⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL10670976 | 0.69 | PARP1 (0.50) | — | |
| SCHEMBL2793120 | 0.65 | PTGS1 (0.45) | — | |
| SCHEMBL7191487 | 0.65 | LPL (0.46) | — | |
| SCHEMBL827748 | 0.61 | — | — | |
| SCHEMBL3627235 | 0.61 | — | — | |
| SCHEMBL15009754 | 0.61 | — | — | |
| SCHEMBL4356639 | 0.61 | MMP2 (0.32) | — | |
| SCHEMBL731623 | 0.60 | — | — | |
| SCHEMBL242032 | 0.60 | — | — | |
| SCHEMBL1543501 | 0.60 | — | — |
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 116 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-1258300-A | Modified benzimidazole nucleosides as antiviral agents | UNIV MICHIGAN (US) | 2000-06-28 | — | — | CN | claimed |
| CN-114920911-B | Method for producing polyisothiaindene conductive polymer | 株式会社力森诺科 | 2024-05-03 | — | — | CN | disclosed |
| CN-114920911-A | Method for producing polyisothianaphthene-based conductive polymer | 昭和电工株式会社 | 2022-08-19 | — | — | CN | disclosed |
| CN-110121516-B | Method for producing polyisothianaphthene-based conductive polymer | 昭和电工株式会社 | 2022-07-01 | — | — | CN | disclosed |
| CN-109627205-B | Preparation method and application of carbazolyl isopropanolamine derivatives | 贵州大学 | 2022-04-12 | — | — | CN | disclosed |
| US-20220037698-A1 | NON-AQUEOUS ELECTROLYTE CONTAINING LIFSI SALT FOR FAST CHARGING/DISCHARGING OF LITHIUM-ION BATTERY | UT-BATTELLE, LLC | 2022-02-03 | — | — | US | disclosed |
| US-11183340-B2 | Method for manufacturing solid electrolytic capacitor | SHOWA DENKO K.K. (JP) | 2021-11-23 | — | — | US | disclosed |
| US-11136432-B2 | Method for producing polyisothianaphthene-based electroconductive polymer | SHOWA DENKO K.K. (JP) | 2021-10-05 | — | — | US | disclosed |
| CN-110121757-B | Method for manufacturing solid electrolytic capacitor | 昭和电工株式会社 | 2021-09-14 | — | — | CN | disclosed |
| WO-2020133013-A1 | CRYSTALLINE FORM B OF CYPYRAFLUONE ISOPROPYLAMINE SALT, AND PREPARATION METHOD AND USE THEREFOR | 青岛清原化合物有限公司 | 2020-07-02 | — | — | WO | disclosed |
| US-20020035295-A1 | PROCESS FOR PRODUCING AROMATIC AMINES | TAKASAGO INTERNATIONAL CORPORATION | 2002-03-21 | — | — | US | disclosed |
| US-20020015279-A1 | Solid electrolytic capacitor and method for producing the same | SHOWA DENKO K.K. | 2002-02-07 | — | — | US | disclosed |
| US-20020003689-A1 | Solid electrolytic capacitor and method for producing the same | SHOWA DENKO K.K. | 2002-01-10 | — | — | US | disclosed |
| US-20020001168-A1 | Solid electrolytic capacitor and method for producing the same | MURATA MANUFACTURING CO., LTD. (JP) | 2002-01-03 | — | — | US | disclosed |
| EP-1167372-A1 | 2,2-(Diaryl)vinylphosphine compound, palladium catalyst thereof, and process for producing arylamine, diaryl, or arylalkyne with the catalyst | Takasago International Corporation (JP) | 2002-01-02 | — | — | EP | disclosed |
| EP-1028440-A1 | CONDUCTIVE POLYMER, SOLID ELECTROLYTIC CAPACITOR, AND PROCESSES FOR PRODUCING THESE | Showa Denko Kabushiki Kaisha (JP) | 2000-08-16 | — | — | EP | disclosed |
| CN-1036398-C | Therapeutic nucleosides | WELLCOME FOUND (GB) | 1997-11-12 | — | — | CN | disclosed |
| CN-1032062-C | Asymmetric synthesis of 3-substituted furanoside compounds | AMERICAN CYANAMID CO (US) | 1996-06-19 | — | — | CN | disclosed |
| CN-1066658-A | The asymmetric synthesis of 3-substituted furanoside compounds | AMERICAN CYANAMID CO (US) | 1992-12-02 | — | — | CN | disclosed |
| US-4454320-A | Process for 5-substituted dialuric acids | PFIZER INC. (US) | 1984-06-12 | — | — | US | disclosed |