Compounds similar to this structure
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)O)CEdit in Covalent
111 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
Ticarcillin monosodium74682-62-556 % similar
Sulbenicillin sodium28002-18-852 % similar
6-APA551-16-652 % similar
Sultamicillin tosylate83105-70-849 % similar
Cloxacillin61-72-349 % similar
Cephalexin15686-71-249 % similar
Dicloxacillin3116-76-548 % similar
Penicillin G procaine54-35-348 % similar
Azlocillin sodium37091-65-947 % similar
Cephalexin monohydrate23325-78-247 % similar
Cefaclor53994-73-346 % similar
Benzylpenicillin procaine monohydrate6130-64-946 % similar
Penicillin G potassium113-98-446 % similar
Penicillin G sodium69-57-845 % similar
Ticarcillin disodium29457-07-645 % similar
Ticillin4697-14-745 % similar
Cefaclor monohydrate70356-03-545 % similar
Flucloxacillin5250-39-545 % similar
Cloxacillin benzathine23736-58-544 % similar
Piperacillin sodium59703-84-344 % similar
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