SCHEMBL699601

SCHEMBL699601

CC(C)(C)OC(=O)NCCCCC(C=O)NC(=O)OCc1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.61
SYK P43405 1/20 0.57
CTSK P43235 5/20 0.53
KLK7 P49862 2/20 0.52
KLK5 Q9Y337 2/20 0.52
L3MBTL1 Q9Y468 1/20 0.50
CTSL P07711 1/20 0.50
CTSB P07858 1/20 0.50
FOLH1 Q04609 1/20 0.49
POLB P06746 1/20 0.49
MAPK1 P28482 1/20 0.49
TGM2 P21980 1/20 0.48
ITGB3 P05106 1/20 0.48
ITGA2B P08514 1/20 0.48

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
SCHEMBL12247705 1.00 MAPT (0.61) MAPTSYKCTSKKLK7KLK5
SCHEMBL5500108 0.97 SYK (0.58) MAPTSYKCTSKKLK7KLK5
SCHEMBL4821212 0.96 MAPT (0.66) MAPTSYKCTSKKLK7KLK5
SCHEMBL4179699 0.93 MAPT (0.62) MAPTSYKCTSKKLK7KLK5
SCHEMBL24152311 0.90 FOLH1 (0.58) CTSKFOLH1TGM2
SCHEMBL8607096 0.90 FOLH1 (0.58) CTSKFOLH1TGM2
SCHEMBL24845372 0.86 MAPT (0.64) MAPTSYKKLK7KLK5L3MBTL1
SCHEMBL23453055 0.85 CTSK (0.54) MAPTSYKCTSKKLK7KLK5
SCHEMBL15670737 0.85 CTSK (0.53) MAPTSYKCTSKCTSLCTSB
SCHEMBL15670736 0.85 CTSK (0.53) MAPTSYKCTSKCTSLCTSB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111349053-A Inhibitors of lysine porphyromonas gingivalis protease 库特克希米公司 2020-06-30 CN disclosed
EP-2051968-B1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES UNIV CALIFORNIA (US) 2020-04-29 EP disclosed
CN-107108468-B Inhibitors of lysine porphyromonas gingivalis protease 库特克希米公司 2020-01-03 CN disclosed
EP-2816038-B1 HOPO CHELATORS LUMIPHORE INC (US) 2019-11-20 EP disclosed
US-10352938-B2 Macrocyclic HOPO chelators LUMIPHORE, INC. (US) 2019-07-16 US disclosed
EP-2423201-B1 Luminescent macrocyclic lanthanide complexes UNIV CALIFORNIA (US) 2017-10-04 EP disclosed
US-20160320399-A1 MACROCYCLIC HOPO CHELATORS LUMIPHORE, INC. 2016-11-03 US disclosed
US-20160320399-A1 MACROCYCLIC HOPO CHELATORS LUMIPHORE, INC. 2016-11-03 US disclosed
US-20160221971-A1 DI-MACROCYCLES LUMIPHORE, INC. (US) 2016-08-04 US disclosed
US-20160221971-A1 DI-MACROCYCLES LUMIPHORE, INC. (US) 2016-08-04 US disclosed
US-8729258-B2 Luminescent macrocyclic lanthanide complexes THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2014-05-20 US disclosed
US-20120329174-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-12-27 US disclosed
US-20120214253-A1 MACROCYCLIC HOPO CHELATORS LUMIPHORE, INC. (US) 2012-08-23 US disclosed
US-20120214253-A1 MACROCYCLIC HOPO CHELATORS LUMIPHORE, INC. (US) 2012-08-23 US disclosed
US-8173800-B2 Hydroxy-isophthalamide moieties; antibodies; high stability, luminescence; kits THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-05-08 US disclosed
EP-2423201-A1 Luminescent macrocyclic lanthanide complexes The Regents of The University of California (US) 2012-02-29 EP disclosed
WO-2011025790-A1 MACROCYCLIC HOPO CHELATORS LUMIPHORE, INC. (US) 2011-03-03 WO disclosed
US-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-09-04 US disclosed
WO-2006044133-A1 ACTIVE KETONE INHIBITORS OF TRYPTASE AXYS PHARMACEUTICALS, INC. (US) 2006-04-27 WO disclosed
WO-2006044133-A1 ACTIVE KETONE INHIBITORS OF TRYPTASE AXYS PHARMACEUTICALS, INC. (US) 2006-04-27 WO 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 (6 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-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES SSB, HACD3, CLTA MAPT 1513/4885SYK 4342/4885CTSK 2374/4885
US-20160221971-A1 DI-MACROCYCLES DLD, NDC1, MCL1 MAPT 1196/4885SYK 2835/4885CTSK 883/4885
US-20120329174-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES SSB, HACD3, CLTA MAPT 1513/4885SYK 4342/4885CTSK 2374/4885
US-20160320399-A1 MACROCYCLIC HOPO CHELATORS PHPT1, SSB, CD69 MAPT 2711/4885SYK 1866/4885CTSK 2474/4885
US-20120214253-A1 MACROCYCLIC HOPO CHELATORS PHPT1, SSB, CD69 MAPT 2711/4885SYK 1866/4885CTSK 2474/4885
US-10352938-B2 Macrocyclic HOPO chelators PHPT1, SSB, CD69 MAPT 2711/4885SYK 1866/4885CTSK 2474/4885

“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.