⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL11064741 | 0.87 | ALDH1A1 (0.44) | — | |
| SCHEMBL11683132 | 0.86 | TSHR (0.50) | — | |
| SCHEMBL15421646 | 0.84 | KMT2A (0.54) | — | |
| SCHEMBL20184219 | 0.84 | TSHR (0.48) | — | |
| SCHEMBL9074783 | 0.82 | KMT2A (0.57) | — | |
| SCHEMBL11512170 | 0.82 | KMT2A (0.57) | — | |
| SCHEMBL29009465 | 0.82 | KMT2A (0.57) | — | |
| SCHEMBL8663105 | 0.82 | — | — | |
| SCHEMBL25174 | 0.78 | — | — | |
| SCHEMBL8119186 | 0.78 | CES2 (0.60) | — |
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 12 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3143055-A2 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP | Bridgestone Corporation (JP) | 2017-03-22 | — | — | EP | claimed |
| WO-2015175280-A2 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP | BRIDGESTONE CORPORATION (JP) | 2015-11-19 | — | — | WO | claimed |
| US-9670171-B2 | Process for preparing fluoxastrobin | ARYSTA LIFESCIENCE CORP (JP) | 2017-06-06 | — | — | US | disclosed |
| EP-3143055-A2 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP | Bridgestone Corporation (JP) | 2017-03-22 | — | — | EP | disclosed |
| US-20160237047-A1 | PROCESS FOR PREPARING FLUOXASTROBIN | ARYSTA LIFESCIENCE CORP (JP) | 2016-08-18 | — | — | US | disclosed |
| WO-2015175280-A2 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP | BRIDGESTONE CORPORATION (JP) | 2015-11-19 | — | — | WO | disclosed |
| US-20100233549-A1 | Non-Aqueous Electrolyte and Electrochemical Device With an Improved Safety | LG CHEM, LTD. (KR) | 2010-09-16 | — | — | US | disclosed |
| EP-1994599-A1 | NON-AQUEOUS ELECTROLYTE AND ELECTROCHEMICAL DEVICE WITH AN IMPROVED SAFETY | LG Chem, Ltd. (KR) | 2008-11-26 | — | — | EP | disclosed |
| WO-2007094626-A1 | NON-AQUEOUS ELECTROLYTE AND ELECTROCHEMICAL DEVICE WITH AN IMPROVED SAFETY | LG CHEM, LTD. (KR) | 2007-08-23 | — | — | WO | disclosed |
| US-6605681-B1 | Process for the continuous production of epoxylated addition polymers, and powder and liquid coating applications containing epoxylated addition polymers | JOHNSON POLYMER, INC. | 2003-08-12 | — | — | US | disclosed |
| US-6552144-B1 | Continuously charging into a reactor monomers consisting ofepoxy-functional acrylic monomer and monoethylenically unsaturated free radical polymerizable monomer; heating to polymerize | JOHNSON POLYMER, INC. | 2003-04-22 | — | — | US | disclosed |
| US-5331103-A | Reaction with hydrogen peroxide, hydroquinone from phenol | RHONE-POULENC CHIMIE (FR) | 1994-07-19 | — | — | US | disclosed |