⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL12678155 | 0.77 | — | — | |
| SCHEMBL15481099 | 0.75 | — | — | |
| SCHEMBL25815739 | 0.75 | — | — | |
| SCHEMBL15481098 | 0.75 | — | — | |
| SCHEMBL15482914 | 0.71 | — | — | |
| SCHEMBL25738197 | 0.70 | — | — | |
| SCHEMBL18681405 | 0.69 | MGAM (0.31) | — | |
| SCHEMBL243965 | 0.69 | — | — | |
| SCHEMBL2480054 | 0.69 | — | — | |
| SCHEMBL15116740 | 0.68 | TSHR (0.31) | — |
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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-11687000-B2 | Sulfonium compound, chemically amplified resist composition, and patterning process | SHIN-ETSU CHEMICAL CO., LTD. (JP) | 2023-06-27 | — | — | US | disclosed |
| US-20210226253-A1 | ELECTROLYTIC SOLUTION FOR LITHIUM-ION SECONDARY BATTERY, AND LITHIUM-ION SECONDARY BATTERY | MURATA MANUFACTURING CO., LTD. (JP) | 2021-07-22 | — | — | US | disclosed |
| US-20200388884-A1 | NONAQUEOUS ELECTROLYTIC SOLUTION AND ENERGY DEVICE INCLUDING THE SAME | MITSUBISHI CHEMICAL CORPORATION (JP) | 2020-12-10 | — | — | US | disclosed |
| US-20200388887-A1 | NONAQUEOUS ELECTROLYTIC SOLUTION AND ELECTRICAL STORAGE DEVICE INCLUDING THE SAME | MITSUBISHI CHEMICAL CORPORATION (JP) | 2020-12-10 | — | — | US | disclosed |
| US-10777850-B2 | Nonaqueous electrolytic solution and nonaqueous electrolyte secondary battery using the same | MITSUBISHI CHEMICAL CORPORATION (JP) | 2020-09-15 | — | — | US | disclosed |
| US-20190051941-A1 | NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTE SECONDARY BATTERY USING THE SAME | MITSUBISHI CHEMICAL CORPORATION (JP) | 2019-02-14 | — | — | US | disclosed |
| US-10177414-B2 | Nonaqueous electrolytic solution and nonaqueous electrolyte secondary battery using the same | MITSUBISHI CHEMICAL CORPORATION (JP) | 2019-01-08 | — | — | US | disclosed |
| EP-3098893-B1 | NON-AQUEOUS ELECTROLYTE SOLUTION AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY USING SAME | MITSUBISHI CHEM CORP (JP) | 2017-11-29 | — | — | EP | disclosed |
| US-9760003-B2 | Pattern forming method and actinic-ray- or radiation-sensitive resin composition | FUJIFILM CORPORATION (JP) | 2017-09-12 | — | — | US | disclosed |
| EP-3098893-A1 | NON-AQUEOUS ELECTROLYTE SOLUTION AND NON-AQUEOUS ELECTROLYTE SOLUTION SECONDARY BATTERY USING SAME | Mitsubishi Chemical Corporation (JP) | 2016-11-30 | — | — | EP | disclosed |
| US-8901038-B2 | Biphenyl-substituted cyclic ketoenols | BAYER CROPSCIENCE AG (DE) | 2014-12-02 | — | — | US | disclosed |
| US-8541617-B2 | Cycloalkylphenyl substituted cyclic ketoenols | BAYER CROPSCIENCE AG (DE) | 2013-09-24 | — | — | US | disclosed |
| US-20110230346-A1 | Biphenyl-Substituted Cyclic Ketoenols | BAYER CROPSCIENCE AG (DE) | 2011-09-22 | — | — | US | disclosed |
| US-20100210633-A1 | CARBOXAMIDE COMPOUNDS AND THEIR USE | EPIX DELAWARE, INC. (US) | 2010-08-19 | — | — | US | disclosed |
| EP-1962590-B1 | HERBICIDAL COMPOSITIONS HAVING IMPROVED EFFECT | BAYER CROPSCIENCE AG (DE) | 2010-08-11 | — | — | EP | disclosed |
| US-6660860-B2 | To ketones and aldehydes, by reacting with alkali hypohalite under alkaline conditions, using selective heterogeneous oxidation catalyst insoluble in the reaction medium that has 4-oxy-2,2,6,6-tetramethylpiperidin-1-oxyl groups | CIBA SPECIALTY CHEMICALS CORPORATION | 2003-12-09 | — | — | US | disclosed |
| EP-1103537-B1 | Process for the selective oxidation of alcohols using easily separable nitroxyl radicals | CIBA SC HOLDING AG (CH) | 2003-05-14 | — | — | EP | disclosed |
| US-20020161265-A1 | Process for the selective oxidation of alcohols using readily removable nitroxyl radicals | SOMMERLADE REINHARD (DE) | 2002-10-31 | — | — | US | disclosed |
| US-6441243-B1 | FORMING KETONES, ALDEHYDES | CIBA SPECIALTY CHEMICALS CORPORATION | 2002-08-27 | — | — | US | disclosed |
| EP-1103537-A1 | Process for the selective oxidation of alcohols using easily separable nitroxyl radicals | Ciba SC Holding AG (CH) | 2001-05-30 | — | — | EP | disclosed |