⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL5962553 | 0.74 | — | — | |
| SCHEMBL15242275 | 0.73 | — | — | |
| SCHEMBL6137133 | 0.72 | — | — | |
| SCHEMBL14900808 | 0.72 | LMNA (0.36) | — | |
| Methylene Chloride SCHEMBL1847548 | 0.72 | — | — | |
| SCHEMBL23795116 | 0.71 | — | — | |
| SCHEMBL129288 | 0.71 | — | — | |
| SCHEMBL11850974 | 0.67 | MAPK1 (0.40) | — | |
| SCHEMBL1304743 | 0.65 | — | — | |
| SCHEMBL592210 | 0.65 | — | — |
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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108440570-B | Preparation method of ceftiofur ester compound or halogen salt thereof | 济宁市化工研究院 | 2020-12-04 | — | — | CN | claimed |
| CN-111249292-A | Antibacterial pharmaceutical composition and preparation method and application thereof | 黑龙江中医药大学 | 2020-06-09 | — | — | CN | claimed |
| CN-108440570-A | A kind of Ceftiofur ester type compound or its haloid and its preparation method and application | 济宁市化工研究院 | 2018-08-24 | — | — | CN | claimed |
| CN-111249292-B | Antibacterial pharmaceutical composition and preparation method and application thereof | 黑龙江中医药大学 | 2021-09-21 | — | — | CN | disclosed |
| CN-213644106-U | A crystallization reaction equipment for production of roxithromycin | 孙慧 | 2021-07-09 | — | — | CN | disclosed |
| CN-108440570-B | Preparation method of ceftiofur ester compound or halogen salt thereof | 济宁市化工研究院 | 2020-12-04 | — | — | CN | disclosed |
| CN-108440570-B | Preparation method of ceftiofur ester compound or halogen salt thereof | 济宁市化工研究院 | 2020-12-04 | — | — | CN | disclosed |
| CN-111249292-A | Antibacterial pharmaceutical composition and preparation method and application thereof | 黑龙江中医药大学 | 2020-06-09 | — | — | CN | disclosed |
| CN-108440570-A | A kind of Ceftiofur ester type compound or its haloid and its preparation method and application | 济宁市化工研究院 | 2018-08-24 | — | — | CN | disclosed |
| CN-108440570-A | A kind of Ceftiofur ester type compound or its haloid and its preparation method and application | 济宁市化工研究院 | 2018-08-24 | — | — | CN | disclosed |
| CN-102686632-A | Process for manufacturing a product derived from epichlorohydrin | SOLVAY | 2012-09-19 | — | — | CN | disclosed |
| WO-2011054769-A2 | PROCESS FOR MANUFACTURING A PRODUCT DERIVED FROM EPICHLOROHYDRIN | SOLVAY SA (BE) | 2011-05-12 | — | — | WO | disclosed |
| US-5741438-A | Optically active biphenyl derivative, process for preparation thereof, liquid crystal composition containing the same as an effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1998-04-21 | — | — | US | disclosed |
| US-5422038-A | Ferroelectric liquid crystal material with sufficient spontaneous polarization, high speed response capability, wide temperature range | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-06-06 | — | — | US | disclosed |
| EP-0416946-B1 | Optically active naphthalene derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL CO (JP) | 1994-11-09 | — | — | EP | disclosed |
| EP-0395390-B1 | Optically active biphenyl derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL CO (JP) | 1994-09-28 | — | — | EP | disclosed |
| US-5238598-A | Having trifluoromethyl group; high speed response | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-08-24 | — | — | US | disclosed |
| EP-0434297-A2 | Optically active aromatic compounds, preparation process thereof, and liquid crystal compositions and elements | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-06-26 | — | — | EP | disclosed |
| EP-0416946-A2 | Optically active naphthalene derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1991-03-13 | — | — | EP | disclosed |
| EP-0395390-A1 | Optically active biphenyl derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-10-31 | — | — | EP | disclosed |