Selumetinib

Selumetinib

SCHEMBL155456

Cn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(C(=O)NOCCO)cc21

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 Selumetinib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
MAP2K1 known ✓ Q02750 20/20 1.00
MAP2K2 known ✓ P36507 3/20 1.00
SMC2 O95347 1/20 1.00
EGFR P00533 1/20 1.00
CSNK2A2 P19784 1/20 1.00
SMC1A Q14683 1/20 1.00
AAK1 Q2M2I8 1/20 1.00
Q6ZSR9 Q6ZSR9 1/20 1.00
BMP2K Q9NSY1 1/20 1.00
ABCB11 O95342 1/20 0.84
NQO2 P16083 1/20 0.84
BRAF P15056 5/20 0.47

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
Selumetinib SCHEMBL29353582 1.00 MAP2K1 (1.00) MAP2K1MAP2K2SMC2EGFRCSNK2A2
Selumetinib SCHEMBL29555068 1.00 MAP2K1 (1.00) MAP2K1MAP2K2SMC2EGFRCSNK2A2
Selumetinib SCHEMBL2354340 0.97 MAP2K1 (0.94) MAP2K1MAP2K2SMC2EGFRCSNK2A2
Selumetinib SCHEMBL29744701 0.97 MAP2K1 (0.94) MAP2K1MAP2K2SMC2EGFRCSNK2A2
SCHEMBL4546029 0.95 MAP2K1 (0.91) MAP2K1MAP2K2SMC2EGFRCSNK2A2
Selumetinib SCHEMBL30487255 0.94 MAP2K1 (0.89) MAP2K1MAP2K2SMC2EGFRCSNK2A2
Selumetinib SCHEMBL30487260 0.93 MAP2K1 (0.88) MAP2K1MAP2K2SMC2EGFRCSNK2A2
SCHEMBL21501424 0.93 MAP2K1 (0.87) MAP2K1MAP2K2SMC2EGFRCSNK2A2
SCHEMBL4546010 0.93 MAP2K1 (0.87) MAP2K1MAP2K2SMC2EGFRCSNK2A2
SCHEMBL19141378 0.92 MAP2K1 (0.86) MAP2K1MAP2K2SMC2EGFRCSNK2A2

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 10031 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-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-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
US-20260130856-A1 LIPOSOME COMPOSITIONS FOR DELIVERY OF COMPOUNDS AND METHODS THEREOF NANOTECH PHARMA INC (US) 2026-05-14 US claimed
EP-4741395-A1 NOVEL COMPOUND SENSITIVE TO NITROGEN MONOXIDE AND PHARMACEUTICAL COMPOSITION COMPRISING SAME Omniamed Co. Ltd (KR) 2026-05-13 EP claimed
US-20260115209-A1 COMBINATION THERAPY INCLUDING COX-2 INHIBITOR FOR THE TREATMENT OF CANCER UNIV CALIFORNIA (US) 2026-04-30 US claimed
WO-2026090321-A1 TREATMENT OF CANCER WITH A KRAS INHIBITOR ALTEROME THERAPEUTICS, INC. (US) 2026-04-30 WO claimed
WO-2026090174-A1 COMPOSITIONS FOR TARGETED DELIVERY OF THERAPEUTIC AGENTS AND METHODS FOR THE SYNTHESIS AND USE THEREOF BRYET US, INC. (US) 2026-04-30 WO claimed
WO-2015169884-A2 COMPOUNDS AND METHODS FOR THE TREATMENT OF ITCH WESTFAELISCHE WILHELMS-UNIVERSITAET MUENSTER (DE) 2015-11-12 WO claimed
US-20150141380-A1 INHIBITORS OF ERK FOR DEVELOPMENTAL DISORDERS OF NEURONAL CONNECTIVITY CASE WESTERN RESERVE UNIVERSITY (US) 2015-05-21 US claimed
WO-2015002729-A2 CELL STABILIZATION BIOMATRICA, INC. (US) 2015-01-08 WO claimed
US-20140200260-A1 METHODS FOR DETERMINING AND INHIBITING RHEUMATOID ARTHRITIS ASSOCIATED WITH THE BRAF ONCOGENE IN A SUBJECT THE UNITED STATES OF AMERICA AS REPRESENTED BY 2014-07-17 US claimed
EP-2600862-A2 INHIBITORS OF ERK FOR DEVELOPMENTAL DISORDERS OF NEURONAL CONNECTIVITY Case Western Reserve University (US) 2013-06-12 EP claimed
WO-2012019113-A2 INHIBITORS OF ERK FOR DEVELOPMENTAL DISORDERS OF NEURONAL CONNECTIVITY CASE WESTERN RESERVE UNIVERSITY (US) 2012-02-09 WO claimed
WO-2011095807-A1 COMBINATIONS OF MEK AND HH INHIBITORS ASTRAZENECA AB (SE) 2011-08-11 WO claimed
US-20110158971-A1 COMPOSITIONS COMPRISING N3 ALKYLATED BENZIMIDAZOLE DERIVATIVES AS MEK INHIBITORS AND METHODS OF USE THEREOF ARRAY BIOPHARMA INC. (US) 2011-06-30 US claimed
JP-2011506420-A 2011-03-03 JP claimed
EP-2271321-A1 PHARMACEUTICAL COMPOSITION 271 AstraZeneca AB (SE) 2011-01-12 EP claimed