SCHEMBL5010110

SCHEMBL5010110

O=C1c2ccccc2C(=O)c2c1cccc2-c1cccc2c1C(=O)c1ccccc1C2=O

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 4/20 0.67
KMT2A Q03164 4/20 0.67
ADORA2A P29274 2/20 0.67
CDC25B P30305 1/20 0.67
MAPT P10636 8/20 0.59
ALDH1A1 P00352 8/20 0.59
MAPK1 P28482 7/20 0.59
SMN1; SMN2 Q16637 6/20 0.59
L3MBTL1 Q9Y468 5/20 0.59
LMNA P02545 4/20 0.59
EGFR P00533 3/20 0.59
TDP1 Q9NUW8 3/20 0.59
RAB9A P51151 3/20 0.59
PABPC1 P11940 1/20 0.59
NSD2 O96028 1/20 0.59
MAOA P21397 7/20 0.56
KDM4E B2RXH2 2/20 0.56
RECQL P46063 2/20 0.56
BCL2 P10415 2/20 0.56
MCL1 Q07820 2/20 0.56

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
SCHEMBL29836726 1.00 MEN1 (0.67) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL9335085 1.00 MEN1 (0.67) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL3925899 0.87 ADORA2A (0.53) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL19146551 0.87 ALDH1A1 (0.56) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL1038974 0.85 ADORA2A (0.57) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL18984668 0.85 DNMT1 (0.58) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL10885242 0.83 ALDH1A1 (0.53) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL1886170 0.82 ADORA2A (0.59) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL10991981 0.82 ADORA2A (0.59) MEN1KMT2AADORA2ACDC25BMAPT
SCHEMBL11101446 0.82 ADORA2A (0.59) MEN1KMT2AADORA2ACDC25BMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106582725-B A kind of preparation method and application of copper/calcium sulfate carriers catalyst 天津大学 2019-08-30 CN claimed
CN-108732867-A Photosensitive polymer combination, photo-sensitive resin and colour filter using it 三星SDI株式会社 2018-11-02 CN claimed
CN-103270119-B The pigment preparation of surface modification BASF SE (DE) 2016-04-20 CN claimed
CN-103270119-A Surface-modified pigment preparations BASF SE 2013-08-28 CN claimed
EP-0525073-B1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA DU PONT (US) 1994-05-25 EP claimed
EP-0525073-A1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA. DU PONT (US) 1993-02-03 EP claimed
WO-1991015954-A1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-31 WO claimed
CN-115151596-B Polymer, photosensitive resin composition comprising the same, photosensitive resin film using the same, color filter and display device 三星SDI株式会社 2025-03-11 CN disclosed
CN-118946460-A Laminate and packaging material DIC株式会社 2024-11-12 CN disclosed
CN-118252882-A Traditional Chinese medicine for treating scar 保定市第五医院(保定市莲池区中心医院) 2024-06-28 CN disclosed
CN-117625025-A Aqueous multi-liquid polyurethane coating composition 关西涂料株式会社 2024-03-01 CN disclosed
CN-117460794-A Releasable coating forming composition DIC株式会社 2024-01-26 CN disclosed
CN-117440995-A Releasable coating forming composition DIC株式会社 2024-01-23 CN disclosed
US-5755875-A Fluorescent chromophores containing cyanimino groups CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-05-26 US disclosed
US-5755875-A Fluorescent chromophores containing cyanimino groups CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-05-26 US disclosed
EP-0673979-A1 Fluorescent dyestuffs having cyanimino groups CIBA-GEIGY AG (CH) 1995-09-27 EP disclosed
US-5385842-A Anthraquinones as inhibitors of sulfide production from sulfate-reducing bacteria E. I. DU PONT DE NEMOURS AND COMPANY (US) 1995-01-31 US disclosed
US-5332574-A Compounds produced by a strain of Streptomyces exfoliatus BRISTOL-MYERS SQUIBB COMPANY (US) 1994-07-26 US disclosed
EP-0525073-A1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA. DU PONT (US) 1993-02-03 EP disclosed
WO-1991015954-A1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-31 WO disclosed