SCHEMBL4881910

SCHEMBL4881910

Nc1ccc(/N=N/c2ccc(S(=O)(=O)[O-])cc2)cc1S(=O)(=O)[O-].[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 20)

geneUniProtsupporting neighboursconfidence
▸ THRB known ✓ P10828 1/20 0.43
▸ CA12 known ✓ O43570 3/20 0.43
▸ CA2 known ✓ P00918 3/20 0.43
▸ PTGS1 known ✓ P23219 3/20 0.42
▸ PTGS2 known ✓ P35354 3/20 0.42
▸ SLC7A11 Q9UPY5 3/20 0.52
▸ PLCG1 P19174 1/20 0.50
▸ APP P05067 2/20 0.46
▸ GLB1 P16278 1/20 0.46
▸ CHAT P28329 1/20 0.46
▸ ENPP2 Q13822 1/20 0.46
▸ PHLPP2 Q6ZVD8 1/20 0.46
▸ CTRC Q99895 1/20 0.46
▸ CA9 Q16790 3/20 0.43
▸ MAPT P10636 3/20 0.41
▸ TDP1 Q9NUW8 3/20 0.41
▸ USP2 O75604 3/20 0.41
▸ KDM4E B2RXH2 2/20 0.41
▸ ALDH1A1 P00352 2/20 0.41
▸ LTA P01374 2/20 0.41

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
SCHEMBL339834 1.00 SLC7A11 (0.52) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL22974903 0.89 SENP2 (0.53) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL29837421 0.89 SENP2 (0.50) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL11200690 0.82 CA12 (0.51) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL11202854 0.82 PTGS1 (0.53) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL11202850 0.82 PTGS1 (0.53) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL11200679 0.82 CA12 (0.51) SLC7A11PLCG1APPGLB1CHAT
SCHEMBL8772805 0.80 LMNA (0.47) SLC7A11CA12CA2CA9MAPT
SCHEMBL9618266 0.78 CA12 (0.68) SLC7A11PLCG1THRBCA12CA2
SCHEMBL2394481 0.78 CA12 (0.68) SLC7A11PLCG1THRBCA12CA2

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-8262201-B2 Micro writing and reading HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. (US) 2012-09-11 — — US disclosed
US-20080252690-A1 Micro Writing And Reading HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2008-10-16 — — US disclosed
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