SCHEMBL3876532

SCHEMBL3876532

COc1ccc(OCC(F)(F)F)c(C(=O)O)c1

nearest known ligand 0.61

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.61
CYP2C9 P11712 1/20 0.61
ALDH1A1 P00352 6/20 0.60
KDM4E B2RXH2 2/20 0.58
MEN1 O00255 2/20 0.56
KMT2A Q03164 2/20 0.56
POLB P06746 3/20 0.55
CYP3A4 P08684 1/20 0.55
HPGD P15428 1/20 0.55
CYP2C19 P33261 1/20 0.55
ATM Q13315 1/20 0.55
SMN1; SMN2 Q16637 3/20 0.51
NPSR1 Q6W5P4 2/20 0.51
RAB9A P51151 1/20 0.51
MAPK1 P28482 1/20 0.50
HTT P42858 2/20 0.48
MAPT P10636 1/20 0.47

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
SCHEMBL978291 0.89 KDM4E (0.71) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
Hydrochloric Acid SCHEMBL10754121 0.88 KDM4E (0.69) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL10470177 0.87 ALDH1A1 (0.63) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL10469100 0.85 ALDH1A1 (0.60) CYP1A2CYP2C9ALDH1A1KDM4EPOLB
SCHEMBL10469508 0.84 ALDH1A1 (0.63) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL7032770 0.83 KDM4E (0.63) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL1487907 0.82 KDM4E (0.51) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL20521847 0.82 KDM4E (0.54) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL7825426 0.82 ALDH1A1 (0.46) CYP1A2CYP2C9ALDH1A1KDM4EMEN1
SCHEMBL3903917 0.81 KDM4E (0.60) ALDH1A1KDM4EMEN1KMT2APOLB

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-7541368-B2 1-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-{3-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-ylmethyl]-phenyl}-urea; use in the treatment of disease states capable of being modulated by the inhibition of p38 kinase and tumor necrosis factor (TNF) AVENTIS PHARMACEUTICALS INC. (US) 2009-06-02 US disclosed
EP-1622610-B1 1-(2H-PYRAZOL-3-YL)-3-{4-[1-(BENZOYL)-PIPERIDIN-4-YLMETHYL]-PHENYL}-UREA DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF INFLAMMATIONS AVENTIS PHARMA INC (US) 2006-12-20 EP disclosed
US-20060063796-A1 Pyrazoles as inhibitors of tumor necrosis factor AVENTIS PHARMACEUTICALS INC. (US) 2006-03-23 US disclosed
EP-1622610-A1 1-(2H-PYRAZOL-3-YL)-3- 4-[1-(BENZOYL)-PIPERIDIN-4-YLMETHYL]-PHENYL -UREA DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF INFLAMMATIONS Aventis Pharmaceuticals Inc. (US) 2006-02-08 EP disclosed
WO-2004100946-A1 1- (2H-PYRAZOL -3-YL) -3YL) {4-`1- (BENZOYL) -PIPERIDIN-4-YLMETHYL!-PHENYL}-UREA DERIVATIVES AND RELATED COMPOUNDS AS INHBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF IMFLAMMATIONS AVENTIS PHARMACEUTICALS INC. (US) 2004-11-25 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-20060063796-A1 Pyrazoles as inhibitors of tumor necrosis factor TNF, LITAF, MAPK1 CYP1A2 374/4885CYP2C9 470/4885ALDH1A1 1448/4885

“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.