SCHEMBL9360481

SCHEMBL9360481

CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(CSc3ncc(-c4ccc(O)cc4)o3)CS[C@H]12)c1csc(N)n1.[Na+]

nearest known ligand 0.67

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 0.57
▸ TDP1 Q9NUW8 6/20 0.67
▸ MAPT P10636 5/20 0.67
▸ APEX1 P27695 3/20 0.67
▸ HSD17B10 Q99714 3/20 0.67
▸ ALDH1A1 P00352 2/20 0.67
▸ POLB P06746 2/20 0.67
▸ RECQL P46063 2/20 0.67
▸ CYP2D6 P10635 1/20 0.67
▸ KDM4E B2RXH2 1/20 0.67
▸ BLM P54132 1/20 0.67
▸ ABCC4 O15439 2/20 0.66
▸ CYP1A2 P05177 1/20 0.66
▸ PKM P14618 1/20 0.66
▸ LMNA P02545 1/20 0.66
▸ NPSR1 Q6W5P4 1/20 0.66
▸ L3MBTL1 Q9Y468 1/20 0.66
▸ NR1I2 O75469 5/20 0.61
▸ ESR1 P03372 1/20 0.61
▸ DRD2 P14416 1/20 0.61

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
SCHEMBL9360487 1.00 TDP1 (0.67) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9365428 0.95 TDP1 (0.68) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9365421 0.95 TDP1 (0.68) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9364726 0.94 TDP1 (0.65) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9364735 0.94 TDP1 (0.65) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9361758 0.88 TDP1 (0.57) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9361750 0.88 TDP1 (0.57) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9361972 0.88 TDP1 (0.71) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9361960 0.88 TDP1 (0.71) TDP1MAPTAPEX1HSD17B10ALDH1A1
SCHEMBL9360460 0.88 NR1I2 (0.64) TDP1MAPTAPEX1HSD17B10ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0241901-B1 Cephalosporin derivatives, processes for their preparation and antibacterial agents BANYU PHARMA CO LTD (JP) 1994-08-24 — — EP disclosed
US-5061794-A Effective against pseudomonads BANYU PHARMACEUTICAL CO., LTD. (JP) 1991-10-29 — — US disclosed
EP-0241901-A2 Cephalosporin derivatives, processes for their preparation and antibacterial agents Banyu Pharmaceutical Co., Ltd. (JP) 1987-10-21 — — EP disclosed
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