SCHEMBL2266038

SCHEMBL2266038

O=C(CCc1ccccc1)CC(=O)C(F)(F)F

nearest known ligand 0.60

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CES1 P23141 5/20 0.60
FAAH O00519 3/20 0.60
MMP12 P39900 1/20 0.53
KEAP1 Q14145 1/20 0.52
HDAC2 Q92769 1/20 0.50
HDAC8 Q9BY41 1/20 0.50
HDAC6 Q9UBN7 1/20 0.50
POLB P06746 1/20 0.49
GAA P10253 1/20 0.49
ALDH1A1 P00352 2/20 0.48
FFAR1 O14842 1/20 0.48
TDP1 Q9NUW8 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
TRPA1 O75762 1/20 0.47
MAPT P10636 1/20 0.47
HTT P42858 1/20 0.47
HDAC1 Q13547 1/20 0.47
TSHR P16473 1/20 0.46
CPA1 P15085 1/20 0.46

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
SCHEMBL1274684 0.85 CES1 (0.73) CES1FAAHKEAP1HDAC2HDAC8
SCHEMBL28142297 0.85 ALDH1A1 (0.47) CES1FAAHMMP12ALDH1A1
SCHEMBL5598977 0.82 KEAP1 (0.67) MMP12KEAP1HDAC2HDAC8HDAC6
SCHEMBL4753311 0.81 CES1 (0.71) CES1FAAHHDAC2HDAC8HDAC6
SCHEMBL27474155 0.81 KEAP1 (0.64) MMP12KEAP1HDAC2HDAC8HDAC6
SCHEMBL10413143 0.80 CES1 (0.44) CES1FAAHTDP1L3MBTL1
SCHEMBL1532408 0.79 MMP12 (0.79) MMP12KEAP1HDAC2HDAC8HDAC6
SCHEMBL497371 0.78 KEAP1 (0.73) MMP12KEAP1HDAC2HDAC8HDAC6
SCHEMBL1171544 0.78 CES1 (0.86) CES1FAAHHDAC2HDAC8HDAC6
Phenyl Propionic Acid SCHEMBL27428011 0.77 KEAP1 (0.79) CES1FAAHKEAP1HDAC2HDAC8

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 5 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
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-20030181420-A1 Heterocyclic compounds, in particular N-substituted pyridones for modulating the activity of nuclear receptors EXELIXIS, INC. 2003-09-25 US disclosed
US-5006254-A Extraction with halogenated beta-diketone RHONE-POULENC CHIMIE (FR) 1991-04-09 US 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 CES1 296/4885FAAH 1611/4885MMP12 4656/4885

“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.