SCHEMBL1015240

SCHEMBL1015240

O=C(COCC(=O)N(c1ccccc1)C1CCCCC1)Nc1ccc(Cl)cc1C(=O)[O-].[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
THRB known ✓ P10828 1/20 0.39
MEN1 O00255 4/20 0.46
KMT2A Q03164 4/20 0.46
ALDH1A1 P00352 3/20 0.46
KDM4E B2RXH2 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
NPC1 O15118 2/20 0.46
RAB9A P51151 2/20 0.46
MITF O75030 1/20 0.46
PAX8 Q06710 1/20 0.46
TRPM8 Q7Z2W7 1/20 0.43
SERPINE1 P05121 1/20 0.43
LMNA P02545 2/20 0.41
MAPT P10636 4/20 0.41
POLB P06746 3/20 0.40
TP53 P04637 2/20 0.40
MAPK1 P28482 1/20 0.39
G6PD P11413 1/20 0.39
GAA P10253 1/20 0.39
CYP1A2 P05177 1/20 0.39

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
SCHEMBL1014856 0.92 SERPINE1 (0.51) MEN1KMT2AALDH1A1KDM4ESMN1; SMN2
SCHEMBL1015239 0.91 SERPINE1 (0.50) MEN1KMT2AALDH1A1KDM4ESMN1; SMN2
SCHEMBL1014777 0.89 ALDH1A1 (0.46) MEN1KMT2AALDH1A1KDM4ESMN1; SMN2
SCHEMBL1013772 0.88 KMT2A (0.44) MEN1KMT2AALDH1A1KDM4ENPC1
SCHEMBL1797139 0.83 MAPT (0.47) MEN1KMT2AALDH1A1KDM4ESMN1; SMN2
SCHEMBL1015397 0.81 SERPINE1 (0.50) MEN1KMT2AALDH1A1KDM4ESERPINE1
SCHEMBL1013771 0.80 SERPINE1 (0.49) MEN1KMT2AALDH1A1KDM4ESERPINE1
SCHEMBL1013555 0.77 KMT2A (0.48) MEN1KMT2AALDH1A1KDM4ESMN1; SMN2
SCHEMBL1012593 0.76 SERPINE1 (0.52) ALDH1A1NPC1MITFSERPINE1
SCHEMBL1798112 0.74 SERPINE1 (0.56) MEN1KMT2AALDH1A1KDM4ENPC1

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
EP-2990057-B1 PAI-1 INHIBITOR FOR USE IN ENHANCING THE ANTITUMOR EFFECT OF AN ANTITUMOR AGENT IN A PATIENT RENASCIENCE CO LTD (JP) 2019-03-20 EP disclosed
EP-2272822-A1 INHIBITOR OF PLASMINOGEN ACTIVATOR INHIBITOR-1 Renascience CO., LTD. (JP) 2011-01-12 EP disclosed