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Daphnane diterpenoid orthoesters with an odd-numbered aliphatic side chain from Daphne pedunculata.
Tan, Lingjian; Otsuki, Kouharu; Kikuchi, Takashi; Zhou, Di; Li, Ning; Huang, Li; Chen, Chin-Ho; Li, Wei.
Afiliación
  • Tan L; Faculty of Pharmaceutical Sciences, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan.
  • Otsuki K; Faculty of Pharmaceutical Sciences, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan. kouharu.otsuki@phar.toho-u.ac.jp.
  • Kikuchi T; Faculty of Pharmaceutical Sciences, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan.
  • Zhou D; School of Traditional Chinese Materia Medica, Key Laboratory of Innovative Traditional Chinese Medicine for Major Chronic Diseases of Liaoning Province, Key Laboratory for TCM Material Basis Study and Innovative, Drug Development of Shenyang City, Shenyang Pharmaceutical University, Shenyang, 110016
  • Li N; School of Traditional Chinese Materia Medica, Key Laboratory of Innovative Traditional Chinese Medicine for Major Chronic Diseases of Liaoning Province, Key Laboratory for TCM Material Basis Study and Innovative, Drug Development of Shenyang City, Shenyang Pharmaceutical University, Shenyang, 110016
  • Huang L; Surgical Sciences, Department of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
  • Chen CH; Surgical Sciences, Department of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
  • Li W; Faculty of Pharmaceutical Sciences, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan. liwei@phar.toho-u.ac.jp.
J Nat Med ; 2024 May 23.
Article en En | MEDLINE | ID: mdl-38780746
ABSTRACT
Daphnane diterpenoids were recognized for their extensive range of potent biological activities. In the present study, phytochemical investigation including LC-MS/MS analysis resulted in the identification of five daphnane diterpenoid orthoesters (1-5). Among the five daphnane diterpenoids, two previously unreported compounds, daphnepedunins I and J (2 and 4) were isolated from Daphne pedunculata. The structure of new compounds was elucidated with extensive physicochemical and spectroscopic analyses. Their structure was characterized by the presence of an unusual odd-numbered aliphatic chain connected to an orthoester. The isolated compounds were evaluated for their anti-HIV activity against HIV-1 infection of MT4 cells, and the results indicated that compound 1 showed the most potent anti-HIV activity with an IC50 value of 0.82 nM.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Nat Med Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Nat Med Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2024 Tipo del documento: Article País de afiliación: Japón
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