SCHEMBL4869116

SCHEMBL4869116

NC(=O)C(=O)Oc1ccccc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 3/20 0.47
TDP1 Q9NUW8 3/20 0.47
L3MBTL1 Q9Y468 2/20 0.47
ATM Q13315 1/20 0.47
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
PRSS1 P07477 2/20 0.46
ACR P10323 1/20 0.46
TMPRSS15 P98073 1/20 0.46
HSD17B10 Q99714 2/20 0.45
HPGD P15428 1/20 0.45
ALOX15 P16050 1/20 0.45
CTNNB1 P35222 1/20 0.44
ELANE P08246 1/20 0.43
MAPT P10636 3/20 0.42
KDM4E B2RXH2 1/20 0.42
NSD2 O96028 1/20 0.42
CYP3A4 P08684 2/20 0.42
POLB P06746 1/20 0.42
PARP1 P09874 1/20 0.42

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
SCHEMBL4963226 0.92 PARP10 (0.60) PARP10KMT2AHPGDCTNNB1TSHR
Diphenyl Ethanedioat SCHEMBL43364 0.85 TDP1 (0.54) TDP1L3MBTL1ATMHSD17B10HPGD
Diphenyl Ethanedioat SCHEMBL2254079 0.84 PARP10 (0.46) PARP10TDP1L3MBTL1ATMMEN1
Diphenyl Ethanedioat SCHEMBL27328178 0.82 TDP1 (0.52) TDP1L3MBTL1ATMHSD17B10HPGD
SCHEMBL27505259 0.82 ELANE (0.49) PARP10TDP1L3MBTL1ATMMEN1
SCHEMBL419381 0.80 TDP1 (0.50) TDP1L3MBTL1ATMHSD17B10HPGD
Carbamic Acid Phenyl Ester SCHEMBL7566 0.80 MEN1 (0.70) PARP10TDP1L3MBTL1ATMMEN1
SCHEMBL131450 0.80 TDP1 (0.50) TDP1L3MBTL1ATMMEN1KMT2A
Diphenyl Ethanedioat SCHEMBL10797780 0.80 TDP1 (0.50) TDP1L3MBTL1ATMHSD17B10HPGD
SCHEMBL28242447 0.79 TDP1 (0.50) PARP10TDP1L3MBTL1ATMMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110003920-A Aligning agent for liquid crystal, the manufacturing method of liquid crystal orientation film and liquid crystal display element 奇美实业股份有限公司 2019-07-12 CN disclosed
CN-107987017-B - 2 (1H)-quinolinones compound of a kind of 3,4-dihydro and the preparation method and application thereof 绍兴文理学院 2019-07-12 CN disclosed
CN-108047133-B A kind of preparation method of quinolinones compound 绍兴文理学院 2019-07-12 CN disclosed
CN-109705022-A A kind of preparation method of aromatic amine intermediate 上海彩迩文生化科技有限公司 2019-05-03 CN disclosed
CN-108047133-A A kind of preparation method of quinolinones compound 绍兴文理学院 2018-05-18 CN disclosed
CN-107987017-A A kind of 3,4-dihydro-2 (1H)-quinolinones compound and preparation method and application 绍兴文理学院 2018-05-04 CN disclosed
US-9268915-B2 Systems and methods for diagnosis or treatment THERANOS, INC. (US) 2016-02-23 US disclosed
US-20130079599-A1 SYSTEMS AND METHODS FOR DIAGNOSIS OR TREATMENT Theranos, Inc., a Delaware Corporation (US) 2013-03-28 US disclosed
US-7361648-B2 Heterocyclylakylamines as muscarinic receptor antagonists ROCHE PALO ALTO LLC (US) 2008-04-22 US disclosed
US-20060287293-A1 Heterocyclylalkylamines as muscarinic receptor antagonists ROCHE PALO ALTO LLC 2006-12-21 US disclosed
WO-2005028502-A1 INHIBITORS OF SERINE PROTEASES, PARTICULARLY HCV NS3-NS4A PROTEASE VERTEX PHARMACEUTICALS, INCORPORATED (US) 2005-03-31 WO disclosed
CN-1178922-C Substituted 1-aminoalkyllactam compounds and their use as muscarinic receptor antagonists - 2004-12-08 CN disclosed
US-20040087581-A1 Heterocyclylalkylamines as muscarinic receptor antagonists DVORAK CHARLES ALOIS (US) 2004-05-06 US disclosed
US-6667301-B2 Therapy for muscular disorders, urogenital disorders, gastrointestinal disorders, respiratory system disorders SYNTEX (U.S.A.) LLC 2003-12-23 US disclosed
CN-1430610-A Substituted 1-aminoalkyllactam compounds and their use as muscarinic receptor antagonists HOFFMANN LA ROCHE (CH) 2003-07-16 CN disclosed
EP-1289965-A1 SUBSTITUTED 1-AMINOALKYL-LACTAMS AND THEIR USE AS MUSCARINIC RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2003-03-12 EP disclosed
US-20020004501-A1 Heterocyclylalkylamines as muscarinic receptor antagonists SYNTEX (U.S.A.) LLC 2002-01-10 US disclosed
WO-2001090081-A1 SUBSTITUTED 1-AMINOALKYL-LACTAMS AND THEIR USE AS MUSCARINIC RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2001-11-29 WO disclosed
EP-0097942-B1 ANTIALLERGIC PYRAZINE-BIS(2-OXOGLYCINE) COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1987-07-22 EP disclosed
EP-0097942-A1 Antiallergic pyrazine-bis(2-oxoglycine) compounds THE DOW CHEMICAL COMPANY (US) 1984-01-11 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 (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-20060287293-A1 Heterocyclylalkylamines as muscarinic receptor antagonists CHRM5, CHRM2, CHRM3 PARP10 2468/4885TDP1 4153/4885L3MBTL1 2437/4885
US-20020004501-A1 Heterocyclylalkylamines as muscarinic receptor antagonists CHRM5, CHRM2, CHRM1 PARP10 2824/4885TDP1 3835/4885L3MBTL1 2339/4885
US-20040087581-A1 Heterocyclylalkylamines as muscarinic receptor antagonists CHRM5, CHRM2, CHRM1 PARP10 2824/4885TDP1 3835/4885L3MBTL1 2339/4885

“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.