Trametinib

Trametinib

SCHEMBL170938

CC(=O)Nc1cccc(-n2c(=O)n(C3CC3)c(=O)c3c(Nc4ccc(I)cc4F)n(C)c(=O)c(C)c32)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MAP2K1MAP2K2

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

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MAP2K1 known ✓ Q02750 17/20 1.00
MAP2K2 known ✓ P36507 2/20 1.00
ABCB1 P08183 1/20 1.00
NOX4 Q9NPH5 1/20 0.39
PIK3CA P42336 1/20 0.38
PRKDC P78527 1/20 0.38
MAP2K5 Q13163 1/20 0.37
EIF2AK1 Q9BQI3 1/20 0.37
GAA P10253 1/20 0.34

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
Trametinib SCHEMBL29363416 1.00 MAP2K1 (1.00) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL29355100 1.00 MAP2K1 (1.00) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL1419085 0.99 MAP2K1 (0.98) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL1419395 0.99 MAP2K1 (0.98) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL21048481 0.99 MAP2K1 (0.98) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL1419392 0.99 MAP2K1 (0.98) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL30035834 0.99 MAP2K1 (0.98) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL30301264 0.99 MAP2K1 (0.98) MAP2K1MAP2K2ABCB1NOX4PIK3CA
Trametinib SCHEMBL1419017 0.98 MAP2K1 (0.97) MAP2K1MAP2K2ABCB1NOX4PIK3CA
SCHEMBL26815709 0.98 MAP2K1 (0.96) MAP2K1MAP2K2ABCB1NOX4PIK3CA

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

Appears in 15624 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260146289-A1 ASSESSING AND TREATING MELANOMA MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2026-05-28 US claimed
EP-4747285-A1 MONOCLONAL ANTIBODIES AGAINST PCDH7 FOR LUNG CANCER THERAPY The Board of Regents of the University of Texas System (US) 2026-05-27 EP claimed
CN-122075716-A Medicine for treating tumor by combining recombinant oncolytic virus and small-molecule anticancer medicine 2026-05-26 CN claimed
US-12636376-B2 Methods and compositions for use of growth factor antibodies in combination with non-tyrosine targeting kinase inhibitors IN3BIO LTD. (BM) 2026-05-26 US claimed
CN-115813930-B Use of macrocyclic compounds in combination with MEK inhibitors in medicaments for the treatment of diseases Sano Hubble Pharmaceutical (Chengdu) Co.,Ltd. (CN) 2026-05-26 CN claimed
CN-122070932-A Application of combination of decitabine and anti-HER 2 antibody in preparation of medicines for treating tumors 上海交通大学 2026-05-22 CN claimed
WO-2026107416-A1 SINGLE DOSAGE FORMS CONTAINING ELRAGLUSIB AND AT LEAST ONE OTHER ACTIVE INGREDIENT ACTUATE THERAPEUTICS, INC. (US) 2026-05-21 WO claimed
US-20260139320-A1 StarTrace: A Multiplex Drug Testing Platform for Personalized Medicine UNIV OF SOUTH CAROLINA (US) 2026-05-21 US claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
EP-2571358-A1 COMBINATION GlaxoSmithKline LLC (US) 2013-03-27 EP claimed
US-20120245180-A1 COMBINATION GLAXOSMITHKLINE LLC (US) 2012-09-27 US claimed
EP-2482819-A2 COMBINATION GlaxoSmithKline LLC (US) 2012-08-08 EP claimed
WO-2012088033-A2 NOVEL PHARMACEUTICAL COMPOSITION GLAXOSMITHKLINE LLC (US) 2012-06-28 WO claimed
WO-2012088030-A1 COMBINATION GLAXOSMITHKLINE LLC (US) 2012-06-28 WO claimed
WO-2012027438-A1 PHARMACEUTICAL COMBINATION OF A VEGFR INHIBITOR AND A MEK INHIBITOR USEFUL FOR TREATING CANCER GLAXOSMITHKLINE LLC (US) 2012-03-01 WO claimed
WO-2011146712-A1 COMBINATION GLAXOSMITHKLINE LLC (US) 2011-11-24 WO claimed
WO-2011038380-A2 COMBINATION GLAXOSMITHKLINE LLC (US) 2011-03-31 WO claimed
US-7378423-B2 Antiproliferative, anticancer, antitumor agents; rheumatism; N-{3-[3-cyclopropyl-5-(2-fluoro-4-iodo-phenylamino)-6,8-dimethyl-2,4,7-trioxo-3,4,6,7-tetrahydro-2H-pyrido[4,3-d]pyrimidin-1-yl]-phenyl}-acetamide; a p15, and/or a protein inducing action, and/or an MEK inhibitory action; side effect reduction JAPAN TOBACCO INC. (JP) 2008-05-27 US claimed
EP-1761528-B1 5-AMINO-2,4,7-TRIOXO-3,4,7,8-TETRAHYDRO-2H-PYRIDO[2,3-D]PYRIMIDINE DERIVATIVES AND RELATED COMPOUNDS FOR THE TREATMENT OF CANCER JAPAN TOBACCO INC (JP) 2008-01-09 EP claimed