SCHEMBL11439995

SCHEMBL11439995

CC(=O)Nc1ccc2c(S(=O)(=O)[O-])cc(S(=O)(=O)[O-])cc2c1NC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)[O-].[Na+].[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
▸ KMT2A Q03164 6/20 0.41
▸ MAPT P10636 4/20 0.41
▸ SMN1; SMN2 Q16637 2/20 0.40
▸ RORC P51449 2/20 0.38
▸ P2RY11 Q96G91 1/20 0.36
▸ CYP19A1 P11511 1/20 0.36
▸ POLB P06746 1/20 0.36
▸ MEN1 O00255 3/20 0.36
▸ F11 P03951 1/20 0.36
▸ HTT P42858 2/20 0.36
▸ LMNA P02545 1/20 0.36
▸ SLC5A1 P13866 1/20 0.36
▸ NCOA1 Q15788 1/20 0.36
▸ NCOA3 Q9Y6Q9 1/20 0.36
▸ KDM4E B2RXH2 1/20 0.36
▸ ALDH1A1 P00352 1/20 0.36
▸ CYP3A4 P08684 1/20 0.36
▸ HPGD P15428 1/20 0.36
▸ TDP1 Q9NUW8 1/20 0.36
▸ DUSP5 Q16690 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
SCHEMBL11439998 0.86 KMT2A (0.41) KMT2AMAPTSMN1; SMN2RORCCYP19A1
SCHEMBL11438055 0.85 NPC1 (0.41) KMT2AMAPTSMN1; SMN2P2RY11POLB
SCHEMBL11439992 0.85 KMT2A (0.41) KMT2AMAPTSMN1; SMN2RORCCYP19A1
SCHEMBL11437642 0.81 F11 (0.42) KMT2AMAPTSMN1; SMN2RORCP2RY11
SCHEMBL11432545 0.79 F11 (0.58) KMT2AMAPTSMN1; SMN2P2RY11POLB
SCHEMBL11437672 0.77 RORC (0.43) KMT2AMAPTSMN1; SMN2RORCPOLB
SCHEMBL11432497 0.76 CA2 (0.41) KMT2AMAPTSMN1; SMN2P2RY11MEN1
SCHEMBL11444087 0.76 APEX1 (0.43) KMT2AMAPTSMN1; SMN2RORCPOLB
SCHEMBL11444112 0.76 F11 (0.48) KMT2AMAPTSMN1; SMN2P2RY11POLB
SCHEMBL11418891 0.75 APEX1 (0.43) KMT2AMAPTSMN1; SMN2RORCP2RY11

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
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