⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL2348244 | 0.83 | — | — | |
| SCHEMBL2350926 | 0.81 | SMN1; SMN2 (0.30) | — | |
| SCHEMBL2343609 | 0.74 | CA1 (0.33) | — | |
| SCHEMBL16003245 | 0.74 | KDM4E (0.30) | — | |
| SCHEMBL2692834 | 0.74 | — | — | |
| SCHEMBL18588303 | 0.74 | — | — | |
| SCHEMBL16657577 | 0.74 | — | — | |
| SCHEMBL16581421 | 0.70 | — | — | |
| SCHEMBL7085873 | 0.69 | CA1 (0.32) | — | |
| SCHEMBL13049849 | 0.69 | — | — |
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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1741000-B1 | AS-INDACENE DERIVATIVES HAVING NEGATIVE DIELECTRIC ANISOTROPY | MERCK PATENT GMBH (DE) | 2012-12-26 | — | — | EP | disclosed |
| EP-1544190-B1 | METHOD FOR PRODUCING CARBOXYLIC ACIDS | NAT INST OF ADVANCED IND SCIEN (JP) | 2011-08-31 | — | — | EP | disclosed |
| US-7732643-B2 | Transition metal complex, catalyst for olefin polymerization, and process for producing olefin polymer with the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2010-06-08 | — | — | US | disclosed |
| EP-1532090-B1 | CYCLOPENTA ¬B NAPHTHALENE DERIVATIVES | MERCK PATENT GMBH (DE) | 2010-03-17 | — | — | EP | disclosed |
| US-7671226-B2 | Transition metal complex, catalyst for olefin polymerization, and process for producing olefin polymer with the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2010-03-02 | — | — | US | disclosed |
| US-20100048933-A1 | TRANSITION METAL COMPLEX, CATALYST FOR OLEFIN POLYMERIZATION, AND PROCESS FOR PRODUCING OLEFIN POLYMER WITH THE SAME | HANAOKA HIDENORI | 2010-02-25 | — | — | US | disclosed |
| EP-1426379-B1 | TRANSITION METAL COMPLEX,CATALYST FOR OLEFIN POLYMERIZATION, AND PROCESS FOR PRODUCING OLEFIN POLYMER WITH THE SAME | SUMITOMO CHEMICAL CO (JP) | 2009-11-11 | — | — | EP | disclosed |
| US-7612243-B2 | Cyclopenta[b]naphthalene derivatives | MERCK PATENT GMBH (DE) | 2009-11-03 | — | — | US | disclosed |
| US-7612243-B2 | Cyclopenta[b]naphthalene derivatives | MERCK PATENT GMBH (DE) | 2009-11-03 | — | — | US | disclosed |
| US-7575785-B2 | use thereof in liquid-crystalline media, and and to electro-optical display elements containing these liquid-crystalline media; negative dielectric anisotropy | MERCK PATENT GMBH (DE) | 2009-08-18 | — | — | US | disclosed |
| US-20070228328-A1 | As-Indacen Derivatives | MERCK PATENT GMBH (DE) | 2007-10-04 | — | — | US | disclosed |
| US-7186858-B2 | Method for producing carboxylic acid | NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) | 2007-03-06 | — | — | US | disclosed |
| US-20050215817-A1 | Method for producing carboxylic acid | NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) | 2005-09-29 | — | — | US | disclosed |
| EP-1544190-A1 | METHOD FOR PRODUCING CARBOXYLIC ACID | National Institute of Advanced Industrial Science and Technology (JP) | 2005-06-22 | — | — | EP | disclosed |
| US-20040242410-A1 | Transition metal complex, catalyst for olefin polymerization, and process for producing olefin polymer with the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2004-12-02 | — | — | US | disclosed |
| EP-1426379-A1 | TRANSITION METAL COMPLEX,CATALYST FOR OLEFIN POLYMERIZATION, AND PROCESS FOR PRODUCING OLEFIN POLYMER WITH THE SAME | Sumitomo Chemical Company, Limited (JP) | 2004-06-09 | — | — | EP | disclosed |
| EP-0437290-B1 | Process for the preparation of 5-oxohexane nitriles and the compound 2,4-dimethyl-5-oxohexane nitrile | DSM NV (NL) | 1998-05-06 | — | — | EP | disclosed |
| US-5334721-A | Reacting a methyl ketone and an alpha,beta-unsaturated nitrile in the presence of a basic catalyst; preparation of a 2-methyl-3,5-dialkylpyridine; cyclization; dehydrogenation | STAMICARBON B.V. (NL) | 1994-08-02 | — | — | US | disclosed |
| US-5254712-A | Using basic catalyst | STAMICARBON B.V. (NL) | 1993-10-19 | — | — | US | disclosed |
| EP-0437290-A1 | Process for the preparation of 5-oxohexane nitriles and the compound 2,4-dimethyl-5-oxohexane nitrile | DSM N.V. (NL) | 1991-07-17 | — | — | EP | disclosed |