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Fulvanines J-K, two rare lactam pyrrole alkaloids from Hemerocallis fulva.
Lei, Ya-E; Wang, Qian; Yaermaimaiti, Saimijiang; Ma, Zi-Hui; Li, Miao-Miao; Lu, Yan; Chen, Dao-Feng; Wang, Qi.
Afiliación
  • Lei YE; Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832002, P. R. China.
  • Wang Q; Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832002, P. R. China.
  • Yaermaimaiti S; Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832002, P. R. China.
  • Ma ZH; Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832002, P. R. China.
  • Li MM; Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832002, P. R. China.
  • Lu Y; Department of Pharmacognosy, School of Pharmacy, Fudan University, Shanghai, 201203, P. R. China.
  • Chen DF; Department of Pharmacognosy, School of Pharmacy, Fudan University, Shanghai, 201203, P. R. China.
  • Wang Q; Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832002, P. R. China.
Chem Biodivers ; 21(2): e202301672, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38116924
ABSTRACT
Two rare jatropham lactam derivatives, named as fulvanines J-K (1-2), together with six known pyrrole alkaloids, 5,5'-oxydi(3-methyl-3-pyrrolin-2-one) (3), (-)-5-hydroxy-3-methyl-3-pyrrolin-2-one (jatropham) (4), (±)-5-O-methyljatropham (5), perlolyrine (6), butyl-2-formyl-5-(hydroxymethyl)-1H-pyrrole-1-butanoate (7), and hemerocallisamine II (8), were isolated from the flower of Hemerocallis fulva. Their structures were elucidated on the basis of spectroscopic methods and compared with the NMR spectra data in the literature. All compounds were evaluated for their anti-complementary activity in vitro, and compounds 1, 4, and 6 exhibited anti-complement effect with CH50 values from 0.61 to 1.42 mM.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hemerocallis / Alcaloides Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hemerocallis / Alcaloides Idioma: En Año: 2024 Tipo del documento: Article