SCHEMBL4888025

SCHEMBL4888025

O=C1c2cccc3cccc(c23)C(=O)N1O.[Na]

nearest known ligand 0.96

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ERCC1 P07992 2/20 0.96
FEN1 P39748 2/20 0.96
ERCC4 Q92889 2/20 0.96
ALDH1A1 P00352 9/20 0.60
KDM4E B2RXH2 6/20 0.60
HPGD P15428 4/20 0.60
KMT2A Q03164 3/20 0.60
HSD17B10 Q99714 3/20 0.60
MEN1 O00255 2/20 0.60
HEXA P06865 3/20 0.56
HEXB P07686 3/20 0.56
CYP1B1 Q16678 1/20 0.55
MAPT P10636 3/20 0.55
CYP1A2 P05177 2/20 0.55
POLB P06746 2/20 0.55
AKR1B1 P15121 1/20 0.55
ALOX15 P16050 1/20 0.55
TSHR P16473 1/20 0.55
ALOX12 P18054 1/20 0.55
TDP1 Q9NUW8 1/20 0.55

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
SCHEMBL29410043 0.98 ERCC1 (1.00) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL132760 0.98 ERCC1 (1.00) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL27984890 0.96 ERCC1 (0.96) ERCC1FEN1ERCC4ALDH1A1KDM4E
Methane SCHEMBL20512282 0.96 ERCC1 (0.96) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL43565 0.96 ERCC1 (0.96) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL65320 0.87 ERCC1 (0.79) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL6761575 0.85 ERCC1 (0.69) ERCC1FEN1ERCC4ALDH1A1KDM4E
Trifluoromethanesulfonic Acid SCHEMBL51719 0.82 ERCC1 (0.71) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL7706742 0.81 ERCC1 (0.70) ERCC1FEN1ERCC4ALDH1A1KDM4E
SCHEMBL7706718 0.81 ERCC1 (0.70) ERCC1FEN1ERCC4ALDH1A1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112094232-B Synthesis method of N-hydroxynaphthalimide mesylate 河北凯力昂生物科技有限公司 2022-04-08 CN disclosed
CN-112094232-A Synthesis method of N-hydroxynaphthalimide mesylate 河北凯力昂生物科技有限公司 2020-12-18 CN disclosed
CN-105814488-B Photosensitive resin composition, method for producing cured film, liquid crystal display device, and organic EL display device 富士胶片株式会社 2019-11-05 CN disclosed
CN-105683838-B Photosensitive resin composition, method for producing cured film, liquid crystal display device, and organic EL display device 富士胶片株式会社 2019-10-25 CN disclosed
CN-106716252-A Photosensitive resin composition, method for producing cured film, liquid crystal display device, organic electroluminescence display device, and touch panel 富士胶片株式会社 2017-05-24 CN disclosed
CN-106687865-A Method for manufacturing TFT substrate, organic EL display device, method for manufacturing organic EL display device, liquid crystal display device, and method for manufacturing liquid crystal display device 富士胶片株式会社 2017-05-17 CN disclosed
CN-106459779-A Process and device for removing water and/or oxygen from organic liquid 埃克森美孚化学专利公司 2017-02-22 CN disclosed
CN-106397132-A PROCESS FOR PRODUCING PHENOL 埃克森美孚化学专利公司 2017-02-15 CN disclosed
CN-106238045-A Dehydrogenation and method 埃克森美孚化学专利公司 2016-12-21 CN disclosed
CN-104640827-B Produce the method for phenol and/or cyclohexanone by cyclohexyl benzene 埃克森美孚化学专利公司 2016-11-09 CN disclosed
CN-101384527-A Process for producing sec-butylbenzene EXXONMOBIL CHEM PATENTS INC (US) 2009-03-11 CN disclosed
CN-101384526-A Process for preparing phenol and methyl ethyl ketone EXXONMOBIL CHEM PATENTS INC (US) 2009-03-11 CN disclosed
US-20080076188-A1 Luminescent compounds SETA BIOMEDICALS, LLC 2008-03-27 US disclosed
CN-101006034-A Process for producing sec-butylbenzene EXXONMOBIL CHEM PATENTS INC (US) 2007-07-25 CN disclosed
CN-101006033-A Process for producing phenol and methyl ethyl ketone EXXONMOBIL CHEM PATENTS INC (US) 2007-07-25 CN disclosed
CN-1906230-A Method for producing carbonyl group-containing organosilicon compound WACKER CHEMIE GMBH (DE) 2007-01-31 CN disclosed
CN-1761787-A Oxidation system comprising macrocyclic metal complexes, method for the production and use thereof LANXESS B V (NL) 2006-04-19 CN disclosed
CN-1547564-A Method for producing saturated alcohols, ketones, aldehydes and carboxylic acids 1 2004-11-17 CN disclosed
CN-1420855-A Process for oxidizing hydrocarbons CREAVIS TECH & INNOVATION GMBH (DE) 2003-05-28 CN disclosed
CN-1205366-A System for electrochemical delignification of lignincontaining materials and process for its application CONSORTIUM FURE ELEKTROCHEMISC (DE) 1999-01-20 CN 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-20080076188-A1 Luminescent compounds REL, QRFPR, RCOR3 ERCC1 550/4885FEN1 3519/4885ERCC4 376/4885

“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.