SCHEMBL17675159

SCHEMBL17675159

O=[N+]([O-])c1cccc(OS(=O)(=O)[O-])c1.[Na+]

nearest known ligand 0.71

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 19)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 1/20 0.49
P2RY2 known ✓ P41231 5/20 0.46
TSHR P16473 3/20 0.53
LMNA P02545 1/20 0.53
GAA P10253 1/20 0.51
HTT P42858 1/20 0.51
KMT2A Q03164 1/20 0.51
SLC6A2 P23975 1/20 0.51
SLC6A4 P31645 1/20 0.51
SLC6A3 Q01959 1/20 0.51
GPR17 Q13304 7/20 0.49
CA5A P35218 1/20 0.49
CHRNB2 P17787 1/20 0.48
CHRNA4 P43681 1/20 0.48
ALDH1A1 P00352 3/20 0.46
ACHE P22303 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
ALOX15 P16050 1/20 0.46
F2 P00734 1/20 0.46

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
SCHEMBL7123260 0.86 TSHR (0.57) TSHRLMNAGAAHTTKMT2A
SCHEMBL22462541 0.83 TSHR (0.53) TSHRLMNAGAAHTTKMT2A
SCHEMBL8690576 0.83 TSHR (0.53) TSHRLMNAGAAHTTKMT2A
SCHEMBL7145541 0.83 TSHR (0.53) TSHRLMNAGAAHTTKMT2A
SCHEMBL9005003 0.83 GPR17 (0.55) TSHRLMNAGAAHTTKMT2A
SCHEMBL9000083 0.83 GPR17 (0.55) TSHRLMNAGAAHTTKMT2A
SCHEMBL9451297 0.83 CA2 (0.64) TSHRLMNAGAAHTTKMT2A
SCHEMBL8966976 0.81 CHRNB2 (0.54) TSHRLMNAGAAHTTKMT2A
SCHEMBL29413045 0.81 KMT2A (0.54) TSHRLMNAGAAHTTKMT2A
SCHEMBL28701811 0.81 TSHR (0.52) TSHRLMNAGAAHTTKMT2A

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117867872-A Low-temperature dyeing auxiliary agent and preparation method thereof 福盈化学(苏州)有限公司 2024-04-12 CN claimed
CN-117867872-A Low-temperature dyeing auxiliary agent and preparation method thereof 福盈化学(苏州)有限公司 2024-04-12 CN disclosed
EP-3203840-A1 MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR Vertex Pharmaceuticals Incorporated (US) 2017-08-16 EP disclosed
WO-2016057572-A1 MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MILLER MARK THOMAS (US) 2016-04-14 WO disclosed