SCHEMBL6131782

SCHEMBL6131782

CC(=O)O[BH-](OC(C)=O)OC(C)=O.COc1ccccc1N1CCN(Cc2ccc(O)c(F)c2)CC1.[Na+]

nearest known ligand 0.58

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 12)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.58
MAPK1 P28482 2/20 0.57
HTR7 P34969 3/20 0.53
POLB P06746 1/20 0.53
KDM4E B2RXH2 4/20 0.53
SMN1; SMN2 Q16637 2/20 0.53
GAA P10253 2/20 0.53
TDP1 Q9NUW8 1/20 0.53
DRD4 P21917 2/20 0.52
DRD2 P14416 1/20 0.52
DRD3 P35462 1/20 0.52
KMT2A Q03164 2/20 0.51

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
SCHEMBL7691290 0.89 ALDH1A1 (0.71) ALDH1A1MAPK1HTR7KDM4ESMN1; SMN2
SCHEMBL9720648 0.79 HTR7 (0.70) ALDH1A1MAPK1HTR7POLBKDM4E
SCHEMBL6132013 0.77 KDM4E (0.63) HTR7KDM4ESMN1; SMN2GAATDP1
SCHEMBL6131871 0.76 ALDH1A1 (0.75) ALDH1A1MAPK1HTR7KDM4ESMN1; SMN2
Hydrochloric Acid SCHEMBL6131815 0.74 ALDH1A1 (0.58) ALDH1A1MAPK1POLBKDM4ESMN1; SMN2
SCHEMBL18177886 0.74 MAPK1 (1.00) ALDH1A1MAPK1HTR7KDM4ESMN1; SMN2
SCHEMBL9720681 0.73 MAPK1 (0.78) ALDH1A1MAPK1HTR7KDM4ETDP1
SCHEMBL9720708 0.73 DRD4 (0.73) ALDH1A1MAPK1HTR7POLBKDM4E
SCHEMBL8403757 0.72 HTR7 (0.63) ALDH1A1MAPK1HTR7POLBKDM4E
SCHEMBL9720726 0.72 KDM4E (0.79) ALDH1A1MAPK1HTR7KDM4ESMN1; SMN2

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-1032559-A4 AMINOALKYLPHENOL DERIVATIVES AND RELATED COMPOUNDS AVENTIS PHARMA INC (US) 2005-05-25 EP disclosed
EP-1032559-A1 AMINOALKYLPHENOL DERIVATIVES AND RELATED COMPOUNDS AVENTIS PHARMACEUTICALS INC. (US) 2000-09-06 EP disclosed
WO-1999016746-A1 AMINOALKYLPHENOL DERIVATIVES AND RELATED COMPOUNDS AVENTIS PHARMACEUTICALS INC. (US) 1999-04-08 WO disclosed