SCHEMBL9513069

SCHEMBL9513069

CCCCCCCCCCCCCCCCCCOc1ccc(C(=O)[O-])cc1OCCCCCCCCCCCCCCCCCC.[Na+]

nearest known ligand 0.65

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 11)

geneUniProtsupporting neighboursconfidence
THRA known ✓ P10827 2/20 0.54
THRB known ✓ P10828 2/20 0.54
PDE4B known ✓ Q07343 1/20 0.50
SMPD1 P17405 6/20 0.59
ALDH1A1 P00352 1/20 0.53
HPGD P15428 1/20 0.53
PTPN11 Q06124 1/20 0.52
CNR2 P34972 1/20 0.52
PLA2G4B P0C869 1/20 0.50
PLA2G2D Q9UNK4 1/20 0.49
S1PR3 Q99500 1/20 0.49

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
SCHEMBL9512878 1.00 SMPD1 (0.59) SMPD1THRATHRBALDH1A1HPGD
Tetramethylammonium Ion SCHEMBL9512800 0.94 SMPD1 (0.56) SMPD1THRATHRBALDH1A1HPGD
SCHEMBL9513086 0.86 SMPD1 (0.49) SMPD1THRATHRBALDH1A1HPGD
SCHEMBL1201602 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B
SCHEMBL1231278 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B
SCHEMBL1200986 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B
SCHEMBL1199953 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B
SCHEMBL1199847 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B
SCHEMBL1199892 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B
SCHEMBL1201534 0.86 ALDH1A1 (0.69) SMPD1ALDH1A1HPGDPTPN11PLA2G4B

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
EP-0308977-B1 Anthracycline derivatives having inhibitory activity against reverse transcriptase of human immunodeficiency virus ZAIDAN HOJIN BISEIBUTSU (JP) 1993-12-08 EP disclosed
US-5003055-A Anthracycline derivatives having inhibitory activity against reverse transcriptase of human immunodeficiency virus ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1991-03-26 US disclosed
EP-0308977-A2 Anthracycline derivatives having inhibitory activity against reverse transcriptase of human immunodeficiency virus ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1989-03-29 EP disclosed