SCHEMBL143100

SCHEMBL143100

O=C1c2ccccc2-c2ccc(O)cc21

nearest known ligand 0.82

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 3/20 0.82
ESR2 Q92731 3/20 0.82
MAOA P21397 2/20 0.82
UGT1A1 P22309 1/20 0.82
MAOB P27338 1/20 0.82
BCL2 P10415 2/20 0.64
MCL1 Q07820 2/20 0.64
TTR P02766 2/20 0.58
PTPRC P08575 4/20 0.57
MEN1 O00255 3/20 0.55
KMT2A Q03164 3/20 0.55
CDC25B P30305 1/20 0.55
RAB9A P51151 4/20 0.54
NPC1 O15118 3/20 0.54
SMN1; SMN2 Q16637 3/20 0.54
ALDH1A1 P00352 3/20 0.54
MAPK1 P28482 2/20 0.54
ELANE P08246 1/20 0.54
TP53 P04637 1/20 0.54
CYP3A4 P08684 1/20 0.54

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
Anthraquinone SCHEMBL28256672 1.00 ESR1 (0.82) ESR1ESR2MAOAUGT1A1MAOB
SCHEMBL30366712 1.00 ESR1 (0.82) ESR1ESR2MAOAUGT1A1MAOB
SCHEMBL28320135 1.00 ESR1 (0.82) ESR1ESR2MAOAUGT1A1MAOB
2-Hydroxyanthraquinone SCHEMBL498619 0.98 ESR1 (0.86) ESR1ESR2MAOAUGT1A1MAOB
2-Hydroxyanthraquinone SCHEMBL28843858 0.98 ESR1 (0.86) ESR1ESR2MAOAUGT1A1MAOB
SCHEMBL2029500 0.95 ESR1 (0.74) ESR1ESR2MAOAUGT1A1MAOB
SCHEMBL8773067 0.95 ESR1 (0.74) ESR1ESR2MAOAUGT1A1MAOB
2-Hydroxyanthraquinone SCHEMBL28853822 0.95 ESR1 (0.82) ESR1ESR2MAOAUGT1A1MAOB
SCHEMBL8210089 0.91 ESR1 (0.67) ESR1ESR2MAOAUGT1A1MAOB
SCHEMBL25270871 0.91 ESR2 (0.90) ESR1ESR2MAOAUGT1A1MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12628491-B2 Organic-inorganic adhesion layer and its use in perovskite solar cells and modules Tandem PV (US) 2026-05-12 US claimed
EP-3494396-B1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF PIERCE BIOTECHNOLOGY INC (US) 2025-06-11 EP claimed
WO-2024081751-A1 ORGANIC-INORGANIC ADHESION LAYER AND ITS USE IN PEROVSKITE SOLAR CELLS AND MODULES Tandem PV (US) 2024-04-18 WO claimed
US-20240121970-A1 ORGANIC-INORGANIC ADHESION LAYER AND ITS USE IN PEROVSKITE SOLAR CELLS AND MODULES Tandem PV 2024-04-11 US claimed
CN-113816843-A 2-hydroxy-9-fluorenone derivative and synthesis method and application thereof 临沂大学 2021-12-21 CN claimed
US-10722882-B2 Chemiluminescent and fluorescent substrate pads and uses thereof PIERCE BIOTECHNOLOGY, INC. (US) 2020-07-28 US claimed
EP-3494396-A1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF Pierce Biotechnology, Inc. (US) 2019-06-12 EP claimed
US-20180043355-A1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF PIERCE BIOTECHNOLOGY, INC. 2018-02-15 US claimed
WO-2018027004-A1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF PIERCE BIOTECHNOLOGY, INC. (US) 2018-02-08 WO claimed
US-20090032774-A1 DEAGGREGATED ELECTRICALLY CONDUCTIVE POLYMERS AND PRECURSORS THEREOF ANGELOPOULOS MARIE 2009-02-05 US claimed
US-20010012867-A1 Methods of fabrication of deaggregated electrically conductive polymers and precursors thereof ANGELOPOULOS MARIE (US) 2001-08-09 US claimed
WO-2001055446-A1 NOVEL STABILIZED FORMULATIONS FOR CHEMILUMINESCENT ASSAYS GIRI BRIJ PAL (US) 2001-08-02 WO claimed
US-5804100-A Deaggregated electrically conductive polymers and precursors thereof INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 1998-09-08 US claimed
US-5736623-A OXIDATIVE POLYMERIZATION; NEUTRALIZATION INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 1998-04-07 US claimed
EP-0721194-A2 Deaggregated electrically conductive polymers and precursors thereof International Business Machines Corporation (US) 1996-07-10 EP claimed
EP-0410287-B1 Polyphosphazene derivatives containing carbonyl groups and variously alkylated tertiary amino groups CONSIGLIO NAZIONALE RICERCHE (IT) 1995-11-02 EP claimed
EP-0422252-B1 Method for detecting a substance using chemiluminescence TORAY INDUSTRIES (JP) 1995-07-26 EP claimed
US-5206149-A Reaction of peroxidase, oxidant, luminol and 2-hydroxy-9-fluorenone enhancer; chemiluminescence TORAY INDUSTRIES, INC. (JP) 1993-04-27 US claimed
EP-0422252-A1 Method for detecting a substance using chemiluminescence TORAY INDUSTRIES, INC. (JP) 1991-04-17 EP claimed
EP-0410287-A2 Polyphosphazene derivatives containing carbonyl groups and variously alkylated tertiary amino groups CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 1991-01-30 EP claimed

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-12628491-B2 Organic-inorganic adhesion layer and its use in perovskite solar cells and modules EPCAM, CDH1, L1CAM ESR1 804/4885ESR2 1557/4885MAOA 1944/4885

“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.