⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL3629050 | 0.85 | TSHR (0.56) | — | |
| SCHEMBL11474968 | 0.84 | ACHE (0.46) | — | |
| SCHEMBL18867407 | 0.84 | PAOX (0.46) | — | |
| SCHEMBL29284296 | 0.82 | PAOX (0.50) | — | |
| Acrylamide SCHEMBL7516464 | 0.78 | ALDH1A1 (0.61) | — | |
| Formaldehyde SCHEMBL2873057 | 0.75 | ALDH1A1 (0.83) | — | |
| SCHEMBL28060459 | 0.74 | ALDH1A1 (1.00) | — | |
| SCHEMBL10001 | 0.74 | — | — | |
| SCHEMBL195813 | 0.74 | — | — | |
| SCHEMBL221762 | 0.74 | — | — |
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 11 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115135717-B | Fluorocopolymer composition, crosslinked product thereof, and compound | ＡＧＣ株式会社 | 2024-07-05 | — | — | CN | disclosed |
| CN-115135717-A | Fluorine-containing copolymer composition, crosslinked product thereof, and compound | ＡＧＣ株式会社 | 2022-09-30 | — | — | CN | disclosed |
| US-20170240668-A1 | METHOD FOR THE CONTINUOUS PRODUCTION OF ANIONIC POLYMERS USING RADICALS | COATEX (FR) | 2017-08-24 | — | — | US | disclosed |
| US-9738617-B2 | Methods for producing fuels, gasoline additives, and lubricants | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2017-08-22 | — | — | US | disclosed |
| EP-2068904-B1 | METHODS FOR PREPARING DIAZONAMIDES | JOYANT PHARMACEUTICALS INC (US) | 2012-12-05 | — | — | EP | disclosed |
| US-7977430-B2 | Prepared by reacting an amine- or isocyanate-capped polyurea with a multifunctional compound having at least one one ethylenically unsaturated group and a function group coreactive with the capping amine or isocyanate groups of the polyurea; soft contact lenses; durability | NOVARTIS AG (CH) | 2011-07-12 | — | — | US | disclosed |
| US-7695863-B2 | rechargeable batteries having excellent battery cycle properties, electrical capacity and storage characteristic during charging, comprising electrodes and a nonaqueous electrolytic solution containing a dicarbonyl compound as an additive | UBE INDUSTRIES, LTD. (JP) | 2010-04-13 | — | — | US | disclosed |
| US-20080102377-A1 | rechargeable batteries having excellent battery cycle properties, electrical capacity and storage characteristic during charging, comprising electrodes and a nonaqueous electrolytic solution containing a dicarbonyl compound as an additive | UBE INDUSTRIES, LTD (JP) | 2008-05-01 | — | — | US | disclosed |
| EP-0630891-A1 | 3-Isothiazolones derivatives and their use as antimicrobial agents | ROHM AND HAAS COMPANY (US) | 1994-12-28 | — | — | EP | disclosed |
| US-5321141-A | Reacting an isothiazole with an a,b-unsaturated ketone or aldehyde | ROHM AND HAAS COMPANY (US) | 1994-06-14 | — | — | US | disclosed |
| US-5288693-A | Microbiocides | ROHM AND HAAS COMPANY (US) | 1994-02-22 | — | — | US | disclosed |