SCHEMBL1793005

SCHEMBL1793005

COC1(OC)Cc2ccccc2C1=O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 4/20 0.46
LMNA P02545 3/20 0.46
NPSR1 Q6W5P4 2/20 0.46
HTT P42858 2/20 0.46
HTR2A P28223 2/20 0.40
HTR2C P28335 2/20 0.40
HTR2B P41595 2/20 0.40
SIGMAR1 Q99720 2/20 0.40
POLB P06746 3/20 0.39
PPIB P23284 1/20 0.38
ALDH1A1 P00352 3/20 0.38
KDM4E B2RXH2 3/20 0.38
MAPT P10636 3/20 0.38
SMN1; SMN2 Q16637 3/20 0.38
RAB9A P51151 2/20 0.38
CES1 P23141 1/20 0.38
MAOA P21397 1/20 0.38
MAP2K7 O14733 1/20 0.38
GMNN O75496 1/20 0.38
TP53 P04637 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
SCHEMBL29498104 1.00 L3MBTL1 (0.46) L3MBTL1LMNANPSR1HTTHTR2A
Hydrochloric Acid SCHEMBL6600350 0.98 L3MBTL1 (0.45) L3MBTL1LMNANPSR1HTTHTR2A
SCHEMBL6629689 0.81 SIGMAR1 (0.53) NPSR1HTR2AHTR2CHTR2BSIGMAR1
SCHEMBL6227380 0.81 POLB (0.46) L3MBTL1LMNAHTTPOLBALDH1A1
SCHEMBL6112888 0.79 SIGMAR1 (0.46) HTR2AHTR2CHTR2BSIGMAR1POLB
SCHEMBL5610431 0.74 L3MBTL1 (0.44) L3MBTL1LMNANPSR1HTTHTR2A
SCHEMBL29661169 0.74 NPSR1 (0.50) L3MBTL1LMNANPSR1HTTHTR2A
SCHEMBL1745254 0.74 NPSR1 (0.50) L3MBTL1LMNANPSR1HTTHTR2A
SCHEMBL6806743 0.73 L3MBTL1 (0.40) L3MBTL1LMNANPSR1HTTHTR2A
SCHEMBL2592743 0.71 HTR2A (0.36) HTR2ASIGMAR1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113825499-B Percutaneous absorption preparation containing high-dose donepezil or salt thereof 株式会社大熊制药 2024-03-08 CN disclosed
US-20220226296-A1 PREPARATION FOR PERCUTANEOUS ABSORPTION COMPRISING HIGH DOSE OF DONEPEZIL OR SALT THEREOF DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2022-07-21 US disclosed
EP-3970704-A1 PREPARATION FOR PERCUTANEOUS ABSORPTION COMPRISING HIGH DOSE OF DONEPEZIL OR SALT THEREOF Daewoong Pharmaceutical Co., Ltd. (KR) 2022-03-23 EP disclosed
WO-2010070511-A3 A PROCESS FOR THE PREPARATION OF DONEPEZIL HYDROCHLORIDE ALEMBIC LIMITED (IN) 2011-10-13 WO disclosed
EP-2370408-A2 A PROCESS FOR THE PREPARATION OF DONEPEZIL HYDROCHLORIDE Alembic Limited (IN) 2011-10-05 EP disclosed
US-20110123929-A1 OXIME COMPOUND, PHOTOSENSITIVE COMPOSITION, COLOR FILTER, PRODUCTION METHOD FOR THE COLOR FILTER, AND LIQUID CRYSTAL DISPLAY ELEMENT FUJIFILM CORPORATION (JP) 2011-05-26 US disclosed
US-7795440-B2 N-substituted tricyclic 1-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders JANSSEN PHARMACEUTICA NV (BE) 2010-09-14 US disclosed
WO-2010070511-A2 A PROCESS FOR THE PREPARATION OF DONEPEZIL HYDROCHLORIDE ALEMBIC LIMITED (IN) 2010-06-24 WO disclosed
EP-2116527-A1 OXIME COMPOUND, PHOTOSENSITIVE COMPOSITION, COLOR FILTER, METHOD FOR PRODUCTION OF THE COLOR FILTER, AND LIQUID CRYSTAL DISPLAY ELEMENT FUJIFILM Corporation (JP) 2009-11-11 EP disclosed
EP-1506175-B1 N-SUBSTITUTED TRICYCLIC 3-AMINOPYRAZOLES AS PDGF RECEPTOR INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2009-04-01 EP disclosed
US-5349090-A Process for preparing arylketoamines HOECHST CELANESE CORPORATION (US) 1994-09-20 US disclosed
US-5338884-A Reacting an arylisonitrosoalkanone with hydrogen then acid, ester inpresence of catalyst HOECHST CELANESE (US) 1994-08-16 US disclosed
EP-0586479-A1 DIHYDROXYINDANONE TYROSINE KINASE INHIBITORS PFIZER INC. (US) 1994-03-16 EP disclosed
US-5220063-A Reacting arylisonitrosoalkanone with hydrogen and acyl doner in presence of transition metal catalyst HOECHST CELANESE CORPORATION (US) 1993-06-15 US disclosed
US-5198585-A Catalytic hydrogenation of arylisonitrosoalkanone HOECHST CELANESE CORPORATION (US) 1993-03-30 US disclosed
WO-1993001158-A1 METHOD FOR THE PREPARATION OF ARYLKETOAMINES HOECHST CELANESE CORPORATION (US) 1993-01-21 WO disclosed
US-5175368-A Hydrogenating aryl alpha-oximinoalkyl ketones in aqueous medium containing hydrochlroic acid, recovering salt HOECHST CELANESE CORPORATION (US) 1992-12-29 US disclosed
EP-0491557-A1 Process for the preparation of arylalkylamines and substituted arylalkylamines HOECHST CELANESE CORPORATION (US) 1992-06-24 EP disclosed
EP-0481705-A1 Process for the preparation of arylalkylamines and substituted arylalkylamines HOECHST CELANESE CORPORATION (US) 1992-04-22 EP disclosed
US-5041669-A Reacting alkyl aryl ketones with alkyl nitrites, extracting product, catalytically hydrogenating/reducing in nonaqueous acid mixture HOECHST CELANESE CORPORATION (US) 1991-08-20 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 (1 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-20110123929-A1 OXIME COMPOUND, PHOTOSENSITIVE COMPOSITION, COLOR FILTER, PRODUCTION METHOD FOR THE COLOR FILTER, AND LIQUID CRYSTAL DISPLAY ELEMENT PPOX, CRY2, HCCS L3MBTL1 3025/4885LMNA 3886/4885NPSR1 2679/4885

“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.