⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL15189032 | 0.75 | — | — | |
| SCHEMBL21077634 | 0.74 | — | — | |
| SCHEMBL24222560 | 0.74 | — | — | |
| SCHEMBL23875536 | 0.72 | — | — | |
| SCHEMBL15039421 | 0.72 | — | — | |
| SCHEMBL21361787 | 0.71 | — | — | |
| SCHEMBL125210 | 0.71 | — | — | |
| SCHEMBL10344416 | 0.71 | — | — | |
| SCHEMBL125209 | 0.71 | — | — | |
| SCHEMBL25468983 | 0.70 | ALDH1A1 (0.42) | — |
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 17 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3224246-B1 | 4-OXOQUINOLINE COMPOUNDS | BASF SE (DE) | 2022-01-12 | — | — | EP | disclosed |
| EP-3101087-B1 | MULTIPLE CHROMOPHORES WITH A PERYLENEDIIMIDE SKELETON | BASF SE (DE) | 2018-01-17 | — | — | EP | disclosed |
| US-20170331049-A1 | 4-OXOQUINOLINE COMPOUNDS | BASF SE (DE) | 2017-11-16 | — | — | US | disclosed |
| US-20170327465-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | BASF SE (DE) | 2017-11-16 | — | — | US | disclosed |
| EP-3072887-B1 | N,N'-BIS(2,6-DIISOPROPYLPHENYL)-1,7-DI(2,6-DIPHENYLPHENOXY)PERYLENE-3,4;9,10-TETRACARBOXIMIDE, N,N'-BIS(2,6-DIISOPROPYLPHENYL)-1,6-DI(2,6-DIPHENYLPHENOXY)PERYLENE-3,4;9,10-TETRACARBOXIMIDE AND THE USE THEREOF | BASF SE (DE) | 2017-10-18 | — | — | EP | disclosed |
| EP-3224247-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | BASF SE (DE) | 2017-10-04 | — | — | EP | disclosed |
| EP-3224246-A1 | 4-OXOQUINOLINE COMPOUNDS | BASF SE (DE) | 2017-10-04 | — | — | EP | disclosed |
| US-20170018717-A1 | NEW CYCLAZINES AND THEIR USE AS SEMICONDUCTORS | MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN E.V. (DE) | 2017-01-19 | — | — | US | disclosed |
| EP-3110817-A1 | NEW CYCLAZINES AND THEIR USE AS SEMICONDUCTORS | BASF SE (DE) | 2017-01-04 | — | — | EP | disclosed |
| EP-3101087-A1 | MULTIPLE CHROMOPHORES WITH A PERYLENEDIIMIDE SKELETON | BASF SE (DE) | 2016-12-07 | — | — | EP | disclosed |
| EP-3072887-A1 | N,N'-BIS(2,6-DIISOPROPYLPHENYL)-1,7-DI(2,6-DIPHENYLPHENOXY)PERYLENE-3,4;9,10-TETRACARBOXIMIDE, N,N'-BIS(2,6-DIISOPROPYLPHENYL)-1,6-DI(2,6-DIPHENYLPHENOXY)PERYLENE-3,4;9,10-TETRACARBOXIMIDE AND THE USE THEREOF | BASF SE (DE) | 2016-09-28 | — | — | EP | disclosed |
| WO-2016083914-A1 | 4-OXOQUINOLINE COMPOUNDS | BASF SE (DE) | 2016-06-02 | — | — | WO | disclosed |
| WO-2016083915-A1 | 4-HYDROXYQUINOLINE COMPOUNDS | BASF SE (DE) | 2016-06-02 | — | — | WO | disclosed |
| WO-2015125125-A1 | NEW CYCLAZINES AND THEIR USE AS SEMICONDUCTORS | BASF SE (DE) | 2015-08-27 | — | — | WO | disclosed |
| CN-101035788-B | Process for the preparation of halogenated rylen-carboximides by halogenation of rylene-carboximides with elemental halogen in a two-phase mixture comprising an organic solvent and water | BASF AG | 2013-01-23 | — | — | CN | disclosed |
| CN-101068790-A | Rylene tetracarboxylic acid diimides substituted by cyclic amino groups | BASF AG (DE) | 2007-11-07 | — | — | CN | disclosed |
| CN-101035788-A | Halogenation of rylen-carboximides with elemental halogen in a two-phase mixture comprising an organic solvent and water, wherein the hydrogen halide formed is continuously removed from the organic solvent | BASF AG (DE) | 2007-09-12 | — | — | CN | disclosed |