B-D-Galactose

B-D-Galactose

SCHEMBL9847381

O=P(O)(O)O.O=P(O)(O)O.OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O.[NaH]

nearest known ligand 0.48

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of B-D-Galactose. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LGALS1 P09382 2/20 0.47
LGALS3 P17931 2/20 0.47
LGALS9 O00182 1/20 0.47
LGALS8 O00214 1/20 0.47
CA12 O43570 3/20 0.42
CA1 P00915 3/20 0.42
CA2 P00918 3/20 0.42
CA9 Q16790 3/20 0.42
FBP1 P09467 1/20 0.41
PYGB P11216 6/20 0.41
GAA P10253 1/20 0.41

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
D-Galactose SCHEMBL17593535 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL361799 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
Beta-D-Glucose SCHEMBL361597 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
Dextrose SCHEMBL7651668 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL361515 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL16429773 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL361340 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
D-Mannose SCHEMBL1772795 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
Dextrose SCHEMBL6038162 0.98 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
Ribose (Furanose) SCHEMBL27896040 0.96 LGALS1 (0.45) LGALS1LGALS3LGALS9LGALS8CA12

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
EP-0456948-A2 Method for the preparation of polyphosphorylated derivatives of galactopyranosides with a potential insulin-like activity EUROPHARMA, S.A. (ES) 1991-11-21 EP disclosed