SCHEMBL10763510

SCHEMBL10763510

O=C([O-])CCCSc1nc(-c2ccccc2)c(-c2ccccc2)n1-c1ccccc1.[Na+]

nearest known ligand 0.50

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 0.39
MEN1 O00255 4/20 0.46
KMT2A Q03164 4/20 0.46
SMN1; SMN2 Q16637 3/20 0.41
HDAC2 Q92769 3/20 0.40
HDAC3 O15379 2/20 0.40
HDAC1 Q13547 2/20 0.40
HDAC8 Q9BY41 2/20 0.40
HDAC6 Q9UBN7 2/20 0.40
PTK2 Q05397 1/20 0.40
FAAH O00519 1/20 0.40
PTGES O14684 1/20 0.40
APLNR P35414 1/20 0.39
USP2 O75604 1/20 0.39
TSHR P16473 1/20 0.39
MAPK1 P28482 1/20 0.39
NPSR1 Q6W5P4 1/20 0.38
RXFP1 Q9HBX9 1/20 0.38
LMNA P02545 2/20 0.38
ALDH1A1 P00352 1/20 0.38

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
SCHEMBL10754201 0.95 HDAC2 (0.46) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10754564 0.89 MEN1 (0.55) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10757516 0.86 HDAC2 (0.55) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10762838 0.85 HDAC2 (0.56) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10755254 0.85 HDAC2 (0.56) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10764814 0.85 HDAC2 (0.56) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10758321 0.85 HDAC2 (0.56) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10754699 0.85 HDAC2 (0.56) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10758403 0.85 HDAC2 (0.56) MEN1KMT2ASMN1; SMN2HDAC2HDAC3
SCHEMBL10758906 0.84 MEN1 (0.64) MEN1KMT2ASMN1; SMN2HDAC2HDAC3

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-0130526-B1 IMIDAZOL-2-YL MERCAPTO ALKANOIC ACIDS, PROCESS FOR PRODUCING THE SAME AND PHARMACEUTICAL PREPARATIONS CONTAINING THE SAME A. Nattermann & Cie. GmbH (DE) 1987-12-09 EP disclosed
US-4654358-A 1,4,5-triphenylimidazol-2-yl mercapto alkanoic acids, useful against inflammation and diseases responding to lipid lowering A. NATTERMANN & CIE GMBH (DE) 1987-03-31 US disclosed
EP-0130526-A1 Imidazol-2-yl mercapto alkanoic acids, process for producing the same and pharmaceutical preparations containing the same A. Nattermann & Cie. GmbH (DE) 1985-01-09 EP disclosed