⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL213399 | 1.00 | — | — | |
| SCHEMBL16768163 | 1.00 | — | — | |
| SCHEMBL2173094 | 0.84 | ALDH1A1 (0.38) | — | |
| SCHEMBL10029807 | 0.84 | ALDH1A1 (0.38) | — | |
| SCHEMBL31686857 | 0.82 | ALDH1A1 (0.36) | — | |
| SCHEMBL22892712 | 0.82 | — | — | |
| SCHEMBL16433945 | 0.82 | — | — | |
| SCHEMBL5593674 | 0.82 | — | — | |
| SCHEMBL9899251 | 0.81 | TDP1 (0.38) | — | |
| SCHEMBL9899250 | 0.81 | TDP1 (0.38) | — |
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 13 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20120077941-A1 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS | BRIDGESTONE CORPORATION (JP) | 2012-03-29 | — | — | US | claimed |
| US-8088868-B2 | oximation of cojugated homopolymers formed by addtion polymerization of conjugated diene monomer in the presence lanthanide copmpounds as polymerization catalysts; polymers used in the manufacture of tires having reduced hysteresis | BRIDGESTONE CORPORATION (JP) | 2012-01-03 | — | — | US | claimed |
| US-20080146745-A1 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS | BRIDGESTONE CORPORATION (JP) | 2008-06-19 | — | — | US | claimed |
| CN-113150792-B | Polymerizable liquid crystal mixture and polymerizable liquid crystal composition | 住友化学株式会社 | 2024-09-20 | — | — | CN | disclosed |
| US-20170205710-A1 | OXIME ESTER PHOTOINITIATORS | BASF SE (DE) | 2017-07-20 | — | — | US | disclosed |
| US-9365515-B2 | Oxime ester photoinitiators | BASF SE (DE) | 2016-06-14 | — | — | US | disclosed |
| US-20150064624-A1 | OXIME ESTER PHOTOINITIATORS | BASF SE (DE) | 2015-03-05 | — | — | US | disclosed |
| US-20140334027-A1 | OXIME ESTER PHOTOINITIATORS | BASF SE (DE) | 2014-11-13 | — | — | US | disclosed |
| US-8541509-B2 | Polymers functionalized with protected oxime compounds | BRIDGESTONE CORPORATION (JP) | 2013-09-24 | — | — | US | disclosed |
| US-20120077941-A1 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS | BRIDGESTONE CORPORATION (JP) | 2012-03-29 | — | — | US | disclosed |
| US-8088868-B2 | oximation of cojugated homopolymers formed by addtion polymerization of conjugated diene monomer in the presence lanthanide copmpounds as polymerization catalysts; polymers used in the manufacture of tires having reduced hysteresis | BRIDGESTONE CORPORATION (JP) | 2012-01-03 | — | — | US | disclosed |
| EP-1963374-B1 | OXIME ESTER PHOTOINITIATORS | BASF SE (DE) | 2010-02-17 | — | — | EP | disclosed |
| US-20080146745-A1 | POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS | BRIDGESTONE CORPORATION (JP) | 2008-06-19 | — | — | US | disclosed |