Compounds similar to this structure
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H](C(C)=O)[C@@]4(C)CC[C@@H]32)C1Edit in Covalent
123 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Cholesteryl nonanoate1182-66-749 % similar
Cholesteryl decanoate1183-04-649 % similar
Cholesteryl stearate1184-05-049 % similar
Cholesteryl laurate1908-11-849 % similar
Cholesteryl myristate1989-52-249 % similar
Cholesteryl stearate35602-69-849 % similar
Cholesteryl palmitate601-34-349 % similar
Cholesteryl behenate61510-09-649 % similar
Cholesteryl phenylacetate33998-26-449 % similar
Ester4351-55-749 % similar
Methandriol dipropionate3593-85-948 % similar
Cholesteryl oleate303-43-547 % similar
Androstenediol521-17-547 % similar
3-Acetyloxypregn-16-en-20-one1169-20-646 % similar
Cholesteryl sodium sulfate2864-50-846 % similar
Cholesteryl sulfate potassium salt6614-96-646 % similar
Cholenic acid5255-17-446 % similar
3β-Acetoxy-5α-androstan-17-one1239-31-246 % similar
7-Oxodehydroepiandrosterone 3-acetate1449-61-246 % similar
Cholesteryl linolenate2545-22-445 % similar
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