⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL6280786 | 0.97 | LMNA (0.50) | — | |
| SCHEMBL9794655 | 0.97 | LMNA (0.50) | — | |
| SCHEMBL5717469 | 0.97 | — | — | |
| SCHEMBL8652515 | 0.97 | LMNA (0.50) | — | |
| SCHEMBL13075202 | 0.97 | LMNA (0.50) | — | |
| SCHEMBL4363756 | 0.97 | LMNA (0.50) | — | |
| Hydrochloric Acid SCHEMBL5345632 | 0.94 | LMNA (0.48) | — | |
| Bromide SCHEMBL5343457 | 0.94 | LMNA (0.48) | — | |
| SCHEMBL2097116 | 0.90 | — | — | |
| SCHEMBL14840292 | 0.83 | HIF1A (0.41) | — |
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 12 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2831128-B1 | PREPARATION OF FUNCTIONAL POLYMERS USING PHOSPHIDE INITIATORS | BRIDGESTONE CORP (JP) | 2016-11-30 | — | — | EP | disclosed |
| US-9163104-B2 | Preparation of functional polymers using phosphide initiators | BRIDGESTONE CORPORATION (JP) | 2015-10-20 | — | — | US | disclosed |
| US-20150065673-A1 | Preparation Of Functional Polymers Using Phosphide Initiators | BRIDGESTONE CORPORATION (JP) | 2015-03-05 | — | — | US | disclosed |
| EP-2831128-A1 | PREPARATION OF FUNCTIONAL POLYMERS USING PHOSPHIDE INITIATORS | Bridgestone Corporation (JP) | 2015-02-04 | — | — | EP | disclosed |
| WO-2013149233-A1 | PREPARATION OF FUNCTIONAL POLYMERS USING PHOSPHIDE INITIATORS | BRIDGESTONE CORPORATION (JP) | 2013-10-03 | — | — | WO | disclosed |
| EP-1650216-B1 | PROCESS FOR PRODUCING OPTICALLY ACTIVE DIMER OF PHOSPHORUS HETEROCYCLE | NIPPON CHEMICAL IND COMPANY LTD (JP) | 2011-12-28 | — | — | EP | disclosed |
| US-20100299783-A1 | FUSION POLYNUCLEOTIDE FOR BIOSYNTHESIS OF BETA-CAROTENE USING BICISTRONIC GENE EXPRESSION AND METHOD FOR PRODUCING BETA-CAROTENE USING THE SAME | REPUBLIC OF KOREA, RURAL DEVELOPMENT ADMINISTRATION (KR) | 2010-11-25 | — | — | US | disclosed |
| US-7411096-B2 | Process for producing optically active phosphorus heterocyclic dimer | NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) | 2008-08-12 | — | — | US | disclosed |
| US-20060211888-A1 | 2,2'-bis-(1-alkylphosphetanes); a primary alkyl or cycloalkyl phosphine is reacted with 1,3-dichloropropane, in the presence of n-butyllithium, and then reacted with boron trihydride, oxygen, or sulfur, dimerizing, removing the boron trihydride, oxygen, or sulfur; assymetric hydrogenation catalysts | NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) | 2006-09-21 | — | — | US | disclosed |
| US-20060189818-A1 | Novel optically active phosphorus-chiral diphosphetanes, intermediates of the same, and transition metal complexes containing the diphosphetanes as the ligand | NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) | 2006-08-24 | — | — | US | disclosed |
| EP-1650217-A1 | NOVEL OPTICALLY ACTIVE PHOSPHORUS-CHIRAL DIPHOSPHETANES, INTERMEDIATES OF THE SAME, AND TRANSITION METAL COMPLEXES CONTAINING THE DIPHOSPHETANES AS THE LIGAND | Nippon Chemical Industrial Co., Ltd. (JP) | 2006-04-26 | — | — | EP | disclosed |
| EP-1650216-A1 | PROCESS FOR PRODUCING OPTICALLY ACTIVE DIMER OF PHOSPHORUS HETEROCYCLE | NIPPON CHEMICAL INDUSTRIAL COMPANY LIMITED (JP) | 2006-04-26 | — | — | EP | disclosed |