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Pestanoid A, a Rearranged Pimarane Diterpenoid Osteoclastogenesis Inhibitor from a Marine Mesophotic Zone Chalinidae Sponge-Associated Fungus, Pestalotiopsis sp. NBUF145.
Wang, Tingting; Feng, Yunping; Huang, Jian; Wu, Sitong; Hu, Kun; Wu, Jiabin; Naman, C Benjamin; Wang, Hong; Lin, Wenhan; He, Shan.
Afiliação
  • Wang T; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo 315211, Zhejiang, China.
  • Feng Y; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo 315211, Zhejiang, China.
  • Huang J; Ningbo Institute of Marine Medicine, Peking University, Ningbo 315832, Zhejiang, China.
  • Wu S; School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, Zhejiang, China.
  • Hu K; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China.
  • Wu J; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo 315211, Zhejiang, China.
  • Naman CB; Department of Science and Conservation, San Diego Botanic Garden, Encinitas, California 92024, United States.
  • Wang H; School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, Zhejiang, China.
  • Lin W; Ningbo Institute of Marine Medicine, Peking University, Ningbo 315832, Zhejiang, China.
  • He S; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo 315211, Zhejiang, China.
J Nat Prod ; 87(1): 160-165, 2024 01 26.
Article em En | MEDLINE | ID: mdl-38194474
ABSTRACT
One novel rearranged pimarane diterpenoid, pestanoid A (1), and two reported molecules, nodulisporenones A (2) and B (3), were discovered from Pestalotiopsis sp. NBUF145 fungus associated with a 62 m deep mesophotic ("twilight") zone Chalinidae sponge. The structures of 1-3 were identified by spectrometry, spectroscopy, quantum-chemical calculations, and X-ray crystallography. Compounds 1 and 2 inhibited bone marrow monocyte osteoclastogenesis in vitro with the IC50 values 4.2 ± 0.2 µM and 3.0 ± 0.4 µM, respectively, without observed cytotoxicity. Both 1 and 2 suppressed the receptor activator of NF-kB ligand-induced MAPK and NF-κB signaling by inhibiting the phosphorylation of ERK1/2-JNK1/2-p38 MAPKs and NF-κB nuclear translocation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoclastos / Osteogênese Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Nat Prod Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoclastos / Osteogênese Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Nat Prod Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China