SCHEMBL7417375

SCHEMBL7417375

CC(C)[C@H](NC(=O)N1CCC(NC(=O)OC(C)(C)C)CC1)C(=O)[O-].[Na+]

nearest known ligand 0.43

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 15)

geneUniProtsupporting neighboursconfidence
CA1 known ✓ P00915 1/20 0.43
CA2 known ✓ P00918 1/20 0.43
CTSK P43235 2/20 0.43
HSD11B1 P28845 6/20 0.42
CYP2C9 P11712 1/20 0.42
NAMPT P43490 1/20 0.41
EPHX1 P07099 1/20 0.41
TSHR P16473 1/20 0.40
PREP P48147 1/20 0.40
KMT2A Q03164 4/20 0.39
PARP1 P09874 1/20 0.39
MEN1 O00255 3/20 0.38
BTK Q06187 1/20 0.38
ALDH1A1 P00352 1/20 0.38
KCNA3 P22001 1/20 0.37

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
SCHEMBL7417378 0.88 TSHR (0.48) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL7417381 0.88 TSHR (0.48) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL7419142 0.87 KMT2A (0.50) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL21184011 0.78 CTSK (0.48) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL10268743 0.77 CTSK (0.51) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL15373447 0.76 CTSK (0.54) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL20093573 0.75 CTSK (0.52) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL15297472 0.75 CTSK (0.52) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL9225867 0.75 HSD11B1 (0.55) CTSKCA1CA2HSD11B1CYP2C9
SCHEMBL8747853 0.74 CTSK (0.54) CTSKCA1CA2PREP

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
WO-1993013066-A1 CYCLIC AMIDES OF 3-AMINO-2-HYDROXY-CARBOXYLIC ACIDS AS HIV-PROTEASE INHIBITORS SYNTEX (U.S.A.) INC. (US) 1993-07-08 WO disclosed