Compounds similar to this structure
[N-]=[N+]=NCC(O)=N[C@@H](C=O)[C@@H](O)[C@@H](O)[C@H](O)COEdit in Covalent
62 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Arabinose147-81-939 % similar
Lyxose1949-78-639 % similar
Arabinose20235-19-239 % similar
L-Ribose24259-59-439 % similar
DL-Xylose25990-60-739 % similar
DL-Xylose41247-05-639 % similar
Ribose50-69-139 % similar
L-Arabinose5328-37-039 % similar
Xylose58-86-639 % similar
L-Xylose609-06-339 % similar
N-Acetylmuramic acid10597-89-439 % similar
Galactosamine hydrochloride1772-03-837 % similar
D-Mannosamine hydrochloride5505-63-537 % similar
Glucosamine hydrochloride66-84-237 % similar
N,N′-Diacetylchitobiose35061-50-836 % similar
Metrizamide31112-62-636 % similar
Gluconic acid526-95-435 % similar
N-Glycolylneuraminic acid1113-83-335 % similar
N-Acetylchitohexaose38854-46-535 % similar
N,N′,N′′-Triacetylchitotriose38864-21-035 % similar
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