SCHEMBL11212331

SCHEMBL11212331

O=C(Nc1ccc2cc(S(=O)(=O)[O-])cc(O)c2c1)c1ccc([N+](=O)[O-])cc1.[Na+]

nearest known ligand 0.54

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
▸ FGF1 known ✓ P05230 1/20 0.48
▸ CA12 known ✓ O43570 1/20 0.47
▸ CA1 known ✓ P00915 2/20 0.47
▸ CA2 known ✓ P00918 2/20 0.47
▸ SIRT1 Q96EB6 1/20 0.54
▸ PRMT1 Q99873 1/20 0.54
▸ ATM Q13315 1/20 0.51
▸ RAB9A P51151 6/20 0.50
▸ MAPT P10636 4/20 0.50
▸ MEN1 O00255 6/20 0.49
▸ KMT2A Q03164 6/20 0.49
▸ NPC1 O15118 3/20 0.48
▸ CASP6 P55212 2/20 0.48
▸ ALDH1A1 P00352 1/20 0.48
▸ CTDSP1 Q9GZU7 1/20 0.48
▸ CASP3 P42574 2/20 0.47
▸ CASP2 P42575 1/20 0.47
▸ CASP7 P55210 1/20 0.47
▸ CASP8 Q14790 1/20 0.47
▸ NT5E P21589 1/20 0.47

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
SCHEMBL11208714 0.90 CASP6 (0.60) PRMT1ATMRAB9AMAPTMEN1
SCHEMBL11346743 0.89 CASP6 (0.59) PRMT1ATMRAB9AMAPTMEN1
SCHEMBL11215154 0.85 MAPT (0.53) SIRT1PRMT1ATMRAB9AMAPT
SCHEMBL11208448 0.85 MEN1 (0.52) SIRT1PRMT1ATMRAB9AMAPT
SCHEMBL11423173 0.84 CASP6 (0.53) ATMRAB9AMAPTMEN1KMT2A
SCHEMBL10823704 0.83 CA2 (0.52) SIRT1PRMT1MAPTMEN1KMT2A
SCHEMBL11431595 0.82 CASP6 (0.71) SIRT1PRMT1ATMRAB9AMAPT
SCHEMBL14418594 0.81 ATM (0.60) ATMRAB9AMAPTMEN1KMT2A
SCHEMBL10907666 0.79 SIRT1 (0.55) SIRT1PRMT1MAPTMEN1KMT2A
SCHEMBL10908133 0.79 MEN1 (0.64) RAB9AMAPTMEN1KMT2ANPC1

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
EP-0013784-B1 C-SUBSTITUTED NAPHTHALENEMONOSULFONIC UREIDES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AMERICAN CYANAMID COMPANY (US) 1983-02-23 — — EP disclosed
US-4297372-A ANTIARTHRITIC AGENTS; COLLAGENASE AND PROTEOLYTIC ENZYME INHIBITORS; BONE, SKIN, AND ORAL DISORDERS AMERICAN CYANAMID COMPANY (US) 1981-10-27 — — US disclosed
EP-0013784-A1 C-Substituted naphthalenemonosulfonic ureides, process for their preparation and pharmaceutical compositions containing them AMERICAN CYANAMID COMPANY (US) 1980-08-06 — — EP disclosed
US-4216165-A Amine precursors to ureide inhibitors of connective tissue destruction AMERICAN CYANAMID COMPANY (US) 1980-08-05 — — US disclosed
US-4216164-A Ureide inhibitors of connective tissue destruction AMERICAN CYANAMID COMPANY (US) 1980-08-05 — — US disclosed
US-4216166-A Nitro precursors to amine precursors to ureide inhibitors of connective tissue destruction AMERICAN CYANAMID COMPANY (US) 1980-08-05 — — US disclosed
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