{"doi":"10.1002/pep2.24292","title":"Issue Information","abstract":"Cyclic depsipeptides (CDPs) are attractive in drug discovery because of their various bioactivities.Hiroaki Suga and team recently developed ribosomal synthesis of CDPs, enabling the construction of a vast library for de novo discovery of bioactive CDPs.However, quantities of the CDPs synthesized by this method are insufficient for downstream biological assays.Here they report the synthesis of CDPs by chemical macrolactonization via the S-to-S-to-O acyl transfer reaction.The up to 91% conversion facilitates the de novo discovery of bioactive CDPs from artificial libraries.","journal":"Peptide Science","year":2022,"id":310242,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":0,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9578,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2022-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[],"reference_count":0,"raw_metadata":null,"created_at":"2026-07-19T00:33:19.712967Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}