SCHEMBL2264159

SCHEMBL2264159

CCc1ccc(Oc2ccc(-c3cc(C(F)(F)F)c(C#N)c(=O)n3Cc3ccc(C)cc3C)cc2)cc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR1H2 P55055 4/20 0.60
NR1H3 Q13133 4/20 0.60
RXRA P19793 3/20 0.60
AR P10275 6/20 0.38
ALDH1A1 P00352 6/20 0.37
HPGD P15428 3/20 0.37
GLA P06280 2/20 0.37
GAA P10253 1/20 0.37
ATM Q13315 1/20 0.37
KDM4E B2RXH2 7/20 0.36
MAPT P10636 2/20 0.36
LMNA P02545 1/20 0.34
HSD17B10 Q99714 1/20 0.34
PPARG P37231 1/20 0.34
NCOA2 Q15596 1/20 0.34
NCOA1 Q15788 1/20 0.34
NPSR1 Q6W5P4 1/20 0.34
RXFP1 Q9HBX9 1/20 0.34
NCOA3 Q9Y6Q9 1/20 0.34
GRM2 Q14416 1/20 0.33

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
SCHEMBL2266726 0.94 NR1H2 (0.65) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2262458 0.92 NR1H2 (0.61) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2262290 0.91 NR1H2 (0.62) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2262577 0.91 NR1H2 (0.62) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2263400 0.90 NR1H2 (0.69) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2266212 0.90 NR1H2 (0.61) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2264983 0.90 NR1H2 (0.61) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2268061 0.90 NR1H2 (0.61) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL2262380 0.90 NR1H2 (0.61) NR1H2NR1H3RXRAARALDH1A1
SCHEMBL4896265 0.90 NR1H2 (0.61) NR1H2NR1H3RXRAARALDH1A1

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 6 patents. 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
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
EP-1465869-A4 MODULATORS OF LXR X CEPTOR THERAPEUTICS INC (US) 2005-12-28 EP disclosed
EP-1465869-A1 MODULATORS OF LXR X-Ceptor Therapeutics, Inc. (US) 2004-10-13 EP disclosed
US-20030181420-A1 Heterocyclic compounds, in particular N-substituted pyridones for modulating the activity of nuclear receptors EXELIXIS, INC. 2003-09-25 US disclosed
WO-2003059884-A1 MODULATORS OF LXR X-CEPTOR THERAPEUTICS, INC. (US) 2003-07-24 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20030181420-A1 Heterocyclic compounds, in particular N-substituted pyridones for modulating the activity of nuclear receptors NR1H2, NR1H3, NCOA1 NR1H2 1/4885NR1H3 2/4885RXRA 16/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.