SCHEMBL1978410

SCHEMBL1978410

CC(O[C@@H](C[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)N(C)Cc1csc(C(C)C)n1)C(C)C)[C@H](Cc1ccccc1)NC(=O)OCc1cncs1)OP(=O)([O-])[O-].[Na+].[Na+]

nearest known ligand 0.77

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
ADORA3 known ✓ P0DMS8 1/20 0.77
SCN5A known ✓ Q14524 1/20 0.77
CYP3A4 P08684 20/20 0.77
CYP2D6 P10635 6/20 0.77
CYP2C19 P33261 3/20 0.77
CYP2C9 P11712 3/20 0.77
MEN1 O00255 1/20 0.77
SLC22A2 O15244 1/20 0.77
SLC22A1 O15245 1/20 0.77
ABCC3 O15438 1/20 0.77
ABCC4 O15439 1/20 0.77
MLNR O43193 1/20 0.77
NR1I2 O75469 1/20 0.77
SLCO2B1 O94956 1/20 0.77
ABCB11 O95342 1/20 0.77
ALDH1A1 P00352 1/20 0.77
PGR P06401 1/20 0.77
ABCB1 P08183 1/20 0.77
HTR1A P08908 1/20 0.77
ADRA2A P08913 1/20 0.77

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
SCHEMBL1977833 0.95 CYP3A4 (0.78) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL14655786 0.94 CYP3A4 (0.77) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL14655919 0.94 CYP3A4 (0.77) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL1978846 0.91 CYP3A4 (0.82) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL1978015 0.91 CYP3A4 (0.77) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL14655920 0.90 CYP3A4 (0.76) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL14655894 0.90 CYP3A4 (0.76) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL1982720 0.90 CYP3A4 (0.76) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL14878352 0.90 CYP3A4 (0.85) CYP3A4CYP2D6CYP2C19CYP2C9MEN1
SCHEMBL26551669 0.90 CYP3A4 (0.85) CYP3A4CYP2D6CYP2C19CYP2C9MEN1

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-2336138-A2 Prodrugs of HIV protease inhibitors ABBOTT LABORATORIES (US) 2011-06-22 EP disclosed