SCHEMBL5314795

SCHEMBL5314795

Cc1cc(-c2ccc(NCCS(=O)(=O)[O-])c(C)c2)ccc1NCCS(=O)(=O)[O-].[Na+].[Na+]

nearest known ligand 0.41

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
CA12 known ✓ O43570 1/20 0.32
CA2 known ✓ P00918 1/20 0.32
P2RY2 known ✓ P41231 1/20 0.32
P2RY4 known ✓ P51582 1/20 0.32
THRB known ✓ P10828 1/20 0.32
MET P08581 2/20 0.41
KIF11 P52732 1/20 0.38
MAPT P10636 3/20 0.35
HTT P42858 1/20 0.35
BBOX1 O75936 1/20 0.34
AR P10275 1/20 0.34
VDR P11473 1/20 0.34
LMNA P02545 2/20 0.33
HPGD P15428 2/20 0.33
HSD17B10 Q99714 2/20 0.33
MAPK1 P28482 2/20 0.33
TDP1 Q9NUW8 1/20 0.33
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
CYP3A4 P08684 2/20 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
SCHEMBL5314416 0.82 KIF11 (0.39) METKIF11MAPTHTTAR
SCHEMBL5314794 0.81 KIF11 (0.38) METKIF11MAPTHTTAR
SCHEMBL5314740 0.76 KIF11 (0.38) KIF11MAPTHTTARVDR
SCHEMBL5313590 0.76 KIF11 (0.38) KIF11MAPTHTTARVDR
SCHEMBL5311924 0.75 VDR (0.38) METKIF11HTTARVDR
SCHEMBL29391622 0.75 VDR (0.38) METKIF11HTTARVDR
SCHEMBL18747679 0.69 SMN1; SMN2 (0.49) MAPTHTTHPGDMAPK1MEN1
SCHEMBL14253796 0.69 L3MBTL1 (0.47) MAPTHTTARVDRMAPK1
SCHEMBL4822328 0.68 L3MBTL1 (0.42) MAPTHTTARVDRTDP1
SCHEMBL3489701 0.67 PKM (0.52) MAPTLMNAMAPK1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070224691-A1 Composition for measuring concentration of residual chlorine MIURA CO., LTD. 2007-09-27 US claimed
EP-1837653-A1 Composition for measuring concentration of residual chlorine MIURA CO., LTD. (JP) 2007-09-26 EP claimed
US-20070224691-A1 Composition for measuring concentration of residual chlorine MIURA CO., LTD. 2007-09-27 US disclosed
US-20070224691-A1 Composition for measuring concentration of residual chlorine MIURA CO., LTD. 2007-09-27 US disclosed
EP-1837653-A1 Composition for measuring concentration of residual chlorine MIURA CO., LTD. (JP) 2007-09-26 EP disclosed
EP-1837653-A1 Composition for measuring concentration of residual chlorine MIURA CO., LTD. (JP) 2007-09-26 EP disclosed