⚠ 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 | |
|---|---|---|---|---|
| Tetramethylammonium Ion SCHEMBL8116837 | 1.00 | CHRNB2 (0.80) | — | |
| Tetramethylammonium Ion SCHEMBL4151392 | 1.00 | — | — | |
| Tetramethylammonium Ion SCHEMBL2556541 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL7710979 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL9850017 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL23832835 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL4151389 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL2111724 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL27855282 | 0.91 | — | — | |
| Tetramethylammonium Ion SCHEMBL16825 | 0.89 | — | — |
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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20230375937-A1 | SUBSTRATE PROCESSING COMPOSITION AND SUBSTRATE PROCESSING METHOD USING THE SAME | SK INC. (KR) | 2023-11-23 | — | — | US | claimed |
| US-20230375937-A1 | SUBSTRATE PROCESSING COMPOSITION AND SUBSTRATE PROCESSING METHOD USING THE SAME | SK INC. (KR) | 2023-11-23 | — | — | US | disclosed |
| US-20230367223-A1 | SUBSTRATE PROCESSING COMPOSITION AND SUBSTRATE PROCESSING METHOD USING THE SAME | SK INC. (KR) | 2023-11-16 | — | — | US | disclosed |
| CN-116895602-A | Reworking method of semiconductor element | 南亚科技股份有限公司 | 2023-10-17 | — | — | CN | disclosed |
| CN-116895520-A | Method for manufacturing semiconductor element | 南亚科技股份有限公司 | 2023-10-17 | — | — | CN | disclosed |
| CN-114539508-B | Low-viscosity polyisocyanate composition for improving water dispersibility | 万华化学集团股份有限公司 | 2023-05-30 | — | — | CN | disclosed |
| CN-114539508-A | Low-viscosity polyisocyanate composition with improved water dispersibility | 万华化学集团股份有限公司 | 2022-05-27 | — | — | CN | disclosed |
| CN-111793182-B | Polyisocyanate composition | 万华化学集团股份有限公司 | 2022-04-22 | — | — | CN | disclosed |
| CN-111809182-A | Etching liquid for copper/molybdenum (niobium)/IGZO film layer and preparation method and application thereof | 江苏和达电子科技有限公司 | 2020-10-23 | — | — | CN | disclosed |
| CN-111793182-A | Polyisocyanate composition | 万华化学集团股份有限公司 | 2020-10-20 | — | — | CN | disclosed |
| US-9475832-B2 | Phosphonates with reduced toxicity for treatment of viral infections | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2016-10-25 | — | — | US | disclosed |
| US-20150080344-A1 | PHOSPHONATES WITH REDUCED TOXICITY FOR TREATMENT OF VIRAL INFECTIONS | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, A CALIFORNIA CORPORATION | 2015-03-19 | — | — | US | disclosed |
| US-8846643-B2 | Phosphonates with reduced toxicity for treatment of viral infections | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2014-09-30 | — | — | US | disclosed |
| EP-2558466-A2 | PHOSPHONATES WITH REDUCED TOXICITY FOR TREATMENT OF VIRAL INFECTIONS | The Regents of the University of California (US) | 2013-02-20 | — | — | EP | disclosed |
| US-20130029940-A1 | PHOSPHONATES WITH REDUCED TOXICITY FOR TREATMENT OF VIRAL INFECTIONS | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2013-01-31 | — | — | US | disclosed |
| WO-2011130557-A2 | PHOSPHONATES WITH REDUCED TOXICITY FOR TREATMENT OF VIRAL INFECTIONS | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2011-10-20 | — | — | WO | disclosed |
| WO-2008134578-A2 | SYNTHESIS OF OPTICALLY ACTIVE RADIO-LABELED REVERSE TRANSCRIPTASE INHIBITORS | THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF (US) | 2008-11-06 | — | — | WO | disclosed |
| US-5008425-A | Trifluoromethylation of carbonyl compounds | ETHYL CORPORATION (US) | 1991-04-16 | — | — | US | disclosed |
| US-4871877-A | Gem-disubstituted cyclohexadienones and their production | ETHYL CORPORATION (US) | 1989-10-03 | — | — | US | disclosed |
| US-4845258-A | Production of gem-disubstituted cyclohexadienones | ETHYL CORPORATION (US) | 1989-07-04 | — | — | US | disclosed |