SCHEMBL7364050

SCHEMBL7364050

O=[N+]([O-])Nc1ccc(S(=O)(=O)[O-])cc1.[Na+]

nearest known ligand 0.39

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
CA2 known ✓ P00918 6/20 0.37
CA1 known ✓ P00915 4/20 0.36
CA12 known ✓ O43570 2/20 0.33
P2RY12 known ✓ Q9H244 1/20 0.33
CA4 known ✓ P22748 1/20 0.33
CA9 Q16790 6/20 0.37
LMNA P02545 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
SIRT1 Q96EB6 1/20 0.35
PRMT1 Q99873 1/20 0.35
KMT2A Q03164 2/20 0.34
MEN1 O00255 1/20 0.33
POLB P06746 1/20 0.33
MMP1 P03956 1/20 0.33
MMP2 P08253 1/20 0.33
MMP9 P14780 1/20 0.33
MMP8 P22894 1/20 0.33
MMP13 P45452 1/20 0.33
CA3 P07451 1/20 0.33
CA6 P23280 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
SCHEMBL7364052 0.82 LMNA (0.45) CA9CA2LMNATDP1CA1
SCHEMBL11567649 0.79 ENPP2 (0.45) CA9CA2LMNACA1CA12
SCHEMBL27460156 0.79 CA2 (0.57) CA9CA2TDP1CA1KMT2A
SCHEMBL7364054 0.79 LMNA (0.46) CA9CA2LMNATDP1CA1
SCHEMBL7359879 0.79 ALDH1A1 (0.43) CA9CA2TDP1CA1KMT2A
SCHEMBL31732365 0.75 ALDH1A1 (0.38) CA9CA2LMNATDP1CA1
SCHEMBL9223945 0.75 HPGD (0.61) CA9CA2TDP1CA1KMT2A
SCHEMBL19953365 0.74 LMNA (0.55) CA9CA2LMNATDP1CA1
SCHEMBL5625358 0.73 CA1 (0.55) CA9CA2LMNATDP1CA1
Sulfuric Acid SCHEMBL1882493 0.72 CA9 (0.52) CA9CA2LMNATDP1CA1

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
EP-1086076-A1 SULFONAMIDE INHIBITORS OF ASPARTYL PROTEASE Vertex Pharmaceuticals Incorporated (US) 2001-03-28 EP disclosed
WO-1999065870-A2 SULFONAMIDE INHIBITORS OF ASPARTYL PROTEASE VERTEX PHARMACEUTICALS INCORPORATED (US) 1999-12-23 WO disclosed