⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL5692930 | 0.95 | — | — | |
| SCHEMBL4943693 | 0.67 | — | — | |
| SCHEMBL29725803 | 0.67 | — | — | |
| SCHEMBL8586649 | 0.63 | — | — | |
| Hydrochloric Acid SCHEMBL2357952 | 0.63 | — | — | |
| Hydrochloric Acid SCHEMBL545334 | 0.63 | — | — | |
| Iodide SCHEMBL2356598 | 0.63 | — | — | |
| Bromide SCHEMBL5190792 | 0.63 | — | — | |
| Bromide SCHEMBL2357681 | 0.63 | — | — | |
| Water SCHEMBL546028 | 0.63 | — | — |
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 13 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1094068-B1 | Silylation of hydroxyl group-containing compounds | SHINETSU CHEMICAL CO (JP) | 2004-12-15 | — | — | EP | claimed |
| US-20250059200-A1 | PROCESS FOR C-H INSERTION BY GEM-HYDROGENATION OF AN INTERNAL ALKYNE | STUDIENGESELLSCHAFT KOHLE GGMBH (DE) | 2025-02-20 | — | — | US | disclosed |
| WO-2024226242-A1 | METHODS FOR MAKING SEMICONDUCTOR DEVICES THAT INCLUDE METAL CAP LAYERS | TOKYO ELECTRON LIMITED (JP) | 2024-10-31 | — | — | WO | disclosed |
| US-20240363410-A1 | METHODS FOR MAKING SEMICONDUCTOR DEVICES THAT INCLUDE METAL CAP LAYERS | TOKYO ELECTRON LIMITED (JP) | 2024-10-31 | — | — | US | disclosed |
| EP-4413012-A1 | PROCESS FOR C-H INSERTION BY GEM-HYDROGENATION OF AN INTERNAL ALKYNE | Studiengesellschaft Kohle gGmbH (DE) | 2024-08-14 | — | — | EP | disclosed |
| WO-2023110394-A1 | PROCESS FOR C-H INSERTION BY GEM-HYDROGENATION OF AN INTERNAL ALKYNE | STUDIENGESELLSCHAFT KOHLE GGMBH (DE) | 2023-06-22 | — | — | WO | disclosed |
| CN-108452801-A | The inexpensive oxidation catalyst controlled for VOC and halogenation VOC emission object | 科莱恩公司 | 2018-08-28 | — | — | CN | disclosed |
| US-8674143-B2 | Synthesis of green ketone intermediate | DSM IP ASSETS, B.V. (NL) | 2014-03-18 | — | — | US | disclosed |
| US-20120283476-A1 | SYNTHESIS OF GREEN KETONE INTERMEDIATE | DSM IP ASSETS, B.V. (NL) | 2012-11-08 | — | — | US | disclosed |
| US-6225488-B1 | CATALYSTS WHICH ARE HIGHLY ACTIVE IN RING-OPENING POLYMERIZATION OF CYCLO-OLEFIN MONOMERS WITHOUT REQUIRING PRESENCE OF CO-CATALYST | NIPPON ZEON CO., LTD. (JP) | 2001-05-01 | — | — | US | disclosed |
| EP-1041078-A2 | Ruthenium or osmium catalysts for olefin metathesis reactions | Zeon Chemicals, L.P. (US) | 2000-10-04 | — | — | EP | disclosed |
| US-5936100-A | METAL CARBENE COMPLEXES OF RUTHENIUM OR OSMIUM | STUDIENGESELLSCHAFT KOHLE MBH (DE) | 1999-08-10 | — | — | US | disclosed |
| US-5113033-A | Ruthenium salt and aluminum halide catalyst system for codimerization of alpha monoolefins and conjugated diolefins | EXXON CHEMICAL PATENTS INC. (US) | 1992-05-12 | — | — | US | disclosed |