SCHEMBL537408

SCHEMBL537408

CCOC(=O)N1C(=O)c2cccc(N)c2C1=O

nearest known ligand 0.56

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 15/20 0.56
LMNA P02545 3/20 0.52
KMT2A Q03164 6/20 0.51
ALDH1A1 P00352 6/20 0.51
MEN1 O00255 5/20 0.51
F2 P00734 1/20 0.51
DPP4 P27487 1/20 0.48
MAPT P10636 7/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
PABPC1 P11940 2/20 0.47
ADORA2A P29274 1/20 0.47
POLB P06746 2/20 0.46
HTT P42858 1/20 0.46
MDM2 Q00987 1/20 0.45
XBP1 P17861 1/20 0.45
HSD17B10 Q99714 1/20 0.44
NPC1 O15118 1/20 0.44
HPGD P15428 1/20 0.44
RAB9A P51151 1/20 0.44

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
SCHEMBL30225703 1.00 KDM4E (0.56) KDM4ELMNAKMT2AALDH1A1MEN1
SCHEMBL23121513 0.85 ANPEP (0.44) KDM4ELMNAKMT2AALDH1A1DPP4
SCHEMBL74973 0.82 L3MBTL1 (0.55) KMT2AALDH1A1MAPTHTTHSD17B10
SCHEMBL31241181 0.82 L3MBTL1 (0.55) KMT2AALDH1A1MAPTHTTHSD17B10
SCHEMBL22635807 0.81 KDM4E (0.51) KDM4ELMNAKMT2AALDH1A1MEN1
SCHEMBL4538988 0.80 PTGS2 (0.39) KDM4EKMT2AALDH1A1DPP4MAPT
SCHEMBL2283350 0.79 LMNA (0.51) KDM4ELMNAKMT2AALDH1A1MEN1
SCHEMBL30048865 0.79 LMNA (0.51) KDM4ELMNAKMT2AALDH1A1MEN1
SCHEMBL18485418 0.78 ALDH1A1 (0.56) KDM4ELMNAKMT2AALDH1A1MEN1
Ethylene Glycol SCHEMBL8989789 0.78 L3MBTL1 (0.51) KDM4ELMNAKMT2AALDH1A1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3411366-B1 METHOD FOR THE PRODUCTION OF POMALIDOMIDE EGYT GYOGYSZERVEGYESZETI GYAR (HU) 2022-11-23 EP disclosed
US-20190040037-A1 METHOD FOR THE PRODUCTION OF POMALIDOMIDE EGIS GYOGYSZERGYAR ZRT. (HU) 2019-02-07 US disclosed
EP-3411366-A1 METHOD FOR THE PRODUCTION OF POMALIDOMIDE Egis Gyógyszergyár Zrt. (HU) 2018-12-12 EP disclosed
WO-2017134476-A1 METHOD FOR THE PRODUCTION OF POMALIDOMIDE EGIS GYÓGYSZERGYÁR ZRT. (HU) 2017-08-10 WO disclosed
US-RE45685-E1 Pharmaceutically active isoindoline derivatives CELGENE CORPORATION (US) 2015-09-29 US disclosed
EP-1228071-B8 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES CELGENE CORP (US) 2012-02-29 EP disclosed
EP-2263669-B1 Pharmaceutically active isoindoline derivatives CELGENE CORP (US) 2012-02-08 EP disclosed
EP-2255801-B1 Pharmaceutically active isoindoline derivatives CELGENE CORP (US) 2012-02-08 EP disclosed
US-8030343-B2 Pharmaceutically active isoindoline derivatives CELGENE CORPORATION (US) 2011-10-04 US disclosed
EP-1698334-B1 Pharmaceutically active isoindoline derivatives CELGENE CORP (US) 2011-04-20 EP disclosed
EP-2255801-A1 Pharmaceutically active isoindoline derivatives CELGENE CORPORATION (US) 2010-12-01 EP disclosed
US-7678825-B2 Pharmaceutically active isoindoline derivates CELGENE CORPORATION (US) 2010-03-16 US disclosed
US-20080221196-A1 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES CELGENE CORPORATION 2008-09-11 US disclosed
EP-1228071-B1 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES CELGENE CORP (US) 2007-03-28 EP disclosed
EP-1698334-A1 Pharmaceutically active isoindoline derivatives CELGENE CORPORATION (US) 2006-09-06 EP disclosed
US-20040147588-A1 Pharmaceutically active isoindoline derivatives MAN HON-WAH 2004-07-29 US disclosed
US-6667316-B1 Amido or imido functionality; tumor necrosis factor alpha, phosphodiesterases, matrix metalloproteases and angiogenesis inhibitors CELGENE CORPORATION 2003-12-23 US disclosed
EP-1228071-A4 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES CELGENE CORP (US) 2002-12-04 EP disclosed
EP-1228071-A1 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES CELGENE CORPORATION (US) 2002-08-07 EP disclosed
WO-2001034606-A1 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES CELGENE CORPORATION (US) 2001-05-17 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 (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-20080221196-A1 PHARMACEUTICALLY ACTIVE ISOINDOLINE DERIVATIVES PDE3A, PDE2A, PDE5A KDM4E 619/4885LMNA 2777/4885KMT2A 1298/4885
US-20040147588-A1 Pharmaceutically active isoindoline derivatives PDE3A, PDE5A, PDE2A KDM4E 771/4885LMNA 3128/4885KMT2A 1774/4885
US-20190040037-A1 METHOD FOR THE PRODUCTION OF POMALIDOMIDE PM20D2, HSD17B14, FUT5 KDM4E 2685/4885LMNA 4316/4885KMT2A 3693/4885

“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.