⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL10905091 | 0.97 | — | — | |
| SCHEMBL9990819 | 0.97 | — | — | |
| SCHEMBL3180439 | 0.97 | — | — | |
| SCHEMBL301090 | 0.97 | — | — | |
| SCHEMBL301018 | 0.97 | — | — | |
| SCHEMBL3171223 | 0.94 | — | — | |
| Hydrochloric Acid SCHEMBL22531839 | 0.94 | — | — | |
| SCHEMBL301250 | 0.94 | — | — | |
| Hydrochloric Acid SCHEMBL17491838 | 0.89 | — | — | |
| SCHEMBL31416085 | 0.87 | — | — |
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 17 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2610248-B1 | METHOD FOR PRODUCING PHENYL-SUBSTITUTED HETEROCYCLIC DERIVATIVE BY MEANS OF COUPLING METHOD USING A PALLADIUM COMPOUND | TEIJIN PHARMA LTD (JP) | 2016-06-08 | — | — | EP | disclosed |
| US-8952174-B2 | Process for producing phenyl-substituted heterocyclic derivative through coupling using transition metal catalyst | TEIJIN PHARMA LIMITED (JP) | 2015-02-10 | — | — | US | disclosed |
| US-8916714-B2 | Method for producing phenyl-substituted heterocyclic derivative by means of coupling method using palladium compound | TEIJIN PHARMA LIMITED (JP) | 2014-12-23 | — | — | US | disclosed |
| US-8580384-B2 | Dielectric materials and methods of preparation and use thereof | POLYERA CORPORATION (US) | 2013-11-12 | — | — | US | disclosed |
| EP-2610248-A1 | METHOD FOR PRODUCING PHENYL-SUBSTITUTED HETEROCYCLIC DERIVATIVE BY MEANS OF COUPLING METHOD USING A PALLADIUM COMPOUND | Teijin Pharma Limited (JP) | 2013-07-03 | — | — | EP | disclosed |
| US-20130158272-A1 | METHOD FOR PRODUCING PHENYL-SUBSTITUTED HETEROCYCLIC DERIVATIVE BY MEANS OF COUPLING METHOD USING PALLADIUM COMPOUND | TEIJIN PHARMA LIMITED (JP) | 2013-06-20 | — | — | US | disclosed |
| EP-2404908-A1 | PROCESS FOR PRODUCING PHENYL-SUBSTITUTED HETEROCYCLIC DERIVATIVE THROUGH COUPLING USING TRANSITION METAL CATALYST | Teijin Pharma Limited (JP) | 2012-01-11 | — | — | EP | disclosed |
| US-8084563-B2 | Cyclic olefin addition copolymer, process for production thereof, and retardation film obtained from the copolymer | JSR CORPORATION (JP) | 2011-12-27 | — | — | US | disclosed |
| US-20110313169-A1 | PROCESS FOR PRODUCING PHENYL-SUBSTITUTED HETEROCYCLIC DERIVATIVE THROUGH COUPLING USING TRANSITION METAL CATALYST | TEIJIN PHARMA LIMITED (JP) | 2011-12-22 | — | — | US | disclosed |
| US-20110175089-A1 | Dielectric Materials and Methods of Preparation and Use Thereof | FLEXTERRA, INC. | 2011-07-21 | — | — | US | disclosed |
| US-20100021707-A1 | CYCLIC OLEFIN ADDITION COPOLYMER, METHOD FOR PRODUCING THE SAME, AND RETARDATION FILM OBTAINED FROM THE COPOLYMER | JSR CORPORATION (JP) | 2010-01-28 | — | — | US | disclosed |
| US-20090292088-A1 | PROCESS FOR PRODUCTION OF CYCLIC OLEFIN ADDITION POLYMER | JSR CORPORATION (JP) | 2009-11-26 | — | — | US | disclosed |
| EP-2039708-A1 | CYCLIC OLEFIN ADDITION COPOLYMER, METHOD FOR PRODUCING THE SAME, AND RETARDATION FILM OBTAINED FROM THE COPOLYMER | JSR Corporation (JP) | 2009-03-25 | — | — | EP | disclosed |
| US-7482412-B2 | Process for manufacturing cycloolefin addition polymer | JSR CORPORATION (JP) | 2009-01-27 | — | — | US | disclosed |
| EP-1961774-A1 | PROCESS FOR PRODUCTION OF CYCLIC OLEFIN ADDITION POLYMER | JSR Corporation (JP) | 2008-08-27 | — | — | EP | disclosed |
| US-20080085979-A1 | PROCESS FOR MANUFACTURING CYCLOOLEFIN ADDITION POLYMER | JSR CORPORATION (JP) | 2008-04-10 | — | — | US | disclosed |
| US-4595701-A | Reacting carbon monoxide and hydrogen in liquid phase in the presence of a rhodium and trialkylphosphine catalyst | AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) | 1986-06-17 | — | — | US | disclosed |