⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL3213 | 0.87 | — | — | |
| SCHEMBL10338627 | 0.87 | — | — | |
| SCHEMBL27653464 | 0.75 | — | — | |
| SCHEMBL27977083 | 0.75 | — | — | |
| SCHEMBL27173194 | 0.75 | — | — | |
| SCHEMBL25351100 | 0.75 | — | — | |
| Ethylene SCHEMBL2287961 | 0.75 | — | — | |
| Hydrochloric Acid SCHEMBL8590292 | 0.75 | — | — | |
| SCHEMBL20837936 | 0.75 | — | — | |
| SCHEMBL27547742 | 0.75 | — | — |
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 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108366561-A | Biocidal activity polymer composition | 路博润先进材料公司 | 2018-08-03 | — | — | CN | disclosed |
| US-8822621-B2 | Method for producing (hydroxymethyl)polysiloxanes | WACKER CHEMIE AG (DE) | 2014-09-02 | — | — | US | disclosed |
| US-20120220793-A1 | Method for Producing (Hydroxymethyl)Polysiloxanes | WACKER CHEMIE AG (DE) | 2012-08-30 | — | — | US | disclosed |
| US-7972682-B2 | Reactive silicic acid suspensions | WACKER CHEMIE AG (DE) | 2011-07-05 | — | — | US | disclosed |
| US-7737242-B2 | Crosslinkable siloxane urea copolymers | WACKER CHEMIE AG (DE) | 2010-06-15 | — | — | US | disclosed |
| US-20080255317-A1 | Polyester-Polysiloxane Copolymers and Process for their Preparation | WACKER CHEMIE AG (DE) | 2008-10-16 | — | — | US | disclosed |
| US-20080113162-A1 | Reactive Silicic Acid Suspensions | WACKER CHEMIE AG (DE) | 2008-05-15 | — | — | US | disclosed |
| US-20070232772-A1 | Crosslinkable Siloxane Urea Copolymers | WACKER CHEMIE AG (DE) | 2007-10-04 | — | — | US | disclosed |
| US-20060122413-A1 | Aminomethylene functional siloxanes | WACKER CHEMIE AG (DE) | 2006-06-08 | — | — | US | disclosed |
| US-6943265-B2 | Method for the production of hydroxyalkyl polysiloxanes | CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE, GMBH (DE) | 2005-09-13 | — | — | US | disclosed |
| US-20050085612-A1 | Aminomethylene-functional siloxanes | CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) | 2005-04-21 | — | — | US | disclosed |
| US-20040073031-A1 | Method for the production of hydroxyalkyl polysiloxanes | WACKER CHEMIE AG (DE) | 2004-04-15 | — | — | US | disclosed |
| US-6534615-B2 | Reacting polydimethylsiloxane, polymethylvinylsiloxane and polymethyltrifluoropropylsiloxane with N-((3-aminopropyl)di-methylsilyl)-2,2-dimethyl-1-aza-2-silacyclopentane | CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) | 2003-03-18 | — | — | US | disclosed |
| US-20020049296-A1 | Preparation of amino-functional siloxanes | CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) | 2002-04-25 | — | — | US | disclosed |