⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL379845 | 1.00 | — | — | |
| SCHEMBL33549 | 1.00 | — | — | |
| SCHEMBL9386322 | 1.00 | — | — | |
| SCHEMBL379844 | 1.00 | — | — | |
| SCHEMBL812021 | 1.00 | — | — | |
| SCHEMBL13894718 | 0.95 | CA1 (0.53) | — | |
| SCHEMBL560334 | 0.95 | CA1 (0.53) | — | |
| SCHEMBL3339811 | 0.95 | — | — | |
| SCHEMBL594309 | 0.95 | CA1 (0.53) | — | |
| SCHEMBL3339455 | 0.95 | CA1 (0.53) | — |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108440251-B | Method for photo/nickel concerted catalysis of monoarylation diol | 陕西师范大学 | 2021-01-01 | — | — | CN | disclosed |
| EP-3468945-A1 | DISCRIMINATION OF CIS- AND TRANS-1, 3-DIAMINOCYCLOHEXANES | BASF SE (DE) | 2019-04-17 | — | — | EP | disclosed |
| CN-108440251-A | A kind of method of light/nickel concerted catalysis list arylation glycol | 陕西师范大学 | 2018-08-24 | — | — | CN | disclosed |
| EP-3286261-A1 | POROUS CYCLODEXTRIN POLYMERIC MATERIALS AND METHODS OF MAKING AND USING SAME | Cornell University (US) | 2018-02-28 | — | — | EP | disclosed |
| EP-3176154-A1 | BENZAMIDES AND NICOTINAMIDES AS SYK MODULATORS | Portola Pharmaceuticals, Inc. (US) | 2017-06-07 | — | — | EP | disclosed |
| WO-2016172118-A1 | POROUS CYCLODEXTRIN POLYMERIC MATERIALS AND METHODS OF MAKING AND USING SAME | CORNELL UNIVERSITY (US) | 2016-10-27 | — | — | WO | disclosed |
| EP-3016942-A1 | FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES | DSM IP Assets B.V. (NL) | 2016-05-11 | — | — | EP | disclosed |
| EP-3016939-A1 | FORMATION OF CHIRAL 4-CHROMANONES USING CHIRAL PYRROLIDINES IN THE PRESENCE OF ACIDS | DSM IP Assets B.V. (NL) | 2016-05-11 | — | — | EP | disclosed |
| EP-3004115-A1 | OPIOID KETAL COMPOUNDS AND USES THEREOF | Rhodes Technologies (US) | 2016-04-13 | — | — | EP | disclosed |
| US-20160068630-A1 | Process for Preparing Polycarbonates by Polymerization of Five-Membered-Ring Cyclic Carbonates | TOTAL RESEARCH & TECHNOLOGY FELUY (BE) | 2016-03-10 | — | — | US | disclosed |
| US-20100247439-A1 | DENDRITIC NANO-ANTIOXIDANTS | NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT | 2010-09-30 | — | — | US | disclosed |
| EP-1133357-B1 | POLYMER-SUPPORTED PHOSPHORUS LIGANDS FOR CATALYSIS | DU PONT (US) | 2009-04-15 | — | — | EP | disclosed |
| US-7238841-B2 | Polymer-supported phosphorus ligands for catalysts | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2007-07-03 | — | — | US | disclosed |
| US-20070099983-A1 | Aminocyclohexyl ether compounds and uses thereof | CARDIOME PHARMA CORP. (CA) | 2007-05-03 | — | — | US | disclosed |
| EP-1753862-A2 | METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM MESO-EPOXIDES | CSIR (ZA) | 2007-02-21 | — | — | EP | disclosed |
| EP-1604738-A2 | Process for the preparation of coumarin | E.I. du Pont de Nemours and Company (US) | 2005-12-14 | — | — | EP | disclosed |
| EP-1593432-A2 | Polymer-supported phosphorus ligands for catalysis | E.I. du Pont de Nemours and Company (US) | 2005-11-09 | — | — | EP | disclosed |
| EP-1593430-A2 | Polymer-Supported phosphorus ligands for catalysts | E.I. DU PONT DE NEMOURS & COMPANY INCORPORATED (US) | 2005-11-09 | — | — | EP | disclosed |
| WO-2005100578-A2 | METHODS FOR OBTAINING OPTICALLY ACTIVE EPOXIDES AND VICINAL DIOLS FROM MESO-EPOXIDES | CSIR (ZA) | 2005-10-27 | — | — | WO | disclosed |
| US-6630604-B1 | Phosphine and phosphine oxide ligands are prepared using polymeric supports. These compounds can be easily cleaved from the support, and along with the corresponding supported compounds, used as ligands in the preparation of novel, | E. I. DU PONT DE NEMOURS AND COMPANY | 2003-10-07 | — | — | US | disclosed |