SCHEMBL7354968

SCHEMBL7354968

O=C(O)C1=Cc2ccccc2C1=O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAOA P21397 2/20 0.50
▸ MAOB P27338 1/20 0.50
▸ CDC25B P30305 3/20 0.44
▸ CDC25A P30304 2/20 0.44
▸ KMT2A Q03164 7/20 0.42
▸ MAPT P10636 5/20 0.42
▸ LMNA P02545 4/20 0.42
▸ PTPRC P08575 4/20 0.42
▸ MEN1 O00255 4/20 0.42
▸ ALDH1A1 P00352 3/20 0.42
▸ KDM4E B2RXH2 3/20 0.42
▸ POLB P06746 3/20 0.42
▸ BCHE P06276 2/20 0.42
▸ THRB P10828 2/20 0.42
▸ CES1 P23141 2/20 0.42
▸ RECQL P46063 2/20 0.42
▸ PKM P14618 1/20 0.42
▸ IDO1 P14902 1/20 0.42
▸ HPGD P15428 1/20 0.42
▸ ALOX15 P16050 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
SCHEMBL28211937 0.94 MAOA (0.49) MAOAMAOBCDC25BCDC25AKMT2A
SCHEMBL503745 0.85 MAOA (0.50) MAOAMAOBKMT2ALMNAPTPRC
SCHEMBL30895284 0.85 MAOA (0.50) MAOAMAOBKMT2ALMNAPTPRC
Hydrochloric Acid SCHEMBL26614007 0.83 MAOA (0.48) MAOAMAOBKMT2ALMNAPTPRC
SCHEMBL8102488 0.82 CDC25B (0.43) MAOAMAOBCDC25BCDC25AKMT2A
SCHEMBL30645249 0.82 CDC25B (0.47) MAOAMAOBCDC25BCDC25AKMT2A
Ethylene SCHEMBL28442445 0.81 MAOA (0.47) MAOAMAOBKMT2ALMNAPTPRC
SCHEMBL20843280 0.81 MAOA (0.41) MAOAMAOBCDC25BCDC25AKMT2A
SCHEMBL1243588 0.79 BACE1 (0.52) MAOAMAOBCDC25BCDC25AKMT2A
SCHEMBL30172862 0.79 BACE1 (0.52) MAOAMAOBCDC25BCDC25AKMT2A

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0015231-B1 INDENONCARBOXYLIC ACIDS, THEIR ESTERS AND PROCESS FOR THE MANUFACTURE THEREOF CIBA-GEIGY AG (CH) 1982-09-01 — — EP claimed
US-4323701-A FROM DIHALOGENOMALEIC ANHYDRIDES OR ACYL HALIDE AND AN AROMATIC COMPOUND CIBA-GEIGY CORPORATION (US) 1982-04-06 — — US claimed
CN-105521826-B A kind of Zr catalyst and its prepare chiral alpha-hydroxy-beta -one ester compound method 大连理工大学 2018-12-21 — — CN disclosed
CN-108997306-A A kind of method that industrialized production prepares fluorine substituted diphenylamine bithiophene S, S- dioxide 浙江九洲药物科技有限公司 2018-12-14 — — CN disclosed
CN-1738795-A Indanone carboxylic acid derivatives and their use in the treatment and prevention of diabetes and dyslipidemia MERCK PATENT GMBH (DE) 2006-02-22 — — CN disclosed
CN-1129428-C Endothelin receptor antagonists SMITHKLINE BEECHAM CORP (US) 2003-12-03 — — CN disclosed
CN-1034569-C ET (ENDOTHELIN) receptor antagonists SMITHKLINE BEECHAM CORP (US) 1997-04-16 — — CN disclosed
CN-1145223-A Endothelin receptor antagonists SMITHKLINE BEECHAM CORP (US) 1997-03-19 — — CN disclosed
CN-1124923-A Endothelin receptor antagonists SMITHKLINE BEECHAM CORP (US) 1996-06-19 — — CN disclosed
EP-0699069-A4 — — 1996-04-03 — — EP disclosed
EP-0699069-A1 ENDOTHELIN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM CORPORATION (US) 1996-03-06 — — EP disclosed
WO-1994025013-A1 ENDOTHELIN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM CORPORATION (US) 1994-11-10 — — WO disclosed
CN-1073161-A ET (ENDOTHELIN) receptor antagonists SMITHKLINE BEECHAM CORP (US) 1993-06-16 — — CN disclosed
US-4463142-A Photocrosslinkable polymers with side groups derived from indenone and the preparation and use of these polymers CIBA-GEIGY CORPORATION (US) 1984-07-31 — — US disclosed
US-4399259-A ACRYLIC ESTER HOMO- AND COPOLYMERS; KETONE RESINS; BROMO- AND CHLOROPOLYMERS; PHOTORESISTS CIBA-GEIGY CORPORATION (US) 1983-08-16 — — US disclosed
US-4323701-A FROM DIHALOGENOMALEIC ANHYDRIDES OR ACYL HALIDE AND AN AROMATIC COMPOUND CIBA-GEIGY CORPORATION (US) 1982-04-06 — — US disclosed
US-4323701-A FROM DIHALOGENOMALEIC ANHYDRIDES OR ACYL HALIDE AND AN AROMATIC COMPOUND CIBA-GEIGY CORPORATION (US) 1982-04-06 — — US disclosed
EP-0015231-A1 Indenoncarboxylic acids, their esters and process for the manufacture thereof CIBA-GEIGY AG (CH) 1980-09-03 — — EP disclosed
EP-0015231-A1 Indenoncarboxylic acids, their esters and process for the manufacture thereof CIBA-GEIGY AG (CH) 1980-09-03 — — EP disclosed
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