SCHEMBL4424337

SCHEMBL4424337

CNc1cc2c(cn1)cc(-c1cc(NC(=O)Nc3nn(C(C)(C)C)c4ccccc34)c(F)cc1Cl)c(=O)n2C

nearest known ligand 0.48

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KIT P10721 1/20 0.48
PDGFRA P16234 1/20 0.48
FGFR1 P11362 9/20 0.47
SRC P12931 7/20 0.47
BRAF P15056 9/20 0.44
RAF1 P04049 8/20 0.44
KRAS P01116 6/20 0.44
KDR P35968 6/20 0.44
MAP2K2 P36507 5/20 0.44
MAP2K1 Q02750 5/20 0.44
ARAF P10398 1/20 0.35
FGFR4 P22455 1/20 0.35

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
SCHEMBL5062175 0.92 BRAF (0.54) KITPDGFRAFGFR1SRCBRAF
SCHEMBL5062161 0.85 FGFR1 (0.55) KITPDGFRAFGFR1SRCBRAF
SCHEMBL5062576 0.84 KIT (0.66) KITPDGFRAFGFR1SRCBRAF
SCHEMBL5065211 0.83 BRAF (0.49) KITPDGFRAFGFR1SRCBRAF
SCHEMBL22538096 0.82 FGFR1 (0.55) KITPDGFRAFGFR1SRCBRAF
SCHEMBL4426658 0.81 BRAF (0.49) KITPDGFRAFGFR1SRCBRAF
SCHEMBL4426394 0.81 BRAF (0.48) KITPDGFRAFGFR1SRCBRAF
SCHEMBL4423868 0.81 FGFR1 (0.56) KITPDGFRAFGFR1SRCBRAF
SCHEMBL4427156 0.81 BRAF (0.49) KITPDGFRAFGFR1SRCBRAF
SCHEMBL5065239 0.81 BRAF (0.46) KITPDGFRAFGFR1SRCBRAF

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-20080114006-A1 Kinase inhibitors useful for the treatment of proliferative diseases DECIPHERA PARMACEUTICALS, LLC (US) 2008-05-15 US claimed
US-20120289540-A1 KINASE INHIBITORS USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES DECIPHERA PHARMACEUTICALS, LLC (US) 2012-11-15 US disclosed
US-8188113-B2 For example, 1-(5-(2-amino-8-methyl-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-6-yl)-2-fluorophenyl)-3-(3-tert-butyl-1-phenyl-1H-pyrazol-5-yl)urea; for treatment of mammalian cancers and inflammatory diseases including rheumatoid arthritis, retinopathies DECIPHERA PHARMACEUTICALS, INC. (US) 2012-05-29 US disclosed
EP-2063897-A2 KINASE INHIBITORS USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES Deciphera Pharmaceuticals, LLC. (US) 2009-06-03 EP disclosed
US-20080114006-A1 Kinase inhibitors useful for the treatment of proliferative diseases DECIPHERA PARMACEUTICALS, LLC (US) 2008-05-15 US disclosed
WO-2008034008-A2 KINASE INHIBITORS USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES DECIPHERA PHARMACEUTICALS, LLC. (US) 2008-03-20 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 (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-20120289540-A1 KINASE INHIBITORS USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES BRAF, PRKDC, RAF1 KIT 2755/4885PDGFRA 2199/4885FGFR1 577/4885
US-20080114006-A1 Kinase inhibitors useful for the treatment of proliferative diseases BRAF, PRKDC, RAF1 KIT 2755/4885PDGFRA 2199/4885FGFR1 577/4885

“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.