Pyrrolo[2,1-<i>a</i>]isoquinoline scaffolds for developing anti-cancer agents-Reference-Cited by-同舟云学术

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Pyrrolo[2,1-a]isoquinoline scaffolds for developing anti-cancer agents

Published:2024 Issue:3 Volume:14 Page:1710-1728
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

García Maza Leidy J.¹,Salgado Arturo Mendoza¹^ORCID,Kouznetsov Vladimir V.²^ORCID,Meléndez Carlos M.¹^ORCID

Affiliation:

1. Facultad de Ciencias Básicas, Grupo de Investigación de Química Orgánica y Biomédica, Universidad del Atlántico, Barranquilla, Colombia

2. Laboratorio de Química Orgánica y Biomolecular, Escuela de Química, Universidad Industrial de Santander, Piedecuesta 680002, Colombia

Abstract

Fused pyrrolo[2,1-a]isoquinolines have emerged as compelling molecules with remarkably potent cytotoxic activity and topoisomerase inhibitors.

Funder

Universidad del Atlántico

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RA/D3RA07047F

Reference90 articles.

1. Anticancer Properties of Lamellarins

2. Lamellarin-inspired potent topoisomerase I inhibitors with the unprecedented benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-one scaffold

3. T.Fukuda , F.Ishibashi and M.Iwao , Lamellarin Alkaloids: Isolation, Synthesis, and Biological Activity , Elsevier Inc. , 1st edn, 2020 , vol. 83

4. Design, Synthesis and Structure-Activity Relationship Studies of Glycosylated Derivatives of Marine Natural Product Lamellarin D

5. Assessing the drug-likeness of lamellarins, a marine-derived natural product class with diverse oncological activities

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cascade Synthesis of Pyrrolo[1,2-a]quinolines and Pyrrolo[2,1-a]isoquinolines via Formal [3 + 2]-Cycloaddition of Push–Pull Nitro Heterocycles with Carbonyl-Stabilized Quinolinium/Isoquinolinium Ylides;The Journal of Organic Chemistry;2024-06-25

2. Photo-induced tungsten-catalyzed cascade synthesis of pyrrolo[2,1-a]isoquinoline-1,3-dicarboxylate and its reaction mechanism;Chemical Communications;2024

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