⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL2164463 | 1.00 | — | — | |
| SCHEMBL6525170 | 0.86 | KMT2A (0.32) | — | |
| SCHEMBL4145192 | 0.85 | — | — | |
| SCHEMBL4145193 | 0.85 | — | — | |
| SCHEMBL9380581 | 0.85 | — | — | |
| SCHEMBL4130255 | 0.83 | EP300 (0.47) | — | |
| SCHEMBL4130257 | 0.83 | EP300 (0.47) | — | |
| SCHEMBL6053800 | 0.81 | EP300 (0.50) | — | |
| SCHEMBL16431472 | 0.81 | EP300 (0.50) | — | |
| SCHEMBL9262187 | 0.81 | EP300 (0.50) | — |
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 41 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2024029475-A1 | WAVELENGTH CONVERSION FILM FORMING COMPOSITION | 日産化学株式会社 | 2024-02-08 | — | — | WO | disclosed |
| US-10326138-B2 | Charge storage material, electrode active material and secondary battery | WASEDA UNIVERSITY (JP) | 2019-06-18 | — | — | US | disclosed |
| EP-3122789-B1 | 9,10-BIS(1,3-DITHIOL-2-YLIDENE)-9,10-DIHYDROANTHRACENE POLYMERS AND USE THEREOF | EVONIK DEGUSSA GMBH (DE) | 2019-05-08 | — | — | EP | disclosed |
| US-10263280-B2 | 9,10-Bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene polymers and use thereof | EVONIK DEGUSSA GMBH (DE) | 2019-04-16 | — | — | 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-9890230-B2 | Tetracyanoanthraquinodimethane polymers and use thereof | EVONIK DEGUSSA GMBH (DE) | 2018-02-13 | — | — | 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-9856336-B2 | — | — | 2018-01-02 | — | — | US | disclosed |
| US-20170179525-A1 | NOVEL 9,10-BIS(1,3-DITHIOL-2-YLIDENE)-9,10-DIHYDROANTHRACENE POLYMERS AND USE THEREOF | EVONIK DEGUSSA GMBH (DE) | 2017-06-22 | — | — | US | disclosed |
| US-20170114162-A1 | NOVEL TETRACYANOANTHRAQUINODIMETHANE POLYMERS AND USE THEREOF | EVONIK DEGUSSA GMBH (DE) | 2017-04-27 | — | — | US | disclosed |
| US-6566110-B1 | Nucleotide sequences coding polypeptide for use tool in halogenating compounds | BASF AKTIENGESELLSCHAFT (DE) | 2003-05-20 | — | — | US | disclosed |
| WO-2000077182-A9 | NUCLEIC ACID FRAGMENT AND VECTOR CONTAINING HALOGENASE AND METHOD FOR THE HALOGENATION OF CHEMICAL COMPOUNDS | BASF AG (DE) | 2002-09-12 | — | — | WO | disclosed |
| EP-1187819-A1 | N-SUBSTITUTED PERHYDRO DIAZINE | BASF AKTIENGESELLSCHAFT (DE) | 2002-03-20 | — | — | EP | disclosed |
| EP-1185629-A1 | NUCLEIC ACID FRAGMENT AND VECTOR CONTAINING HALOGENASE AND METHOD FOR THE HALOGENATION OF CHEMICAL COMPOUNDS | BASF AKTIENGESELLSCHAFT (DE) | 2002-03-13 | — | — | EP | disclosed |
| EP-1123386-A1 | METHOD FOR PRODUCING CHIRAL CARBOXYLIC ACIDS FROM NITRILES WITH THE ASSISTANCE OF A NITRILASE OR MICROORGANISMS WHICH CONTAIN A GENE FOR THE NITRILASE | BASF AKTIENGESELLSCHAFT (DE) | 2001-08-16 | — | — | EP | disclosed |
| WO-2001000600-A1 | N-SUBSTITUTED PERHYDRO DIAZINE | BASF AKTIENGESELLSCHAFT (DE) | 2001-01-04 | — | — | WO | disclosed |
| WO-2000077182-A1 | NUCLEIC ACID FRAGMENT AND VECTOR CONTAINING HALOGENASE AND METHOD FOR THE HALOGENATION OF CHEMICAL COMPOUNDS | BASF AKTIENGESELLSCHAFT (DE) | 2000-12-21 | — | — | WO | disclosed |
| WO-2000028330-A1 | METHOD FOR SELECTING CATALYTIC ANTIBODIES | BASF AKTIENGESELLSCHAFT (DE) | 2000-05-18 | — | — | WO | disclosed |
| WO-2000023577-A1 | METHOD FOR PRODUCING CHIRAL CARBOXYLIC ACIDS FROM NITRILES WITH THE ASSISTANCE OF A NITRILASE OR MICROORGANISMS WHICH CONTAIN A GENE FOR THE NITRILASE | BASF AKTIENGESELLSCHAFT (DE) | 2000-04-27 | — | — | WO | disclosed |
| US-4203898-A | ANTICARCINOGENIC | ELI LILLY AND COMPANY (US) | 1980-05-20 | — | — | US | disclosed |