⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL2476669 | 0.85 | CYP2D6 (0.32) | — | |
| SCHEMBL1349276 | 0.83 | CYP2D6 (0.33) | — | |
| SCHEMBL1151138 | 0.82 | CYP2D6 (0.33) | — | |
| SCHEMBL14142720 | 0.78 | — | — | |
| SCHEMBL17948249 | 0.71 | MEN1 (0.30) | — | |
| SCHEMBL1206903 | 0.70 | CYP2D6 (0.36) | — | |
| SCHEMBL5318549 | 0.68 | CYP2D6 (0.32) | — | |
| SCHEMBL14859877 | 0.67 | CYP2D6 (0.31) | — | |
| SCHEMBL7201976 | 0.67 | HSD11B1 (0.32) | — | |
| SCHEMBL18772329 | 0.64 | CYP2C19 (0.33) | — |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-9994538-B2 | Latent acids and their use | BASF SE (DE) | 2018-06-12 | — | — | US | disclosed |
| US-20180009775-A1 | LATENT ACIDS AND THEIR USE | BASF SE (DE) | 2018-01-11 | — | — | US | disclosed |
| WO-2016124493-A1 | LATENT ACIDS AND THEIR USE | BASF SE (DE) | 2016-08-11 | — | — | WO | disclosed |
| EP-1595182-B1 | HALOGENATED OXIME DERIVATIVES AND THE USE THEREOF AS LATENT ACIDS | BASF SE (DE) | 2015-09-30 | — | — | EP | disclosed |
| EP-1769286-B1 | OXIME DERIVATIVES AND THE USE THEROF AS LATENT ACIDS | BASF SE (DE) | 2015-09-09 | — | — | EP | disclosed |
| US-8652752-B2 | Sulphonium salt initiators | BASF SE (DE) | 2014-02-18 | — | — | US | disclosed |
| EP-2197840-B1 | SULPHONIUM SALT INITIATORS | BASF SE (DE) | 2013-11-06 | — | — | EP | disclosed |
| US-8512934-B2 | Sulphonium salt initiators | BASF SE (DE) | 2013-08-20 | — | — | US | disclosed |
| EP-2197869-B1 | SULPHONIUM SALT INITIATORS | BASF SE (DE) | 2013-04-24 | — | — | EP | disclosed |
| EP-2539316-A1 | LATENT ACIDS AND THEIR USE | BASF SE (DE) | 2013-01-02 | — | — | EP | disclosed |
| EP-2197839-B1 | SULPHONIUM SALT INITIATORS | BASF SE (DE) | 2013-01-02 | — | — | EP | disclosed |
| US-20110300484-A1 | SULFONIUM DERIVATIVES AND THE USE THEROF AS LATENT ACIDS | BASF SE (DE) | 2011-12-08 | — | — | US | disclosed |
| WO-2011104127-A1 | LATENT ACIDS AND THEIR USE | BASF SE (DE) | 2011-09-01 | — | — | WO | disclosed |
| US-20110171569-A1 | SULFONIUM DERIVATIVES AND THE USE THEROF AS LATENT ACIDS | BASF SE (DE) | 2011-07-14 | — | — | US | disclosed |
| US-20100297542-A1 | SULPHONIUM SALT INITIATORS | BASF SE (DE) | 2010-11-25 | — | — | US | disclosed |
| US-20100297540-A1 | SULPHONIUM SALT INITIATORS | BASF SE (DE) | 2010-11-25 | — | — | US | disclosed |
| US-7687220-B2 | Oxime derivatives and use thereof as latent acids | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2010-03-30 | — | — | US | disclosed |
| US-20090042114-A1 | Halogenated oxime derivatives and the use therof as latent acids | YAMATO HITOSHI | 2009-02-12 | — | — | US | disclosed |
| US-20080085458-A1 | Oxime Derivatives And Use Thereof As Latent Acids | CIBA SPECIALTY CHEMICALS CORPORATION | 2008-04-10 | — | — | US | disclosed |