Compounds similar to this structure
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(c4cccnc4)=CC[C@@H]32)C1Edit in Covalent
63 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Cholesteryl butyrate521-13-138 % similar
Cholesterol ethyl carbonate23836-43-338 % similar
Cholesteryl valerate7726-03-638 % similar
Cholesteryl caproate1062-96-038 % similar
Cholesteryl 2,4-dichlorobenzoate32832-01-237 % similar
Cholesteryl heptanoate1182-07-637 % similar
Cholesteryl caprylate1182-42-937 % similar
Cholesteryl nonanoate1182-66-737 % similar
Cholesteryl decanoate1183-04-637 % similar
Cholesteryl stearate1184-05-037 % similar
Cholesteryl hemisuccinate1510-21-037 % similar
Cholesteryl laurate1908-11-837 % similar
Cholesteryl myristate1989-52-237 % similar
Cholesteryl stearate35602-69-837 % similar
Cholesteryl palmitate601-34-337 % similar
Cholesteryl behenate61510-09-637 % similar
17-Iodoandrosta-5,16-dien-3beta-ol32138-69-537 % similar
Dehydroepiandrosterone53-43-037 % similar
17-Hydroxypregnenolone387-79-137 % similar
Ester4351-55-736 % similar
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