SCHEMBL1032816

SCHEMBL1032816

Fc1ccc(/N=C/c2ccc(OCc3ccccc3)cc2)cc1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.77
ALDH1A1 P00352 3/20 0.77
MEN1 O00255 3/20 0.77
KMT2A Q03164 3/20 0.77
L3MBTL1 Q9Y468 2/20 0.77
GAA P10253 1/20 0.77
MAPT P10636 1/20 0.77
THRB P10828 1/20 0.77
PKM P14618 1/20 0.77
CASP3 P42574 1/20 0.77
RECQL P46063 1/20 0.77
BLM P54132 1/20 0.77
PLEC Q15149 1/20 0.77
SENP8 Q96LD8 1/20 0.77
SENP7 Q9BQF6 1/20 0.77
SENP6 Q9GZR1 1/20 0.77
CA12 O43570 1/20 0.67
CA9 Q16790 1/20 0.67
MAOB P27338 13/20 0.65
SMN1; SMN2 Q16637 1/20 0.62

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
SCHEMBL525302 1.00 KDM4E (0.77) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL12275030 1.00 KDM4E (0.77) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL13980482 0.90 KDM4E (0.83) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL8806871 0.86 KDM4E (0.77) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL8806870 0.86 KDM4E (0.77) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL23785508 0.85 KDM4E (0.76) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL7828469 0.82 KDM4E (0.76) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL7828471 0.82 KDM4E (0.76) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL3824529 0.81 MAOB (0.67) KDM4EALDH1A1MEN1KMT2AL3MBTL1
SCHEMBL4299698 0.81 MAOB (0.67) KDM4EALDH1A1MEN1KMT2AL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109810038-A A kind of preparation method of azetidinone class blood lipid-lowering medicine ezetimibe 南通常佑药业科技有限公司 2019-05-28 CN claimed
CN-109810038-A A kind of preparation method of azetidinone class blood lipid-lowering medicine ezetimibe 南通常佑药业科技有限公司 2019-05-28 CN disclosed
EP-2414326-B1 INTERMEDIATES IN THE PREPARATION OF 1,4-DIPHENYL AZETIDINONE LUPIN LTD (IN) 2017-12-20 EP disclosed
EP-2326616-B1 PROCESS FOR THE SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USEFUL THEREFORE LEK PHARMACEUTICALS (SI) 2017-03-08 EP disclosed
EP-2326616-B1 PROCESS FOR THE SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USEFUL THEREFORE LEK PHARMACEUTICALS (SI) 2017-03-08 EP disclosed
US-9518014-B2 Process for synthesis of ezetimibe and intermediates used in said process SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) 2016-12-13 US disclosed
US-20150166479-A1 PROCESS FOR SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USED IN SAID PROCESS SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) 2015-06-18 US disclosed
US-9040688-B2 Intermediates in the preparation of 1,4-diphenyl azetidinone LUPIN LIMITED (IN) 2015-05-26 US disclosed
CN-102112430-B Process for synthesis of ezetimibe and intermediates useful therefor LEK PHARMACEUTICALS 2014-05-28 CN disclosed
WO-2012076030-A1 PROCESS FOR THE PREPARATION OF INTERMEDIATE COMPOUNDS USEFUL IN THE PREPARATION OF EZETIMIBE PHARMATHEN S.A. (GR) 2012-06-14 WO disclosed
US-20090216009-A1 PROCESS FOR THE PRODUCTION OF EZETIMIBE AND INTERMEDIATES USED IN THIS PROCESS RICHTER GEDEON NYRT. (HU) 2009-08-27 US disclosed
US-7544667-B2 Hypocholesterolemic compounds LIPIDEON BIOTECHNOLOGY AG (CH) 2009-06-09 US disclosed
WO-2009067960-A2 A METHOD OF MANUFACTURING (3R,4S)-L-(4-FLUOROPHENYL)-3-[(3S)-3-(4-FLUOROPHENYL)-3- HYDROXYPROPYL)]-4-(4-HYDROXYPHENYL)-2-AZETIDINONE AND ITS INTERMEDIATES ZENTIVA, A.S. (CZ) 2009-06-04 WO disclosed
WO-2008106900-A1 METHOD OF MANUFACTURING (3R, 4S) -1- (4-FLUOROPHENYL) -3- [ (3S) -3- (4 -FLUOROPHENYL) -3-HYDROXYPROPYL) ] -4- (4-HYD ROXYPHENYL) -2-AZETIDINONE ZENTIVA, A.S. (CZ) 2008-09-12 WO disclosed
US-20080214547-A1 METHODS AND COMPOSITIONS OF TRAIL-DEATH RECEPTOR AGONISTS/ACTIVATORS UNIVERSITY OF MARYLAND, BALTIMORE 2008-09-04 US disclosed
US-20080214547-A1 METHODS AND COMPOSITIONS OF TRAIL-DEATH RECEPTOR AGONISTS/ACTIVATORS UNIVERSITY OF MARYLAND, BALTIMORE 2008-09-04 US disclosed
EP-1963260-A1 PROCESS FOR THE PRODUCTION OF EZETIMIBE AND INTERMEDIATES USED IN THIS PROCES Richter Gedeon NYRT (HU) 2008-09-03 EP disclosed
WO-2008094319-A2 METHODS AND COMPOSITIONS OF TRAIL-DEATH RECEPTOR AGONISTS/ACTIVATORS THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYTEM (US) 2008-08-07 WO disclosed
US-20070275909-A1 Useful in the treatment and prevention of atherosclerosis and for the reduction of cholesterol levels; carbohydrate-containing pyrazolidinone or oxazolidinone derivatives, for example LIPIDEON BIOTECHNOLOGY AG (CH) 2007-11-29 US disclosed
WO-2007072088-A1 PROCESS FOR THE PRODUCTION OF EZETIMIBE AND INTERMEDIATES USED IN THIS PROCES RICHTER GEDEON NYRT. (HU) 2007-06-28 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-20150166479-A1 PROCESS FOR SYNTHESIS OF EZETIMIBE AND INTERMEDIATES USED IN SAID PROCESS HMGCR, COASY, APOB KDM4E 138/4885ALDH1A1 268/4885MEN1 1286/4885
US-20090216009-A1 PROCESS FOR THE PRODUCTION OF EZETIMIBE AND INTERMEDIATES USED IN THIS PROCESS APOB, HMGCR, PCSK9 KDM4E 733/4885ALDH1A1 342/4885MEN1 2791/4885
US-20080214547-A1 METHODS AND COMPOSITIONS OF TRAIL-DEATH RECEPTOR AGONISTS/ACTIVATORS BID, BAD, MCL1 KDM4E 3451/4885ALDH1A1 3768/4885MEN1 392/4885
US-20070275909-A1 Useful in the treatment and prevention of atherosclerosis and for the reduction of cholesterol levels; carbohydrate-containing pyrazolidinone or oxazolidinone derivatives, for example PCSK9, APOB, HMGCR KDM4E 3847/4885ALDH1A1 1933/4885MEN1 2233/4885

“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.