Design, synthesis, and antitumor evaluation of novel naphthalimide derivatives-Reference-Cited by-同舟云学术

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Design, synthesis, and antitumor evaluation of novel naphthalimide derivatives

Published:2019-11-09 Issue:2 Volume:29 Page:180-188
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Li Xin,Wu Zheng,Xu Lu,Chi Chun-Lan,Chen Bao-Quan

Funder

Tianjin Municipal Natural Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-019-02471-w.pdf

Reference47 articles.

1. Abo-Bakr AM, Hashem HE (2019) New 1,3,4-thiadiazole derivatives: synthesis, characterization, and antimicrobial activity. J Heterocycl Chem 56:1038–1047

2. Adhikari S, Ta S, Ghosh A, Guria S, Pal A, Ahir M, Adhikary A, Hira SK, Manna PP, Das D (2019) A 1,8 naphthalimide anchor rhodamine B based FRET probe for ratiometric detection of Cr 3+ ion in living cells. J Photochem Photobio A 372:49–58

3. Al-Salahi R, Alswaidan I, Ghabbour HA, Ezzeldin E, Elaasser M, Marzouk M (2015) Docking and antiherpetic activity of 2-aminobenzo[de]-isoquinoline-1,3-diones. Molecules 20:5099–5111

4. Banerjee S, Veale EB, Phelan CM, Murphy SA, Tocci GM, Gillespie LJ, Frimannsson DO, Kelly JM, Gunnlaugsson T (2013) Recent advances in the development of 1,8-naphthalimide based DNA targeting binders, anticancer and fluorescent cellular imaging agents. Chem Soc Rev 42:1601–1618

5. Cesarini S, Spallarossa A, Ranise A, Schenone S, Bruno O, Colla PL, Casula L, Collu G, Sanna G, Loddo R (2008) Parallel one-pot synthesis and structure–activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors. Bioorg Med Chem 16:6353–6363

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4. Design, synthesis, antiproliferative and antimicrobial evaluation of a new class of disulfides containing 1,3,4-thiadiazole units;Medicinal Chemistry Research;2022-07-28

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