Compounds similar to this structure
C=C1CC[C@@H]2[C@](C)(CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)CCC[C@@]2(C)[C@@H]1CCC1=CCOC1=OEdit in Covalent
57 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Neoandrographolide27215-14-1100 % similar
Deoxyandrographolide4176-97-054 % similar
Rubusoside64849-39-437 % similar
Gentiopicroside20831-76-937 % similar
14-Deoxy-11,12-dehydroandrographolide42895-58-936 % similar
Darutoside59219-65-736 % similar
Andrographolide5508-58-736 % similar
Steviolbioside41093-60-136 % similar
Stevioside57817-89-735 % similar
Rebaudioside B58543-17-235 % similar
Rebaudioside M1220616-44-335 % similar
Rebaudioside G127345-21-535 % similar
Rebaudioside A58543-16-135 % similar
Dehydroandrographolide134418-28-335 % similar
Rebaudioside D63279-13-034 % similar
Rebaudioside N1220616-46-534 % similar
Rebaudioside C63550-99-234 % similar
(-)-Sweroside14215-86-233 % similar
Ginsenoside rk2364779-14-633 % similar
Allyl α-D-glucopyranoside7464-56-433 % similar
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