SCHEMBL10140852

SCHEMBL10140852

CCCCCNC(=O)COCC(=O)O

nearest known ligand 0.59

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
FAAH O00519 1/20 0.59
EPHX2 P34913 4/20 0.55
CASP2 P42575 1/20 0.53
NAAA Q02083 1/20 0.50
EPHX1 P07099 5/20 0.48
GLP1R P43220 5/20 0.47
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47
TSHR P16473 1/20 0.47
RECQL P46063 1/20 0.47

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
SCHEMBL15613427 0.98 FAAH (0.62) FAAHEPHX2CASP2NAAAEPHX1
SCHEMBL17817086 0.98 FAAH (0.62) FAAHEPHX2CASP2NAAAEPHX1
SCHEMBL17817084 0.98 FAAH (0.62) FAAHEPHX2CASP2NAAAEPHX1
SCHEMBL24622918 0.98 FAAH (0.62) FAAHEPHX2CASP2NAAAEPHX1
SCHEMBL3273924 0.94 FAAH (0.51) FAAHEPHX2CASP2NAAAEPHX1
SCHEMBL13857031 0.92 FAAH (0.67) FAAHCASP2NAAAEPHX1MEN1
SCHEMBL21096710 0.90 FAAH (0.65) FAAHCASP2NAAAEPHX1MEN1
SCHEMBL27986572 0.90 FAAH (0.70) FAAHCASP2NAAAEPHX1MEN1
SCHEMBL9356724 0.90 MEN1 (0.44) FAAHEPHX2CASP2GLP1RMEN1
SCHEMBL15552174 0.88 ALDH1A1 (0.48) FAAHEPHX2CASP2GLP1RMEN1

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
WO-2023150540-A1 HYDROXAMIC ACID MACROCYCLIC AGENTS WITH PENDANT CHELATING MOIETIES AND COMPLEXES THEREOF LUMIPHORE, INC. (US) 2023-08-10 WO disclosed
WO-2022087317-A1 THIOHYDROXYPYRIDINE CHELATES LUMIPHORE, INC. (US) 2022-04-28 WO disclosed
EP-3129350-B1 MACROCYCLES LUMIPHORE INC (US) 2021-10-27 EP disclosed
US-20210290787-A1 MACROCYCLE CONJUGATES LUMIPHORE, INC. 2021-09-23 US disclosed
EP-2816038-B1 HOPO CHELATORS LUMIPHORE INC (US) 2019-11-20 EP disclosed
WO-2019173639-A1 MACROCYCLIC LIGANDS WITH PENDANT CHELATING MOIETIES AND COMPLEXES THEREOF LUMIPHORE, INC. (US) 2019-09-12 WO disclosed
EP-2920157-B1 DI-MACROCYCLES LUMIPHORE INC (US) 2019-09-11 EP disclosed
WO-2018045385-A1 MACROCYCLIC LIGANDS WITH PENDANT CHELATING MOIETIES AND COMPLEXES THEREOF LUMIPHORE, INC. (US) 2018-03-08 WO disclosed
US-20170360956-A1 FUNCTIONALIZED LINEAR LIGANDS AND COMPLEXES THEREOF LUMIPHORE, INC. 2017-12-21 US disclosed
EP-2423201-B1 Luminescent macrocyclic lanthanide complexes UNIV CALIFORNIA (US) 2017-10-04 EP disclosed
US-20160221971-A1 DI-MACROCYCLES LUMIPHORE, INC. (US) 2016-08-04 US disclosed
US-9273059-B2 Macrocyclic HOPO chelators LUMIPHORE, INC. (US) 2016-03-01 US disclosed
US-20150157746-A1 MACROCYCLES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2015-06-11 US disclosed
EP-2816038-A1 Hopo chelators Lumiphore, Inc. (US) 2014-12-24 EP disclosed
EP-2470513-B1 MACROCYCLIC HOPO CHELATORS LUMIPHORE INC (US) 2014-10-08 EP 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-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
US-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-09-04 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 (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 FAAH 1287/4885EPHX2 2965/4885CASP2 2679/4885
US-20210290787-A1 MACROCYCLE CONJUGATES FOLH1, KLK3, CD47 FAAH 4170/4885EPHX2 2132/4885CASP2 3704/4885
US-20160221971-A1 DI-MACROCYCLES DLD, NDC1, MCL1 FAAH 4748/4885EPHX2 1930/4885CASP2 1035/4885
US-20170360956-A1 FUNCTIONALIZED LINEAR LIGANDS AND COMPLEXES THEREOF CLTB, CLTA, EPCAM FAAH 4839/4885EPHX2 3366/4885CASP2 3804/4885
US-20120329174-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES SSB, HACD3, CLTA FAAH 1287/4885EPHX2 2965/4885CASP2 2679/4885
US-20150157746-A1 MACROCYCLES SLC39A14, SLC39A3, SLC40A1 FAAH 4686/4885EPHX2 3539/4885CASP2 4146/4885

“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.