Lifirafenib

Lifirafenib

SCHEMBL15085288

O=C1CCc2c(Oc3ccc4c(c3)[C@@H]3[C@H](O4)[C@H]3c3nc4ccc(C(F)(F)F)cc4[nH]3)ccnc2N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BRAF

The experimentally established mechanism targets of Lifirafenib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
BRAF known ✓ P15056 20/20 1.00
RAF1 P04049 17/20 1.00
ARAF P10398 1/20 1.00

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
Lifirafenib SCHEMBL29464034 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL15085317 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL29749194 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL20133921 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL15085289 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL24916576 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL20129833 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL15085287 1.00 BRAF (1.00) BRAFRAF1ARAF
Lifirafenib SCHEMBL29750805 0.94 BRAF (0.89) BRAFRAF1ARAF
Lifirafenib SCHEMBL29750807 0.94 BRAF (0.89) BRAFRAF1ARAF

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 62 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4119559-A1 MALEATE SALTS OF A B-RAF KINASE INHIBITOR, CRYSTALLINE FORMS, METHODS OF PREPARATION, AND USES THEREFORE BeiGene, Ltd. (KY) 2023-01-18 EP claimed
EP-3283486-B1 MALEATE SALTS OF A B-RAF KINASE INHIBITOR, CRYSTALLINE FORMS, METHODS OF PREPARATION, AND USES THEREFORE BEIGENE LTD (KY) 2022-07-27 EP claimed
CN-113307805-A Maleate salts of B-RAF kinase inhibitors, crystalline forms, processes for their preparation and their use 百济神州有限公司 2021-08-27 CN claimed
CN-107531682-B Maleate salts of B-RAF kinase inhibitors, crystalline forms, processes for their preparation and their use 百济神州有限公司 2021-05-04 CN claimed
US-10351559-B2 Maleate salts of a B-RAF kinase inhibitor, crystalline forms, methods of preparation, and uses therefore BEIGENE, LTD. (KY) 2019-07-16 US claimed
US-20190170752-A1 METHOD FOR PREDICTING EFFICACY OF IMMUNE CHECKPOINT INHIBITORS IN CANCER PATIENTS BEIGENE, LTD. (KY) 2019-06-06 US claimed
US-20180127412-A1 MALEATE SALTS OF A B-RAF KINASE INHIBITOR, CRYSTALLINE FORMS, METHODS OF PREPARATION, AND USES THEREFORE BEONE MEDICINES I GMBH (CH) 2018-05-10 US claimed
EP-3402822-B1 AXL-SPECIFIC ANTIBODY-DRUG CONJUGATES FOR CANCER TREATMENT GENMAB AS (DK) 2025-03-12 EP disclosed
EP-4125842-B1 CO-ADMINISTRATION OF MIRDAMETINIB AND LIFIRAFENIB FOR USE IN TREATING CANCERS BEIGENE LTD (US) 2024-06-05 EP disclosed
WO-2023212071-A1 COMBINATION AND THE USE THEREOF BEIGENE SWITZERLAND GMBH (CH) 2023-11-02 WO disclosed
WO-2023209611-A1 METHODS OF TREATING CANCER WITH A B-RAF INHIBITOR, IN PARTICULAR LIFIRAFENIB BEIGENE SWITZERLAND GMBH (CH) 2023-11-02 WO disclosed
US-20230321261-A1 AXL-SPECIFIC ANTIBODY-DRUG CONJUGATES FOR CANCER TREATMENT WILMINGTON TRUST, NATIONAL ASSOCIATION 2023-10-12 US disclosed
WO-2023076991-A1 COMBINATION THERAPY FOR TREATING ABNORMAL CELL GROWTH VERASTEM, INC. (US) 2023-05-04 WO disclosed
EP-2797888-B1 FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS BEIGENE LTD (KY) 2016-06-08 EP disclosed
US-9273046-B2 Fused tricyclic compounds as Raf kinase inhibitors BEIGENE, LTD. (KY) 2016-03-01 US disclosed
US-9273046-B2 Fused tricyclic compounds as Raf kinase inhibitors BEIGENE, LTD. (KY) 2016-03-01 US disclosed
US-9273046-B2 Fused tricyclic compounds as Raf kinase inhibitors BEIGENE, LTD. (KY) 2016-03-01 US disclosed
US-20150045355-A1 FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS BEONE MEDICINES I GMBH (CH) 2015-02-12 US disclosed
US-20150045355-A1 FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS BEONE MEDICINES I GMBH (CH) 2015-02-12 US disclosed
WO-2013097224-A1 FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS BEIGENE, LTD. (KY) 2013-07-04 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 (5 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-10351559-B2 Maleate salts of a B-RAF kinase inhibitor, crystalline forms, methods of preparation, and uses therefore BRAF, RAF1, NRAS BRAF 1/4885RAF1 2/4885ARAF 6/4885
US-20190170752-A1 METHOD FOR PREDICTING EFFICACY OF IMMUNE CHECKPOINT INHIBITORS IN CANCER PATIENTS CD274, PDCD1LG2, PDCD1 BRAF 171/4885RAF1 1014/4885ARAF 1012/4885
US-20150045355-A1 FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS BRAF, RAF1, ARAF BRAF 1/4885RAF1 2/4885ARAF 3/4885
US-20230321261-A1 AXL-SPECIFIC ANTIBODY-DRUG CONJUGATES FOR CANCER TREATMENT AXL, BRAF, MAPK1 BRAF 2/4885RAF1 72/4885ARAF 55/4885
US-20180127412-A1 MALEATE SALTS OF A B-RAF KINASE INHIBITOR, CRYSTALLINE FORMS, METHODS OF PREPARATION, AND USES THEREFORE BRAF, RAF1, NRAS BRAF 1/4885RAF1 2/4885ARAF 6/4885

“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.