SCHEMBL4995728

SCHEMBL4995728

COc1c(C(=O)O)ccc(C)c1C(=O)O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 2/20 0.49
MAPT P10636 1/20 0.49
ALDH1A1 P00352 6/20 0.47
HSD17B10 Q99714 4/20 0.47
KDM4E B2RXH2 4/20 0.47
HPGD P15428 3/20 0.43
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA7 P43166 1/20 0.42
CA9 Q16790 1/20 0.42
CA14 Q9ULX7 1/20 0.42
POLB P06746 2/20 0.41
CYP2C9 P11712 2/20 0.39
NOTUM Q6P988 1/20 0.39
CDC25B P30305 1/20 0.39
HAAO P46952 1/20 0.39
CYP1A2 P05177 2/20 0.38
MEN1 O00255 1/20 0.38
GFER P55789 1/20 0.38

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
SCHEMBL31643643 0.86 ALDH1A1 (0.52) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL6646160 0.84 TDP1 (0.52) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL1919502 0.82 TDP1 (0.50) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL1505827 0.81 TDP1 (0.61) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL28902668 0.81 KDM4E (0.47) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL14612801 0.81 TDP1 (0.53) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL28841565 0.81 TDP1 (0.58) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL27673090 0.80 ALDH1A1 (0.40) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL27392561 0.80 KDM4E (0.44) TDP1MAPTALDH1A1HSD17B10KDM4E
SCHEMBL195882 0.79 CYP1A2 (0.44) TDP1ALDH1A1HSD17B10KDM4EHPGD

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2051968-B1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES UNIV CALIFORNIA (US) 2020-04-29 EP disclosed
CN-107835812-A Target mutant K RAS composition and method 南特生物科学股份有限公司 2018-03-23 CN disclosed
EP-2423201-B1 Luminescent macrocyclic lanthanide complexes UNIV CALIFORNIA (US) 2017-10-04 EP disclosed
US-8729258-B2 Luminescent macrocyclic lanthanide complexes THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2014-05-20 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-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
US-8173800-B2 Hydroxy-isophthalamide moieties; antibodies; high stability, luminescence; kits THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2012-05-08 US disclosed
US-20080293155-A1 SALICYLAMIDE-LANTHANIDE COMPLEXES FOR USE AS LUMINESCENT MARKERS THE REGENTS OF THE UNIVERISTY OF CALIFORNIA (US) 2008-11-27 US disclosed
US-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-09-04 US disclosed
US-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-09-04 US disclosed
US-7404912-B2 Salicylamide-lanthanide complexes for use as luminescent markers THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-07-29 US disclosed
US-20060286567-A1 Salicylamide-lanthanide complexes for use as luminescent markers THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2006-12-21 US disclosed
US-7018850-B2 Salicylamide-lanthanide complexes for use as luminescent markers THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2006-03-28 US disclosed
EP-1154991-B1 SALICYLAMIDE-LANTHANIDE COMPLEXES FOR USE AS LUMINESCENT MARKERS UNIV CALIFORNIA (US) 2004-07-28 EP disclosed
US-20030027189-A1 Salicylamide-lanthanide complexes for use as luminescent markers THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2003-02-06 US disclosed
US-6406297-B1 USED FOR DETECTING AND QUANTIFYING CHEMICAL, BIOCHEMICAL AND BIOLOGICAL SUBSTANCES AS ANALYTES IN RESEARCH AND DIAGNOSTIC MIXTURES. THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2002-06-18 US disclosed
EP-1154991-A1 SALICYLAMIDE-LANTHANIDE COMPLEXES FOR USE AS LUMINESCENT MARKERS The Regents of the University of California (US) 2001-11-21 EP disclosed
WO-2000048991-A1 SALICYLAMIDE-LANTHANIDE COMPLEXES FOR USE AS LUMINESCENT MARKERS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2000-08-24 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 (4 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 TDP1 4027/4885MAPT 1513/4885ALDH1A1 4586/4885
US-20120329174-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES SSB, HACD3, CLTA TDP1 4027/4885MAPT 1513/4885ALDH1A1 4586/4885
US-20060286567-A1 Salicylamide-lanthanide complexes for use as luminescent markers SCLY, SSB, LIG3 TDP1 1659/4885MAPT 3987/4885ALDH1A1 869/4885
US-20030027189-A1 Salicylamide-lanthanide complexes for use as luminescent markers SCLY, SSB, LIG3 TDP1 1659/4885MAPT 3987/4885ALDH1A1 869/4885

“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.