

Nc1c(S(=O)(=O)[O-])cc(NS(=O)(=O)c2ccccc2)c2c1C(=O)c1ccccc1C2=O.[Na+]

nearest known ligand 0.84

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
P2RY4 known ✓ P51582 10/20 0.71
P2RY12 known ✓ Q9H244 8/20 0.71
P2RY2 known ✓ P41231 4/20 0.71
P2RY1 known ✓ P47900 2/20 0.71
P2RY6 known ✓ Q15077 2/20 0.71
CDK2 P24941 3/20 0.84
MEN1 O00255 1/20 0.65
POLB P06746 1/20 0.65
CCR6 P51684 1/20 0.65
BLM P54132 1/20 0.65
KMT2A Q03164 1/20 0.65
RXFP1 Q9HBX9 1/20 0.65
MET P08581 2/20 0.65
HGF P14210 2/20 0.65

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
SCHEMBL7538900 0.91 CDK2 (1.00) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL7535057 0.86 CDK2 (0.71) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL11612508 0.86 GNG2 (0.64) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL7534351 0.85 GNG2 (0.63) CDK2P2RY4P2RY12P2RY2P2RY1
Acid Blue 25 SCHEMBL790822 0.83 P2RY4 (1.00) CDK2P2RY4P2RY12P2RY2P2RY1
Acid Blue 25 SCHEMBL29355038 0.83 P2RY4 (1.00) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL11348172 0.83 P2RY4 (0.72) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL3026030 0.81 P2RY12 (1.00) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL11343912 0.81 P2RY4 (0.69) CDK2P2RY4P2RY12P2RY2P2RY1
SCHEMBL3032350 0.81 P2RY4 (0.80) CDK2P2RY4P2RY12P2RY2P2RY1

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
EP-0463993-B1 Process for the preparation of aminoanthraquinone derivatives CIBA SC HOLDING AG (CH) 2002-05-02 EP disclosed
US-5196553-A From bromaminic acid and a benzenesulfonamide or an amide, copper/I/ catalyst formed by in situ reduction of a copper/II/ salt, less copper required CIBA-GEIGY CORPORATION (US) 1993-03-23 US disclosed
EP-0463993-A1 Process for the preparation of aminoanthraquinone derivatives CIBA-GEIGY AG (CH) 1992-01-02 EP disclosed