SCHEMBL3564478

SCHEMBL3564478

COP(=O)(CC(=O)c1ccc(C(F)(F)F)cc1)OC

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 2/20 0.53
GSK3B P49841 1/20 0.53
MAPT P10636 2/20 0.48
ALDH1A1 P00352 1/20 0.48
CES2 O00748 1/20 0.47
CES1 P23141 1/20 0.47
MMP1 P03956 1/20 0.46
LMNA P02545 1/20 0.46
POLB P06746 1/20 0.46
KDM4E B2RXH2 2/20 0.46
HTT P42858 1/20 0.46
KMT2A Q03164 1/20 0.46
MMP2 P08253 1/20 0.46
MMP8 P22894 1/20 0.46
HSD11B1 P28845 1/20 0.43
HDAC1 Q13547 1/20 0.43
HDAC8 Q9BY41 1/20 0.43
TRPV1 Q8NER1 1/20 0.43
MAOB P27338 1/20 0.42
SRD5A2 P31213 1/20 0.42

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
SCHEMBL5734467 0.82 NPSR1 (0.54) ALDH1A1CES2LMNAPOLBHTT
SCHEMBL2322443 0.81 LMNA (0.50) PTPN1MAPTALDH1A1CES2CES1
SCHEMBL10357072 0.80 LMNA (0.51) GSK3BMAPTALDH1A1CES2CES1
SCHEMBL15438643 0.78 KIF11 (0.46) PTPN1MAPTALDH1A1LMNAKDM4E
SCHEMBL9548021 0.78 GSK3B (0.50) GSK3BMAPTALDH1A1CES2CES1
SCHEMBL9257364 0.78 LMNA (0.50) GSK3BMAPTALDH1A1CES2CES1
SCHEMBL5734842 0.78 POLB (0.73) PTPN1GSK3BMAPTALDH1A1CES1
SCHEMBL3564484 0.77 PTPN1 (0.49) PTPN1GSK3BMAPTALDH1A1CES2
SCHEMBL3391803 0.76 ALDH1A1 (0.60) PTPN1GSK3BMAPTALDH1A1CES2
SCHEMBL11830641 0.76 ALDH1A1 (0.55) PTPN1ALDH1A1MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118126080-A Chiral gamma-carbonyl phosphate derivative and preparation method and application thereof 武汉大学 2024-06-04 CN disclosed
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 PTPN1 2323/4885GSK3B 1321/4885MAPT 658/4885
US-20090318474-A1 PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR 2 ANTAGONISTS GRM2, GRM1, GRM3 PTPN1 590/4885GSK3B 1615/4885MAPT 1080/4885

“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.