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Isolation and target identification of anti-renal fibrosis compounds from Cordyceps militaris.
Yang, Wei; Zhu, Kun-Fang; Tao, Cheng-Tian; Yan, Yong-Ming; Cheng, Yong-Xian.
Afiliação
  • Yang W; Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen 518055, Guangdong, PR China.
  • Zhu KF; Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen 518055, Guangdong, PR China.
  • Tao CT; Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen 518055, Guangdong, PR China.
  • Yan YM; Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen 518055, Guangdong, PR China.
  • Cheng YX; Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen 518055, Guangdong, PR China. Electronic address: yxcheng@szu.edu.cn.
Bioorg Chem ; 144: 107169, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38330722
ABSTRACT
Four undescribed compounds including one aromatic glucoside derivative, cordyceglycoside A (1), one new isoleucine derivative inner salt, cordycepisosalt A (2), a rare four-membered lactam, cinerealactam B (3), and one sesquiterpene derivative, cordycepsetp A (4), together with six known compounds were isolated from Cordyceps militaris. The structures including absolute configurations of these new compounds, were unambiguously elucidated by spectroscopic data analysis and single crystal X-ray diffraction. Biological evaluation of compounds 1-4 showed that 3 displays anti-renal fibrotic activities in TGF-ß1 induced NRK-52e cells. Furthermore, DARTS coupled with LC-MS/MS analysis was used to identify candidate target proteins for 3. Subsequently, C1qbp knockdown using siRNA allowed us to validate the target protein of 3.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cordyceps Tipo de estudo: Diagnostic_studies Idioma: En Revista: Bioorg Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cordyceps Tipo de estudo: Diagnostic_studies Idioma: En Revista: Bioorg Chem Ano de publicação: 2024 Tipo de documento: Article