⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL4809041 | 1.00 | — | — | |
| SCHEMBL5573466 | 1.00 | — | — | |
| SCHEMBL51549 | 1.00 | — | — | |
| SCHEMBL15738515 | 1.00 | — | — | |
| SCHEMBL8906969 | 1.00 | — | — | |
| SCHEMBL5573465 | 1.00 | — | — | |
| SCHEMBL51917 | 0.85 | — | — | |
| SCHEMBL51994 | 0.84 | — | — | |
| SCHEMBL1486297 | 0.84 | — | — | |
| SCHEMBL1486296 | 0.84 | — | — |
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-0583591-A2 | Process for the preparation of oxiranalcohols of high enantiomeric purity | HOECHST AKTIENGESELLSCHAFT (DE) | 1994-02-23 | — | — | EP | claimed |
| EP-0618914-B1 | OXIRANYL METHYL ETHERS EXHIBITING CHIRALITY, AND THEIR USE AS DOPANTS IN LIQUID-CRYSTAL MIXTURES | AVENTIS RES & TECH GMBH & CO (DE) | 2001-10-17 | — | — | EP | disclosed |
| WO-1999067410-A1 | BIOCATALYTIC METHOD FOR THE PRODUCTION OF ALDEHYDES USING CHLORPEROXIDASE | NESTE CHEMICALS OY (FI) | 1999-12-29 | — | — | WO | disclosed |
| US-5707545-A | OPTICAL APPARATUS FOR ELCTRONICS | HOECHST AKTIENGESELLSCHAFT (DE) | 1998-01-13 | — | — | US | disclosed |
| EP-0583591-B1 | Process for the preparation of oxiranalcohols of high enantiomeric purity | HOECHST AG (DE) | 1996-10-09 | — | — | EP | disclosed |
| US-5478954-A | Recrystallizing mixture of two enantiomers in an organic solvent mixture comprising aliphatic and aromatic hydrocarbons, halogenated aliphatic and aromatic hydrocarbons, ethers. esters, and amides | HOECHST AKTIENGESELLSCHAFT (DE) | 1995-12-26 | — | — | US | disclosed |
| US-5422037-A | For electro-optical and display devices | DISPLAYTECH, INC. (US) | 1995-06-06 | — | — | US | disclosed |
| EP-0618914-A1 | OXIRANYL METHYL ETHERS EXHIBITING CHIRALITY, AND THEIR USE AS DOPANTS IN LIQUID-CRYSTAL MIXTURES | HOECHST AKTIENGESELLSCHAFT (DE) | 1994-10-12 | — | — | EP | disclosed |
| EP-0583591-A2 | Process for the preparation of oxiranalcohols of high enantiomeric purity | HOECHST AKTIENGESELLSCHAFT (DE) | 1994-02-23 | — | — | EP | disclosed |
| WO-1993013093-A1 | OXIRANYL METHYL ETHERS EXHIBITING CHIRALITY, AND THEIR USE AS DOPANTS IN LIQUID-CRYSTAL MIXTURES | HOECHST AKTIENGESELLSCHAFT (DE) | 1993-07-08 | — | — | WO | disclosed |
| US-5180520-A | Ferroelectric liquid crystal compositions containing halogenated cores and chiral halogenated cores and chiral haloalkoxy tail units | UNIVERSITY RESEARCH CORPORATION (US) | 1993-01-19 | — | — | US | disclosed |
| WO-1992001766-A1 | FERROELECTRIC LIQUID CRYSTAL COMPOSITIONS CONTAINING HALOGENATED CORES AND CHIRAL HALOALKOXY TAIL UNITS | DISPLAYTECH, INC. (US) | 1992-02-06 | — | — | WO | disclosed |