SCHEMBL550351

SCHEMBL550351

O=C(O)NC(=O)OCc1ccccc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 1/20 0.60
RAB9A P51151 1/20 0.60
LMNA P02545 1/20 0.59
SMN1; SMN2 Q16637 1/20 0.59
CA12 O43570 2/20 0.57
CA1 P00915 2/20 0.57
CA2 P00918 2/20 0.57
CA9 Q16790 2/20 0.57
ALDH1A1 P00352 4/20 0.57
POLB P06746 1/20 0.56
HTT P42858 1/20 0.56
L3MBTL1 Q9Y468 2/20 0.55
MAPK1 P28482 1/20 0.55
SLC6A2 P23975 1/20 0.55
SLC6A3 Q01959 1/20 0.55
KMT2A Q03164 1/20 0.55
TDP1 Q9NUW8 1/20 0.55
CTRB1 P17538 2/20 0.53
MGLL Q99685 1/20 0.53
GAA P10253 1/20 0.51

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
SCHEMBL234454 0.92 LMNA (0.62) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL8775653 0.88 LMNA (0.59) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL344303 0.87 NPC1 (0.59) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL3068668 0.86 LMNA (0.57) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL2295789 0.85 CA12 (0.66) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL11388818 0.85 ALDH1A1 (0.58) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL7355501 0.85 ALDH1A1 (0.63) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL2185920 0.85 CA12 (0.58) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL8815917 0.85 SLC6A2 (0.61) NPC1RAB9ALMNASMN1; SMN2CA12
SCHEMBL308290 0.85 ALDH1A1 (0.63) NPC1RAB9ALMNASMN1; SMN2CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2694524-B1 2'-O-AMINOOXYMETHYL NUCLEOSIDE DERIVATIVES FOR USE IN THE SYNTHESIS AND MODIFICATION OF NUCLEOSIDES, NUCLEOTIDES AND OLIGONUCLEOTIDES US HEALTH (US) 2016-05-18 EP claimed
US-9284343-B2 2′-O-aminooxymethyl nucleoside derivatives for use in the synthesis and modification of nucleosides, nucleotides and oligonucleotides THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2016-03-15 US claimed
US-20140051846-A1 2'-O-AMINOOXYMETHYL NUCLEOSIDE DERIVATIVES FOR USE IN THE SYNTHESIS AND MODIFICATION OF NUCLEOSIDES, NUCLEOTIDES AND OLIGONUCLEOTIDES TheUnited ofAmerica,asrepresentedbythe Secre -tary,Department ofHealthand Human Service (US) 2014-02-20 US claimed
EP-1797068-B1 PROCESSES FOR THE PREPARATION OF SUBSTITUTED 2-(2,6-DIOXOPIPERIDIN-3-YL)-1-OXOISOINDOLINES CELGENE CORP (US) 2013-10-09 EP claimed
US-7863451-B2 Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines CELGENE CORPORATION (US) 2011-01-04 US claimed
CN-101080400-A Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines CELGENE CORP (US) 2007-11-28 CN claimed
EP-1797068-A1 PROCESSES FOR THE PREPARATION OF SUBSTITUTED 2-(2,6-DIOXOPIPERIDIN-3-YL)-1-OXOISOINDOLINES CELGENE CORPORATION (US) 2007-06-20 EP claimed
WO-2006028964-A1 PROCESSES FOR THE PREPARATION OF SUBSTITUTED 2-(2,6-DIOXOPIPERIDIN-3-YL)-1-OXOISOINDOLINES CELGENE CORPORATION (US) 2006-03-16 WO claimed
US-20060052609-A1 Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines CELGENE CORPORATION 2006-03-09 US claimed
US-20040034246-A1 Nucleophilic approach for preparing radiolabeled imaging agents and associated compounds NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-02-19 US claimed
WO-2002044144-A2 NUCLEOPHILIC APPROACH FOR PREPARING RADIOLABELED IMAGING AGENTS AND ASSOCIATED COMPOUNDS ADVANCED RESEARCH AND TECHNOLOGY INSTITUTE, INC. (US) 2002-06-06 WO claimed
EP-4619374-A1 SYNTHESIS OF A-BETA-UNSATURATED CARBONYLS FROM ALKENES VIA SULFONIUM INTERMEDIATES AND THEIR APPLICATION IN THE SYNTHESIS OF CONJUGATED DIENE PHEROMONES, KAIROMONES, AND RELATED COMPOUNDS HUN-REN TERMÉSZETTUDOMÁNYI KUTATÓKÖZPONT (HU) 2025-09-24 EP disclosed
EP-4480537-A2 METHOD OF TREATING OR AMELIORATING METABOLIC DISORDERS USING GLP-1 RECEPTOR AGONISTS CONJUGATED TO ANTAGONISTS FOR GASTRIC INHIBITORY PEPTIDE RECEPTOR (GIPR) Amgen Inc. (US) 2024-12-25 EP disclosed
WO-2024105421-A1 SYNTHESIS OF α,β-UNSATURATED CARBONYLS FROM ALKENES VIA SULFONIUM INTERMEDIATES AND THEIR APPLICATION IN THE SYNTHESIS OF CONJUGATED DIENE PHEROMONES, KAIROMONES, AND RELATED COMPOUNDS Természettudományi Kutatóközpont (HU) 2024-05-23 WO disclosed
US-20240115711-A1 Novel Bifunctional Molecules For Targeted Protein Degradation AMPHISTA THERAPEUTICS LIMITED (GB) 2024-04-11 US disclosed
WO-2001085706-A1 SUBSTITUTED PHENYLACETAMIDES AND THEIR USE AS GLUCOKINASE ACTIVATORS F. HOFFMANN-LA ROCHE AG (CH) 2001-11-15 WO disclosed
WO-2001044216-A1 TRANS OLEFINIC GLUCOKINASE ACTIVATORS F. HOFFMANN-LA ROCHE AG (CH) 2001-06-21 WO disclosed
US-5508432-A TREATING GASTROINTESTINAL DISORDERS, CENTRAL NERVOUS SYSTEM DISORDERS GLAXO WELLCOME INC. (US) 1996-04-16 US disclosed
US-5380872-A Appetite suppresant, gall bladder disorders, CNS disorders GLAXO INC. (US) 1995-01-10 US disclosed
EP-0173522-B1 PROCESS AND INTERMEDIATES FOR SORBINIL PFIZER INC. (US) 1988-12-07 EP 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-20040034246-A1 Nucleophilic approach for preparing radiolabeled imaging agents and associated compounds SNCA, PARK7, SAMHD1 NPC1 344/4885RAB9A 54/4885LMNA 3586/4885
US-20060052609-A1 Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines TNF, IL1A, TRAF2 NPC1 2170/4885RAB9A 3887/4885LMNA 2234/4885
US-20240115711-A1 Novel Bifunctional Molecules For Targeted Protein Degradation PSMG3, MYCBP2, PSME2 NPC1 3374/4885RAB9A 2146/4885LMNA 3987/4885
US-20140051846-A1 2'-O-AMINOOXYMETHYL NUCLEOSIDE DERIVATIVES FOR USE IN THE SYNTHESIS AND MODIFICATION OF NUCLEOSIDES, NUCLEOTIDES AND OLIGONUCLEOTIDES NSUN2, RNGTT, RNMT NPC1 3669/4885RAB9A 2348/4885LMNA 1313/4885

“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.