Refametinib

Refametinib

SCHEMBL29360059

COc1cc(F)c(F)c(Nc2ccc(I)cc2F)c1NS(=O)(=O)C1(CC(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 SCHEMBL29358040 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL346872 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL10314890 1.00 MAP2K1 (1.00) MAP2K1MAP2K2CHEK1MAPK10PRKAG1
Refametinib SCHEMBL29398471 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 91 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114807035-B Reproducible differentiation method of clinical grade retinal pigment epithelial cells (由卫生与公众服务部部长代表的)美利坚合众国 2024-02-02 CN claimed
EP-3347456-B1 METHOD FOR REPRODUCIBLE DIFFERENTIATION OF CLINICAL-GRADE RETINAL PIGMENT EPITHELIUM CELLS US HEALTH (US) 2023-12-27 EP claimed
CN-122059926-A Heterocyclic degradation determinants for target protein degradation C4医药公司 2026-05-19 CN disclosed
EP-4735438-A2 HETEROBIFUNCTIONAL COMPOUNDS FOR THE DEGRADATION OF KRAS Merck Patent GmbH (DE) 2026-05-06 EP disclosed
EP-4735452-A2 HETEROBIFUNCTIONAL COMPOUNDS FOR THE DEGRADATION OF KRAS PROTEIN Merck Patent GmbH (DE) 2026-05-06 EP disclosed
US-12605387-B2 Treatment of cancers using PI3 kinase isoform modulators SECURA BIO, INC. (US) 2026-04-21 US disclosed
EP-4346928-B1 BIODEGRADABLE TISSUE SCAFFOLD WITH SECONDARY MATRIX TO HOST WEAKLY ADHERENT CELLS US HEALTH (US) 2026-01-14 EP disclosed
EP-4665720-A2 ISOINDOLINONE GLUTARIMIDE AND PHENYL GLUTARIMIDE ANALOGS AS DEGRADERS OF RET KINASE Bristol-Myers Squibb Company (US) 2025-12-24 EP disclosed
US-12454521-B2 Targeted protein degradation C4 THERAPEUTICS, INC. 2025-10-28 US disclosed
EP-4611901-A1 RET-LDD PROTEIN DEGRADERS Bristol-Myers Squibb Company (US) 2025-09-10 EP disclosed
EP-4611900-A1 RET-LDD PROTEIN INHIBITORS Bristol-Myers Squibb Company (US) 2025-09-10 EP disclosed
WO-2022066774-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS ACHILLION PHARMACEUTICALS, INC. (US) 2022-03-31 WO disclosed
CN-114230571-A Solid forms of isoquinolinones, methods of making, compositions containing, and methods of use thereof 无限药品股份有限公司 2022-03-25 CN disclosed
EP-3966315-A1 METHODS FOR THE PRODUCTION OF HEPATOCYTES FUJIFILM Cellular Dynamics, Inc. (US) 2022-03-16 EP disclosed
CN-108699024-B Benzothienyl selective estrogen receptor down-regulator compounds 伊利诺伊大学评议会 2022-03-11 CN disclosed
WO-2022035997-A1 IN VIVO ASSEMBLY OF ASGPR BINDING THERAPEUTICS AVILAR THERAPEUTICS, INC. (US) 2022-02-17 WO disclosed
WO-2022032132-A1 ADVANTAGEOUS THERAPIES FOR DISORDERS MEDIATED BY IKAROS OR AIOLOS C4 THERAPEUTICS, INC. (US) 2022-02-10 WO disclosed
WO-2022032026-A1 COMPOUNDS FOR TARGETED DEGRADATION OF RET C4 THERAPEUTICS, INC. (US) 2022-02-10 WO disclosed
WO-2022019920-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS VERASTEM, INC. (US) 2022-01-27 WO disclosed
EP-3941462-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS Achillion Pharmaceuticals, Inc. (US) 2022-01-26 EP 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 (2 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-12605387-B2 Treatment of cancers using PI3 kinase isoform modulators PIK3R5, PIK3R4, PIK3CD MAP2K1 73/4885MAP2K2 74/4885CHEK1 430/4885
US-12454521-B2 Targeted protein degradation STUB1, MDM2, UBE3A MAP2K1 3832/4885MAP2K2 3630/4885CHEK1 1593/4885

“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.