SCHEMBL11432583

SCHEMBL11432583

O=C([O-])c1cc(C(=O)Nc2ccc(S(=O)(=O)O)c3cc(S(=O)(=O)[O-])cc(O)c23)cc([N+](=O)[O-])c1.[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
F11 P03951 1/20 0.46
SIRT2 Q8IXJ6 3/20 0.45
SIRT1 Q96EB6 3/20 0.45
KMT2A Q03164 8/20 0.44
MAPT P10636 6/20 0.44
RECQL P46063 5/20 0.44
HSD17B10 Q99714 5/20 0.44
TDP1 Q9NUW8 5/20 0.44
POLB P06746 5/20 0.44
ALDH1A1 P00352 4/20 0.44
LMNA P02545 4/20 0.44
PKM P14618 4/20 0.44
NFKB1 P19838 4/20 0.44
APEX1 P27695 4/20 0.44
P2RX1 P51575 4/20 0.44
BLM P54132 4/20 0.44
CYP3A4 P08684 3/20 0.44
TSHR P16473 3/20 0.44
P2RX3 P56373 3/20 0.44
GAA P10253 2/20 0.44

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
SCHEMBL11432585 0.86 TIMP3 (0.49) SIRT2SIRT1KMT2AMAPTRECQL
SCHEMBL10413972 0.81 TIMP3 (0.58) F11SIRT2SIRT1KMT2AMAPT
SCHEMBL11593396 0.81 TIMP3 (0.63) F11SIRT2SIRT1KMT2AMAPT
SCHEMBL10413406 0.81 MEN1 (0.58) SIRT2SIRT1KMT2AMAPTRECQL
SCHEMBL11444112 0.77 F11 (0.48) F11SIRT2SIRT1KMT2AMAPT
SCHEMBL11444114 0.76 TIMP3 (0.46) SIRT2SIRT1KMT2AMAPTRECQL
SCHEMBL11425899 0.76 TIMP3 (0.56) SIRT2SIRT1KMT2AMAPTRECQL
SCHEMBL11444111 0.75 TIMP3 (0.45) SIRT2SIRT1KMT2AMAPTRECQL
SCHEMBL11407259 0.75 TIMP3 (0.55) SIRT2SIRT1KMT2AMAPTRECQL
SCHEMBL11587242 0.75 P2RY11 (0.53) F11SIRT2SIRT1KMT2AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4229584-A Ureylenebis(anionic substituted phenylene carbonyl)imino naphthalene sulfonic acids and naphthalene carboxylic acids and their salts AMERICAN CYANAMID COMPANY (US) 1980-10-21 US disclosed
US-4177209-A COMPLEMENT INHIBITORS AMERICAN CYANAMID COMPANY (US) 1979-12-04 US disclosed
US-4129590-A INHIBITORS OF THE COMPLEMENT SYSTEM AMERICAN CYANAMID COMPANY (US) 1978-12-12 US disclosed