⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL13856027 | 0.69 | — | — | |
| SCHEMBL20161010 | 0.68 | MAOB (0.34) | — | |
| SCHEMBL14204541 | 0.67 | — | — | |
| SCHEMBL11918093 | 0.66 | — | — | |
| SCHEMBL16132612 | 0.65 | — | — | |
| SCHEMBL762708 | 0.65 | — | — | |
| SCHEMBL10135096 | 0.65 | — | — | |
| SCHEMBL11880417 | 0.63 | — | — | |
| SCHEMBL11601128 | 0.63 | — | — | |
| SCHEMBL21086704 | 0.63 | — | — |
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 10 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1183223-B1 | PROCESS FOR THE MANUFACTURE OF FLUOROOLEFINS | DU PONT (US) | 2005-04-27 | — | — | EP | claimed |
| US-6624337-B1 | Fluorination of 1,1,2,2-tetrafluorocyclobutane in electrolytic cells, then thermocracking the perfluorocyclobutane in the presence of carbon or metals, to form chemical intermediates for fluoropolymers | E. I. DU PONT DE NEMOURS AND COMPANY | 2003-09-23 | — | — | US | claimed |
| EP-1183223-A1 | PROCESS FOR THE MANUFACTURE OF FLUOROOLEFINS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2002-03-06 | — | — | EP | claimed |
| WO-2000075092-A1 | PROCESS FOR THE MANUFACTURE OF FLUOROOLEFINS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-12-14 | — | — | WO | claimed |
| EP-1183223-B1 | PROCESS FOR THE MANUFACTURE OF FLUOROOLEFINS | DU PONT (US) | 2005-04-27 | — | — | EP | disclosed |
| US-6624337-B1 | Fluorination of 1,1,2,2-tetrafluorocyclobutane in electrolytic cells, then thermocracking the perfluorocyclobutane in the presence of carbon or metals, to form chemical intermediates for fluoropolymers | E. I. DU PONT DE NEMOURS AND COMPANY | 2003-09-23 | — | — | US | disclosed |
| EP-1183223-A1 | PROCESS FOR THE MANUFACTURE OF FLUOROOLEFINS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2002-03-06 | — | — | EP | disclosed |
| WO-2000075092-A1 | PROCESS FOR THE MANUFACTURE OF FLUOROOLEFINS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-12-14 | — | — | WO | disclosed |
| US-4086407-A | CYCLODIMERIZING HEXAFLUOROPROPYLENE AND ETHYLENE TO FORM CYCLOBUTANE DERIVATIVE, POLYMERIZATION | PHILLIPS PETROLEUM COMPANY (US) | 1978-04-25 | — | — | US | disclosed |
| US-3996299-A | CHEMICAL INTERMEDIATE FOR 2,3,3,3-TETRAFLUOROPROPYLENE | PHILLIPS PETROLEUM COMPANY (US) | 1976-12-07 | — | — | US | disclosed |