⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL5845578 | 0.70 | — | — | |
| SCHEMBL9580258 | 0.69 | — | — | |
| SCHEMBL702562 | 0.67 | — | — | |
| SCHEMBL3257468 | 0.65 | — | — | |
| SCHEMBL3370693 | 0.63 | — | — | |
| SCHEMBL13661891 | 0.55 | — | — | |
| SCHEMBL1738884 | 0.55 | — | — | |
| SCHEMBL442819 | 0.55 | — | — | |
| SCHEMBL11913224 | 0.53 | — | — | |
| SCHEMBL4594727 | 0.53 | TSHR (0.37) | — |
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 50 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3643401-A1 | COBALT CATALYST COMPRISING A SUPPORT WITH A MIXED OXIDE PHASE CONTAINING COBALT AND/OR NICKEL PREPARED FROM A DILACTONE COMPOUND | IFP Energies nouvelles (FR) | 2020-04-29 | — | — | EP | claimed |
| CN-1960982-A | Method for producing 1,3-dioxolan-4,6-dione compound | FUJI PHOTO FILM CO LTD (JP) | 2007-05-09 | — | — | CN | claimed |
| EP-3643401-B1 | COBALT CATALYST COMPRISING A SUPPORT WITH A MIXED OXIDE PHASE CONTAINING COBALT AND/OR NICKEL PREPARED FROM A DILACTONE COMPOUND | IFP ENERGIES NOW (FR) | 2023-03-15 | — | — | EP | disclosed |
| US-11235312-B2 | Cobalt catalyst comprising a support comprising a mixed oxide phase including cobalt and/or nickel produced from a dilactone compound | IFP Energies Nouvelles (FR) | 2022-02-01 | — | — | US | disclosed |
| CN-113557238-A | Lithium borate compound, additive for lithium secondary battery, nonaqueous electrolyte for lithium secondary battery, lithium secondary battery precursor, and method for producing lithium secondary battery | 三井化学株式会社 | 2021-10-26 | — | — | CN | disclosed |
| CN-112004928-A | Oligonucleotide compositions and methods of use thereof | 波涛生命科学有限公司 | 2020-11-27 | — | — | CN | disclosed |
| CN-104661664-B | Chiral control | 波涛生命科学有限公司 | 2020-07-03 | — | — | CN | disclosed |
| CN-111372942-A | β -catenin function modulating agents and methods thereof | 弗格制药有限公司 | 2020-07-03 | — | — | CN | disclosed |
| US-20200129966-A1 | COBALT CATALYST COMPRISING A SUPPORT COMPRISING A MIXED OXIDE PHASE INCLUDING COBALT AND/OR NICKEL PRODUCED FROM A DILACTONE COMPOUND | IFP Energies Nouvelles (FR) | 2020-04-30 | — | — | US | disclosed |
| EP-3643401-A1 | COBALT CATALYST COMPRISING A SUPPORT WITH A MIXED OXIDE PHASE CONTAINING COBALT AND/OR NICKEL PREPARED FROM A DILACTONE COMPOUND | IFP Energies nouvelles (FR) | 2020-04-29 | — | — | EP | disclosed |
| US-20150361063-A1 | TREATMENT OF AMYLOIDOSIS BY COMPOUNDS THAT REGULATE RETROMER STABILIZATION | THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK | 2015-12-17 | — | — | US | disclosed |
| WO-2002010096-A1 | KINETIC RESOLUTIONS OF CHIRAL 2- AND 3-SUBSTITUTED CARBOXYLIC ACIDS | BRANDEIS UNIVERSITY (US) | 2002-02-07 | — | — | WO | disclosed |
| US-6331570-B1 | PREVENTION OF SPONTANEOUS SQUAMOUS CELL CARCINOMA IN IMMUNOCOMPROMISED HUMAN TRANSPLANT PATIENTS | BRISTOL-MYERS SQUIBB COMPANY | 2001-12-18 | — | — | US | disclosed |
| EP-1115395-A1 | ACTIVE ENANTIOMER OF RARgamma-SPECIFIC AGONIST | BRISTOL-MYERS SQUIBB COMPANY (US) | 2001-07-18 | — | — | EP | disclosed |
| US-6200997-B1 | CYCLIZATION TO GIVE OXAZOLIDINEDIONES AND TRIAZOLIDINEDIONES | BASF AKTIENGESELLSCHAFT (DE) | 2001-03-13 | — | — | US | disclosed |
| WO-2000016769-A1 | ACTIVE ENANTIOMER OF RARη-SPECIFIC AGONIST | BRISTOL-MYERS SQUIBB COMPANY (US) | 2000-03-30 | — | — | WO | disclosed |
| WO-1998029396-A1 | HETEROCYCLIC AROMATIC ANION SALTS, AND THEIR USES AS IONIC CONDUCTING MATERIALS | HYDRO-QUEBEC (CA) | 1998-07-09 | — | — | WO | disclosed |
| EP-0219070-B1 | A PROCESS FOR PREPARING N-GLYCOLYLNEURAMINIC ACID DERIVATIVES | MECT CORPORATION (JP) | 1989-06-21 | — | — | EP | disclosed |
| US-4774326-A | ANTITUMOR ANTIGENS, AMIDATION WITH GLYCOLIC ACID | MECT CORPORATION (JP) | 1988-09-27 | — | — | US | disclosed |
| EP-0219070-A2 | A process for preparing N-glycolylneuraminic acid derivatives | MECT CORPORATION (JP) | 1987-04-22 | — | — | EP | disclosed |