Compounds similar to this structure
CC(=O)[C@@]12O[C@@H]1C[C@H]1[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@@]12CEdit in Covalent
93 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Hydroxyprogesterone caproate630-56-833 % similar
Cholesteryl bromide516-91-632 % similar
Cholesteryl chloride910-31-632 % similar
Epiandrosterone481-29-832 % similar
Androsterone53-41-832 % similar
Etiocholanolone53-42-932 % similar
Cholesteryl heptanoate1182-07-632 % similar
Cholesteryl caprylate1182-42-932 % similar
Cholesteryl nonanoate1182-66-732 % similar
Cholesteryl decanoate1183-04-632 % similar
Cholesteryl stearate1184-05-032 % similar
Cholesteryl laurate1908-11-832 % similar
Cholesteryl myristate1989-52-232 % similar
Cholesteryl stearate35602-69-832 % similar
Ruscogenin472-11-732 % similar
Cholesteryl palmitate601-34-332 % similar
Cholesteryl behenate61510-09-632 % similar
21-(Acetyloxy)-17-hydroxypregn-4-ene-3,20-dione640-87-932 % similar
Medroxyprogesterone acetate71-58-932 % similar
Methyltestosterone58-18-432 % similar
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