Mirdametinib

Mirdametinib

SCHEMBL453656

O=C(NOCC(O)CO)c1ccc(F)c(F)c1Nc1ccc(I)cc1F

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

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MAP2K1 known ✓ Q02750 17/20 1.00
MAP2K2 known ✓ P36507 6/20 1.00
MAPK1 P28482 2/20 1.00
BRAF P15056 1/20 1.00
MAP2K5 Q13163 1/20 1.00
PIM1 P11309 1/20 0.67
CAMK2B Q13554 1/20 0.67
HDAC3 O15379 2/20 0.64
HDAC4 P56524 2/20 0.64
HDAC1 Q13547 2/20 0.64
HDAC7 Q8WUI4 2/20 0.64
HDAC2 Q92769 2/20 0.64
HDAC10 Q969S8 2/20 0.64
HDAC11 Q96DB2 2/20 0.64
HDAC8 Q9BY41 2/20 0.64
HDAC6 Q9UBN7 2/20 0.64
HDAC9 Q9UKV0 2/20 0.64
HDAC5 Q9UQL6 2/20 0.64

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
Mirdametinib SCHEMBL172904 1.00 MAP2K1 (1.00) MAP2K1MAP2K2MAPK1BRAFMAP2K5
Mirdametinib SCHEMBL29358470 1.00 MAP2K1 (1.00) MAP2K1MAP2K2MAPK1BRAFMAP2K5
Mirdametinib SCHEMBL895854 1.00 MAP2K1 (1.00) MAP2K1MAP2K2MAPK1BRAFMAP2K5
Mirdametinib SCHEMBL29352748 1.00 MAP2K1 (1.00) MAP2K1MAP2K2MAPK1BRAFMAP2K5
SCHEMBL4859890 0.92 MAP2K1 (0.85) MAP2K1MAP2K2MAPK1BRAFMAP2K5
SCHEMBL20435083 0.92 MAP2K1 (0.85) MAP2K1MAP2K2MAPK1BRAFMAP2K5
SCHEMBL6295227 0.91 MAP2K1 (0.84) MAP2K1MAP2K2MAPK1BRAFMAP2K5
SCHEMBL21067871 0.91 MAP2K1 (0.84) MAP2K1MAP2K2MAPK1BRAFMAP2K5
SCHEMBL13667024 0.91 MAP2K1 (0.84) MAP2K1MAP2K2MAPK1BRAFMAP2K5
SCHEMBL6292221 0.91 MAP2K1 (0.84) MAP2K1MAP2K2MAPK1BRAFMAP2K5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260083690-A1 DISPERSIBLE FORMULATIONS OF N-((R)-2,3-DIHYDROXYPROPOXY)-3,4-DIFLUORO-2-(2- FLUORO-4-IODO-PHENYLAMINO)-BENAZMIDE AND USES THEREOF SPRINGWORKS THERAPEUTICS INC (US) 2026-03-26 US claimed
US-20250270166-A1 CRYSTALLINE SOLIDS OF MEK INHIBITOR N-((R)-2,3-DIHYDROXYPROPOXY)-3,4-DIFLUORO-2-(2-FLUORO-4-IODO--PHENYLAMINO)-BENZAMIDE AND USES THEREOF SPRINGWORKS THERAPEUTICS, INC. 2025-08-28 US claimed
US-12275688-B2 Crystalline solids of MEK inhibitor N-((R)-2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide and uses thereof SPRINGWORKS THERAPEUTICS, INC. (US) 2025-04-15 US claimed
US-12195771-B2 Combination chemotherapy for the treatment of cancer WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2025-01-14 US claimed
US-20240382484-A1 COMPOSITION FOR TREATING, PREVENTING, OR AMELIORATING MELANOMA AND METHOD THEREOF THOMAS JEFFERSON UNIVERSITY 2024-11-21 US claimed
US-12090128-B2 Dispersible formulations of n-((r)-2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benazmide and uses thereof SPRINGWORKS THERAPEUTICS, INC. (US) 2024-09-17 US claimed
US-20240279201-A1 DUAL WNT SIGNALING PATHWAY INHIBITORS AND AMPK ACTIVATORS FOR TREATMENTS OF DISEASE UNIVERSITY OF MARYLAND, BALTIMORE 2024-08-22 US claimed
CN-118355110-A Method for producing cartilage and bone 默多克儿童研究所 2024-07-16 CN claimed
US-12037306-B2 Methods of treating neurofibromatosis type 1 with N-((R))-2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-benzamide WARNER-LAMBERT COMPANY LLC (US) 2024-07-16 US claimed
US-20240216307-A1 DISPERSIBLE FORMULATIONS OF N-((R)-2,3-DIHYDROXYPROPOXY)-3,4-DIFLUORO-2-(2- FLUORO-4-IODO-PHENYLAMINO)-BENAZMIDE AND USES THEREOF SPRINGWORKS THERAPEUTICS, INC. 2024-07-04 US claimed
US-20050222163-A1 Combinations of signal transduction inhibitors PFIZER INC 2005-10-06 US claimed
EP-1562601-A1 COMBINATION CHEMOTHERAPY COMPRISING A MEK INHIBITOR AND CAPECITABINE FOR TREATING CANCER Warner-Lambert Company LLC (US) 2005-08-17 EP claimed
US-20050176820-A1 Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids WARNER-LAMBERT COMPANY 2005-08-11 US claimed
WO-2004045617-A1 COMBINATION CHEMOTHERAPY COMPRISING A MEK INHIBITOR AND CAPECITABINE FOR TREATING CANCER WARNER-LAMBERT COMPANY LLC (US) 2004-06-03 WO claimed
US-20040054172-A1 Oxygenated esters of 4-lodo phenylamino benzhydroxamic acids WARNER-LAMBERT COMPANY 2004-03-18 US claimed
CN-1446197-A Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids WARNER LAMBERT CO (US) 2003-10-01 CN claimed
EP-1301472-A2 OXYGENATED ESTERS OF 4-IODO PHENYLAMINO BENZHYDROXAMIC ACIDS WARNER-LAMBERT COMPANY (US) 2003-04-16 EP claimed
US-20030055095-A1 Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor BARAGI VIJAYKUMAR M (US) 2003-03-20 US claimed
EP-1262176-A1 Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor WARNER-LAMBERT COMPANY (US) 2002-12-04 EP claimed
WO-2002006213-A2 OXYGENATED ESTERS OF 4-IODO PHENYLAMINO BENZHYDROXAMIC ACIDS WARNER-LAMBERT COMPANY (US) 2002-01-24 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (12 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-12275688-B2 Crystalline solids of MEK inhibitor N-((R)-2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide and uses thereof NRAS, BRAF, KSR2 MAP2K1 34/4885MAP2K2 16/4885MAPK1 121/4885
US-20260083690-A1 DISPERSIBLE FORMULATIONS OF N-((R)-2,3-DIHYDROXYPROPOXY)-3,4-DIFLUORO-2-(2- FLUORO-4-IODO-PHENYLAMINO)-BENAZMIDE AND USES THEREOF TAS2R5, TAS2R14, TAS2R1 MAP2K1 1219/4885MAP2K2 861/4885MAPK1 4625/4885
US-20250270166-A1 CRYSTALLINE SOLIDS OF MEK INHIBITOR N-((R)-2,3-DIHYDROXYPROPOXY)-3,4-DIFLUORO-2-(2-FLUORO-4-IODO--PHENYLAMINO)-BENZAMIDE AND USES THEREOF NRAS, BRAF, KSR2 MAP2K1 36/4885MAP2K2 17/4885MAPK1 115/4885
US-20050176820-A1 Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids CYP4X1, CYP2A7, CYP4B1 MAP2K1 4341/4885MAP2K2 4268/4885MAPK1 4734/4885
US-12037306-B2 Methods of treating neurofibromatosis type 1 with N-((R))-2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-benzamide VHL, NRAS, KRAS MAP2K1 3438/4885MAP2K2 3378/4885MAPK1 4542/4885
US-20040054172-A1 Oxygenated esters of 4-lodo phenylamino benzhydroxamic acids CYP4X1, ALOX5, HAAO MAP2K1 4312/4885MAP2K2 4025/4885MAPK1 4233/4885
US-20240279201-A1 DUAL WNT SIGNALING PATHWAY INHIBITORS AND AMPK ACTIVATORS FOR TREATMENTS OF DISEASE PRKAB2, PRKAB1, PRKAG2 MAP2K1 51/4885MAP2K2 48/4885MAPK1 698/4885
US-12090128-B2 Dispersible formulations of n-((r)-2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benazmide and uses thereof QDPR, DHFR, NEFM MAP2K1 4337/4885MAP2K2 3323/4885MAPK1 4873/4885
US-20240382484-A1 COMPOSITION FOR TREATING, PREVENTING, OR AMELIORATING MELANOMA AND METHOD THEREOF PDPK1, PLK3, PLK2 MAP2K1 207/4885MAP2K2 205/4885MAPK1 91/4885
US-20240216307-A1 DISPERSIBLE FORMULATIONS OF N-((R)-2,3-DIHYDROXYPROPOXY)-3,4-DIFLUORO-2-(2- FLUORO-4-IODO-PHENYLAMINO)-BENAZMIDE AND USES THEREOF QDPR, DHFR, NEFM MAP2K1 4337/4885MAP2K2 3323/4885MAPK1 4873/4885
US-20030055095-A1 Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor MMP8, SERPINB1, CXCR2 MAP2K1 105/4885MAP2K2 89/4885MAPK1 33/4885
US-20050222163-A1 Combinations of signal transduction inhibitors CDK4, CDK3, CDK2 MAP2K1 12/4885MAP2K2 6/4885MAPK1 23/4885

“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.