SCHEMBL3887709

SCHEMBL3887709

CC(=O)C=CC(=O)c1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RECQL P46063 2/20 0.59
MAPT P10636 7/20 0.57
LMNA P02545 5/20 0.57
PLIN1 O60240 2/20 0.57
PLIN5 Q00G26 2/20 0.57
ABHD5 Q8WTS1 2/20 0.57
BCHE P06276 1/20 0.57
TNFRSF1A P19438 1/20 0.57
ACHE P22303 1/20 0.57
MAOB P27338 1/20 0.57
CYP1B1 Q16678 1/20 0.57
ALDH1A1 P00352 8/20 0.54
TDP1 Q9NUW8 3/20 0.54
MAPK1 P28482 2/20 0.54
GLA P06280 1/20 0.54
HPGD P15428 4/20 0.53
AKT1 P31749 2/20 0.53
CYP3A4 P08684 2/20 0.53
RAB9A P51151 5/20 0.53
NPC1 O15118 4/20 0.53

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
SCHEMBL11073619 0.88 MAPT (0.70) RECQLMAPTLMNAPLIN1PLIN5
SCHEMBL2954318 0.88 MAPT (0.70) RECQLMAPTLMNAPLIN1PLIN5
SCHEMBL2954324 0.88 MAPT (0.70) RECQLMAPTLMNAPLIN1PLIN5
SCHEMBL8534126 0.88 SMN1; SMN2 (0.59) RECQLMAPTLMNACYP1B1ALDH1A1
SCHEMBL8536033 0.88 SMN1; SMN2 (0.59) RECQLMAPTLMNACYP1B1ALDH1A1
SCHEMBL8534131 0.88 SMN1; SMN2 (0.59) RECQLMAPTLMNACYP1B1ALDH1A1
Chalcone SCHEMBL4635269 0.82 CYP1B1 (0.81) RECQLMAPTLMNAPLIN1PLIN5
SCHEMBL312429 0.81 ALDH1A1 (0.68) RECQLMAPTLMNAPLIN1PLIN5
SCHEMBL5585936 0.81 ALDH1A1 (0.68) RECQLMAPTLMNAPLIN1PLIN5
SCHEMBL312430 0.81 ALDH1A1 (0.68) RECQLMAPTLMNAPLIN1PLIN5

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-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 claimed
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 claimed
US-20060063796-A1 Pyrazoles as inhibitors of tumor necrosis factor AVENTIS PHARMACEUTICALS INC. (US) 2006-03-23 US claimed
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

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 RECQL 4334/4885MAPT 1770/4885LMNA 2887/4885

“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.