Synthesis and anti-plasmodial activity of isoandrographolide acetals-Reference-Cited by-同舟云学术

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Synthesis and anti-plasmodial activity of isoandrographolide acetals

Published:2023-02-01 Issue: Volume: Page:
ISSN:0366-6352
Container-title:Chemical Papers
language:en
Short-container-title:Chem. Pap.

Author:

Tamang Nitesh,Mavileti Sai Kiran,Yadav Mamta,Nanduri Srinivas,Sahal Dinkar,Golakoti Nageswara Rao

Funder

Council of Scientific & Industrial Research

Publisher

Springer Science and Business Media LLC

Subject

Materials Chemistry,Industrial and Manufacturing Engineering,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s11696-023-02684-9.pdf

Reference45 articles.

1. Akowuah GA, Zhari I, Mariam A, Yam MF (2009) Absorption of andrographolides from Andrographis paniculata and its effect on CCl4-induced oxidative stress in rats. Food Chem Toxicol 47:2321–2326. https://doi.org/10.1016/j.fct.2009.06.022

2. Arsakhant P, Sirion U, Chairoungdua A et al (2020) Design and synthesis of C-12 dithiocarbamate andrographolide analogues as an anticancer agent. Bioorg Med Chem Lett 30:127263. https://doi.org/10.1016/j.bmcl.2020.127263

3. Cai W, Li J, Chen C et al (2021) Design, synthesis, and anticancer evaluation of novel andrographolide derivatives bearing an α, β-unsaturated ketone moiety. Bioorg Chem 112:104941. https://doi.org/10.1016/j.bioorg.2021.104941

4. Chao W-W, Lin B-F (2010) Isolation and identification of bioactive compounds in Andrographis paniculata (Chuanxinlian). Chin Med 5:1–15. https://doi.org/10.1186/1749-8546-5-17

5. Chen Z-G, Zhu Q, Zong M-H et al (2011) Enzymatic synthesis and antibacterial activity of andrographolide derivatives. Process Biochem 46:1649–1653. https://doi.org/10.1016/j.procbio.2011.05.011

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