SCHEMBL2010223

SCHEMBL2010223

COc1cc(OC)c(Cl)c(NC(=O)Nc2cc(Nc3ccc(OCCN4CCOCC4)cc3)ncn2)c1Cl

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FGFR3 P22607 8/20 0.65
CYP3A4 P08684 3/20 0.65
BRAF P15056 5/20 0.51
MAPK14 Q16539 1/20 0.51
KDR P35968 7/20 0.50
EGFR P00533 5/20 0.50
ABL1 P00519 4/20 0.50
KIT P10721 3/20 0.50
FGFR1 P11362 3/20 0.50
SRC P12931 3/20 0.50
TEK Q02763 3/20 0.50
RET P07949 3/20 0.50
JAK2 O60674 2/20 0.50
INSR P06213 2/20 0.50
LCK P06239 2/20 0.50
FYN P06241 2/20 0.50
YES1 P07947 2/20 0.50
LYN P07948 2/20 0.50
MET P08581 2/20 0.50
ROS1 P08922 2/20 0.50

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
SCHEMBL374572 0.93 FGFR3 (0.75) FGFR3CYP3A4BRAFKDREGFR
SCHEMBL374717 0.92 FGFR3 (0.67) FGFR3CYP3A4BRAFKDREGFR
SCHEMBL374427 0.90 FGFR3 (0.69) FGFR3CYP3A4BRAFMAPK14KDR
SCHEMBL2015731 0.87 FGFR3 (0.87) FGFR3CYP3A4BRAFKDRABL1
SCHEMBL374879 0.86 EGFR (0.64) FGFR3CYP3A4BRAFMAPK14KDR
SCHEMBL374465 0.85 FGFR3 (0.62) FGFR3CYP3A4BRAFKDREGFR
SCHEMBL15127726 0.83 EGFR (0.57) FGFR3CYP3A4BRAFMAPK14KDR
SCHEMBL374534 0.82 EPHX2 (0.67) BRAFKDREGFRABL1KIT
SCHEMBL374477 0.82 FGFR3 (0.54) FGFR3BRAFMAPK14KDREGFR
SCHEMBL374200 0.82 FGFR3 (0.63) FGFR3CYP3A4BRAFMAPK14KDR

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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1976847-B1 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS NOVARTIS AG (CH) 2015-06-17 EP claimed
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors NOVARTIS AG 2008-12-18 US claimed
EP-1976847-A2 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS Novartis AG (CH) 2008-10-08 EP claimed
WO-2007071752-A2 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS NOVARTIS AG (CH) 2007-06-28 WO claimed
EP-1976847-B1 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS NOVARTIS AG (CH) 2015-06-17 EP disclosed
US-8759517-B2 Pyrirnidinyl aryl urea derivatives being FGF inhibitors NOVARTIS AG (CH) 2014-06-24 US disclosed
US-8759517-B2 Pyrirnidinyl aryl urea derivatives being FGF inhibitors NOVARTIS AG (CH) 2014-06-24 US disclosed
US-8759517-B2 Pyrirnidinyl aryl urea derivatives being FGF inhibitors NOVARTIS AG (CH) 2014-06-24 US disclosed
US-20130030171-A1 Pyrimidinyl Aryl Urea Derivatives being FGF Inhibitors NOVARTIS AG (CH) 2013-01-31 US disclosed
US-20130030171-A1 Pyrimidinyl Aryl Urea Derivatives being FGF Inhibitors NOVARTIS AG (CH) 2013-01-31 US disclosed
US-20130030171-A1 Pyrimidinyl Aryl Urea Derivatives being FGF Inhibitors NOVARTIS AG (CH) 2013-01-31 US disclosed
EP-2512476-A1 METHOD FOR TREATING HAEMATOLOGICAL CANCERS Novartis AG (CH) 2012-10-24 EP disclosed
US-8293746-B2 Pyrimidinyl aryl urea derivatives being FGF inhibitors NOVARTIS AG (CH) 2012-10-23 US disclosed
US-20120258940-A1 METHOD FOR TREATING HAEMATOLOGICAL CANCERS NOVARTIS AG (CH) 2012-10-11 US disclosed
WO-2011075620-A1 METHOD FOR TREATING HAEMATOLOGICAL CANCERS NOVARTIS AG (CH) 2011-06-23 WO disclosed
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors NOVARTIS AG 2008-12-18 US disclosed
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors NOVARTIS AG 2008-12-18 US disclosed
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors NOVARTIS AG 2008-12-18 US disclosed
EP-1976847-A2 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS Novartis AG (CH) 2008-10-08 EP disclosed
WO-2007071752-A2 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS NOVARTIS AG (CH) 2007-06-28 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 (3 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-20120258940-A1 METHOD FOR TREATING HAEMATOLOGICAL CANCERS FGFR3, FGFR2, FGFR1 FGFR3 1/4885CYP3A4 2057/4885BRAF 91/4885
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors FGFR1, FGF1, FGF2 FGFR3 5/4885CYP3A4 2061/4885BRAF 136/4885
US-20130030171-A1 Pyrimidinyl Aryl Urea Derivatives being FGF Inhibitors FGFR1, FGF1, FGF2 FGFR3 5/4885CYP3A4 2061/4885BRAF 136/4885

“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.