Mk-2461

Mk-2461

SCHEMBL93526

CN(C[C@@H]1COCCO1)S(=O)(=O)Nc1ccc2ccc3ncc(-c4cnn(C)c4)cc3c(=O)c2c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MET

The experimentally established mechanism targets of Mk-2461. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MET known ✓ P08581 20/20 1.00
MST1R Q04912 2/20 1.00
AURKA O14965 1/20 1.00
JAK2 O60674 1/20 1.00
ABL1 P00519 1/20 1.00
NTRK1 P04629 1/20 1.00
RET P07949 1/20 1.00
CYP3A4 P08684 1/20 1.00
PDGFRB P09619 1/20 1.00
FGFR1 P11362 1/20 1.00
CYP2C9 P11712 1/20 1.00
NQO2 P16083 1/20 1.00
FLT1 P17948 1/20 1.00
FGFR2 P21802 1/20 1.00
FGFR3 P22607 1/20 1.00
FECH P22830 1/20 1.00
FLT4 P35916 1/20 1.00
KDR P35968 1/20 1.00
FLT3 P36888 1/20 1.00
MAPK9 P45984 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
Mk-2461 SCHEMBL2326906 1.00 MET (1.00) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL29529144 1.00 MET (1.00) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL29394185 1.00 MET (1.00) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL29356324 1.00 MET (1.00) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL2326614 1.00 MET (1.00) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL1270766 0.99 MET (0.98) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL1270764 0.99 MET (0.98) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL1269865 0.99 MET (0.98) METMST1RAURKAJAK2ABL1
Mk-2461 SCHEMBL1269863 0.99 MET (0.98) METMST1RAURKAJAK2ABL1
SCHEMBL4316174 0.92 MET (0.84) METMST1RAURKAJAK2ABL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160046672-A1 STAPLING eIF4E INTERACTING PEPTIDES AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2016-02-18 US claimed
EP-2976354-A1 STAPLING eIF4E INTERACTING PEPTIDES Agency For Science, Technology And Research (SG) 2016-01-27 EP claimed
EP-2904000-A1 PEPTIDES AND METHODS FOR TREATING CANCER Agency for Science, Technology and Research (SG) 2015-08-12 EP claimed
WO-2014149001-A1 STAPLING eIF4E INTERACTING PEPTIDES AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2014-09-25 WO claimed
WO-2014055039-A1 PEPTIDES AND METHODS FOR TREATING CANCER AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2014-04-10 WO claimed
US-8207186-B2 Benzocycloheptapyridines as inhibitors of the receptor tyrosine kinase MET MERCK SHARP & DOHME CORP. (US) 2012-06-26 US claimed
EP-2425830-A1 Synergistic drug combination for the treatment of cancer Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2012-03-07 EP claimed
EP-1896421-B1 BENZOCYCLOHEPTAPYRIDINES AS INHIBITORS OF THE RECEPTOR TYROSINE KINASE MET MERCK SHARP & DOHME (US) 2011-09-14 EP claimed
EP-1896422-B1 TYROSINE KINASE INHIBITORS MERCK SHARP & DOHME (US) 2011-08-17 EP claimed
US-7550478-B2 Tyrosine kinase inhibitors MERCK & CO. INC. (US) 2009-06-23 US claimed
US-12570625-B2 3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof NOVARTIS AG (CH) 2026-03-10 US disclosed
EP-4541381-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2026-02-04 EP disclosed
EP-4545101-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2025-12-10 EP disclosed
EP-4545100-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2025-12-10 EP disclosed
EP-4541380-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2025-12-10 EP disclosed
US-7550478-B2 Tyrosine kinase inhibitors MERCK & CO. INC. (US) 2009-06-23 US disclosed
US-7550478-B2 Tyrosine kinase inhibitors MERCK & CO. INC. (US) 2009-06-23 US disclosed
US-7550478-B2 Tyrosine kinase inhibitors MERCK & CO. INC. (US) 2009-06-23 US disclosed
WO-2007002254-A2 BENZOCYCLOHEPTAPYRIDINES AS INHIBITORS OF THE RECEPTOR TYROSINE KINASE MET MERCK & CO., INC. (US) 2007-01-04 WO disclosed
US-20060293358-A1 Tyrosine kinase inhibitors MERCK SHARP & DOHME LLC 2006-12-28 US 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 (3 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-12570625-B2 3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof IKZF1, IKZF2, BCL6 MET 1078/4885MST1R 3238/4885AURKA 2758/4885
US-20160046672-A1 STAPLING eIF4E INTERACTING PEPTIDES EIF4EBP1, EIF4E, EIF4G2 MET 2104/4885MST1R 2787/4885AURKA 2719/4885
US-20060293358-A1 Tyrosine kinase inhibitors ABL1, ERBB2, RET MET 4/4885MST1R 163/4885AURKA 464/4885

“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.