SCHEMBL680378

SCHEMBL680378

Cc1cc(-c2cc3[nH]ncc3cc2Oc2ccc(NC(=O)c3ccnn(-c4ccc(F)cc4)c3=O)cc2F)n(C)n1

nearest known ligand 0.55

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
AXL P30530 20/20 0.55
MERTK Q12866 19/20 0.52
TYRO3 Q06418 18/20 0.52
MET P08581 17/20 0.52
PLK4 O00444 1/20 0.51
NTRK1 P04629 1/20 0.51
RET P07949 1/20 0.51
KDR P35968 1/20 0.51
FLT3 P36888 1/20 0.51
MST1R Q04912 1/20 0.51
DDR1 Q08345 1/20 0.51
CAMK4 Q16566 1/20 0.51
DDR2 Q16832 1/20 0.51
MKNK1 Q9BUB5 1/20 0.51
MKNK2 Q9HBH9 1/20 0.51

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
SCHEMBL2496266 0.87 AXL (0.55) AXLMERTKTYRO3MET
SCHEMBL12214704 0.86 AXL (0.59) AXLMERTKTYRO3MET
SCHEMBL681035 0.84 AXL (0.55) AXLMERTKTYRO3MET
SCHEMBL679258 0.84 AXL (0.60) AXLMERTKTYRO3MET
SCHEMBL12190694 0.84 AXL (0.51) AXLMERTKTYRO3METPLK4
SCHEMBL680768 0.84 AXL (0.56) AXLMERTKTYRO3MET
SCHEMBL2496790 0.82 AXL (0.49) AXLMERTKTYRO3METPLK4
SCHEMBL12190671 0.81 AXL (0.60) AXLMERTKTYRO3METPLK4
SCHEMBL680526 0.80 AXL (0.57) AXLMERTKTYRO3MET
SCHEMBL680267 0.79 AXL (0.57) AXLMERTKTYRO3METPLK4

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-RE43878-E1 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2012-12-25 US disclosed
US-RE43878-E1 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2012-12-25 US disclosed
US-RE43878-E1 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2012-12-25 US disclosed
EP-2310382-B1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET LILLY CO ELI (US) 2012-02-22 EP disclosed
US-8030302-B2 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2011-10-04 US disclosed
US-8030302-B2 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2011-10-04 US disclosed
US-8030302-B2 Amidophenoxyindazoles useful as inhibitors of c-Met ELI LILLY AND COMPANY (US) 2011-10-04 US disclosed
US-20100022529-A1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET ELI LILLY AND COMPANY 2010-01-28 US disclosed
US-20100022529-A1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET ELI LILLY AND COMPANY 2010-01-28 US disclosed
US-20100022529-A1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET ELI LILLY AND COMPANY 2010-01-28 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-20100022529-A1 AMIDOPHENOXYINDAZOLES USEFUL AS INHIBITORS OF C-MET MET, MYCBP, MYC AXL 113/4885MERTK 10/4885TYRO3 67/4885

“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.