Refametinib

Refametinib

SCHEMBL29398471

COc1cc(F)c(F)c(Nc2ccc(I)cc2F)c1NS(=O)(=O)C1(C[C@H](O)CO)CC1

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

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
MAP2K1 known ✓ Q02750 20/20 1.00
MAP2K2 known ✓ P36507 6/20 1.00
CHEK1 O14757 1/20 1.00
MAPK10 P53779 1/20 1.00
PRKAG1 P54619 1/20 1.00
ADCK1 Q86TW2 1/20 1.00
PRKAG2 Q9UGJ0 1/20 1.00
MAP2K5 Q13163 2/20 0.45
BRAF P15056 1/20 0.45
MAPK1 P28482 1/20 0.45
CA2 P00918 1/20 0.41

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
Refametinib SCHEMBL345334 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL29385439 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL345333 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL29360059 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL29358040 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL346872 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL10314890 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL29368551 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
SCHEMBL16127640 0.94 MAP2K1 (0.89) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL3691191 0.94 MAP2K1 (0.88) MAP2K1MAP2K2CHEK1MAPK10PRKAG1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023044386-A1 COMPOSITION FOR TREATING, PREVENTING, OR AMELIORATING MELANOMA AND METHOD THEREOF THOMAS JEFFERSON UNIVERSITY (US) 2023-03-23 WO claimed
WO-2025090966-A1 MEK INHIBITORS, ALONE OR IN COMBINATION WITH CDK4/5 INHIBITORS, FOR USE IN TREATING CANCER VEVO THERAPEUTICS, INC. (US) 2025-05-01 WO disclosed
EP-4504777-A1 COMBINATION OF A GREMLIN-1 ANTAGONIST WITH AN INHIBITOR OF RAS-RAF-MEK-ERK SIGNALLING UCB Biopharma SRL (BE) 2025-02-12 EP disclosed
CN-118973580-A Combination therapy comprising SOS1 inhibitor and MEK inhibitor 米拉蒂治疗股份有限公司 2024-11-15 CN disclosed
WO-2024171957-A1 TRANSPLANTATION OF PITUITARY HORMONE-PRODUCING CELLS 国立大学法人東海国立大学機構 2024-08-22 WO disclosed
EP-4410962-A1 CELL AGGREGATE INCLUDING PITUITARY HORMONE-PRODUCING CELLS AND METHOD FOR PRODUCING SAME Sumitomo Pharma Co., Ltd. (JP) 2024-08-07 EP disclosed
CN-118318033-A Cell aggregate comprising pituitary hormone-producing cells and method for producing the same 住友制药株式会社 2024-07-09 CN disclosed
CN-118043447-A Method for preparing cell population containing pituitary tissue and cell population 住友化学株式会社 2024-05-14 CN disclosed
EP-4346826-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2024-04-10 EP disclosed
CN-117615762-A Combination therapy 米拉蒂治疗股份有限公司 2024-02-27 CN disclosed
EP-4157448-A1 METHODS AND COMPOSITIONS FOR TREATING RNA VIRAL INFECTIONS Model Medicines, Inc. (US) 2023-04-05 EP disclosed
WO-2023044386-A1 COMPOSITION FOR TREATING, PREVENTING, OR AMELIORATING MELANOMA AND METHOD THEREOF THOMAS JEFFERSON UNIVERSITY (US) 2023-03-23 WO disclosed
WO-2023008462-A1 MEDICAMENT FOR TREATMENT AND/OR PREVENTION OF CANCER 東レ株式会社 2023-02-02 WO disclosed
WO-2023277135-A1 METHOD FOR PRODUCING CELLS CONSTITUTING NASAL EPITHELIUM, AND CELL POPULATION INCLUDING CELLS CONSTITUTING NASAL EPITHELIUM OR PROGENITOR CELLS THEREOF 住友化学株式会社 2023-01-05 WO disclosed
WO-2022251193-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2022-12-01 WO disclosed
WO-2022195551-A1 BIOMARKERS FOR CANCER AND METHODS OF USE THEREOF NOVARTIS AG (CH) 2022-09-22 WO disclosed
WO-2022165142-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2022-08-04 WO disclosed
WO-2022159763-A1 SARS-COV-2 THERAPEUTICS MODEL MEDICINES, INC. (US) 2022-07-28 WO disclosed
US-20220096590-A1 NOVEL-ANTI-INFECTIVE STRATEGY AGAINST INFLUENZA VIRUS AND S. AUREUS COINFECTIONS ATRIVA THERAPEUTICS GMBH (DE) 2022-03-31 US disclosed
CN-114127266-A Selective differentiation regulating method for musculoskeletal system stem cells 雪拉托兹治疗株式会社 2022-03-01 CN 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 (1 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-20220096590-A1 NOVEL-ANTI-INFECTIVE STRATEGY AGAINST INFLUENZA VIRUS AND S. AUREUS COINFECTIONS MAPK1, MAP2K1, MAP2K6 MAP2K1 2/4885MAP2K2 11/4885CHEK1 824/4885

“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.