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Lysidrhodosides A-I, acylphloroglucinol glucosides with anti-inflammatory activities from the leaves of Lysidice rhodostegia.
Fu, Jin-Tao; Hao, Yi-Kun; Zhan, Zhao-Chun; Yang, Si-Yu; Tang, Qing; Lin, Qiang; Zhao, Hai-Yue; Du, Jing-Yi; Zhu, Tian-Xi; Li, Yao-Lan; Zhang, Yu-Bo; Wang, Guo-Cai.
Afiliação
  • Fu JT; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Hao YK; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Zhan ZC; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Yang SY; Guangdong Clinical Translational Center for Targeted Drug, Department of Pharmacology, School of Medicine, Jinan University, Guangzhou 510632, PR China.
  • Tang Q; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Lin Q; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Zhao HY; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Du JY; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Zhu TX; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Li YL; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
  • Zhang YB; Guangdong Clinical Translational Center for Targeted Drug, Department of Pharmacology, School of Medicine, Jinan University, Guangzhou 510632, PR China. Electronic address: ybzhang99@126.com.
  • Wang GC; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, PR Chin
Fitoterapia ; 172: 105768, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38056698
Lysidrhodosides A-I (1-9), nine acylphloroglucinol glucoside derivatives along with three known analogues (10-12) were isolated from the leaves of Lysidice rhodostegia. Their structures and absolute configuration were elucidated by spectroscopic data analysis (NMR, UV, IR, HR-ESI-MS), single-crystal X-ray diffraction, and acid hydrolysis with HPLC analysis. Notably, compounds 7-9 represent the first examples of 3-methylbutyryl phloroglucinol glucoside dimers isolated from this plant. Additionally, compounds 1-12 were assessed for their inhibitory effects on nitric oxide (NO) in the LPS-induced BV-2 cells. The results showed that compounds 6 and 12 significantly inhibited the production of the inflammatory mediator NO, with an inhibitory rate of 95.96 and 91.13% at a concentration of 50 µM, respectively.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glucosídeos / Fabaceae Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glucosídeos / Fabaceae Idioma: En Ano de publicação: 2024 Tipo de documento: Article