⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL1036966 | 1.00 | — | — | |
| SCHEMBL1036967 | 1.00 | — | — | |
| SCHEMBL21021468 | 1.00 | — | — | |
| SCHEMBL1039600 | 1.00 | — | — | |
| SCHEMBL10500856 | 0.95 | ALDH1A1 (0.36) | — | |
| SCHEMBL9845738 | 0.95 | — | — | |
| SCHEMBL7618246 | 0.95 | ALDH1A1 (0.36) | — | |
| SCHEMBL15848099 | 0.91 | ALDH1A1 (0.33) | — | |
| SCHEMBL1040973 | 0.90 | — | — | |
| SCHEMBL1040971 | 0.90 | — | — |
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 66 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10392455-B2 | Process for controlling the polymer composition of an ethylene copolymer obtained by a catalyst system comprising a transition metal catalyst component and a Ziegler catalyst component | BASELL POLYOLEFINE GMBH (DE) | 2019-08-27 | — | — | US | disclosed |
| EP-2143707-B1 | Secondary diamine | LINE X LLC (US) | 2018-04-11 | — | — | EP | disclosed |
| EP-2794691-B1 | PROCESS FOR CONTROLLING THE POLYMER COMPOSITION OF AN ETHYLENE COPOLYMER OBTAINED BY A CATALYST SYSTEM COMPRISING A TRANSITION METAL CATALYST COMPONENT AND A ZIEGLER CATALYST COMPONENT | BASELL POLYOLEFINE GMBH (DE) | 2016-06-22 | — | — | EP | disclosed |
| EP-1419184-B1 | PROCESS FOR THE POLYMERIZATION OF ETHYLENE AND INTERPOLYMERS THEREOF | WESTLAKE LONGVIEW CORP (US) | 2014-11-26 | — | — | EP | disclosed |
| US-20140329978-A1 | PROCESS FOR CONTROLLING THE POLYMER COMPOSITION OF AN ETHYLENE COPOLYMER OBTAINED BY A CATALYST SYSTEM COMPRISING A TRANSITION METAL CATALYST COMPONENT AND A ZIEGLER CATALYST COMPONENT | BASELL POLYOLEFINE GMBH (DE) | 2014-11-06 | — | — | US | disclosed |
| EP-2794691-A1 | PROCESS FOR CONTROLLING THE POLYMER COMPOSITION OF AN ETHYLENE COPOLYMER OBTAINED BY A CATALYST SYSTEM COMPRISING A TRANSITION METAL CATALYST COMPONENT AND A ZIEGLER CATALYST COMPONENT | Basell Polyolefine GmbH (DE) | 2014-10-29 | — | — | EP | disclosed |
| WO-2013092453-A1 | PROCESS FOR CONTROLLING THE POLYMER COMPOSITION OF AN ETHYLENE COPOLYMER OBTAINED BY A CATALYST SYSTEM COMPRISING A TRANSITION METAL CATALYST COMPONENT AND A ZIEGLER CATALYST COMPONENT | BASELL POLYOLEFINE GMBH (DE) | 2013-06-27 | — | — | WO | disclosed |
| EP-2607391-A1 | Process for controlling the polymer composition of an ethylene copolymer obtained by a catalyst system comprising a transition metal catalyst component and a Ziegler catalyst component | Basell Polyolefine GmbH (DE) | 2013-06-26 | — | — | EP | disclosed |
| US-8212078-B2 | Making chain extenders with slower cure rates; reacting a ketone and/or aldehyde with a primary amine in the presence of an acidic ion exchange resin and hydrogenation agent; making diimine same way but excluding hydrogenation agent; e.g. N,N'-di-5-nonyl-isophoronediamine | ALBEMARLE CORPORATION (US) | 2012-07-03 | — | — | US | disclosed |
| EP-1417241-B1 | PROCESS FOR THE POLYMERIZATION OF ETHYLENE AND INTERPOLYMERS THEREOF | WESTLAKE LONGVIEW CORP (US) | 2011-01-26 | — | — | EP | disclosed |
| WO-2000052067-A1 | PROCESS FOR PRODUCING POLYETHYLENE | EASTMAN CHEMICAL COMPANY (US) | 2000-09-08 | — | — | WO | disclosed |
| EP-0843592-A4 | DEHALOGENATION OF HALOGENATED HYDROCARBONS IN AQUEOUS COMPOSITIONS | MONSANTO CO (US) | 1999-02-17 | — | — | EP | disclosed |
| EP-0843592-A1 | DEHALOGENATION OF HALOGENATED HYDROCARBONS IN AQUEOUS COMPOSITIONS | MONSANTO COMPANY (US) | 1998-05-27 | — | — | EP | disclosed |
| WO-1997004868-A1 | DEHALOGENATION OF HALOGENATED HYDROCARBONS IN AQUEOUS COMPOSITIONS | MONSANTO COMPANY (US) | 1997-02-13 | — | — | WO | disclosed |
| US-4785121-A | Preparation of halophthalic anhydrides | STAUFFER CHEMICAL COMPANY (US) | 1988-11-15 | — | — | US | disclosed |
| US-4739057-A | USING AN ARYLPHOSPHORUSHALIDE | STAUFFER CHEMICAL CO. (US) | 1988-04-19 | — | — | US | disclosed |
| US-4730046-A | FROM ARYL NITRO COMPOUNDS | STAUFFER CHEMICAL COMPANY (US) | 1988-03-08 | — | — | US | disclosed |
| EP-0251246-A1 | Process for converting organohydroxyl compounds to halides | STAUFFER CHEMICAL COMPANY (US) | 1988-01-07 | — | — | EP | disclosed |
| EP-0249257-A1 | Preparation of aryl halides | STAUFFER CHEMICAL COMPANY (US) | 1987-12-16 | — | — | EP | disclosed |
| US-4176027-A | INSULATION | RAYCHEM CORPORATION (US) | 1979-11-27 | — | — | US | disclosed |