SCHEMBL9436604

SCHEMBL9436604

O=C(O)c1cc(Cl)c(Cl)c(S(=O)(=O)[O-])c1.O=C(O)c1cc(Cl)c(Cl)c(S(=O)(=O)[O-])c1.[Na+].[Na+]

nearest known ligand 0.47

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 16)

geneUniProtsupporting neighboursconfidence
TTR P02766 3/20 0.47
ACLY P53396 3/20 0.44
TSHR P16473 1/20 0.41
TPMT P51580 2/20 0.41
TDP1 Q9NUW8 1/20 0.40
KMT2A Q03164 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
WDR5 P61964 1/20 0.37
LCK P06239 1/20 0.37
FYN P06241 1/20 0.37
SRD5A2 P31213 1/20 0.37
PLAU P00749 1/20 0.37
POLB P06746 1/20 0.36
HSD17B10 Q99714 1/20 0.36
PKM P14618 1/20 0.36
HCAR1 Q9BXC0 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
SCHEMBL9436607 0.86 CA2 (0.38) TTRACLY
SCHEMBL9040901 0.81 TTR (0.50) TTRACLYTSHRTPMTTDP1
SCHEMBL9436611 0.80 TTR (0.48) TTRACLYTSHRTPMTTDP1
SCHEMBL9038640 0.80 TTR (0.48) TTRACLYTSHRTPMTTDP1
SCHEMBL9042101 0.80 CA1 (0.56) TTRACLYTSHRTPMTTDP1
SCHEMBL1602825 0.77 LCK (0.42) TTRTSHRTPMTTDP1KMT2A
SCHEMBL7263572 0.76 TTR (0.68) TTRTSHRTPMTTDP1SMN1; SMN2
SCHEMBL10674447 0.75 ALDH1A1 (0.46) ACLYTSHRKMT2ASMN1; SMN2HSD17B10
Fluoride SCHEMBL27668632 0.74 TTR (0.65) TTRTSHRTPMTTDP1SMN1; SMN2
SCHEMBL11855494 0.72 CYP3A4 (0.43) TSHRTDP1HSD17B10

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-5373024-A 3,5-Substituted benzoylguanidines, process for their preparation, their use as a medicament of diagnostic and medicament containing them HOECHST AKTIENGESELLSCHAFT (DE) 1994-12-13 US disclosed