SCHEMBL21571376

SCHEMBL21571376

FC(OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)I)=C(F)C(F)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)I

nearest known ligand 0.00

⚠ 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.

Compoundsimilaritytop predictedshared targets
SCHEMBL16792448 0.82
SCHEMBL443402 0.81
SCHEMBL9800681 0.79
SCHEMBL4113076 0.78
SCHEMBL16792446 0.76
SCHEMBL677666 0.75
SCHEMBL17065484 0.72
SCHEMBL5794184 0.71
SCHEMBL160134 0.71
SCHEMBL11229856 0.70

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022259087-A1 METHOD OF MAKING A FLUOROPOLYMER DISPERSION HAVING A LOW AMOUNT OF PERFLUOROALKANOIC ACIDS OR SALTS THEREOF AND THE FLUOROPOLYMER COMPRISES A LOW IONIC END GROUP RATIO 3M INNOVATIVE PROPERTIES COMPANY (US) 2022-12-15 WO claimed
US-20220372193-A1 A Method of Functionalizing Fluorinated Polymers, a Functionalized Fluorinated Polymer and Coating Compositions Thereof 3M INNOVATIVE PROPERTIES COMPANY 2022-11-24 US disclosed
US-11267922-B2 Fluorinated block copolymers derived from nitrile cure-site monomers 3M INNOVATIVE PROPERTIES COMPANY (US) 2022-03-08 US disclosed
US-20190352444-A1 FLUORINATED BLOCK COPOLYMERS DERIVED FROM NITRILE CURE-SITE MONOMERS 3M INNOVATIVE PROPERTIES COMPANY 2019-11-21 US disclosed