⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL640791 | 1.00 | — | — | |
| SCHEMBL642477 | 1.00 | — | — | |
| SCHEMBL18074135 | 0.75 | — | — | |
| SCHEMBL18074131 | 0.75 | — | — | |
| SCHEMBL13762165 | 0.72 | — | — | |
| SCHEMBL13762169 | 0.72 | — | — | |
| SCHEMBL5028673 | 0.72 | — | — | |
| SCHEMBL12660411 | 0.69 | KDM4E (0.31) | — | |
| SCHEMBL31293584 | 0.69 | — | — | |
| SCHEMBL18911283 | 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 93 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-11865530-B2 | Process for preparing a fischer-tropsch catalyst in the presence of an additive and of a specific calcining step | IFP Energies Nouvelles (FR) | 2024-01-09 | — | — | US | claimed |
| EP-4043537-A1 | METHOD FOR PREPARING A FISCHER-TROPSCH CATALYST IN THE PRESENCE OF AN ADDITIVE AND A SPECIFIC CALCINATION STEP | IFP Energies nouvelles (FR) | 2022-08-17 | — | — | EP | claimed |
| US-20220250047-A1 | Process for preparing a Fischer-Tropsch catalyst in the presence of an additive and of a specific calcining step | IFP Energies Nouvelles (FR) | 2022-08-11 | — | — | US | claimed |
| US-11161099-B2 | Cobalt catalyst comprising a support comprising a mixed oxide phase including cobalt and/or nickel produced from an organic compound from the family of carboyxyanhydrides | IFP Energies Nouvelles (FR) | 2021-11-02 | — | — | US | claimed |
| US-20210331145-A1 | HYDROGENATION PROCESS COMPRISING A CATALYST PREPARED BY ADDITION OF AN ORGANIC COMPOUND IN THE GAS PHASE | IFP Energies Nouvelles (FR) | 2021-10-28 | — | — | US | claimed |
| US-11111442-B2 | Fischer-Tropsch synthesis process comprising a catalyst prepared by addition of an organic compound in gas phase | TOTAL RESEARCH & TECHNOLOGY FELUY (BE) | 2021-09-07 | — | — | US | claimed |
| CN-113242766-A | Hydrogenation process comprising a catalyst prepared by adding an organic compound in the gas phase | IFP 新能源公司 | 2021-08-10 | — | — | CN | claimed |
| US-20200129967-A1 | COBALT CATALYST COMPRISING A SUPPORT COMPRISING A MIXED OXIDE PHASE INCLUDING COBALT AND/OR NICKEL PRODUCED FROM AN ORGANIC COMPOUND FROM THE FAMILY OF CARBOYXYANHYDRIDES | IFP Energies Nouvelles (FR) | 2020-04-30 | — | — | US | claimed |
| US-20200131441-A1 | FISCHER-TROPSCH SYNTHESIS PROCESS COMPRISING A CATALYST PREPARED BY ADDITION OF AN ORGANIC COMPOUND IN GAS PHASE | IFP Energies Nouvelles (FR) | 2020-04-30 | — | — | US | claimed |
| EP-1913002-B9 | METHOD OF ACYLATING MAYTANSINOL WITH CHIRAL AMINO ACIDS | MILLENNIUM PHARM INC (US) | 2012-04-25 | — | — | EP | claimed |
| EP-1913002-B1 | METHOD OF ACYLATING MAYTANSINOL WITH CHIRAL AMINO ACIDS | MILLENNIUM PHARM INC (US) | 2011-11-30 | — | — | EP | claimed |
| US-7598375-B2 | Method of acylating maytansinol with chiral amino acids | MILLENIUM PHARMACEUTICALS, INC. (US) | 2009-10-06 | — | — | US | claimed |
| EP-1913002-A2 | METHOD OF ACYLATING MAYTANSINOL WITH CHIRAL AMINO ACIDS | MILLENNIUM PHARMACEUTICALS, INC. (US) | 2008-04-23 | — | — | EP | claimed |
| WO-2007021674-A2 | METHOD OF ACYLATING MAYTANSINOL WITH CHIRAL AMINO ACIDS | MILLENNIUM PHARMACEUTICALS, INC. (US) | 2007-02-22 | — | — | WO | claimed |
| US-20070037972-A1 | For making maytansinoids with chiral amino acid side chains; maytansinoids may be conjugated to cell-binding agents such as antibodies and are useful therapeutics, especially for treatment of cancer; high yielding methods that avoid or reduce epimerization in coupling of side chain linker | MILLENNIUM PHARMACEUTICALS, INC. | 2007-02-15 | — | — | US | claimed |
| EP-4685150-A1 | METHOD FOR PRODUCING AMIDE GROUP-CONTAINING COMPOUND USING N-CARBOXYAMINO ACID ANHYDRIDE | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2026-01-28 | — | — | EP | disclosed |
| EP-4678240-A2 | BRIDGE LINKERS FOR CONJUGATION OF CELL-BINDING MOLECULES | Hangzhou Dac Biotech Co., Ltd. (CN) | 2026-01-14 | — | — | EP | disclosed |
| EP-1341034-A1 | Silver halide color photographic light-sensitive material | FUJI PHOTO FILM CO., LTD. (JP) | 2003-09-03 | — | — | EP | disclosed |
| US-20020058819-A1 | METHOD OF PRODUCING 2,4-OXAZOLIDINEDIONES AND METAL SALTS THEREOF | SUMITOMO CHEMICAL COMPANY, LIMITED | 2002-05-16 | — | — | US | disclosed |
| WO-2002014292-A1 | METHOD FOR PRODUCING 5, 5-DIMETHYLOXAZOLIDINE-2, 4-DIONE | SHOWA DENKO K.K. (JP) | 2002-02-21 | — | — | WO | disclosed |