⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL7205584 | 0.82 | — | — | |
| SCHEMBL1991784 | 0.82 | — | — | |
| SCHEMBL7205228 | 0.75 | — | — | |
| SCHEMBL652993 | 0.75 | — | — | |
| SCHEMBL1991255 | 0.75 | — | — | |
| SCHEMBL4729870 | 0.75 | — | — | |
| SCHEMBL9292281 | 0.72 | — | — | |
| SCHEMBL8780340 | 0.72 | — | — | |
| SCHEMBL17518173 | 0.69 | — | — | |
| SCHEMBL2454904 | 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 12 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-2002539096-A | — | — | 2002-11-19 | — | — | JP | claimed |
| EP-1159239-A1 | METHOD OF PRODUCING FLUORINATED COMPOUNDS | AlliedSignal Inc. (US) | 2001-12-05 | — | — | EP | claimed |
| US-6203671-B1 | REACTING A MOLAR EXCESS OF AN ALIPHATIC STARTING COMPOUND IN LIQUID PHASE WITH FLUORINE IN PRESENCE OF ULTRAVIOLET RADIATION TO PRODUCE PRODUCT MIXTURE CONTAINING FLUORINATED PRODUCT HAVING HYDROGEN ATOM; RECOVERING PRODUCT | ALLIEDSIGNAL INC. | 2001-03-20 | — | — | US | claimed |
| WO-2000053549-A1 | METHOD OF PRODUCING FLUORINATED COMPOUNDS | ALLIEDSIGNAL INC. (US) | 2000-09-14 | — | — | WO | claimed |
| EP-0892771-B1 | PROCESS FOR THE MANUFACTURE OF HALOGENATED PROPANES CONTAINING END-CARBON FLUORINE | DU PONT (US) | 2003-06-25 | — | — | EP | disclosed |
| EP-1159239-A1 | METHOD OF PRODUCING FLUORINATED COMPOUNDS | AlliedSignal Inc. (US) | 2001-12-05 | — | — | EP | disclosed |
| US-6203671-B1 | REACTING A MOLAR EXCESS OF AN ALIPHATIC STARTING COMPOUND IN LIQUID PHASE WITH FLUORINE IN PRESENCE OF ULTRAVIOLET RADIATION TO PRODUCE PRODUCT MIXTURE CONTAINING FLUORINATED PRODUCT HAVING HYDROGEN ATOM; RECOVERING PRODUCT | ALLIEDSIGNAL INC. | 2001-03-20 | — | — | US | disclosed |
| WO-2000053549-A1 | METHOD OF PRODUCING FLUORINATED COMPOUNDS | ALLIEDSIGNAL INC. (US) | 2000-09-14 | — | — | WO | disclosed |
| US-6066769-A | PRE-FLUORINATING A CHLORINATED PROPANE COMPOUND OF GIVEN FORMULA IN A FIRST STEP AND COMPLETING THE FLUORINATION IN A SECOND, VAPOR PHASE STEP | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-05-23 | — | — | US | disclosed |
| EP-0388140-B1 | A PROCESS FOR PREPARING ADSORPTIVE POROUS RESIN BEADS | THE DOW CHEMICAL COMPANY (US) | 1993-04-14 | — | — | EP | disclosed |
| US-5079274-A | Haloalkylation of crosslinked beads, purification and post-crosslinking | THE DOW CHEMICAL COMPANY (US) | 1992-01-07 | — | — | US | disclosed |
| EP-0388140-A1 | A process for preparing adsorptive porous resin beads | THE DOW CHEMICAL COMPANY (US) | 1990-09-19 | — | — | EP | disclosed |