SCHEMBL13646602

SCHEMBL13646602

CO[C@@H]1OC(CO[C@H]2OC(CO)[C@H](O)[C@H](O)C2O)[C@@H](O[C@@H]2OC(CO)[C@@H](OC)[C@H](O)C2O)[C@H](O)C1O

nearest known ligand 0.55

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ LGALS3 P17931 2/20 0.55
▸ LGALS8 O00214 1/20 0.55
▸ LGALS4 P56470 1/20 0.55
▸ ENGASE Q8NFI3 1/20 0.52
▸ AMY2A P04746 3/20 0.49
▸ CD209 Q9NNX6 2/20 0.49
▸ FGF1 P05230 1/20 0.48
▸ LGALS9 O00182 1/20 0.47
▸ LGALS1 P09382 1/20 0.47
▸ LGALS7; LGALS7B P47929 1/20 0.47
▸ GAA P10253 1/20 0.47
▸ MEN1 O00255 1/20 0.44
▸ KMT2A Q03164 1/20 0.44
▸ AMY1A P0DUB6 1/20 0.44

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
SCHEMBL19959375 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL19618053 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL19542759 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL12709335 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL20225006 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL13251421 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL12381500 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL16626033 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL12767553 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A
SCHEMBL19958924 1.00 LGALS3 (0.55) LGALS3LGALS8LGALS4ENGASEAMY2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7598372-B2 using a highly inexpensive natural polysaccharide having a mannose beta -1,4-bond as the starting material, a beta -1,4-glycoside bond of mannose is formed; preparing trisaccharide moiety of the reducing terminal utilizing galactomannan, guar gum and/or mannan derivatives SHIONOGI & CO., LTD. (JP) 2009-10-06 — — US disclosed
US-20070166783-A1 Synthesis of core sugar chain structure of aspargine-linked glycoprotein NISHIMURA, SHIN-ICHIRO (JP) 2007-07-19 — — US disclosed
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