⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL3026361 | 0.85 | SCN4A (1.00) | — | |
| SCHEMBL17279815 | 0.83 | NOTUM (0.74) | — | |
| SCHEMBL6055861 | 0.82 | SCN4A (0.52) | — | |
| SCHEMBL6055605 | 0.82 | SCN4A (0.52) | — | |
| SCHEMBL17279817 | 0.81 | POLB (0.77) | — | |
| SCHEMBL3392174 | 0.80 | PDPK1 (1.00) | — | |
| SCHEMBL23105893 | 0.78 | PDPK1 (0.68) | — | |
| SCHEMBL27876939 | 0.76 | SCN4A (0.73) | — | |
| SCHEMBL980356 | 0.74 | NOTUM (0.62) | — | |
| SCHEMBL21415566 | 0.74 | NOTUM (0.62) | — |
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 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114276286-A | Method for preparing N, N-disubstituted-alpha, beta-unsaturated enamine from arone and secondary nitrogen compound | 长沙资材科技有限公司 | 2022-04-05 | — | — | CN | claimed |
| US-20250304567-A1 | PYRROLIDIONE DERIVATIVES AS INHIBITORS OF NF KAPPA B INDUCING KINASE | JANSSEN PHARMACEUTICA NV (BE) | 2025-10-02 | — | — | US | disclosed |
| US-20240383875-A1 | Benzimidazole Pyridine Derivatives | HOFFMANN-LA ROCHE INC. (US) | 2024-11-21 | — | — | US | disclosed |
| WO-2024208143-A1 | TRIAZOLE COMPOUND, AND PREPARATION METHOD THEREFOR, HERBICIDAL COMPOSITION AND USE THEREOF | 青岛清原化合物有限公司 | 2024-10-10 | — | — | WO | disclosed |
| WO-2024169666-A1 | BENZENE RING-SUBSTITUTED PYRIMIDINE CARBOXYLIC ACID COMPOUND, AND PREPARATION METHOD THEREFOR, HERBICIDAL COMPOSITION COMPRISING SAME, AND USE THEREOF | 青岛清原化合物有限公司 | 2024-08-22 | — | — | WO | disclosed |
| WO-2024169667-A1 | SUBSTITUTED PYRROLIDONE COMPOUND AND PREPARATION METHOD THEREFOR, HERBICIDAL COMPOSITION, AND USE | 青岛清原化合物有限公司 | 2024-08-22 | — | — | WO | disclosed |
| CN-114276286-A | Method for preparing N, N-disubstituted-alpha, beta-unsaturated enamine from arone and secondary nitrogen compound | 长沙资材科技有限公司 | 2022-04-05 | — | — | CN | disclosed |
| US-7833331-B2 | Non-toxic corrosion-protection pigments based on cobalt | UNIVERSITY OF DAYTON (US) | 2010-11-16 | — | — | US | disclosed |
| US-7789958-B2 | Non-toxic corrosion-protection pigments based on manganese | UNIVERSITY OF DAYTON (US) | 2010-09-07 | — | — | US | disclosed |
| US-20090163628-A1 | NON-TOXIC CORROSION-PROTECTION PIGMENTS BASED ON COBALT | STURGILL JEFFREY ALLEN | 2009-06-25 | — | — | US | disclosed |
| US-20030234063-A1 | Non-toxic corrosion-protection conversion coats based on cobalt | DAYTON, UNIVERSITY OF | 2003-12-25 | — | — | US | disclosed |
| US-20030230363-A1 | Non-toxic corrosion-protection rinses and seals based on cobalt | UNIVERSITY OF DAYTON | 2003-12-18 | — | — | US | disclosed |
| US-6627573-B2 | Useful as a cocatalyst for addition coordination polymerization comprising an anion containing at least two Lewis basic sites which are coordinated to Lewis acids, and further containing a hydroxyl group for support attachment | THE DOW CHEMICAL COMPANY | 2003-09-30 | — | — | US | disclosed |
| WO-2003060192-A1 | NON-TOXIC CORROSION-PROTECTION RINSES AND SEALS BASED ON COBALT | UNIVERSITY OF DAYTON (US) | 2003-07-24 | — | — | WO | disclosed |
| WO-2003060191-A2 | NON-TOXIC CORROSION-PROTECTION CONVERSION COATINGES ABSED ON COBALT | UNIVERSITY OF DAYTON (US) | 2003-07-24 | — | — | WO | disclosed |
| WO-2003060019-A1 | NON-TOXIC CORROSION PROTECTION PIGMENTS BASED ON COBALT | UNIVERSITY OF DAYTON (US) | 2003-07-24 | — | — | WO | disclosed |
| US-20020032120-A1 | Expanded anionic compounds comprising hydroxyl or quiescent reactive functionality and catalyst activators therefrom | DOW CHEMICAL COMPANY, THE | 2002-03-14 | — | — | US | disclosed |
| WO-2002008303-A1 | EXPANDED ANIONIC COMPOUNDS COMPRISING HYDROXYL OR QUIESCENT REACTIVE FUNCTIONALITY AND CATALYST ACTIVATORS THEREFROM | THE DOW CHEMICAL COMPANY (US) | 2002-01-31 | — | — | WO | disclosed |
| EP-0650480-A1 | 1-ARYLSULPHONYL, ARYLCARBONYL AND 1-ARYLPHOSPHONYL-3-PHENYL-1,4,5,6-TETRAHYDROPYRIDAZINES | ORTHO PHARMACEUTICAL CORPORATION (US) | 1995-05-03 | — | — | EP | disclosed |
| WO-1994001412-A1 | 1-ARYLSULPHONYL, ARYLCARBONYL AND 1-ARYLPHOSPHONYL-3-PHENYL-1,4,5,6-TETRAHYDROPYRIDAZINES | ORTHO PHARMACEUTICAL CORPORATION (US) | 1994-01-20 | — | — | WO | disclosed |