SCHEMBL3795531

SCHEMBL3795531

COc1cc2nccc(Oc3ccc(C(N)=O)cc3OC)c2cc1OC

nearest known ligand 0.67

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ PDGFRA P16234 3/20 0.61
▸ PDGFRB P09619 1/20 0.61
▸ SRC P12931 5/20 0.60
▸ TGFBR1 P36897 5/20 0.60
▸ FGFR2 P21802 1/20 0.57
▸ KDR P35968 3/20 0.56
▸ AURKA O14965 1/20 0.56
▸ ABL1 P00519 1/20 0.56
▸ LCK P06239 1/20 0.56
▸ LYN P07948 1/20 0.56
▸ MET P08581 1/20 0.56
▸ TEK Q02763 1/20 0.56
▸ AURKB Q96GD4 1/20 0.56
▸ MAPK1 P28482 1/20 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
SCHEMBL3794339 0.91 SRC (0.61) PDGFRAPDGFRBSRCTGFBR1FGFR2
SCHEMBL3794835 0.90 MET (0.59) PDGFRAPDGFRBSRCTGFBR1FGFR2
SCHEMBL14967511 0.88 PDGFRA (0.54) PDGFRAPDGFRBSRCTGFBR1FGFR2
SCHEMBL14967748 0.87 PDGFRB (0.53) PDGFRAPDGFRBSRCTGFBR1FGFR2
SCHEMBL3794599 0.87 FGFR2 (0.69) PDGFRAPDGFRBFGFR2KDRAURKA
SCHEMBL14966460 0.86 PDGFRA (0.52) PDGFRAPDGFRBSRCTGFBR1FGFR2
SCHEMBL14966992 0.83 FLT3 (0.58) PDGFRAPDGFRBKDRMET
SCHEMBL1591160 0.83 AXL (0.60) PDGFRAPDGFRBSRCFGFR2KDR
SCHEMBL4575945 0.83 MET (0.52) PDGFRASRCTGFBR1FGFR2KDR
SCHEMBL14966613 0.82 SRC (0.59) PDGFRAPDGFRBSRCTGFBR1FGFR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2780338-B1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA INC (US) 2016-11-09 — — EP claimed
US-9206130-B2 Quinoline derivatives as AXL kinase inhibitors MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2015-12-08 — — US claimed
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 — — US claimed
EP-2262772-A1 QUINOLINE DERIVATIVES AS AXL KINASE INHIBITORS Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2010-12-22 — — EP claimed
WO-2009127417-A1 QUINOLINE DERIVATIVES AS AXL KINASE INHIBITORS MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2009-10-22 — — WO claimed
US-10017496-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2018-07-10 — — US disclosed
US-20170320853-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA, INC. (US) 2017-11-09 — — US disclosed
US-9745283-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2017-08-29 — — US disclosed
US-20170050949-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2017-02-23 — — US disclosed
US-9522902-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2016-12-20 — — US disclosed
EP-2780338-B1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA INC (US) 2016-11-09 — — EP disclosed
EP-3045453-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2016-07-20 — — EP disclosed
US-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2015-07-30 — — US disclosed
US-9029538-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2015-05-12 — — US disclosed
EP-2780338-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS Cephalon, Inc. (US) 2014-09-24 — — EP disclosed
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 — — US disclosed
WO-2013074633-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2013-05-23 — — WO disclosed
EP-2262772-B1 QUINOLINE DERIVATIVES AS AXL KINASE INHIBITORS MAX PLANCK GESELLSCHAFT (DE) 2012-07-18 — — EP disclosed
EP-2262772-A1 QUINOLINE DERIVATIVES AS AXL KINASE INHIBITORS Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2010-12-22 — — EP disclosed
WO-2009127417-A1 QUINOLINE DERIVATIVES AS AXL KINASE INHIBITORS MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2009-10-22 — — 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 (5 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-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PDGFRA 103/4885PDGFRB 34/4885SRC 14/4885
US-20170050949-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PDGFRA 103/4885PDGFRB 34/4885SRC 14/4885
US-20170320853-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, FLT3 PDGFRA 72/4885PDGFRB 28/4885SRC 15/4885
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PDGFRA 103/4885PDGFRB 34/4885SRC 14/4885
US-10017496-B2 Uracil derivatives as AXL and c-MET kinase inhibitors AXL, RET, FLT3 PDGFRA 72/4885PDGFRB 28/4885SRC 15/4885

“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.

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