Cobimetinib

Cobimetinib

SCHEMBL189565

O=C(c1ccc(F)c(F)c1Nc1ccc(I)cc1F)N1CC(O)([C@@H]2CCCCN2)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 Cobimetinib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MAP2K1 known ✓ Q02750 20/20 1.00
MAP2K2 known ✓ P36507 19/20 1.00
CHRM2 P08172 1/20 1.00
CHRM1 P11229 1/20 1.00
BRAF P15056 1/20 1.00
DRD1 P21728 1/20 1.00
TBXA2R P21731 1/20 1.00
SLC6A2 P23975 1/20 1.00
SLC6A4 P31645 1/20 1.00
ADRA1A P35348 1/20 1.00
OPRM1 P35372 1/20 1.00
DRD3 P35462 1/20 1.00
ACTR3 P61158 1/20 1.00
SLC6A3 Q01959 1/20 1.00
KCNH2 Q12809 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
Cobimetinib SCHEMBL29839406 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL188704 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL29358284 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL29413366 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL1488831 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL29413464 0.99 MAP2K1 (0.98) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL1489148 0.99 MAP2K1 (0.98) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL30220897 0.99 MAP2K1 (0.98) MAP2K1MAP2K2CHRM2CHRM1BRAF
Cobimetinib SCHEMBL1488436 0.99 MAP2K1 (0.98) MAP2K1MAP2K2CHRM2CHRM1BRAF
SCHEMBL189480 0.97 MAP2K1 (0.95) MAP2K1MAP2K2CHRM2CHRM1BRAF

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 10326 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-4747408-A1 DIAGNOSTIC AND THERAPEUTIC METHODS FOR CANCER GENENTECH, INC. (US) 2026-05-27 EP 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
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-122075716-A Medicine for treating tumor by combining recombinant oncolytic virus and small-molecule anticancer medicine 2026-05-26 CN claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
US-20260139315-A1 DIAGNOSTIC AND THERAPEUTIC METHODS FOR CANCER GENENTECH, INC. (US) 2026-05-21 US 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
EP-4743074-A1 METHODS OF TREATING HEMATOLOGIC CANCER Foghorn Therapeutics Inc. (US) 2026-05-20 EP claimed
US-20260130891-A1 PIM KINASE INHIBITOR IN COMBINATION WITH KRAS INHIBITOR NINGBO NEWBAY TECH DEVELOPMENT CO LTD (CN) 2026-05-14 US claimed
US-20120302545-A1 Method of Using PI3K and MEK Modulators EXELIXIS, INC. (US) 2012-11-29 US claimed
EP-2056829-B9 USING PI3K AND MEK MODULATORS IN TREATMENTS OF CANCER EXELIXIS INC (US) 2012-09-26 EP claimed
EP-2056829-B1 USING PI3K AND MEK MODULATORS IN TREATMENTS OF CANCER EXELIXIS INC (US) 2012-01-04 EP claimed
US-7999006-B2 Anticancer agents; mitogen-activated protein kinases (MEK) EXELIXIS, INC. (US) 2011-08-16 US claimed
EP-1934174-B1 AZETIDINES AS MEK INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISEASES EXELIXIS INC (US) 2011-04-06 EP claimed
US-7803839-B2 anticarcinogenic agent; 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}-carbonyl)azetidin-3-ol EXELIXIS, INC. (US) 2010-09-28 US claimed
US-20100075947-A1 Methods of Using PI3K and MEK Modulators EXELIXIS, INC. (US) 2010-03-25 US claimed
US-20090156576-A1 anticarcinogenic agent; 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}-carbonyl)azetidin-3-ol EXELIXIS INC. (US) 2009-06-18 US claimed
WO-2008124085-A2 METHODS OF USING COMBINATIONS OF MEK AND JAK-2 INHIBITORS EXELIXIS, INC. (US) 2008-10-16 WO claimed
US-20080166359-A1 Methods of using MEK inhibitors EXELIXIS, INC. 2008-07-10 US claimed