SCHEMBL13480225

SCHEMBL13480225

CC(=O)N[C@@H]1OC(COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)C1OC(C)=O

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA12 O43570 13/20 0.67
▸ CA1 P00915 13/20 0.67
▸ CA2 P00918 13/20 0.67
▸ CA9 Q16790 13/20 0.67
▸ CA14 Q9ULX7 10/20 0.55
▸ CYP2D6 P10635 1/20 0.55
▸ THRB P10828 1/20 0.55
▸ HSD17B10 Q99714 1/20 0.55
▸ TSHR P16473 1/20 0.53
▸ NR3C1 P04150 1/20 0.53
▸ FYN P06241 1/20 0.53
▸ ADRA2A P08913 1/20 0.53
▸ ADORA3 P0DMS8 1/20 0.53
▸ ADRA2B P18089 1/20 0.53
▸ DRD4 P21917 1/20 0.53
▸ DRD3 P35462 1/20 0.53
▸ LMNA P02545 2/20 0.50
▸ KMT2A Q03164 1/20 0.50
▸ ALDH1A1 P00352 1/20 0.49
▸ POLB P06746 1/20 0.49

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL13163929 1.00 CA12 (0.67) CA12CA1CA2CA9CA14
SCHEMBL7151935 1.00 CA12 (0.67) CA12CA1CA2CA9CA14
SCHEMBL7151688 1.00 CA12 (0.67) CA12CA1CA2CA9CA14
SCHEMBL8763428 1.00 CA12 (0.67) CA12CA1CA2CA9CA14
SCHEMBL3267262 1.00 CA12 (0.67) CA12CA1CA2CA9CA14
SCHEMBL13866730 0.86 CA12 (0.68) CA12CA1CA2CA9CA14
SCHEMBL18880346 0.86 CA12 (0.68) CA12CA1CA2CA9CA14
SCHEMBL16009180 0.86 CA12 (0.64) CA12CA1CA2CA9CA14
SCHEMBL7623838 0.86 CA12 (0.61) CA12CA1CA2CA9CA14
SCHEMBL13903999 0.86 CA12 (0.61) CA12CA1CA2CA9CA14

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-7655611-B2 Structural family on non-ionic carbohydrate based surfactants (NICBS) and a novel process for their synthesis THE UNIVERSITY OF HOUSTON SYSTEM (US) 2010-02-02 — — US disclosed
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