SCHEMBL3563221

SCHEMBL3563221

Fc1ccc(-c2cc(C(F)(F)F)nc(Cl)n2)cc1F

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 8/20 0.53
HSD17B10 Q99714 5/20 0.53
ALDH1A1 P00352 3/20 0.53
SMN1; SMN2 Q16637 4/20 0.48
TP53 P04637 3/20 0.48
MAPT P10636 2/20 0.48
ADORA2A P29274 1/20 0.48
TDP1 Q9NUW8 1/20 0.48
MITF O75030 1/20 0.44
LMNA P02545 1/20 0.44
STAT3 P40763 1/20 0.44
STAT1 P42224 1/20 0.44
RAB9A P51151 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
TLR9 Q9NR96 1/20 0.44
POLB P06746 1/20 0.43
MAPK1 P28482 3/20 0.43
CYP11B1 P15538 1/20 0.42
CYP11B2 P19099 1/20 0.42
TSHR P16473 1/20 0.41

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
SCHEMBL3562596 0.88 CYP11B2 (0.57) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL3557132 0.85 KDM4E (0.71) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL3561619 0.85 KDM4E (0.68) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL3557053 0.82 KMO (0.53) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL3566819 0.81 CYP3A4 (0.52) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL3567866 0.80 KDM4E (0.55) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL21058802 0.80 ALDH1A1 (0.42) KDM4EALDH1A1SMN1; SMN2MAPTTDP1
SCHEMBL3562786 0.79 KDM4E (0.45) KDM4EHSD17B10ALDH1A1
SCHEMBL3566799 0.78 KDM4E (0.47) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53
SCHEMBL2849704 0.78 MEN1 (0.66) KDM4EHSD17B10ALDH1A1SMN1; SMN2TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2001849-B1 PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR2 ANTAGONISTS HOFFMANN LA ROCHE (CH) 2014-11-26 EP disclosed
EP-2468727-A1 Pyridine and pyrimidine derivatives as MGLUR2 antagonists F. Hoffmann-La Roche AG (CH) 2012-06-27 EP disclosed
US-8183262-B2 Central nervous system disorders; metabotropic glutamate receptors (mGluR); 2-(4-Pyridin-3-yl-imidazol-1-yl)-4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidine HOFFMANN-LA ROCHE INC. (US) 2012-05-22 US disclosed
US-7642264-B2 Phenyl-substituted pyrimidine derivatives as mGluR antagonists HOFFMAN-LA ROCHE INC. (US) 2010-01-05 US disclosed
US-20090318474-A1 PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR 2 ANTAGONISTS GATTI MCARTHUR SILVIA 2009-12-24 US disclosed
EP-2001849-A1 PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR2 ANTAGONISTS F. Hoffmann-Roche AG (CH) 2008-12-17 EP disclosed
US-20070232583-A1 Pyridine and pyrimidine derivatives as mGIuR2 antagonists HOFFMANN-LA ROCHE INC. 2007-10-04 US disclosed
WO-2007110337-A1 PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR2 ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2007-10-04 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 (2 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-20070232583-A1 Pyridine and pyrimidine derivatives as mGIuR2 antagonists P2RX2, P2RY2, P2RX1 KDM4E 2568/4885HSD17B10 3931/4885ALDH1A1 1138/4885
US-20090318474-A1 PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR 2 ANTAGONISTS GRM2, GRM1, GRM3 KDM4E 1276/4885HSD17B10 3932/4885ALDH1A1 3286/4885

“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.