SCHEMBL9236846

SCHEMBL9236846

CC(=O)Nc1cc(N)ccc1N=Nc1cc2c(S(=O)(=O)[O-])cc(S(=O)(=O)[O-])cc2cc1S(=O)(=O)[O-].[Na+].[Na+].[Na+]

nearest known ligand 0.46

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 3/20 0.38
▸ CA1 known ✓ P00915 2/20 0.35
▸ THRB known ✓ P10828 2/20 0.34
▸ APEX1 P27695 2/20 0.46
▸ ENPP2 Q13822 2/20 0.40
▸ PTPN1 P18031 2/20 0.39
▸ USP2 O75604 1/20 0.39
▸ ATM Q13315 1/20 0.39
▸ L3MBTL1 Q9Y468 1/20 0.39
▸ NPC1 O15118 1/20 0.38
▸ CA3 P07451 1/20 0.38
▸ SIRT1 Q96EB6 3/20 0.36
▸ SIRT2 Q8IXJ6 2/20 0.36
▸ PRMT1 Q99873 1/20 0.35
▸ CASP6 P55212 1/20 0.35
▸ CA9 Q16790 2/20 0.35
▸ MAPT P10636 2/20 0.35
▸ P2RY13 Q9BPV8 2/20 0.35
▸ TDP1 Q9NUW8 2/20 0.35
▸ TSHR P16473 2/20 0.35

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
SCHEMBL9238786 0.92 APEX1 (0.47) APEX1ENPP2PTPN1USP2ATM
SCHEMBL11750615 0.84 ENPP2 (0.44) APEX1ENPP2PTPN1USP2ATM
SCHEMBL8047831 0.84 ENPP2 (0.49) ENPP2NPC1CA2CA3CASP6
SCHEMBL9236858 0.84 ENPP2 (0.49) ENPP2NPC1CA2CA3CASP6
SCHEMBL5889361 0.84 ENPP2 (0.49) ENPP2NPC1CA2CA3CASP6
SCHEMBL9236836 0.83 ENPP2 (0.48) ENPP2NPC1CA2CA3CASP6
SCHEMBL4699280 0.76 NT5E (0.41) ENPP2CASP6TDP1THRBALDH1A1
SCHEMBL9238793 0.76 NT5E (0.41) ENPP2CASP6TDP1THRBALDH1A1
SCHEMBL6030186 0.76 NT5E (0.41) ENPP2CASP6TDP1THRBALDH1A1
SCHEMBL9238781 0.76 NT5E (0.41) ENPP2CASP6TDP1THRBALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0681006-A1 Process for continuously reacting organic dyestuffs containing amino groups with trifluorotriazine HOECHST AKTIENGESELLSCHAFT (DE) 1995-11-08 — — EP disclosed
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