SCHEMBL10918877

SCHEMBL10918877

Cn1nnnc1SCC1=C(C(=O)[O-])N2C(=O)C(NC(=O)C(=CCl)c3csc(N)n3)[C@@H]2SC1.[Na+]

nearest known ligand 0.66

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
▸ PPARG known ✓ P37231 1/20 0.51
▸ NR1I2 O75469 2/20 0.66
▸ PGR P06401 2/20 0.66
▸ TDP1 Q9NUW8 12/20 0.60
▸ MAPT P10636 8/20 0.60
▸ HSD17B10 Q99714 6/20 0.60
▸ POLB P06746 6/20 0.60
▸ ALDH1A1 P00352 5/20 0.60
▸ APEX1 P27695 4/20 0.60
▸ KDM4E B2RXH2 2/20 0.60
▸ RECQL P46063 2/20 0.60
▸ CYP2D6 P10635 1/20 0.60
▸ BLM P54132 1/20 0.60
▸ CYP3A4 P08684 1/20 0.59
▸ HPGD P15428 1/20 0.59
▸ PTPN7 P35236 1/20 0.59
▸ LMNA P02545 2/20 0.52
▸ ABCC4 O15439 2/20 0.52
▸ L3MBTL1 Q9Y468 2/20 0.52
▸ CYP1A2 P05177 1/20 0.52

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
SCHEMBL11177589 1.00 NR1I2 (0.66) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10918636 0.93 NR1I2 (0.76) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10918642 0.93 NR1I2 (0.76) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10918875 0.93 NR1I2 (0.75) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL11176448 0.91 NR1I2 (0.56) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL11176453 0.91 NR1I2 (0.56) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL11200899 0.91 NR1I2 (0.64) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL11165488 0.90 NR1I2 (0.54) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL11165481 0.90 NR1I2 (0.54) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10919936 0.90 NR1I2 (0.67) NR1I2PGRTDP1MAPTHSD17B10

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0082498-A2 Beta-lactam compounds and process for the preparation thereof SAGAMI CHEMICAL RESEARCH CENTER (JP) 1983-06-29 — — EP claimed
EP-0048954-B1 BETA-LACTAM COMPOUNDS, PROCESS FOR THE PREPARATION THEREOF AND INTERMEDIATE PRODUCTS FOR THE PREPARATION THEREOF SAGAMI CHEMICAL RESEARCH CENTER (JP) 1986-12-30 — — EP disclosed
EP-0082498-A2 Beta-lactam compounds and process for the preparation thereof SAGAMI CHEMICAL RESEARCH CENTER (JP) 1983-06-29 — — EP disclosed
EP-0048954-A2 Beta-lactam compounds, process for the preparation thereof and intermediate products for the preparation thereof SAGAMI CHEMICAL RESEARCH CENTER (JP) 1982-04-07 — — EP disclosed
Send feedback