Synthesis of new dihydroberberine and tetrahydroberberine analogues and evaluation of their antiproliferative activity on NCI-H1975 cells
Beilstein Journal of Organic Chemistry, ISSN: 1860-5397, Vol: 16, Page: 1606-1616
2020
- 12Citations
- 7Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations12
- Citation Indexes12
- 12
- CrossRef3
- Captures7
- Readers7
Article Description
Dihydroberberine (DHBER), the partially reduced form of the alkaloid berberine (BER), is known to exhibit important biological activities. Despite this fact, there have been only few studies that concern the biological properties of functionalized DHBER. Attracted by the potentiality of this latter compound, we have realized the preparation of new arylhydrazono-functionalized DHBERs, starting from BER and some α-bromohydrazones. On the other hand, also the fully reduced form of BER, namely tetrahydroberberine (THBER), and its derivatives have proven to present different biological activities. Therefore, the obtained arylhydrazono-functionalized DHBERs were reduced to the corresponding arylhydrazono-THBERs. The antiproliferative activity of both arylhydrazono-DHBERs and -THBERs has been evaluated on NCI-H1975 lung cancer cells.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1860539721020703; http://dx.doi.org/10.3762/bjoc.16.133; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85090332321&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/32704327; https://www.beilstein-journals.org/bjoc/articles/16/133; https://dx.doi.org/10.3762/bjoc.16.133
Beilstein Institut
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