{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,12,12]],"date-time":"2024-12-12T00:40:13Z","timestamp":1733964013964,"version":"3.30.2"},"reference-count":31,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Bioorganic & Medicinal Chemistry Letters"],"published-print":{"date-parts":[[2025,2]]},"DOI":"10.1016\/j.bmcl.2024.130040","type":"journal-article","created":{"date-parts":[[2024,11,24]],"date-time":"2024-11-24T02:17:32Z","timestamp":1732414652000},"page":"130040","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"special_numbering":"C","title":["Synthesis of drimanyl indole fragments of drimentine alkaloids and their antibacterial activities"],"prefix":"10.1016","volume":"116","author":[{"given":"Jili","family":"Feng","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nini","family":"Qu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Summia","family":"Kalsoom","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zunjun","family":"Zhou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shiyi","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhe","family":"Cui","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chongmin","family":"Zhong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Miaofeng","family":"Ma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.bmcl.2024.130040_b0005","unstructured":"Lacey E, Power M, Wu Z, Rickards RW. Terpenylated diketopiperazines, (Drimentines). WIPO patent, WO 98009968 A1; 1998."},{"key":"10.1016\/j.bmcl.2024.130040_b0010","doi-asserted-by":"crossref","first-page":"3438","DOI":"10.1021\/ol301396h","article-title":"Hybrid isoprenoids from a reeds rhizosphere soil derived actinomycete Streptomyces sp. CHQ-64","volume":"14","author":"Che","year":"2012","journal-title":"Org Lett"},{"key":"10.1016\/j.bmcl.2024.130040_b0015","doi-asserted-by":"crossref","first-page":"759","DOI":"10.1021\/np3008864","article-title":"Polycyclic hybrid isoprenoids from a reed rhizosphere soil derived Streptomyces sp. CHQ-64","volume":"76","author":"Che","year":"2013","journal-title":"J Nat Prod"},{"key":"10.1016\/j.bmcl.2024.130040_b0020","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1038\/ja.2015.133","article-title":"Structure and absolute configuration of drimentine I, an alkaloid from Streptomyces sp. CHQ-64","volume":"69","author":"Che","year":"2016","journal-title":"J Antibiot"},{"key":"10.1016\/j.bmcl.2024.130040_b0025","doi-asserted-by":"crossref","first-page":"26569","DOI":"10.1021\/jacs.3c06088","article-title":"Total synthesis of four classes of Daphniphyllum alkaloids","volume":"145","author":"Zhang","year":"2023","journal-title":"J Am Chem Soc"},{"key":"10.1016\/j.bmcl.2024.130040_b0030","doi-asserted-by":"crossref","first-page":"6053","DOI":"10.1002\/anie.201901086","article-title":"Total syntheses of echitamine, akuammiline, rhazicine, and pseudoakuammigine","volume":"58","author":"Zhang","year":"2019","journal-title":"Angew Chem Int Ed"},{"key":"10.1016\/j.bmcl.2024.130040_b0035","doi-asserted-by":"crossref","first-page":"15555","DOI":"10.1021\/jacs.6b10880","article-title":"Total syntheses of aflavazole and 14-hydroxyaflavinine","volume":"138","author":"Li","year":"2016","journal-title":"J Am Chem Soc"},{"key":"10.1016\/j.bmcl.2024.130040_b0040","doi-asserted-by":"crossref","first-page":"2851","DOI":"10.1002\/anie.201510568","article-title":"Total synthesis of ileabethoxazole, pseudopteroxazole, and seco-pseudopteroxazole","volume":"55","author":"Yang","year":"2016","journal-title":"Angew Chem Int Ed"},{"key":"10.1016\/j.bmcl.2024.130040_b0045","doi-asserted-by":"crossref","first-page":"3982","DOI":"10.1021\/jacs.6b00764","article-title":"Asymmetric total syntheses of aspidodasycarpine, lonicerine, and the proposed structure of lanciferine","volume":"138","author":"Li","year":"2016","journal-title":"J Am Chem Soc"},{"key":"10.1016\/j.bmcl.2024.130040_b0050","doi-asserted-by":"crossref","first-page":"6096","DOI":"10.1038\/ncomms7096","article-title":"Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families","volume":"6","author":"Meng","year":"2015","journal-title":"Nat Commun"},{"key":"10.1016\/j.bmcl.2024.130040_b0055","doi-asserted-by":"crossref","first-page":"13764","DOI":"10.1021\/jacs.5b09198","article-title":"Total synthesis of epoxyeujindole A","volume":"137","author":"Lu","year":"2015","journal-title":"J Am Chem Soc"},{"key":"10.1016\/j.bmcl.2024.130040_b0060","doi-asserted-by":"crossref","first-page":"6878","DOI":"10.1002\/anie.201501021","article-title":"Asymmetric total synthesis of mycoleptodiscin A","volume":"54","author":"Zhou","year":"2015","journal-title":"Angew Chem Int Ed"},{"key":"10.1016\/j.bmcl.2024.130040_b0065","doi-asserted-by":"crossref","first-page":"9201","DOI":"10.1002\/anie.201303334","article-title":"Total synthesis of indotertine A and drimentines A, F, and G","volume":"52","author":"Sun","year":"2013","journal-title":"Angew Chem Int Ed"},{"key":"10.1016\/j.bmcl.2024.130040_b0070","doi-asserted-by":"crossref","first-page":"2448","DOI":"10.1002\/ejoc.202000158","article-title":"Studies towards the total synthesis of drimentine C. Preparation of the AB and CDEF ring fragments","author":"Pound","year":"2020","journal-title":"Eur J Org Chem"},{"key":"10.1016\/j.bmcl.2024.130040_b0075","doi-asserted-by":"crossref","first-page":"4091","DOI":"10.1038\/s41467-018-06411-x","article-title":"Genome mining of cyclodipeptide synthases unravels unusual tRNA-dependent diketopiperazine-terpene biosynthetic machinery","volume":"9","author":"Yao","year":"2018","journal-title":"Nat Commun"},{"key":"10.1016\/j.bmcl.2024.130040_b0080","doi-asserted-by":"crossref","first-page":"101323","DOI":"10.1016\/j.isci.2020.101323","article-title":"Expanding the structural diversity of drimentines by exploring the promiscuity of two N-methyltransferases","volume":"23","author":"Yao","year":"2020","journal-title":"iScience"},{"key":"10.1016\/j.bmcl.2024.130040_b0085","doi-asserted-by":"crossref","first-page":"133213","DOI":"10.1016\/j.tet.2022.133213","article-title":"Characterization of the cyclodipeptide synthase gene cluster in Streptomyces sp. NRRL F-5123 by unraveling the biosynthesis of drimentine B","volume":"131","author":"Jiang","year":"2023","journal-title":"Tetrahedron"},{"key":"10.1016\/j.bmcl.2024.130040_b0090","doi-asserted-by":"crossref","first-page":"155049","DOI":"10.1016\/j.tetlet.2024.155049","article-title":"An efficient and concise method to 2-methylmycoleptodiscin A from (\u2013)-sclareol","volume":"141","author":"Feng","year":"2024","journal-title":"Tetrahedron Lett"},{"key":"10.1016\/j.bmcl.2024.130040_b0095","doi-asserted-by":"crossref","first-page":"1509","DOI":"10.1039\/c3np70067d","article-title":"Sesquiterpenyl indoles","volume":"30","author":"Marcos","year":"2013","journal-title":"Nat Prod Rep"},{"key":"10.1016\/j.bmcl.2024.130040_b0100","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1021\/np9604893","article-title":"Natural products in drug discovery and development","volume":"60","author":"Cragg","year":"1997","journal-title":"J Nat Prod"},{"key":"10.1016\/j.bmcl.2024.130040_b0105","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1021\/cc000097l","article-title":"Scaffold architecture and pharmacophoric properties of natural products and trade drugs: application in the design of natural","volume":"3","author":"Lee","year":"2001","journal-title":"J Comb Chem"},{"key":"10.1016\/j.bmcl.2024.130040_b0110","doi-asserted-by":"crossref","first-page":"6392","DOI":"10.1021\/acs.orglett.6b03292","article-title":"Biomimetic enantioselective total synthesis of (\u2212)-Mycoleptodiscin A","volume":"18","author":"Dethe","year":"2016","journal-title":"Org Lett"},{"key":"10.1016\/j.bmcl.2024.130040_b0115","doi-asserted-by":"crossref","first-page":"2684","DOI":"10.1021\/acs.orglett.6b01145","article-title":"Expanding diversity without protecting groups: (+)-sclareolide to indolosesquiterpene alkaloid Mycoleptodiscin A and analogues","volume":"18","author":"Nagaraju","year":"2016","journal-title":"Org Lett"},{"key":"10.1016\/j.bmcl.2024.130040_b0120","doi-asserted-by":"crossref","first-page":"4826","DOI":"10.1021\/jo070527v","article-title":"Synthesis of chinensines A-E","volume":"72","author":"Margaros","year":"2007","journal-title":"J Org Chem"},{"key":"10.1016\/j.bmcl.2024.130040_b0125","doi-asserted-by":"crossref","first-page":"2736","DOI":"10.1016\/j.bmc.2007.01.031","article-title":"Synthesis of DL-standishinal and its related compounds for the studies on structure\u2013activity relationship of inhibitory activity against aromatase","volume":"15","author":"Katoh","year":"2007","journal-title":"Bioorgan Med Chem"},{"key":"10.1016\/j.bmcl.2024.130040_b0130","first-page":"892","article-title":"Synthesis and biological evaluation of hexahydropyrrolo[2,3-b]indole derivatives as fungicides against phytopathogenic fungi","volume":"18","author":"Feng","year":"2015","journal-title":"Comb Chem High Trans Scr"},{"key":"10.1016\/j.bmcl.2024.130040_b0135","doi-asserted-by":"crossref","first-page":"11864","DOI":"10.1039\/C9CC05652A","article-title":"Switchable regioselection of C\u2013H thiolation of indoles using different TMS counterions","volume":"55","author":"Ji","year":"2019","journal-title":"Chem Commun"},{"key":"10.1016\/j.bmcl.2024.130040_b0140","doi-asserted-by":"crossref","first-page":"13872","DOI":"10.1002\/anie.201707309","article-title":"Transition-metal-free ring-opening silylation of indoles and benzofurans with (diphenyl-tert-butylsilyl)lithium","volume":"56","author":"Xu","year":"2017","journal-title":"Angew Chem Int Ed"},{"key":"10.1016\/j.bmcl.2024.130040_b0145","doi-asserted-by":"crossref","DOI":"10.1093\/hr\/uhad053","article-title":"CaREM1.4 interacts with CaRIN4 to regulate Ralstonia solanacearum tolerance by triggering cell death in pepper","volume":"10","author":"Zhang","year":"2023","journal-title":"Hortic Res"},{"key":"10.1016\/j.bmcl.2024.130040_b0150","doi-asserted-by":"crossref","first-page":"176","DOI":"10.1016\/j.fm.2017.12.002","article-title":"Antimicrobial efficacy of Syzygium antisepticum plant extract against Staphylococcus aureus and methicillin-resistant S. aureus and its application potential with cooked chicken","volume":"72","author":"Yuan","year":"2018","journal-title":"Food Microbiol"},{"key":"10.1016\/j.bmcl.2024.130040_b0155","doi-asserted-by":"crossref","first-page":"38506","DOI":"10.1021\/acsami.8b14986","article-title":"Facile and versatile modification of cotton fibers for persistent antibacterial activity and enhanced hygroscopicity","volume":"10","author":"Cai","year":"2018","journal-title":"ACS Appl Mater Interfaces"}],"container-title":["Bioorganic & Medicinal Chemistry Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960894X24004426?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960894X24004426?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,12,12]],"date-time":"2024-12-12T00:19:28Z","timestamp":1733962768000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0960894X24004426"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,2]]},"references-count":31,"alternative-id":["S0960894X24004426"],"URL":"https:\/\/doi.org\/10.1016\/j.bmcl.2024.130040","relation":{},"ISSN":["0960-894X"],"issn-type":[{"type":"print","value":"0960-894X"}],"subject":[],"published":{"date-parts":[[2025,2]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Synthesis of drimanyl indole fragments of drimentine alkaloids and their antibacterial activities","name":"articletitle","label":"Article Title"},{"value":"Bioorganic & Medicinal Chemistry Letters","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.bmcl.2024.130040","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.","name":"copyright","label":"Copyright"}],"article-number":"130040"}}