SCHEMBL103903

SCHEMBL103903

COCCNCc1ccc(-c2cc3nccc(Oc4ccc(N(C(=O)C5(C(N)=O)CC5)c5ccc(F)cc5)cc4F)c3s2)nc1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MET P08581 6/20 0.73
▸ KDR P35968 6/20 0.73
▸ AXL P30530 2/20 0.73
▸ FLT3 P36888 2/20 0.73
▸ NTRK1 P04629 1/20 0.73
▸ KIT P10721 1/20 0.73
▸ NTRK2 Q16620 1/20 0.73
▸ MST1R Q04912 15/20 0.62
▸ PLK4 O00444 1/20 0.62
▸ MAP4K4 O95819 1/20 0.62
▸ ABL1 P00519 1/20 0.62
▸ LCK P06239 1/20 0.62
▸ FYN P06241 1/20 0.62
▸ LYN P07948 1/20 0.62
▸ HCK P08631 1/20 0.62
▸ PDGFRB P09619 1/20 0.62
▸ BCR P11274 1/20 0.62
▸ SRC P12931 1/20 0.62
▸ ABL2 P42684 1/20 0.62
▸ FRK P42685 1/20 0.62

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
SCHEMBL29514769 1.00 MET (0.73) METKDRAXLFLT3NTRK1
SCHEMBL104989 0.96 MET (0.67) METKDRAXLFLT3NTRK1
SCHEMBL2534615 0.94 MET (0.65) METKDRAXLFLT3NTRK1
SCHEMBL2670680 0.94 MET (0.64) METKDRAXLFLT3NTRK1
Malic Acid SCHEMBL29910999 0.94 MET (0.65) METKDRAXLFLT3NTRK1
Malic Acid SCHEMBL29910932 0.94 MET (0.65) METKDRAXLFLT3NTRK1
Malic Acid SCHEMBL26110839 0.94 MET (0.65) METKDRAXLFLT3NTRK1
SCHEMBL2670825 0.92 MET (0.61) METKDRAXLFLT3NTRK1
SCHEMBL105538 0.90 MET (0.64) METKDRAXLFLT3NTRK1
SCHEMBL1479218 0.88 MET (0.57) 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 175 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4027999-B1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF MIRATI THERAPEUTICS INC (US) 2026-03-04 — — EP claimed
US-11787819-B2 Crystalline salt of a multi-tyrosine kinase inhibitor, method of preparation, and use thereof MIRATI THERAPEPEUTICS, INC. (US) 2023-10-17 — — US claimed
EP-4213844-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2023-07-26 — — EP claimed
US-20220402936-A1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF Mirati Therapeutics, Inc. 2022-12-22 — — US claimed
US-20220289760-A1 CRYSTALLINE SALT OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF Mirati Therapeutics, Inc. 2022-09-15 — — US claimed
EP-4027999-A1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF Mirati Therapeutics, Inc. (US) 2022-07-20 — — EP claimed
US-20210164055-A1 POINT MUTATIONS IN TRK INHIBITOR-RESISTANT CANCER AND METHODS RELATING TO THE SAME ARRAY BIOPHARMA, INC. 2021-06-03 — — US claimed
WO-2021050580-A1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF Mirati Therapeutics, Inc. (US) 2021-03-18 — — WO claimed
EP-3773725-A1 TREATMENT OF TRK-ASSOCIATED CANCERS Loxo Oncology Inc. (US) 2021-02-17 — — EP claimed
US-20210023086-A1 TREATMENT OF TRK-ASSOCIATED CANCERS LOXO ONCOLOGY, INC. 2021-01-28 — — US claimed
US-10724102-B2 Point mutations in TRK inhibitor-resistant cancer and methods relating to the same LOXO ONCOLOGY, INC. (US) 2020-07-28 — — US claimed
WO-2019191659-A1 TREATMENT OF TRK-ASSOCIATED CANCERS LOXO ONCOLOGY, INC. (US) 2019-10-03 — — WO claimed
US-20170260589-A1 POINT MUTATIONS IN TRK INHIBITOR-RESISTANT CANCER AND METHODS RELATING TO THE SAME ARRAY BIOPHARMA, INC. 2017-09-14 — — US claimed
EP-4027999-B1 CRYSTALLINE FORM OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF MIRATI THERAPEUTICS INC (US) 2026-03-04 — — EP disclosed
US-12466838-B2 Crystalline form of a multi-tyrosine kinase inhibitor, method of preparation, and use thereof Mirati Therapeutics, Inc. (US) 2025-11-11 — — US disclosed
US-12466838-B2 Crystalline form of a multi-tyrosine kinase inhibitor, method of preparation, and use thereof Mirati Therapeutics, Inc. (US) 2025-11-11 — — US disclosed
EP-2183254-A1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY MethylGene Inc. (CA) 2010-05-12 — — 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-2009026717-A1 INHIBITORS OF PROTEIN TYROSINE KINASE ACTIVITY 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 (10 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-20210164055-A1 POINT MUTATIONS IN TRK INHIBITOR-RESISTANT CANCER AND METHODS RELATING TO THE SAME NTRK3, NTRK1, NTRK2 MET 220/4885KDR 661/4885AXL 1642/4885
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-12466838-B2 Crystalline form of a multi-tyrosine kinase inhibitor, method of preparation, and use thereof ABL1, LCK, SRC MET 148/4885KDR 262/4885AXL 57/4885
US-20220289760-A1 CRYSTALLINE SALT OF A MULTI-TYROSINE KINASE INHIBITOR, METHOD OF PREPARATION, AND USE THEREOF LCK, MAP2K5, SRC MET 14/4885KDR 733/4885AXL 206/4885
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
US-11787819-B2 Crystalline salt of a multi-tyrosine kinase inhibitor, method of preparation, and use thereof LCK, MAP2K5, SRC MET 14/4885KDR 733/4885AXL 206/4885
US-20210023086-A1 TREATMENT OF TRK-ASSOCIATED CANCERS TP53, NCOA3, NCOA1 MET 7/4885KDR 297/4885AXL 2198/4885
US-20170260589-A1 POINT MUTATIONS IN TRK INHIBITOR-RESISTANT CANCER AND METHODS RELATING TO THE SAME NTRK3, NTRK1, NTRK2 MET 227/4885KDR 645/4885AXL 1509/4885
US-10724102-B2 Point mutations in TRK inhibitor-resistant cancer and methods relating to the same NTRK3, NTRK1, NTRK2 MET 220/4885KDR 661/4885AXL 1642/4885

“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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