SCHEMBL9165684

SCHEMBL9165684

CC(N)O.[SnH4]

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
SCHEMBL13208844 0.94 — —
SCHEMBL15047 0.94 — —
SCHEMBL8227653 0.94 — —
Hydrogen Sulfide SCHEMBL10900824 0.89 — —
Fluoride SCHEMBL922905 0.89 — —
Bromide SCHEMBL478157 0.89 — —
Hydrochloric Acid SCHEMBL96757 0.89 — —
Methyl Alcohol SCHEMBL18438701 0.89 — —
SCHEMBL2567762 0.89 — —
SCHEMBL413098 0.89 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0448413-B1 Selective 6-acylation of sucrose mediated by cyclic adducts of dialkyltin oxides and diols NORAMCO INC (US) 1995-05-17 — — EP disclosed
US-5089608-A Preparing cyclic adduct by reacting a di(hydrocarbyl)tin oxide with a dihydric alcohol, alkanolamine, or an enolizable alpha-hydroxy ketone MCNEIL-PPC, INC. (US) 1992-02-18 — — US disclosed
EP-0448413-A1 Selective 6-acylation of sucrose mediated by cyclic adducts of dialkyltin oxides and diols NORAMCO, INC. (US) 1991-09-25 — — EP disclosed
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