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Scalalactams A⁻D, Scalarane Sesterterpenes with a γ-Lactam Moiety from a Korean Spongia Sp. Marine Sponge.
Yang, Inho; Lee, Jusung; Lee, Jihye; Hahn, Dongyup; Chin, Jungwook; Won, Dong Hwan; Ko, Jaeyoung; Choi, Hyukjae; Hong, Ahreum; Nam, Sang-Jip; Kang, Heonjoong.
Afiliación
  • Yang I; Department of Convergence Study on the Ocean Science and Technology, Korea Maritime and Ocean University, Busan 49112, Korea. ihyang@kmou.ac.kr.
  • Lee J; The Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Science, Seoul National University, NS-80, Seoul 08826, Korea. leejusung@snu.ac.kr.
  • Lee J; The Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Science, Seoul National University, NS-80, Seoul 08826, Korea. jl3414@gmail.com.
  • Hahn D; School of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea. dohahn@knu.ac.kr.
  • Chin J; Institute of Agricultural Science & Technology, Kyungpook National University, Daegu 41566, Korea. dohahn@knu.ac.kr.
  • Won DH; New Drug Development Center, Daegu-Gyeongbuk Medicinal Innovation Foundation, Daegu 41061, Korea. jwchin@dgmif.re.kr.
  • Ko J; The Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Science, Seoul National University, NS-80, Seoul 08826, Korea. dongfal2@gmail.com.
  • Choi H; Basic Research & Innovation Division, Amorepacific R&D Unit, Yongin 17074, Korea. jaeyoungko@amorepacific.com.
  • Hong A; College of Pharmacy, Yeungnam University, Gyeongsan 38541, Korea. h5choi@yu.ac.kr.
  • Nam SJ; Graduate School of Industrial Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Korea. lyzenne@gmail.com.
  • Kang H; Department of Chemistry and Nanoscience, Ewha Womans University, Seoul 03760, Korea. sjnam@ewha.ac.kr.
Molecules ; 23(12)2018 Dec 03.
Article en En | MEDLINE | ID: mdl-30513974
ABSTRACT
Intensive study on the chemical components of a Korean marine sponge, Spongia sp., has led to the isolation of four new scalarane sesterterpenes, scalalactams A⁻D (1⁻4). Their chemical structures were elucidated from the analysis of spectroscopic data including 1D-and 2D-NMR as well as MS data. Scalalactams A⁻D (1⁻4) possess a scalarane carbon skeleton with a rare structural feature of a γ-lactam moiety within the molecules. Scalalactams A and B (1 and 2) have an extended isopropanyl chain at the lactam ring, and scalalactams C and D (3 and 4) possess a phenethyl group at the lactam ring moiety. Scalalactams A⁻D (1⁻4) did not show FXR antagonistic activity nor cytotoxicity up to 100 µM.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Poríferos / Sesterterpenos Límite: Animals / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Poríferos / Sesterterpenos Límite: Animals / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2018 Tipo del documento: Article