⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL8442362 | 0.88 | BBOX1 (0.43) | — | |
| SCHEMBL28676675 | 0.82 | ALDH1A1 (0.50) | — | |
| SCHEMBL150725 | 0.69 | BBOX1 (0.60) | — | |
| SCHEMBL76857 | 0.69 | BBOX1 (1.00) | — | |
| SCHEMBL7567805 | 0.69 | BBOX1 (0.53) | — | |
| SCHEMBL4452735 | 0.67 | MAOA (0.46) | — | |
| SCHEMBL9516339 | 0.67 | CA1 (0.38) | — | |
| SCHEMBL6477690 | 0.67 | BBOX1 (0.56) | — | |
| Hydrochloric Acid SCHEMBL3629169 | 0.67 | BBOX1 (0.56) | — | |
| Bromide SCHEMBL9069066 | 0.67 | BBOX1 (0.56) | — |
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 57 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113930790-A | Synthetic method of aryl selenide compound | 南昌大学 | 2022-01-14 | — | — | CN | disclosed |
| US-11192908-B2 | Octamolybdate compounds exhibiting bright emission | NANOCO 2D MATERIALS LIMITED (GB) | 2021-12-07 | — | — | US | disclosed |
| EP-3837267-A1 | POLYOXOMETALATE COMPOUNDS EXHIBITING BRIGHT EMISSION AND METHODS OF PRODUCING THE SAME | Nanoco 2D Materials Limited (GB) | 2021-06-23 | — | — | EP | disclosed |
| US-20200055884-A1 | Octamolybdate Compounds Exhibiting Bright Emission | NANOCO TECHNOLOGIES LIMITED (GB) | 2020-02-20 | — | — | US | disclosed |
| WO-2020035670-A1 | POLYOXOMETALATE COMPOUNDS EXHIBITING BRIGHT EMISSION AND METHODS OF PRODUCING THE SAME | NANOCO 2D MATERIALS LIMITED (GB) | 2020-02-20 | — | — | WO | disclosed |
| US-10337030-B2 | Microbially-mediated method for synthesis of metal chalcogenide nanoparticles | UT-BATTELLE, LLC (US) | 2019-07-02 | — | — | US | disclosed |
| US-9909221-B2 | Controllable reductive method for synthesizing metal-containing particles | UT-BATTELLE, LLC (US) | 2018-03-06 | — | — | US | disclosed |
| US-20180010153-A1 | MICROBIALLY-MEDIATED METHOD FOR SYNTHESIS OF METAL CHALCOGENIDE NANOPARTICLES | U.S. DEPARTMENT OF ENERGY | 2018-01-11 | — | — | US | disclosed |
| US-9768333-B2 | Microbially-mediated method for synthesis of non-oxide semiconductor nanoparticles | UT-BATTELLE, LLC (US) | 2017-09-19 | — | — | US | disclosed |
| US-9637828-B2 | Electrochemical method for synthesizing metal-containing particles and other objects | UT-BATTELLE, LLC (US) | 2017-05-02 | — | — | US | disclosed |
| EP-0954558-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR, William C. (US) | 1999-11-10 | — | — | EP | disclosed |
| WO-1998026028-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR WILLIAM C (US) | 1998-06-18 | — | — | WO | disclosed |
| US-5492652-A | Dithiopentacene derivatives, their preparation and the use thereof as electron acceptors in charge transfer complexes | CIBA-GEIGY CORPORATION (US) | 1996-02-20 | — | — | US | disclosed |
| US-5482984-A | ELECTROCONDUCTIVE POLYMER BLENDS WITH MOISTURE AND HEAT STABILITY | CIBA-GEIGY CORPORATION (US) | 1996-01-09 | — | — | US | disclosed |
| US-5436353-A | Dithiopentacene derivatives, their preparation and the use thereof as electron acceptors on charge transfer complexes | CIBA-GEIGY CORPORATION (US) | 1995-07-25 | — | — | US | disclosed |
| US-5378744-A | Thermosetting or thermoplastic resins for electroconductive elements | CIBA-GEIGY CORPORATION (US) | 1995-01-03 | — | — | US | disclosed |
| EP-0588759-A1 | Dithiopentacene derivatives, their preparation and their use in charge-transfer complexes | CIBA-GEIGY AG (CH) | 1994-03-23 | — | — | EP | disclosed |
| EP-0554219-A1 | Resin composition containing charge-transfer complexes, their preparation and their use | CIBA-GEIGY AG (CH) | 1993-08-04 | — | — | EP | disclosed |
| US-4601860-A | Method for producing selenoethers from selenoalcohols or their salts, and carbonates | PPG INDUSTRIES, INC. (US) | 1986-07-22 | — | — | US | disclosed |
| US-4278517-A | Osmium catalyzed hydroxylation of olefins with selenoxide cooxidants | UNION CARBIDE CORPORATION (US) | 1981-07-14 | — | — | US | disclosed |