⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| SCHEMBL26624 | 0.61 | — | — | |
| SCHEMBL3483813 | 0.55 | — | — | |
| SCHEMBL9082350 | 0.55 | — | — | |
| SCHEMBL31165841 | 0.55 | — | — | |
| Arsenic SCHEMBL9006140 | 0.55 | — | — | |
| SCHEMBL2933743 | 0.55 | — | — | |
| Ethane SCHEMBL6423263 | 0.55 | — | — | |
| Methyl Alcohol SCHEMBL3482738 | 0.55 | — | — | |
| Ammonia Solution, Strong SCHEMBL3501220 | 0.55 | — | — | |
| Tetramethylammonium Ion SCHEMBL22360983 | 0.50 | — | — |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-4931573-A | CATALYTIC HYDROGENATION OF DICARBOXYLIC ACID, ESTER OR ANHYDRIDE WITH RUTHENIUM, PHOSPHINES AND GROUPS 3,4,5 COMPOUNDS | MITSUBISHI KASEI CORPORATION (JP) | 1990-06-05 | — | — | US | claimed |
| US-20260125794-A1 | METHOD FOR FORMING METAL OXIDE | SEMICONDUCTOR ENERGY LAB (JP) | 2026-05-07 | — | — | US | disclosed |
| US-20260052673-A1 | MEMORY DEVICE AND METHOD FOR MANUFACTURING THE MEMORY DEVICE | SEMICONDUCTOR ENERGY LAB (JP) | 2026-02-19 | — | — | US | disclosed |
| US-12540397-B2 | Method for forming metal oxide | SEMICONDUCTOR ENERGY LABORATORY CO., LTD. (JP) | 2026-02-03 | — | — | US | disclosed |
| CN-119769187-A | Memory device and method for manufacturing the same | 株式会社半导体能源研究所 | 2025-04-04 | — | — | CN | disclosed |
| WO-2025022294-A1 | OXIDE SEMICONDUCTOR LAYER, METHOD FOR MANUFACTURING OXIDE SEMICONDUCTOR LAYER, SEMICONDUCTOR DEVICE, AND METHOD FOR MANUFACTURING SEMICONDUCTOR DEVICE | 株式会社半導体エネルギー研究所 | 2025-01-30 | — | — | WO | disclosed |
| WO-2024084366-A1 | SEMICONDUCTOR DEVICE AND STORAGE DEVICE | 株式会社半導体エネルギー研究所 | 2024-04-25 | — | — | WO | disclosed |
| WO-2024047500-A1 | STORAGE DEVICE AND STORAGE DEVICE PRODUCTION METHOD | 株式会社半導体エネルギー研究所 | 2024-03-07 | — | — | WO | disclosed |
| US-20240026537-A1 | METHOD FOR FORMING METAL OXIDE | SEMICONDUCTOR ENERGY LABORATORY CO., LTD. (JP) | 2024-01-25 | — | — | US | disclosed |
| EP-4306677-A1 | METHOD FOR FORMING METAL OXIDE | Semiconductor Energy Laboratory Co., Ltd. (JP) | 2024-01-17 | — | — | EP | disclosed |
| CN-117403206-A | Method for depositing metal oxide | 株式会社半导体能源研究所 | 2024-01-16 | — | — | CN | disclosed |
| EP-0372617-B2 | Synthesis of methylaluminoxanes | TEXAS ALKYLS INC (US) | 2002-12-18 | — | — | EP | disclosed |
| EP-0372617-B1 | Synthesis of methylaluminoxanes | TEXAS ALKYLS INC (US) | 1995-06-28 | — | — | EP | disclosed |
| US-5086024-A | Metallocene and methyl aluminoxane | TEXAS ALKYLS, INC. (US) | 1992-02-04 | — | — | US | disclosed |
| US-5079372-A | Hydrogenation of dicarboxylic acid, dicarboxylic acid anhydride and/or dicarboxylic acid ester | MITSUBISHI KASEI CORPORATION (JP) | 1992-01-07 | — | — | US | disclosed |
| US-5041584-A | Reacting tetraalkyldialuminoxane with trimethylaluminum | TEXAS ALKYLS, INC. (US) | 1991-08-20 | — | — | US | disclosed |
| US-4960878-A | REACTING TETRAALKYLALUMINOXANE WITH TRIMETHYLALUMINUM; USEFUL AS COCATALYSTS FOR OLEFIN POLYMERIZATION | TEXAS ALKYLS, INC. (US) | 1990-10-02 | — | — | US | disclosed |
| EP-0372617-A2 | Synthesis of methylaluminoxanes | TEXAS ALKYLS, INC. (US) | 1990-06-13 | — | — | EP | disclosed |
| US-4931573-A | CATALYTIC HYDROGENATION OF DICARBOXYLIC ACID, ESTER OR ANHYDRIDE WITH RUTHENIUM, PHOSPHINES AND GROUPS 3,4,5 COMPOUNDS | MITSUBISHI KASEI CORPORATION (JP) | 1990-06-05 | — | — | US | disclosed |