SCHEMBL8927293

SCHEMBL8927293

CCC=C(C(=O)OCC)C(=O)c1c(F)cc(F)c(C(F)(F)F)c1F

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 5/20 0.38
MEN1 O00255 5/20 0.37
KMT2A Q03164 5/20 0.37
MAPT P10636 5/20 0.37
LMNA P02545 4/20 0.37
CYP1A2 P05177 2/20 0.37
CYP2C19 P33261 2/20 0.37
CYP2C9 P11712 1/20 0.37
MAPK1 P28482 3/20 0.33
KDM4E B2RXH2 2/20 0.33
GPR35 Q9HC97 1/20 0.33
POLB P06746 2/20 0.32
ALDH1A1 P00352 1/20 0.32
S1PR4 O95977 1/20 0.32
S1PR1 P21453 1/20 0.32
GLO1 Q04760 1/20 0.32
GAA P10253 3/20 0.32
HPGD P15428 1/20 0.32
DHODH Q02127 2/20 0.32
CYP3A4 P08684 1/20 0.30

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
SCHEMBL8927287 0.87 NPSR1 (0.38) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL8927289 0.87 NPSR1 (0.38) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL5504515 0.82 MAPT (0.40) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL8925622 0.81 NPSR1 (0.41) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL8927296 0.81 ALDH1A1 (0.39) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL8741019 0.77 NPSR1 (0.44) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL8740982 0.77 NPSR1 (0.38) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL7011227 0.76 MAPT (0.44) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL7054038 0.74 MEN1 (0.42) NPSR1MEN1KMT2AMAPTLMNA
SCHEMBL8102795 0.73 NPSR1 (0.41) NPSR1MEN1KMT2AMAPTLMNA

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
US-5648567-A INTERMEDIATES FOR BACTERICIDES BAYER AKTIENGESELLSCHAFT (DE) 1997-07-15 US disclosed
US-5493048-A REACTING METALLIZED FLUORO-TRIFLUOROMETHYLBENZENE DERIVATIVE WITH CARBON DIOXIDE AND PRODUCT IS THEN HYDROLYSED WITH AN ACID TO FORM ACID, SIMILARLY HALOGENATION GIVE ACID HALIDE AND WITH ALCOHOL GIVES ESTER BAYER AKTIENGESELLSCHAFT (DE) 1996-02-20 US disclosed
US-5457104-A Antibacterials BAYER AKTIENGESELLSCHAFT (DE) 1995-10-10 US disclosed