SCHEMBL2929432

SCHEMBL2929432

O=C1COc2ccccc2-c2ccccc21

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PKM P14618 2/20 0.52
TSHR P16473 1/20 0.52
MAOB P27338 11/20 0.48
MAOA P21397 2/20 0.48
MAPT P10636 4/20 0.45
ATM Q13315 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
MIF P14174 1/20 0.42
ACHE P22303 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
KDM4E B2RXH2 1/20 0.42
CASP1 P29466 1/20 0.42
CASP7 P55210 1/20 0.42
HSD17B10 Q99714 1/20 0.42
ALDH1A1 P00352 1/20 0.42
RAB9A P51151 1/20 0.42
CYP19A1 P11511 1/20 0.42
TP53 P04637 1/20 0.41

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
3-Coumaranone SCHEMBL69412 0.91 PKM (0.56) PKMTSHRMAOBMAOAMAPT
3-Coumaranone SCHEMBL29420742 0.91 PKM (0.56) PKMTSHRMAOBMAOAMAPT
Acetic Acid SCHEMBL8221392 0.89 HSD17B10 (0.44) PKMTSHRMAOBMAOAMAPT
SCHEMBL28709151 0.83 PKM (0.63) PKMTSHRMAOBMAOAMAPT
SCHEMBL28425814 0.80 RAB9A (0.49) PKMMAOBMAPTSMN1; SMN2KMT2A
SCHEMBL28426296 0.80 CYP19A1 (0.49) MAOBMAPTATMSMN1; SMN2KMT2A
SCHEMBL7380169 0.79 MAOA (0.60) PKMTSHRMAOBMAOAMAPT
SCHEMBL31218602 0.79 MAOA (0.60) PKMTSHRMAOBMAOAMAPT
3-Coumaranone SCHEMBL31042958 0.75 MAOB (0.41) PKMTSHRMAOBMAOAMAPT
SCHEMBL10460744 0.75 PKM (0.48) PKMTSHRMAOBMAOAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108191887-B Synthetic method of dibenzospiro [5,6] dodecanone derivative 黑龙江大学 2020-07-28 CN claimed
EP-0041410-B1 TRICYCLIC ETHERS, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS SCIENCE UNION ET Cie SOCIETE FRANCAISE DE RECHERCHE MEDICALE (FR) 1983-11-09 EP claimed
US-20230167447-A1 Compositions for FNIP1/FNIP2 Gene Modulation and Methods Thereof GENETIC INTELLIGENCE INC (US) 2023-06-01 US disclosed
US-11471323-B2 Combination treatments SCION NEUROSTIM, LLC (US) 2022-10-18 US disclosed
CN-112111410-B Preparation method of dibenzooxepinone compound 扬州大学 2022-06-14 CN disclosed
CN-112111410-B Preparation method of dibenzooxepinone compound 扬州大学 2022-06-14 CN disclosed
CN-112111410-B Preparation method of dibenzooxepinone compound 扬州大学 2022-06-14 CN disclosed
CN-112111410-A Preparation method of dibenzoxepin compound 扬州大学 2020-12-22 CN disclosed
CN-112111410-A Preparation method of dibenzoxepin compound 扬州大学 2020-12-22 CN disclosed
CN-108485987-B Dibenzoxepin compound and preparation method and application thereof 扬州大学 2020-10-09 CN disclosed
CN-108191887-B Synthetic method of dibenzospiro [5,6] dodecanone derivative 黑龙江大学 2020-07-28 CN disclosed
US-20090087571-A1 LOW SHRINKAGE EPOXY-CATIONIC CURABLE COMPOSITION HENKEL AG & CO., KGAA (DE) 2009-04-02 US disclosed
EP-2021394-A1 LOW SHRINKAGE EPOXY-CATIONIC CURABLE COMPOSITIONS Henkel AG & Co. KGaA (DE) 2009-02-11 EP disclosed
WO-2007135094-A1 LOW SHRINKAGE EPOXY-CATIONIC CURABLE COMPOSITIONS HENKEL AG & CO. KGAA (DE) 2007-11-29 WO disclosed
EP-0526402-B1 Heteroaryl substituted hydroxylamine derivatives as lipoxygenase inhibitors CIBA GEIGY AG (CH) 1998-01-21 EP disclosed
US-4977158-A Dibenzoxepinon and dibenzothiepino-pyridinol or - pyrrotol derivatives with anti-depressant action AKZO N.V. (NL) 1990-12-11 US disclosed
EP-0014053-B1 SYNTHESIS OF VINDESINE; VINCALEUKOBLASTINE COMPOUNDS ELI LILLY AND COMPANY (US) 1983-12-14 EP disclosed
US-4089961-A Antipsychotically useful quinolizidylidene derivatives of xanthenes, thioxanthenes and dibenzoxepins SMITHKLINE CORPORATION (US) 1978-05-16 US disclosed
US-4086350-A FLUORO, CHLORO AND CYANO SUBSTITUTED 4-(9-XANTHENYLIDENE, 9-THIOXANTHENYLIDENE OR 11(6H)-DIBENZO(B,E)OXEPINYLIDENE)-1-METHYL-PIPERIDINES SMITHKLINE CORPORATION (US) 1978-04-25 US disclosed
US-4073912-A Piperidylidene derivatives of benzo-fused xanthenes, thioxanthenes and dibenzoxepins and antipsychotic use thereof SMITHKLINE CORPORATION (US) 1978-02-14 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 (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-20230167447-A1 Compositions for FNIP1/FNIP2 Gene Modulation and Methods Thereof FNIP1, FN1, TNNC1 PKM 3915/4885TSHR 3697/4885MAOB 1788/4885

“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.