SCHEMBL16089916

SCHEMBL16089916

Cc1cc2nccc(Oc3ccc([N+](=O)[O-])cc3Br)c2cc1C

nearest known ligand 0.50

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PDGFRA P16234 3/20 0.44
KDR P35968 2/20 0.44
SRC P12931 2/20 0.41
TGFBR1 P36897 2/20 0.41
ALDH1A1 P00352 5/20 0.40
TDP1 Q9NUW8 3/20 0.40
GAA P10253 3/20 0.40
MAPT P10636 3/20 0.40
HTT P42858 3/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
TSHR P16473 1/20 0.40
CYP3A4 P08684 1/20 0.38
MEN1 O00255 2/20 0.37
KMT2A Q03164 2/20 0.37
MAPK1 P28482 2/20 0.37
PDGFRB P09619 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.36
EGFR P00533 1/20 0.36
TBXA2R P21731 1/20 0.36

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
SCHEMBL14966986 0.87 PDGFRA (0.59) PDGFRAKDRSRCTGFBR1PDGFRB
SCHEMBL20022397 0.86 HSPB1 (0.47) PDGFRAKDRSRCTGFBR1ALDH1A1
SCHEMBL557790 0.83 PDGFRA (0.61) PDGFRAKDRHTTMEN1KMT2A
SCHEMBL16089917 0.82 PDGFRA (0.42) PDGFRAKDRSRCTGFBR1ALDH1A1
SCHEMBL29487138 0.79 KDR (0.50) PDGFRAKDRPDGFRB
SCHEMBL22960033 0.79 KDR (0.50) PDGFRAKDRPDGFRB
SCHEMBL5824446 0.79 PDGFRA (0.60) PDGFRAKDRSRCTGFBR1PDGFRB
SCHEMBL20032552 0.77 PDGFRA (0.51) PDGFRAKDRSRCTGFBR1PDGFRB
SCHEMBL29683621 0.77 HSPB1 (0.49) ALDH1A1TDP1GAAMAPTHTT
SCHEMBL23882405 0.74 MEN1 (0.42) PDGFRAKDRSRCTGFBR1ALDH1A1

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
US-9120778-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2015-09-01 US disclosed
US-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2015-07-30 US disclosed
US-20150209358-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
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 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 (6 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 103/4885KDR 109/4885SRC 14/4885
US-20170050949-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PDGFRA 103/4885KDR 109/4885SRC 14/4885
US-20170320853-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, FLT3 PDGFRA 72/4885KDR 83/4885SRC 15/4885
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PDGFRA 103/4885KDR 109/4885SRC 14/4885
US-10017496-B2 Uracil derivatives as AXL and c-MET kinase inhibitors AXL, RET, FLT3 PDGFRA 72/4885KDR 83/4885SRC 15/4885
US-20150209358-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PDGFRA 103/4885KDR 109/4885SRC 14/4885

“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.