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Dergiler / Records of Natural Products / 2021 / Cilt: 15 - Sayı: 3

Trimacoside A, a High Molecular Weight Antioxidant Phenylpropanoid Glycoside from Tricyrtis maculata

Yunze WANG
Wei ZHANG
Li REN
Dongbo ZHANG
Sayfa
194–201
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Compounds 1, 4, 5, 7, 8, and 10 showed significant antioxidant activities by DPPH and ABTS assays

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Trimacoside A (1), a new phenylpropanoid glycoside, together with nine known compounds (2−10) was isolated from Tricyrtis maculata.
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Temel Bulgular & Veri:All compounds, except for 8, were firstly isolated from this plant.
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Sonuç & Katkı:Compounds 1, 4, 5, 7, 8, and 10 showed significant antioxidant activities by DPPH and ABTS assays
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Trimacoside A (1), a new phenylpropanoid glycoside, together with nine known compounds (2−10) was isolated from Tricyrtis maculata. All compounds, except for 8, were firstly isolated from this plant. The structure elucidation of the new compound was carried out by the analysis of spectroscopic data, including 1D, 2D NMR, and HRESIMS. Compounds 1, 4, 5, 7, 8, and 10 showed significant antioxidant activities by DPPH and ABTS assays

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Bu Makaleye Atıf Yap

WANG, Y., ZHANG, W., REN, L., ZHANG, D. (2021). Trimacoside A, a High Molecular Weight Antioxidant Phenylpropanoid Glycoside from Tricyrtis maculata. Records of Natural Products, Cilt: 15 - Sayı: 3, 194–201. https://ajindex.com/articles/308221

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Kaynakça (2)

  1. S. W. Hong and S. L. Jury (2011). Phylogeny and divergence times inferred from rps16 sequence data analyses for Tricyrtis (Liliaceae), an endemic genus of North-East Asia, Aob. Plants. 25, 1–11 [2] J. Sun and T. Q. Jia (2016). A preliminary study on the material basis of activating blood-circulation of Tricyrits maculata (D. Don) Machride, J. Chin. Med. Mater. 39, 419–421. [3] J. Sun, J. Q. Liu, X. H.Xia and L. M. Zhang (2012). Study on the extraction technology of its flavonoids parts from Tricyrtis maculata growing in shaanxi province, J. Chin. Mater. Met. 35, 641–644. [4] T. Q. Jia, M. Tian, S. C. Zhang, L. Ren and J. Sun (2019). Determine the concentration, pharmacokinetics and bioavailability of nicotiflorin in rat plasma by LC-MS/MS, Mod. Chin. Med. 21, 1625–1629. [5] J. Yang, D. D. Zhang, X. Zhang and J. Sun (2017). Chemical constituents of Tricyrtis maculata (D. Don) Machride, Cent. South Pharm. 15, 922–924. [6] R. Yan and H. Zhao (2018). Optimization of extraction technology by response surface methodology and inoxidizability of total flavonoids from Tricyrtis maculata Machride. Sci. Technol. Food. Ind. 13, 483– 490. [7] L. Ren, Y. Z. Wang, W. Zhang. R. Zhou, M. Zhao, Z. S. Tang, J. Sun and D. B. Zhang (2020).
  2. Triculata A, A novel compound from Tricyrtis maculata (D. Don) J. F. Macbr. with biological properties, Nat. Prod. Res. 1–9. 10.1080/14786419.2020.1736059. [8] S. M. Jia, X. F. Liu, D. M. Kong and H. X. Shen (2012). A simple, post-additional antioxidant capacity assay using adenosine triphosphate-stabilized 2,2'-azinobis(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS) radical cation in a G-quadruplex DNAzyme catalyzed ABTS-H2O2 system, Biosens. Bioelectron. 35, 407–412. [9] H. Kumagai, Y. Kawai, R. Sawano, H. Kurihara, K. Yamazaki and N. Inoue (2005). Antimicrobial substances from rhizomes of the giant knotweed Polygonum sachalinense against the fish pathogen Photobacterium damselae subsp. Piscicida, Z. Naturforsch. 60, 39−44. [10] S. P. Ovenden, J. Yu, J. Bernays, S. S. Wan, L. J. Christophidis, G. Sberna, R. M. Tait, H. G. Wildman, D. Lebeller, J. Lowther, N. G. Walsh and B. M. Meurer-Grimes (2005). Physaloside A, an acylated sucrose ester from Physalis viscosa, J. Nat. Prod. 68, 282–284. [11] M. Takasaki, S. Kuroki, M. Kozuka and T. Konoshima (2001). New phenylpropanoid esters of sucrose from Polygonum lapathifolium, J. Nat. Prod. 64, 1305–1308. [12] E. Maldonado, R. F. Torres, M. Martínez and L. A. Pérez-Castorena (2006). Sucrose este