SCHEMBL12366226

SCHEMBL12366226

[C-]#[N+]c1c(C(F)(F)F)cc(-c2cccc(C(F)(F)F)c2)n(Cc2ccccc2)c1=O

nearest known ligand 0.45

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
RGS4 P49798 1/20 0.43
RGS8 P57771 1/20 0.43
CTSK P43235 1/20 0.41
CXCR2 P25025 1/20 0.40
TP53 P04637 2/20 0.40
MAPT P10636 2/20 0.40
LMNA P02545 1/20 0.40
RXFP1 Q9HBX9 1/20 0.40
GRIN1 Q05586 6/20 0.40
GRIN2B Q13224 6/20 0.40
S1PR5 Q9H228 1/20 0.38
CFTR P13569 1/20 0.38
EGLN1 Q9GZT9 1/20 0.38
CNR1 P21554 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
SCHEMBL12366278 0.94 MAPT (0.45) RGS4RGS8CTSKTP53MAPT
SCHEMBL12366212 0.91 CNR1 (0.44) RGS4RGS8LMNARXFP1CFTR
SCHEMBL12366275 0.89 CFTR (0.42) RGS4RGS8CFTRCNR1
SCHEMBL12366571 0.88 CNR1 (0.37) RGS4RGS8CNR1
SCHEMBL12366582 0.88 CNR1 (0.37) RGS4RGS8CFTRCNR1
SCHEMBL12366233 0.88 CNR1 (0.42) RGS4RGS8TP53MAPTCNR1
SCHEMBL12366220 0.88 CNR1 (0.39) RGS4RGS8TP53RXFP1CFTR
SCHEMBL12366945 0.88 CNR1 (0.37) RGS4RGS8CTSKRXFP1CFTR
SCHEMBL12366286 0.88 MAPT (0.45) TP53MAPTLMNARXFP1GRIN1
SCHEMBL12366238 0.86 DCTPP1 (0.42) RXFP1S1PR5CFTRCNR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7998986-B2 Heterocyclic compounds, in particular N-substituted pyridones for modulating the activity of nuclear receptors EXELIXIS PATENT COMPANY LLC (US) 2011-08-16 US disclosed