SCHEMBL1027115

SCHEMBL1027115

O=C(O)Cc1coc2ccccc12

nearest known ligand 0.67

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.62
ALOX15 P16050 2/20 0.61
SMN1; SMN2 Q16637 2/20 0.61
MAPT P10636 1/20 0.61
MAOB P27338 2/20 0.56
PSMB8 P28062 1/20 0.50
PSMB5 P28074 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
CA2 P00918 1/20 0.49
PPARD Q03181 1/20 0.48

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
Ammonia Solution, Strong SCHEMBL6385399 0.98 KDM4E (0.60) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL10339724 0.86 KDM4E (0.56) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL21836463 0.84 MAOB (0.51) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL28205795 0.84 ALOX15 (0.50) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL4036348 0.84 KDM4E (0.54) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL4036347 0.84 KDM4E (0.54) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL3147413 0.84 MAOB (0.54) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL18331257 0.84 MAOB (0.54) KDM4EALOX15SMN1; SMN2MAPTMAOB
SCHEMBL5762073 0.82 MAOB (0.53) KDM4EMAOBPSMB8PSMB5CA2
SCHEMBL11500783 0.82 KDM4E (0.51) KDM4EALOX15SMN1; SMN2MAPTMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090293157-A1 PRODUCTION OF PROGENITOR CEREAL CELLS CSIR (ZA) 2009-11-26 US claimed
WO-2009093200-A2 PRODUCTION OF PROGENITOR CEREAL CELLS CSIR (ZA) 2009-07-30 WO claimed
US-20040237133-A1 Method for transformation of mono-and di-cotyledonous plants using meristematic tissue and nodal callus from dicotyledonous plants TOLEDO, UNIVERSITY OF 2004-11-25 US claimed
EP-1455568-A2 METHOD FOR TRANSFORMATION OF MONO- AND DI- COTYLEDONOUS PLANTS USING MERISTEMATIC TISSUE AND NODAL CALLUS FROM DYCOTILEDONOUS PLANTS THE UNIVERSITY OF TOLEDO (US) 2004-09-15 EP claimed
WO-2002102979-A2 TRANSFORMATION OF MONO- AND DI- COTYLEDONOUS PLANTS UNIVERSITY OF TOLEDO, THE a University instrumentality of the State of Ohio (US) 2002-12-27 WO claimed
JP-7324073-A None JP disclosed
WO-2025122501-A1 BENZOTHIOPHENE-3-YL- AND BENZOSELENOPHENE-3-YL (BICLYCLIC HETEROARYL) MALEMIDES AS GSK-3 INHIBITORS MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2025-06-12 WO disclosed
US-20220007607-A1 HIGH THROUGHPUT PROTOPLAST ISOLATION AND TRANSFORMATION OF PLANT CELLS FROM A NOVEL LEAF-BASED CELL CULTURE-DERIVED SYSTEM UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2022-01-13 US disclosed
CN-112955142-A Functionalized heterocyclic compounds as antiviral agents 英安塔制药有限公司 2021-06-11 CN disclosed
US-20200223837-A1 BENZOFURAN AMIDES AND HETEROAROMATIC ANALOGUES THEREOF FOR USE IN THERAPY EUROPEAN MOLECULAR BIOLOGY LABORATORY (DE) 2020-07-16 US disclosed
US-20200216434-A1 BENZOFURAN UREAS OR CARBAMATES AND HETEROAROMATIC ANALOGUES THEREOF FOR USE IN THERAPY EUROPEAN MOLECULAR BIOLOGY LABORATORY (DE) 2020-07-09 US disclosed
EP-3638664-A1 BENZOFURAN AMIDES AND HETEROAROMATIC ANALOGUES THEREOF FOR USE IN THERAPY European Molecular Biology Laboratory (DE) 2020-04-22 EP disclosed
EP-0048954-B1 BETA-LACTAM COMPOUNDS, PROCESS FOR THE PREPARATION THEREOF AND INTERMEDIATE PRODUCTS FOR THE PREPARATION THEREOF SAGAMI CHEMICAL RESEARCH CENTER (JP) 1986-12-30 EP disclosed
EP-0009780-B1 OCTAHYDRO-1H-BENZO(4,5)FURO(3,2-E)ISOQUINOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM E.I. DU PONT DE NEMOURS AND COMPANY (US) 1982-02-24 EP disclosed
US-4260761-A Intermediates for the preparation of octahydro-1H-benzo[4,5]furo[3,2,-e]-isoquinoline analgesic and narcotic antagonistic compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1981-04-07 US disclosed
US-4243668-A Octahydro-1H-benzo[4,5]furo[3,2-e]-isoquinoline analgesic and narcotic antagonistic compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1981-01-06 US disclosed
EP-0009780-A2 Octahydro-1H-benzo(4,5)furo(3,2-e)isoquinoline derivatives, process for their preparation and pharmaceutical compositions containing them E.I. DU PONT DE NEMOURS AND COMPANY (US) 1980-04-16 EP disclosed
US-4172145-A ANALGESICS, ANTIPYRETICS KYOWA HAKKO KOGYO KABUSHIKI KAISHA (JP) 1979-10-23 US disclosed
US-4172145-A ANALGESICS, ANTIPYRETICS KYOWA HAKKO KOGYO KABUSHIKI KAISHA (JP) 1979-10-23 US disclosed
US-4126625-A ANTIPHLOGISTIC, ANALGESIC KYOWA HAKKO KOGYO KABUSHIKI KAISHA (JP) 1978-11-21 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 (2 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-20200216434-A1 BENZOFURAN UREAS OR CARBAMATES AND HETEROAROMATIC ANALOGUES THEREOF FOR USE IN THERAPY NR0B1, NR4A3, NR0B2 KDM4E 2462/4885ALOX15 339/4885SMN1; SMN2 2277/4885
US-20200223837-A1 BENZOFURAN AMIDES AND HETEROAROMATIC ANALOGUES THEREOF FOR USE IN THERAPY SUCNR1, CBR1, CYP2A13 KDM4E 3266/4885ALOX15 126/4885SMN1; SMN2 1329/4885

“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.