SCHEMBL5380374

SCHEMBL5380374

CSC(=O)c1cc(C)cc(C)c1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TPMT P51580 1/20 0.54
HCAR1 Q9BXC0 1/20 0.41
PRSS1 P07477 1/20 0.41
PRSS2 P07478 1/20 0.41
C1S P09871 1/20 0.41
PRSS3 P35030 1/20 0.41
HPGD P15428 1/20 0.41
RXRA P19793 1/20 0.39
RXRB P28702 1/20 0.39
ALDH1A1 P00352 3/20 0.38
NPSR1 Q6W5P4 1/20 0.36
NPC1 O15118 2/20 0.36
RAB9A P51151 2/20 0.36
SMN1; SMN2 Q16637 2/20 0.36
LMNA P02545 1/20 0.36
PARP1 P09874 1/20 0.35
HCAR2 Q8TDS4 1/20 0.35
KMT2A Q03164 3/20 0.35
MEN1 O00255 2/20 0.35
THRB P10828 1/20 0.35

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
SCHEMBL9169866 0.87 HCAR1 (0.61) TPMTHCAR1HPGDALDH1A1NPC1
SCHEMBL28709440 0.78 TPMT (0.52) TPMTHCAR1PRSS1PRSS2C1S
SCHEMBL775679 0.78 PARP1 (0.59) HPGDNPC1RAB9ASMN1; SMN2PARP1
SCHEMBL775142 0.75 ALDH1A1 (0.56) HPGDALDH1A1NPSR1NPC1RAB9A
SCHEMBL28709441 0.73 TPMT (0.46) TPMTHCAR1PRSS1PRSS2C1S
SCHEMBL28709442 0.73 TPMT (0.46) TPMTHCAR1PRSS1PRSS2C1S
SCHEMBL16305559 0.73 TPMT (0.65) TPMTHCAR1PRSS1PRSS2C1S
SCHEMBL7937175 0.73 TPMT (0.65) TPMTHCAR1PRSS1PRSS2C1S
SCHEMBL31054325 0.72 MAPT (0.65) TPMTHPGDALDH1A1NPSR1NPC1
SCHEMBL133987 0.70 TPMT (0.62) TPMTHCAR1PRSS1PRSS2C1S

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2020126591-A1 SUBSTITUTED PYRIMIDINIUM COMPOUNDS FOR COMBATING ANIMAL PESTS BASF SE (DE) 2020-06-25 WO disclosed
US-7205428-B2 Thioether derivatives, their method for production and use NATIONAL INSTITUTE OF INFORMATION AND COMMUNICATIONS TECHNOLOGY, INCORPORATED ADMINISTRATIVE AGENCY (JP) 2007-04-17 US disclosed
EP-1219667-B1 Novel thioether derivatives, their method for production and use COMM RES LAB INDEPENDENT ADMIN (JP) 2004-08-04 EP disclosed
US-6630578-B2 Which respond immediately by emission of light when stimulated with light or electric energy, and are useful as switching material of memory COMMUNICATIONS RESEARCH LABORATORY, INDEPENDENT ADMINISTRATIVE INSTITUTION (JP) 2003-10-07 US disclosed
US-20030171507-A1 Novel thioether derivatives, their method for production and use NATIONAL INSTITUTE OF INFORMATION AND COMMUNICATIONS TECHNOLOGY, INCORPORATED ADMINISTRATIVE AGENCY (JP) 2003-09-11 US disclosed
EP-1219667-A2 Novel thioether derivatives, their method for production and use Communications Research Laboratory, Independent Administrative Institution (JP) 2002-07-03 EP disclosed
US-20020072583-A1 Novel thioether derivatives, their method for production and use NATIONAL INSTITUTE OF INFORMATION AND COMMUNICATIONS TECHNOLOGY, INCORPORATED ADMINISTRATIVE AGENCY (JP) 2002-06-13 US disclosed