SCHEMBL10632562

SCHEMBL10632562

Cn1nnnc1SCC1=C(C(=O)[O-])N2C(=O)[C@@H](NC(=O)/C(=N\OC3CCNC3=O)c3csc(N)n3)[C@@H]2SC1.[Na+]

nearest known ligand 0.70

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 2/20 0.56
▸ NR1I2 O75469 4/20 0.70
▸ PGR P06401 3/20 0.70
▸ TDP1 Q9NUW8 9/20 0.64
▸ MAPT P10636 6/20 0.64
▸ HSD17B10 Q99714 6/20 0.64
▸ APEX1 P27695 4/20 0.64
▸ ALDH1A1 P00352 4/20 0.64
▸ POLB P06746 3/20 0.64
▸ RECQL P46063 2/20 0.64
▸ KDM4E B2RXH2 2/20 0.64
▸ CYP2D6 P10635 1/20 0.64
▸ BLM P54132 1/20 0.64
▸ ABCC4 O15439 2/20 0.57
▸ CYP1A2 P05177 1/20 0.56
▸ PKM P14618 1/20 0.56
▸ LMNA P02545 1/20 0.56
▸ NPSR1 Q6W5P4 1/20 0.56
▸ L3MBTL1 Q9Y468 1/20 0.56
▸ DAO P14920 1/20 0.56

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
SCHEMBL10640931 0.97 NR1I2 (0.69) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10633665 0.94 NR1I2 (0.80) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10999424 0.94 NR1I2 (0.61) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL11000502 0.94 NR1I2 (0.61) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10996849 0.94 NR1I2 (0.61) NR1I2PGRTDP1MAPTHSD17B10
SCHEMBL10640295 0.93 NR1I2 (0.73) NR1I2PGRTDP1MAPTHSD17B10
Cefmenoxime SCHEMBL10776181 0.89 NR1I2 (0.88) NR1I2PGRTDP1MAPTHSD17B10
Cefmenoxime SCHEMBL10776170 0.89 NR1I2 (0.88) NR1I2PGRTDP1MAPTHSD17B10
Cefmenoxime SCHEMBL9651055 0.89 NR1I2 (0.88) NR1I2PGRTDP1MAPTHSD17B10
Cefmenoxime SCHEMBL15660878 0.89 NR1I2 (0.88) 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
US-4742174-A MICROBTOCIDES TANABE SEIYAKU CO., LTD. (JP) 1988-05-03 — — US disclosed
US-4727071-A MICROBIOCIDES TANABE SEIYAKU CO., LTD. (JP) 1988-02-23 — — US disclosed
US-4598154-A Thiazole intermediates for cephalosporin compounds TANABE SEIYAKU CO., LTD. (JP) 1986-07-01 — — US disclosed
US-4598075-A ANTIMICROBIAL TANABE SEIYAKU CO., LTD. (JP) 1986-07-01 — — US disclosed
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