SCHEMBL2011760

SCHEMBL2011760

CCN1CCN(c2cccc(Nc3cc(N(C)C(=O)Nc4c(C)c(OC)cc(OC)c4Cl)ncn3)c2)CC1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FGFR1 P11362 12/20 0.77
FGFR3 P22607 10/20 0.77
FGFR4 P22455 8/20 0.77
CYP3A4 P08684 5/20 0.77
FGFR2 P21802 4/20 0.77
CYP2C19 P33261 4/20 0.77
JAK2 O60674 2/20 0.77
ABL1 P00519 2/20 0.77
INSR P06213 2/20 0.77
LCK P06239 2/20 0.77
FYN P06241 2/20 0.77
YES1 P07947 2/20 0.77
LYN P07948 2/20 0.77
RET P07949 2/20 0.77
MET P08581 2/20 0.77
ROS1 P08922 2/20 0.77
KIT P10721 2/20 0.77
SRC P12931 2/20 0.77
BRAF P15056 2/20 0.77
PDGFRA P16234 2/20 0.77

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
SCHEMBL2014363 0.96 FGFR1 (0.84) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL2013451 0.92 FGFR3 (0.91) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL374711 0.87 FGFR3 (1.00) FGFR1FGFR3FGFR4CYP3A4FGFR2
Infigratinib SCHEMBL374435 0.87 FGFR3 (1.00) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL374257 0.85 FGFR3 (0.88) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL16383021 0.85 FGFR3 (0.92) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL19338005 0.84 FGFR3 (0.91) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL2011033 0.84 FGFR3 (0.91) FGFR1FGFR3FGFR4CYP3A4FGFR2
Infigratinib SCHEMBL14893408 0.84 FGFR3 (1.00) FGFR1FGFR3FGFR4CYP3A4FGFR2
SCHEMBL2014816 0.84 FGFR1 (0.83) FGFR1FGFR3FGFR4CYP3A4FGFR2

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
EP-1976847-B1 PYRIMIDINYL ARYL UREA DERIVATIVES BEING FGF INHIBITORS NOVARTIS AG (CH) 2015-06-17 EP claimed
CN-101336237-A Pyrimidinyl aryl urea derivatives being fgf inhibitors NOVARTIS AG (CH) 2008-12-31 CN claimed
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors NOVARTIS AG 2008-12-18 US 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-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

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 FGFR1 3/4885FGFR3 1/4885FGFR4 5/4885
US-20080312248-A1 Pyrimidinyl Aryl Urea Derivatives Being Fgf Inhibitors FGFR1, FGF1, FGF2 FGFR1 1/4885FGFR3 5/4885FGFR4 6/4885
US-20130030171-A1 Pyrimidinyl Aryl Urea Derivatives being FGF Inhibitors FGFR1, FGF1, FGF2 FGFR1 1/4885FGFR3 5/4885FGFR4 6/4885

“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.