SCHEMBL11750615

SCHEMBL11750615

CC(=O)Nc1cc(N)ccc1N=Nc1cc(S(=O)(=O)[O-])ccc1S(=O)(=O)[O-].[Na+].[Na+]

nearest known ligand 0.44

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
▸ CA1 known ✓ P00915 4/20 0.40
▸ CA2 known ✓ P00918 4/20 0.40
▸ P2RY2 known ✓ P41231 2/20 0.37
▸ DHFR known ✓ P00374 1/20 0.36
▸ THRB known ✓ P10828 1/20 0.35
▸ ENPP2 Q13822 1/20 0.44
▸ NPC1 O15118 2/20 0.43
▸ APEX1 P27695 2/20 0.41
▸ CA9 Q16790 4/20 0.40
▸ PKM P14618 2/20 0.39
▸ CYP2C19 P33261 2/20 0.39
▸ AMY1A P0DUB6 2/20 0.37
▸ TDP1 Q9NUW8 2/20 0.36
▸ TSHR P16473 1/20 0.36
▸ SMN1; SMN2 Q16637 1/20 0.36
▸ SIRT2 Q8IXJ6 1/20 0.36
▸ SIRT1 Q96EB6 1/20 0.36
▸ MAPT P10636 2/20 0.36
▸ KDM4E B2RXH2 1/20 0.36
▸ MEN1 O00255 1/20 0.36

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
SCHEMBL9236846 0.84 APEX1 (0.46) ENPP2NPC1APEX1CA1CA2
SCHEMBL11750629 0.84 ENPP2 (0.52) ENPP2NPC1CA1CA2CA9
SCHEMBL9626814 0.80 ENPP2 (0.56) ENPP2NPC1CA1CA2CA9
SCHEMBL14004209 0.77 ENPP2 (0.60) ENPP2NPC1CA1CA2CA9
SCHEMBL11424803 0.76 ENPP2 (0.43) ENPP2APEX1TDP1TSHRMAPT
SCHEMBL9238786 0.75 APEX1 (0.47) ENPP2APEX1PKMTDP1TSHR
SCHEMBL9626740 0.73 ENPP2 (0.47) ENPP2NPC1TDP1MAPTKDM4E
SCHEMBL9626874 0.73 ENPP2 (0.47) ENPP2NPC1TDP1MAPTKDM4E
SCHEMBL8047831 0.73 ENPP2 (0.49) ENPP2NPC1CA2MEN1KMT2A
SCHEMBL9236858 0.73 ENPP2 (0.49) ENPP2NPC1CA2MEN1KMT2A

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
US-4065446-A Reactive dyestuffs containing urea alkylene linkage between chromophore and reactive radical BAYER AKTIENGESELLSCHAFT (DT) 1977-12-27 — — US disclosed
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