Compounds similar to this structure
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1OEdit in Covalent
200 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Rosiridin100462-37-138 % similar
Barium ribose 5′-phosphate15673-79-738 % similar
Sodium lactobionate27297-39-837 % similar
Aucubin479-98-137 % similar
Lithospermoside63492-69-337 % similar
Arbutin497-76-737 % similar
α-Arbutin84380-01-837 % similar
D-Galactopyranose10257-28-037 % similar
β-D-Glucose492-61-537 % similar
α-D-Glucose492-62-637 % similar
β-D-Allopyranose7283-09-237 % similar
Beta-D-glucose9001-37-037 % similar
β-Galactosidase9031-11-237 % similar
Galactosamine hydrochloride1772-03-837 % similar
D-Mannosamine hydrochloride5505-63-537 % similar
Glucosamine hydrochloride66-84-237 % similar
Lactose, monohydrate10039-26-637 % similar
Alpha-Lactose monohydrate5989-81-137 % similar
α-Cyclodextrin10016-20-336 % similar
Gamma-cyclodextrin17465-86-036 % similar
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