SCHEMBL3878006

SCHEMBL3878006

CCOC(=O)c1cc2ccoc2cn1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GABRA1 P14867 8/20 0.55
GABRG2 P18507 8/20 0.55
GABRB3 P28472 8/20 0.55
GABRA5 P31644 8/20 0.55
GABRA3 P34903 8/20 0.55
GABRA2 P47869 8/20 0.55
GABRA4 P48169 8/20 0.55
GABRA6 Q16445 8/20 0.55
GABRP O00591 6/20 0.55
GABRD O14764 6/20 0.55
GABRB1 P18505 6/20 0.55
GABRB2 P47870 6/20 0.55
GABRE P78334 6/20 0.55
GABRG1 Q8N1C3 6/20 0.55
GABRG3 Q99928 6/20 0.55
GABRQ Q9UN88 6/20 0.55
CYP1A2 P05177 1/20 0.47
ALDH1A1 P00352 3/20 0.46
MAPT P10636 2/20 0.46
KDM4E B2RXH2 2/20 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
SCHEMBL5918048 0.87 TSHR (0.50) GABRA1GABRG2GABRB3GABRA5GABRA3
SCHEMBL7507673 0.84 MIF (0.46) GABRA1GABRG2GABRB3GABRA5GABRA3
SCHEMBL27867975 0.81 CHRNA7 (0.46) GABRA1GABRG2GABRB3GABRA5GABRA3
SCHEMBL55605 0.79 CHRNA7 (0.48) ALDH1A1CHRNA7HTR3AHTR3EHTR3B
SCHEMBL29890580 0.77 KMO (0.57) ALDH1A1MAPTKDM4ESMN1; SMN2CHRNA7
SCHEMBL842797 0.77 KMO (0.57) ALDH1A1MAPTKDM4ESMN1; SMN2CHRNA7
SCHEMBL7504438 0.76 CHRNA7 (0.45) GABRA1GABRG2GABRB3GABRA5GABRA3
SCHEMBL30712292 0.76 GABRA1 (0.59) GABRA1GABRG2GABRB3GABRA5GABRA3
SCHEMBL30712301 0.76 GABRA1 (0.59) GABRA1GABRG2GABRB3GABRA5GABRA3
SCHEMBL2201127 0.76 GABRA1 (0.59) GABRA1GABRG2GABRB3GABRA5GABRA3

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 11 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
EP-0911335-B1 Method for producing furopyridine derivatives and intermediate compounds KURARAY CO (JP) 2002-04-17 EP disclosed
US-6342606-B2 REACTING PYRIDINE ESTER DERIVATIVE WITH A REDUCING AGENT, AN ALKYLATING AGENT, AN ALKENYLATING AGENT, AN ARYLATING AGENT OR AN ARALKYLATING AGENT TO OBTAIN A PYRIDINE CARBONYL DERIVATIVE, REDUCING KURARAY CO., LTD. (JP) 2002-01-29 US disclosed
US-20010031871-A1 Method for producing pyridine derivatives KURARAY CO., LTD. (JP) 2001-10-18 US disclosed
US-6265580-B1 REACTING AMINE DERIVATIVE WITH CARBONYLATING AGENT AND NITRILE DERIVATIVE KURARAY CO., LTD. (JP) 2001-07-24 US disclosed
US-6111111-A Intermediates for producing pyridine derivatives KURARAY CO., LTD. (JP) 2000-08-29 US disclosed
EP-0911335-A2 Method for producing furopyridine derivatives and intermediate compounds KURARAY CO., LTD. (JP) 1999-04-28 EP 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-20060063796-A1 Pyrazoles as inhibitors of tumor necrosis factor TNF, LITAF, MAPK1 GABRA1 3970/4885GABRG2 4187/4885GABRB3 3497/4885
US-20010031871-A1 Method for producing pyridine derivatives CYP2E1, CBR1, CBR3 GABRA1 2437/4885GABRG2 2662/4885GABRB3 3248/4885

“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.