⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL278204 | 0.74 | — | — | |
| SCHEMBL22803776 | 0.73 | — | — | |
| SCHEMBL7057949 | 0.70 | — | — | |
| SCHEMBL19661047 | 0.70 | — | — | |
| SCHEMBL21586404 | 0.70 | — | — | |
| SCHEMBL8279441 | 0.70 | — | — | |
| SCHEMBL483235 | 0.70 | — | — | |
| SCHEMBL25150335 | 0.69 | — | — | |
| SCHEMBL21755013 | 0.69 | — | — | |
| Acrylamide SCHEMBL27872530 | 0.68 | — | — |
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 76 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0743172-B1 | Novel creping adhesive formulations, method of creping and creped fibrous web | FORT JAMES CORP (US) | 1999-08-04 | — | — | EP | claimed |
| US-12435181-B2 | Formulations capable of reacting with or removal of molecular oxygen | LI SHENSHEN (US) | 2025-10-07 | — | — | US | disclosed |
| WO-2023129877-A1 | FLOW CELL SURFACE PATTERNING | ILLUMINA, INC. (US) | 2023-07-06 | — | — | WO | disclosed |
| WO-2023129878-A1 | FLOW CELL SURFACE PATTERNING | ILLUMINA, INC. (US) | 2023-07-06 | — | — | WO | disclosed |
| EP-3980475-B1 | CLEANING COMPOSITION FOR HARD SURFACES | FATER SPA (IT) | 2023-05-24 | — | — | EP | disclosed |
| WO-2023081845-A1 | AKT3 MODULATORS | GEORGIAMUNE LLC (US) | 2023-05-11 | — | — | WO | disclosed |
| US-20220235174-A1 | Formulations capable of reacting with or removal of molecular oxygen | LI ZHENZHEN (CN) | 2022-07-28 | — | — | US | disclosed |
| WO-2022101400-A1 | INCORPORATION AND IMAGING MIXES | ILLUMINA, INC. (US) | 2022-05-19 | — | — | WO | disclosed |
| WO-2021258199-A1 | VANILLIN-DERIVED FLAME RETARDANT MONOMERS, RESINS, PREPOLYMERS, AND POLYMERS | THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) | 2021-12-30 | — | — | WO | disclosed |
| WO-2021133768-A1 | NANOPARTICLE WITH SINGLE SITE FOR TEMPLATE POLYNUCLEOTIDE ATTACHMENT | ILLUMINA, INC. (US) | 2021-07-01 | — | — | WO | disclosed |
| EP-0073961-B1 | HYDROFORMYLATION PROCESS USING A RHODIUM COMPLEX CATALYST WITH BIPHOSPHINE MONOXIDE LIGANDS | UNION CARBIDE CORPORATION (US) | 1985-08-21 | — | — | EP | disclosed |
| US-4522933-A | Hydroformylation catalyst containing bisphosphine monooxide ligands | UNION CARBIDE CORPORATION (US) | 1985-06-11 | — | — | US | disclosed |
| EP-0072560-B1 | PROCESS FOR PREPARING ORGANIC TERTIARY POLYPHOSPHINE MONOOXIDES | UNION CARBIDE CORPORATION (US) | 1985-01-16 | — | — | EP | disclosed |
| US-4491675-A | RHODIUM CATALYZED REACTION | UNION CARBIDE CORPORATION (US) | 1985-01-01 | — | — | US | disclosed |
| EP-0073398-B1 | HYDROFORMYLATION PROCESS USING A RHODIUM COMPLEX CATALYST WITH TRIARYLPHOSPHINE AND BIPHOSPHINE MONOXIDE LIGANDS | UNION CARBIDE CORPORATION (US) | 1984-12-19 | — | — | EP | disclosed |
| US-4429161-A | QUATERNIZATION OF POLYPHOSPHINE, ALKALINE HYDROLYSIS | UNION CARBIDE CORPORATION (US) | 1984-01-31 | — | — | US | disclosed |
| US-4400548-A | Hydroformylation process using bisphosphine monooxide ligands | UNION CARBIDE CORPORATION (US) | 1983-08-23 | — | — | US | disclosed |
| EP-0073961-A1 | Hydroformylation process using a rhodium complex catalyst with biphosphine monoxide ligands | UNION CARBIDE CORPORATION (US) | 1983-03-16 | — | — | EP | disclosed |
| EP-0073398-A1 | Hydroformylation process using a rhodium complex catalyst with triarylphosphine and biphosphine monoxide ligands | UNION CARBIDE CORPORATION (US) | 1983-03-09 | — | — | EP | disclosed |
| EP-0072560-A2 | Process for preparing organic tertiary polyphosphine monooxides | UNION CARBIDE CORPORATION (US) | 1983-02-23 | — | — | EP | disclosed |