⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL1785562 | 0.79 | — | — | |
| SCHEMBL6572587 | 0.77 | — | — | |
| Acetic Acid SCHEMBL15327823 | 0.74 | FFAR3 (0.39) | — | |
| SCHEMBL6719964 | 0.74 | — | — | |
| SCHEMBL6719970 | 0.74 | — | — | |
| SCHEMBL11871590 | 0.74 | — | — | |
| SCHEMBL2920720 | 0.70 | SMN1; SMN2 (0.41) | — | |
| SCHEMBL28860484 | 0.69 | — | — | |
| SCHEMBL1984184 | 0.67 | — | — | |
| SCHEMBL714475 | 0.65 | — | — |
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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10326138-B2 | Charge storage material, electrode active material and secondary battery | WASEDA UNIVERSITY (JP) | 2019-06-18 | — | — | US | disclosed |
| US-10164258-B2 | Fused-ring quinone-substituted polynorbornene, electrode active material and secondary battery | WASEDA UNIVERSITY (JP) | 2018-12-25 | — | — | US | disclosed |
| US-9871253-B2 | Ion-conductive fused-ring quinone polymer, electrode active material and secondary battery | WASEDA UNIVERSITY (JP) | 2018-01-16 | — | — | US | disclosed |
| US-20170104214-A1 | FUSED-RING QUINONE-SUBSTITUTED POLYNORBORNENE, ELECTRODE ACTIVE MATERIAL AND SECONDARY BATTERY | WASEDA UNIVERSITY (JP) | 2017-04-13 | — | — | US | disclosed |
| US-20170077518-A1 | CHARGE STORAGE MATERIAL, ELECTRODE ACTIVE MATERIAL AND SECONDARY BATTERY | WASEDA UNIVERSITY (JP) | 2017-03-16 | — | — | US | disclosed |
| US-20170077517-A1 | ION-CONDUCTIVE FUSED-RING QUINONE POLYMER, ELECTRODE ACTIVE MATERIAL AND SECONDARY BATTERY | WASEDA UNIVERSITY (JP) | 2017-03-16 | — | — | US | disclosed |
| US-20040097728-A1 | Method for producing anellated tetrahydro-{1h}-triazoles | BASF AKTIENGESELLSCHAFT (DE) | 2004-05-20 | — | — | US | disclosed |
| US-6737544-B1 | HEATING ABOVE MELTING POINT | BASF AKTIENGESELLSCHAFT (DE) | 2004-05-18 | — | — | US | disclosed |
| US-6639070-B1 | 4-substituted 1,3,4-oxadiazines; herbicides | BASF AKTIENGESELLSCHAFT (DE) | 2003-10-28 | — | — | US | disclosed |
| EP-1187819-B1 | N-SUBSTITUTED PERHYDRO DIAZINE | BASF AG (DE) | 2003-07-23 | — | — | EP | disclosed |
| WO-2001000600-A1 | N-SUBSTITUTED PERHYDRO DIAZINE | BASF AKTIENGESELLSCHAFT (DE) | 2001-01-04 | — | — | WO | disclosed |
| US-6150303-A | Substituted 3-phenylisoxazolines | BASF AKTIENGESELLSCHAFT (DE) | 2000-11-21 | — | — | US | disclosed |
| EP-0998468-A1 | SUBSTITUTED 3-PHENYL ISOXAZOLINES | BASF AKTIENGESELLSCHAFT (DE) | 2000-05-10 | — | — | EP | disclosed |
| WO-2000023413-A1 | METHOD FOR DRYING PHENOXYMETHYLBENZOIC ACIDS | BASF AKTIENGESELLSCHAFT (DE) | 2000-04-27 | — | — | WO | disclosed |
| WO-1999005130-A1 | SUBSTITUTED 3-PHENYL ISOXAZOLINES | BASF AKTIENGESELLSCHAFT (DE) | 1999-02-04 | — | — | WO | disclosed |
| EP-0891336-A1 | SUBSTITUTED 1-METHYL-3-BENZYLURACILS | BASF AKTIENGESELLSCHAFT (DE) | 1999-01-20 | — | — | EP | disclosed |
| CN-1189824-A | 1-amino-3-benzyluracils | BASF AG (DE) | 1998-08-05 | — | — | CN | disclosed |
| EP-0835248-A1 | 1-AMINO-3-BENZYLURACILS | BASF AKTIENGESELLSCHAFT (DE) | 1998-04-15 | — | — | EP | disclosed |
| WO-1997035845-A1 | SUBSTITUTED 1-METHYL-3-BENZYLURACILS | BASF AKTIENGESELLSCHAFT (DE) | 1997-10-02 | — | — | WO | disclosed |
| WO-1997001543-A1 | 1-AMINO-3-BENZYLURACILS | BASF AKTIENGESELLSCHAFT (DE) | 1997-01-16 | — | — | WO | disclosed |