SCHEMBL169838

SCHEMBL169838

COCCN(Cc1ccc(-c2cc3nccc(Oc4ccc(NC(=O)C5(C(=O)Nc6ccc(F)cc6)CC5)cc4F)c3s2)nc1)C(=O)OC(C)(C)C

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MET P08581 8/20 0.72
KDR P35968 8/20 0.72
AXL P30530 3/20 0.72
FLT3 P36888 2/20 0.72
NTRK1 P04629 1/20 0.72
KIT P10721 1/20 0.72
NTRK2 Q16620 1/20 0.72
MST1R Q04912 13/20 0.71
PLK4 O00444 1/20 0.55
MAP4K4 O95819 1/20 0.55
ABL1 P00519 1/20 0.55
LCK P06239 1/20 0.55
FYN P06241 1/20 0.55
LYN P07948 1/20 0.55
HCK P08631 1/20 0.55
PDGFRB P09619 1/20 0.55
BCR P11274 1/20 0.55
SRC P12931 1/20 0.55
ABL2 P42684 1/20 0.55
FRK P42685 1/20 0.55

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
SCHEMBL29998555 1.00 MET (0.72) METKDRAXLFLT3NTRK1
SCHEMBL23118270 0.95 MST1R (0.68) METKDRAXLFLT3NTRK1
SCHEMBL19026748 0.95 MET (0.65) METKDRAXLFLT3NTRK1
SCHEMBL2537860 0.95 MET (0.72) METKDRAXLFLT3NTRK1
SCHEMBL105450 0.92 MET (0.77) METKDRAXLFLT3NTRK1
SCHEMBL13926736 0.92 MET (0.64) METKDRAXLFLT3NTRK1
SCHEMBL13608234 0.91 MST1R (0.60) METKDRAXLFLT3NTRK1
SCHEMBL171374 0.90 MET (0.61) METKDRAXLFLT3NTRK1
SCHEMBL13664120 0.89 MST1R (0.71) METKDRAXLFLT3NTRK1
SCHEMBL12806823 0.88 MST1R (0.68) METKDRAXLFLT3NTRK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230022859-A1 TREATMENT OF CANCER WITH ANTI-OX40 ANTIBODIES AND MULTI-KINASE INHIBITORS BEIGENE, LTD. (KY) 2023-01-26 US disclosed
US-20220402936-A1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF Mirati Therapeutics, Inc. 2022-12-22 US disclosed
US-20220387404-A1 TREATMENT OF CANCER USING A COMBINATION COMPRISING MULTI-TYROSINE KINASE INHIBITOR AND IMMUNE CHECKPOINT INHIBITOR BEIGENE, LTD. (KY) 2022-12-08 US disclosed
WO-2021098769-A1 TREATMENT OF CANCER WITH ANTI-OX40 ANTIBODIES AND MULTI-KINASE INHIBITORS BEIGENE, LTD. (KY) 2021-05-27 WO disclosed
WO-2021047623-A1 TREATMENT OF CANCER USING A COMBINATION COMPRISING MULTI-TYROSINE KINASE INHIBITOR AND IMMUNE CHECKPOINT INHIBITOR BEIGENE, LTD. (KY) 2021-03-18 WO disclosed
EP-2183254-B1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY METHYLGENE INC (CA) 2017-06-21 EP disclosed
EP-2426108-B1 Processes and intermediates for preparing fused heterocyclic kinase inhibitors METHYLGENE INC (CA) 2016-08-10 EP disclosed
US-9018378-B2 Processes and intermediates for preparing fused heterocyclic kinase inhibitors METHYLGENE INC. (CA) 2015-04-28 US disclosed
US-8907091-B2 Processes and intermediates for preparing fused heterocyclic kinase inhibitors METHYLGENE INC. (CA) 2014-12-09 US disclosed
US-8846927-B2 Inhibitors of protein tyrosine kinase activity METHYLGENE INC. (CA) 2014-09-30 US disclosed
US-20130165477-A1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY METHYLGENE INC. (CA) 2013-06-27 US disclosed
US-8404846-B2 Inhibitors of protein tyrosine kinase activity METHYLGENE INC. (CA) 2013-03-26 US disclosed
EP-2426108-A1 Processes and intermediates for preparing fused heterocyclic kinase inhibitors MethylGene Inc. (CA) 2012-03-07 EP disclosed
US-20090286984-A1 Processes and intermediates for preparing fused heterocyclic kinase inhibitors Mirati Therapeutics, Inc. 2009-11-19 US disclosed
US-20090264440-A1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY Mirati Therapeutics, Inc. 2009-10-22 US disclosed
WO-2009026720-A1 PROCESSES AND INTERMEDIATES FOR PREPARING FUSED HETEROCYCLIC KINASE INHIBITORS METHYLGENE INC. (CA) 2009-03-05 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 (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-20220387404-A1 TREATMENT OF CANCER USING A COMBINATION COMPRISING MULTI-TYROSINE KINASE INHIBITOR AND IMMUNE CHECKPOINT INHIBITOR PDCD1, LCK, CD274 MET 235/4885KDR 1276/4885AXL 164/4885
US-20130165477-A1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY HGF, ERBB2, MET MET 3/4885KDR 11/4885AXL 130/4885
US-20230022859-A1 TREATMENT OF CANCER WITH ANTI-OX40 ANTIBODIES AND MULTI-KINASE INHIBITORS TNFRSF9, TNFRSF1A, TNFSF11 MET 330/4885KDR 579/4885AXL 204/4885
US-20090286984-A1 Processes and intermediates for preparing fused heterocyclic kinase inhibitors MAP3K19, MAP3K9, MAP4K2 MET 1062/4885KDR 526/4885AXL 418/4885
US-20090264440-A1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY HGF, ERBB2, MET MET 3/4885KDR 11/4885AXL 130/4885
US-20220402936-A1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF ABL1, LCK, SRC MET 148/4885KDR 262/4885AXL 57/4885

“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.