SCHEMBL20514980

SCHEMBL20514980

Cn1cc([N+](=O)[O-])cc1C(=O)Nc1cc(C(=O)Nc2ccc3c(S(=O)(=O)[O-])cccc3c2S(=O)(=O)[O-])n(C)c1.[Na+].[Na+]

nearest known ligand 0.83

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
HPSE Q9Y251 8/20 0.83
CD40 P25942 1/20 0.37
CD40LG P29965 1/20 0.37
MAPT P10636 5/20 0.35
KMT2A Q03164 5/20 0.35
LMNA P02545 4/20 0.35
TDP1 Q9NUW8 4/20 0.35
POLB P06746 3/20 0.35
PKM P14618 3/20 0.35
TSHR P16473 3/20 0.35
NFKB1 P19838 3/20 0.35
APEX1 P27695 3/20 0.35
RECQL P46063 3/20 0.35
BLM P54132 3/20 0.35
HSD17B10 Q99714 3/20 0.35
ALDH1A1 P00352 3/20 0.35
CYP3A4 P08684 2/20 0.35
GAA P10253 2/20 0.35
P2RX1 P51575 2/20 0.35
P2RX3 P56373 2/20 0.35

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
SCHEMBL20514950 0.95 HPSE (0.75) HPSECD40CD40LGMAPTKMT2A
SCHEMBL20514940 0.92 HPSE (0.80) HPSEMAPTKMT2ALMNATDP1
SCHEMBL20514939 0.92 HPSE (0.78) HPSEMAPTKMT2ATDP1POLB
SCHEMBL20514961 0.88 HPSE (0.79) HPSEMAPTKMT2ALMNATDP1
SCHEMBL20514976 0.87 HPSE (0.80) HPSEMAPTKMT2ALMNATDP1
SCHEMBL20514932 0.86 HPSE (0.84) HPSEMAPTKMT2ALMNATDP1
SCHEMBL20514929 0.86 HPSE (0.90) HPSEMAPTKMT2ALMNATDP1
Hydrochloric Acid SCHEMBL20515018 0.86 HPSE (0.83) HPSEMAPTKMT2ALMNATDP1
SCHEMBL20514934 0.85 HPSE (0.79) HPSEMAPTKMT2APOLBALDH1A1
SCHEMBL20514941 0.83 HPSE (0.81) HPSEMAPTKMT2ALMNATDP1

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
EP-3381897-A1 DERIVATIVES OF THE DISODIUM 2,2'-{CARBONYLBIS[IMINO-3,1-PHENYLENECARBONYLIMINO(1-METHYL-1H-PYRROLE-4,2-DIYL)CARBONYLIMINO]}DINAPHTHALENE-1,5-DISULFONATE SALT AND RELATED COMPOUNDS AS HEPARANASE INHIBITORS FOR THE TREATMENT OF CANCER Leadiant Biosciences SA (CH) 2018-10-03 EP disclosed