Compounds similar to this structure
O=C[C@H](O)[C@@H](O)[C@H](O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)COEdit in Covalent
200 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Chitobiose577-76-459 % similar
Neoagarobiose484-58-257 % similar
Chitotriose41708-93-456 % similar
Lactulose4618-18-255 % similar
D-Arabinose10323-20-354 % similar
D-Lyxose1114-34-754 % similar
Arabinose147-81-954 % similar
Lyxose1949-78-654 % similar
Arabinose20235-19-254 % similar
L-Ribose24259-59-454 % similar
DL-Xylose25990-60-754 % similar
Sodium lactobionate27297-39-854 % similar
DL-Xylose41247-05-654 % similar
Ribose50-69-154 % similar
L-Arabinose5328-37-054 % similar
Xylose58-86-654 % similar
L-Xylose609-06-354 % similar
Trehalose99-20-753 % similar
L-Mannose10030-80-553 % similar
L-Galactose15572-79-953 % similar
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