Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.52 |
| ▸ | HSP90AA1 | P07900 | 2/20 | 0.52 |
| ▸ | NPC1 | O15118 | 1/20 | 0.52 |
| ▸ | TOP1 | P11387 | 1/20 | 0.43 |
| ▸ | CCR1 | P32246 | 3/20 | 0.42 |
| ▸ | CCR8 | P51685 | 3/20 | 0.42 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.42 |
| ▸ | ENPP1 | P22413 | 1/20 | 0.42 |
| ▸ | CKS1B | P61024 | 1/20 | 0.41 |
| ▸ | GLO1 | Q04760 | 1/20 | 0.41 |
| ▸ | SKP2 | Q13309 | 1/20 | 0.41 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.41 |
| ▸ | LMNA | P02545 | 3/20 | 0.41 |
| ▸ | MAPT | P10636 | 2/20 | 0.41 |
| ▸ | GMNN | O75496 | 1/20 | 0.41 |
| ▸ | TP53 | P04637 | 1/20 | 0.41 |
| ▸ | MMP2 | P08253 | 1/20 | 0.41 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.41 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.41 |
| ▸ | MMP9 | P14780 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL31026593 | 1.00 | L3MBTL1 (0.52) | L3MBTL1HSP90AA1NPC1TOP1CCR1 | |
| SCHEMBL1102824 | 0.87 | L3MBTL1 (0.43) | L3MBTL1HSP90AA1NPC1TOP1CCR1 | |
| SCHEMBL1103081 | 0.85 | L3MBTL1 (0.42) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1103115 | 0.85 | L3MBTL1 (0.42) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1103109 | 0.85 | L3MBTL1 (0.42) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1103120 | 0.85 | L3MBTL1 (0.42) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1102789 | 0.84 | L3MBTL1 (0.41) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1102990 | 0.84 | L3MBTL1 (0.41) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1102949 | 0.84 | L3MBTL1 (0.41) | L3MBTL1HSP90AA1NPC1TOP1KDM4E | |
| SCHEMBL1103097 | 0.84 | L3MBTL1 (0.41) | L3MBTL1HSP90AA1NPC1TOP1KDM4E |
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 17 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4735170-A1 | METATHESIS COMPOSITIONS COMPRISING AIR-STABLE IMIDO ALKYLIDENE COMPLEXES | Verbio SE (DE) | 2026-05-06 | — | — | EP | disclosed |
| WO-2025003441-A1 | METATHESIS COMPOSITIONS COMPRISING AIR-STABLE IMIDO ALKYLIDENE COMPLEXES | VERBIO VEREINIGTE BIOENERGIE AG (DE) | 2025-01-02 | — | — | WO | disclosed |
| US-20230389409-A1 | ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME AND ELECTRONIC APPARATUS INCLUDING THE ORGANIC LIGHT-EMITTING DEVICE | SAMSUNG DISPLAY CO., LTD. (KR) | 2023-11-30 | — | — | US | disclosed |
| US-20230203072-A1 | AIR-STABLE IMIDO ALKYLIDENE COMPLEXES AND USE THEREOF IN OLEFIN METATHESIS REACTIONS | VERBIO SE (DE) | 2023-06-29 | — | — | US | disclosed |
| US-20230203072-A1 | AIR-STABLE IMIDO ALKYLIDENE COMPLEXES AND USE THEREOF IN OLEFIN METATHESIS REACTIONS | VERBIO SE (DE) | 2023-06-29 | — | — | US | disclosed |
| CN-101663265-B | The manufacture method of aryl-hydroxy amine | 和光纯药工业株式会社 | 2016-06-08 | — | — | CN | disclosed |
| US-8455690-B2 | Method for producing arylhydroxylamine | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2013-06-04 | — | — | US | disclosed |
| US-20100113830-A1 | METHOD FOR PRODUCING ARYLHYDROXYLAMINE | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2010-05-06 | — | — | US | disclosed |
| EP-2154125-A1 | METHOD FOR PRODUCING ARYLHYDROXYLAMINE | Wako Pure Chemical Industries, Ltd. (JP) | 2010-02-17 | — | — | EP | disclosed |
| US-7491450-B2 | Organic electroluminescent device | CANON KABUSHIKI KAISHA (JP) | 2009-02-17 | — | — | US | disclosed |
| US-7491450-B2 | Organic electroluminescent device | CANON KABUSHIKI KAISHA (JP) | 2009-02-17 | — | — | US | disclosed |
| EP-0813608-B1 | OSMIUM-CONTAINING REDOX MEDIATOR | ROCHE DIAGNOSTICS CORP (US) | 2002-09-04 | — | — | EP | disclosed |
| EP-0813608-A4 | OSMIUM-CONTAINING REDOX MEDIATOR | ROCHE DIAGNOSTICS CORP (US) | 2000-02-09 | — | — | EP | disclosed |
| US-5846702-A | Reagent including an osmium-containing redox mediator | BOEHRINGER MANNHEIM CORPORATION (US) | 1998-12-08 | — | — | US | disclosed |
| EP-0813608-A1 | OSMIUM-CONTAINING REDOX MEDIATOR | BOEHRINGER MANNHEIM CORPORATION (US) | 1997-12-29 | — | — | EP | disclosed |
| US-5589326-A | FOR ELECTROCHEMICAL BIOSENSORS | BOEHRINGER MANNHEIM CORPORATION (US) | 1996-12-31 | — | — | US | disclosed |
| WO-1996025514-A1 | OSMIUM-CONTAINING REDOX MEDIATOR | BOEHRINGER MANNHEIM CORPORATION (US) | 1996-08-22 | — | — | WO | 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 (3 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20230203072-A1 | AIR-STABLE IMIDO ALKYLIDENE COMPLEXES AND USE THEREOF IN OLEFIN METATHESIS REACTIONS | SOD1, ZRANB2, ZNF277 | L3MBTL1 1999/4885HSP90AA1 4328/4885NPC1 2068/4885 |
| US-20100113830-A1 | METHOD FOR PRODUCING ARYLHYDROXYLAMINE | PAH, APEH, HPD | L3MBTL1 1549/4885HSP90AA1 2119/4885NPC1 3771/4885 |
| US-20230389409-A1 | ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME AND ELECTRONIC APPARATUS INCLUDING THE ORGANIC LIGHT-EMITTING DEVICE | L1CAM, NOM1, MSL1 | L3MBTL1 12/4885HSP90AA1 4240/4885NPC1 1780/4885 |
“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.