SCHEMBL10929620

SCHEMBL10929620

CCN1CCN(C(=O)NC(C(=O)N[C@@H]2C(=O)N3[C@@H]2SC(C)(C)[C@]3(NC=O)C(=O)[O-])c2ccc3c(c2)OCO3)C(=O)C1=O.[Na+]

nearest known ligand 0.51

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 19)

geneUniProtsupporting neighboursconfidence
▸ PDE3A known ✓ Q14432 1/20 0.38
▸ THRB known ✓ P10828 1/20 0.37
▸ TDP1 Q9NUW8 1/20 0.41
▸ LMNA P02545 1/20 0.38
▸ MAPT P10636 1/20 0.38
▸ SLC22A6 Q4U2R8 1/20 0.38
▸ SLC22A8 Q8TCC7 1/20 0.38
▸ SLC22A11 Q9NSA0 1/20 0.38
▸ TSHR P16473 1/20 0.37
▸ HSD17B10 Q99714 1/20 0.37
▸ MEN1 O00255 1/20 0.35
▸ KMT2A Q03164 1/20 0.35
▸ CCKBR P32239 1/20 0.35
▸ SMN1; SMN2 Q16637 2/20 0.31
▸ MGLL Q99685 1/20 0.31
▸ F2 P00734 1/20 0.30
▸ ELANE P08246 1/20 0.30
▸ NPSR1 Q6W5P4 1/20 0.30
▸ GFER P55789 1/20 0.30

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
SCHEMBL11052540 0.93 MAPT (0.40) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10834184 0.82 MAPT (0.42) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10493262 0.82 MAPT (0.42) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10492989 0.81 MAPT (0.49) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10493259 0.81 MAPT (0.39) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10813565 0.80 TDP1 (0.40) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10493151 0.79 TDP1 (0.46) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10813371 0.79 TDP1 (0.37) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10493045 0.77 MEN1 (0.44) TDP1LMNAMAPTPDE3ASLC22A6
SCHEMBL10493026 0.77 LMNA (0.65) TDP1LMNAHSD17B10MEN1KMT2A

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-0131611-A1 $g(b)-LACTAM ANTIBACTERIAL AGENTS BEECHAM GROUP PLC (GB) 1985-01-23 — — EP disclosed
WO-1984002911-A1 beta-LACTAM ANTIBACTERIAL AGENTS BEECHAM GROUP PLC (GB) 1984-08-02 — — WO disclosed
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