SCHEMBL12899673

SCHEMBL12899673

CC1CO[C@H](CO)[C@@H]1O

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
SCHEMBL18541686 1.00
SCHEMBL13212419 1.00
SCHEMBL12929237 1.00
SCHEMBL15594501 1.00
SCHEMBL14217586 1.00
SCHEMBL23705209 0.93 LGALS3 (0.44)
SCHEMBL13295915 0.93 LGALS3 (0.44)
SCHEMBL15966159 0.93 LGALS3 (0.44)
SCHEMBL13344935 0.93 LGALS3 (0.44)
SCHEMBL24916892 0.93 LGALS3 (0.44)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7884202-B2 Nucleobases are perfluoroalkylated in a one step process with a perfluoroalkyl halide in the presence of a sulfoxide, a peroxide and an iron compound; useful as medicinal drugs, intermediates for medicinal drugs and agricultural chemicals TOSOH CORPORATION (JP) 2011-02-08 US disclosed