SCHEMBL1920290

SCHEMBL1920290

O=Cc1cccc(N2C(=O)CCC2=O)c1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 1/20 0.58
▸ ALDH1A1 P00352 6/20 0.47
▸ KMT2A Q03164 5/20 0.45
▸ SMN1; SMN2 Q16637 2/20 0.45
▸ MAPK1 P28482 1/20 0.44
▸ FGFR1 P11362 1/20 0.43
▸ MEN1 O00255 3/20 0.41
▸ KDM4E B2RXH2 1/20 0.41
▸ PKM P14618 1/20 0.41
▸ HPGD P15428 1/20 0.41
▸ HSD17B10 Q99714 1/20 0.41
▸ FAAH O00519 1/20 0.39
▸ MGLL Q99685 1/20 0.39
▸ UNG P13051 1/20 0.39
▸ LMNA P02545 2/20 0.39
▸ NPC1 O15118 1/20 0.39
▸ TP53 P04637 1/20 0.39
▸ NPSR1 Q6W5P4 1/20 0.39
▸ CA1 P00915 2/20 0.38
▸ CA9 Q16790 2/20 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
SCHEMBL29749910 0.82 L3MBTL1 (0.73) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MAPK1
SCHEMBL9171144 0.81 MGLL (0.50) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MAPK1
SCHEMBL7754070 0.80 ALDH1A1 (0.42) L3MBTL1ALDH1A1FGFR1KDM4EFAAH
SCHEMBL1728478 0.79 MGLL (0.67) ALDH1A1FGFR1PKMFAAHMGLL
SCHEMBL18367729 0.79 ALDH1A1 (0.46) L3MBTL1ALDH1A1KMT2ASMN1; SMN2FGFR1
SCHEMBL22236845 0.76 CA12 (0.52) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MAPK1
SCHEMBL2518610 0.76 ALDH1A1 (0.59) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MEN1
SCHEMBL28257396 0.75 ALDH1A1 (0.54) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MEN1
SCHEMBL3791105 0.75 KMT2A (0.66) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MEN1
SCHEMBL6798021 0.73 L3MBTL1 (0.61) L3MBTL1ALDH1A1KMT2ASMN1; SMN2MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210023094-A1 PSMA ANTIBODY-DRUG CONJUGATES PSMA DEVELOPMENT COMPANY, LLC (US) 2021-01-28 — — US claimed
EP-2727606-A2 Compounds for killing psma-expressing, taxane-resistant cancer cells Psma Development Company, L.L.C. (US) 2014-05-07 — — EP claimed
EP-1912677-B1 PSMA antibody-drug conjugates PSMA DEV COMPANY L L C (US) 2013-10-02 — — EP claimed
EP-2326350-B1 COMPOUNDS FOR KILLING PSMA-EXPRESSING, TAXANE-RESISTANT CANCER CELLS PSMA DEV COMPANY L L C (US) 2013-09-04 — — EP claimed
EP-1718667-B1 HETEROCYCLIC SELF-IMMOLATIVE LINKERS AND CONJUGATES GENENTECH INC (US) 2013-01-09 — — EP claimed
EP-2326350-A2 METHODS FOR KILLING PSMA-EXPRESSING, TAXANE-RESISTANT CANCER CELLS Psma Development Company, L.L.C. (US) 2011-06-01 — — EP claimed
US-7754681-B2 Heterocyclic self-immolative linkers and conjugates SEATTLE GENETICS, INC. (US) 2010-07-13 — — US claimed
WO-2010027513-A2 METHODS FOR KILLING PSMA-EXPRESSING, TAXANE-RESISTANT CANCER CELLS PSMA DEVELOPMENT COMPANY, LLC (US) 2010-03-11 — — WO claimed
EP-1718667-A4 HETEROCYCLIC SELF-IMMOLATIVE LINKERS AND CONJUGATES GENENTECH INC (US) 2009-04-08 — — EP claimed
US-20090041791-A1 Heterocyclic self-immolative Linkers and Conjugates SEAGEN INC. 2009-02-12 — — US claimed
EP-1912677-A2 PSMA ANTIBODY-DRUG CONJUGATES Psma Development Company, L.L.C. (US) 2008-04-23 — — EP claimed
WO-2007002222-A2 PSMA ANTIBODY-DRUG CONJUGATES PSMA DEVELOPMENT COMPANY, LLC (US) 2007-01-04 — — WO claimed
EP-1718667-A2 HETEROCYCLIC SELF-IMMOLATIVE LINKERS AND CONJUGATES GENENTECH, INC. (US) 2006-11-08 — — EP claimed
US-20050256030-A1 for linking drug moieties to ligands; comprises a peptide sequence that is a substrate for an intracellular enzyme, for example a cathepsin, that cleaves the peptide at an amide bond SEAGEN INC. 2005-11-17 — — US claimed
WO-2005082023-A2 HETEROCYCLIC SELF-IMMOLATIVE LINKERS AND CONJUGATES GENENTECH, INC. (US) 2005-09-09 — — WO claimed
EP-0624377-B1 Lysosomal enzyme-cleavable antitumor drug conjugates BRISTOL MYERS SQUIBB CO (US) 2002-01-23 — — EP claimed
US-6214345-B1 ANTITUMOR AGENTS; DRUG CONJUGATES WHICH ARE SELECTIVELY ACTIVATIBLE AT THE SITE OF THE TUMOR BRISTOL-MYERS SQUIBB CO. 2001-04-10 — — US claimed
EP-0624377-A2 Lysosomal enzyme-cleavable antitumor drug conjugates Bristol-Myers Squibb Company (US) 1994-11-17 — — EP claimed
EP-3827844-A1 COMBINATION THERAPIES WITH PSMA LIGAND CONJUGATES Psma Development Company, L.L.C. (US) 2021-06-02 — — EP disclosed
US-20070160617-A1 PSMA antibody-drug conjugates PSMA DEVELOPMENT COMPANY, LLC (US) 2007-07-12 — — 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 (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-20210023094-A1 PSMA ANTIBODY-DRUG CONJUGATES FOLH1, PSMA3, PSMA2 L3MBTL1 1683/4885ALDH1A1 2734/4885KMT2A 411/4885
US-20090041791-A1 Heterocyclic self-immolative Linkers and Conjugates CTSL, DNPEP, CTSE L3MBTL1 892/4885ALDH1A1 2008/4885KMT2A 4159/4885
US-20050256030-A1 for linking drug moieties to ligands; comprises a peptide sequence that is a substrate for an intracellular enzyme, for example a cathepsin, that cleaves the peptide at an amide bond CTSS, CTSE, CTSL L3MBTL1 1587/4885ALDH1A1 2102/4885KMT2A 4454/4885
US-20070160617-A1 PSMA antibody-drug conjugates FOLH1, PSMA3, PSMA2 L3MBTL1 1683/4885ALDH1A1 2734/4885KMT2A 411/4885

“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.

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