SCHEMBL12899516

SCHEMBL12899516

CC1O[C@H](CO)[C@H](C)C1F

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
SCHEMBL25966083 1.00 — —
SCHEMBL13941424 1.00 — —
SCHEMBL13941423 0.81 — —
SCHEMBL15962116 0.79 OGA (0.41) —
SCHEMBL21738820 0.79 OGA (0.41) —
SCHEMBL12899657 0.79 OGA (0.41) —
SCHEMBL12150224 0.79 OGA (0.41) —
SCHEMBL14732693 0.79 OGA (0.41) —
SCHEMBL16708418 0.79 OGA (0.41) —
SCHEMBL7603749 0.79 OGA (0.41) —

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
Send feedback