SCHEMBL2218463

SCHEMBL2218463

COc1nc(Cl)nc(Nc2ccc(C=Cc3ccc(Nc4nc(Nc5ccccc5)nc(OC)n4)cc3S(=O)(=O)[O-])c(S(=O)(=O)[O-])c2)n1.[Na+].[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
P2RY2 known ✓ P41231 4/20 0.54
P2RY12 known ✓ Q9H244 3/20 0.54
CA1 known ✓ P00915 3/20 0.47
CA2 known ✓ P00918 3/20 0.47
CA12 known ✓ O43570 2/20 0.47
P2RY4 known ✓ P51582 4/20 0.44
THRB known ✓ P10828 1/20 0.44
P2RY6 known ✓ Q15077 2/20 0.43
P2RY1 known ✓ P47900 1/20 0.41
CA9 Q16790 3/20 0.47
RAD51 Q06609 2/20 0.46
CARM1 Q86X55 1/20 0.45
PRMT1 Q99873 1/20 0.45
MAPT P10636 3/20 0.44
MEN1 O00255 2/20 0.44
MAPK1 P28482 2/20 0.44
KMT2A Q03164 2/20 0.44
LMNA P02545 2/20 0.44
USP2 O75604 1/20 0.44
TP53 P04637 1/20 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
SCHEMBL2206062 0.94 P2RY12 (0.54) P2RY2P2RY12CA1CA2CA9
SCHEMBL29363604 0.94 RAD51 (0.51) P2RY2P2RY12CA1CA2CA9
SCHEMBL3141243 0.94 RAD51 (0.51) P2RY2P2RY12CA1CA2CA9
SCHEMBL30860146 0.94 RAD51 (0.51) P2RY2P2RY12CA1CA2CA9
SCHEMBL8411103 0.94 RAD51 (0.51) P2RY2P2RY12CA1CA2CA9
SCHEMBL2221118 0.93 CA1 (0.50) P2RY2P2RY12CA1CA2CA9
Potassium Ion SCHEMBL2219759 0.92 P2RY12 (0.52) P2RY2P2RY12CA1CA2CA9
Potassium Ion SCHEMBL2217018 0.91 CA1 (0.50) P2RY2P2RY12CA1CA2CA9
Potassium Ion SCHEMBL2220070 0.91 P2RY2 (0.51) P2RY2P2RY12CA1CA2CA9
SCHEMBL11879420 0.91 CA12 (0.56) P2RY2P2RY12CA1CA2CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8546300-B2 Thermosensitive recording material and image recording method RICOH COMPANY, LTD. (JP) 2013-10-01 US disclosed
US-20110177941-A1 THERMOSENSITIVE RECORDING MATERIAL AND IMAGE RECORDING METHOD RICOH COMPANY, LTD. (JP) 2011-07-21 US disclosed