SCHEMBL362296

SCHEMBL362296

Nc1ccc(Nc2ccnc3cc4c(cc23)OCCOCCOCCO4)c(F)c1

nearest known ligand 0.46

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
EGFR P00533 16/20 0.46
KDM4E B2RXH2 1/20 0.42
GAA P10253 1/20 0.42
MAPT P10636 1/20 0.42
CCNC P24863 1/20 0.40
CDK8 P49336 1/20 0.40
GAK O14976 1/20 0.39
RIPK2 O43353 1/20 0.39
BUB1 O43683 1/20 0.39
STK10 O94804 1/20 0.39
CARS1 P49589 1/20 0.39
MAP3K1 Q13233 1/20 0.39
PIP4K2C Q8TBX8 1/20 0.39
SLK Q9H2G2 1/20 0.39
RAF1 P04049 1/20 0.38
BRAF P15056 1/20 0.38
FGFR1 P11362 1/20 0.37
FLT1 P17948 1/20 0.37
KDR P35968 1/20 0.37

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
SCHEMBL363708 0.84 EGFR (0.65) EGFRGAKRIPK2BUB1STK10
SCHEMBL14937427 0.84 TSHR (0.42) EGFRCCNCCDK8RIPK2RAF1
SCHEMBL361752 0.77 AXL (0.55) EGFRKDM4EGAAMAPTKDR
SCHEMBL362781 0.77 PLK4 (0.42) EGFRKDM4EGAAMAPTGAK
SCHEMBL14966611 0.73 AXL (0.53) EGFRKDR
SCHEMBL12469296 0.71 AXL (0.73) EGFRMAPTGAKRIPK2STK10
SCHEMBL27533397 0.70 RAF1 (0.54) EGFRGAKRIPK2RAF1BRAF
SCHEMBL368095 0.70 MET (0.51) EGFRKDR
SCHEMBL361802 0.70 EGFR (0.47) EGFRKDM4EGAAMAPTGAK
SCHEMBL14937611 0.69 EGFR (0.57) EGFRGAKRIPK2BUB1STK10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2593462-B1 NOVEL FUSED HETEROCYCLIC DERIVATIVES USEFUL AS C-MET TYROSINE KINASE INHIBITORS BETTA PHARMACEUTICALS CO LTD (CN) 2016-09-07 EP claimed
US-9242991-B2 Substituted fused heterocycles as c-Met tyrosine kinase inhibitors BETTA PHARMACEUTICALS CO., LTD (CN) 2016-01-26 US claimed
EP-2593462-B1 NOVEL FUSED HETEROCYCLIC DERIVATIVES USEFUL AS C-MET TYROSINE KINASE INHIBITORS BETTA PHARMACEUTICALS CO LTD (CN) 2016-09-07 EP disclosed
US-9242991-B2 Substituted fused heterocycles as c-Met tyrosine kinase inhibitors BETTA PHARMACEUTICALS CO., LTD (CN) 2016-01-26 US disclosed
US-20130123286-A1 Novel Fused Heterocyclic Derivatives Useful as c-Met Tyrosine Kinase Inhibitors BETTA PHARMACEUTICALS CO., LTD. (CN) 2013-05-16 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 (1 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-20130123286-A1 Novel Fused Heterocyclic Derivatives Useful as c-Met Tyrosine Kinase Inhibitors MET, RET, ABL1 EGFR 30/4885KDM4E 1318/4885GAA 2687/4885

“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.