Design and synthesis of analogues of natural products

ME Maier - Organic & Biomolecular Chemistry, 2015 - pubs.rsc.org
In this article strategies for the design and synthesis of natural product analogues are
summarized and illustrated with some selected examples. Proven strategies include …

Dynamically shaping chaperones. Allosteric modulators of HSP90 family as regulatory tools of cell metabolism in neoplastic progression

C Sanchez-Martin, SA Serapian, G Colombo… - Frontiers in …, 2020 - frontiersin.org
Molecular chaperones have recently emerged as fundamental regulators of salient
biological routines, including metabolic adaptations to environmental changes. Yet, many of …

Possibilities to increase the effectiveness of doxorubicin in cancer cells killing

V Hanušová, I Boušová, L Skálová - Drug metabolism reviews, 2011 - Taylor & Francis
Anthracycline antibiotic doxorubicin (DOX) belongs among the most important
antineoplastics used in cancer therapy. Unfortunately, its cytostatic effect in therapeutic …

Cinnamic acid derivatives as chemosensitising agents against DOX-treated lung cancer cells–Involvement of carbonyl reductase 1

P Koczurkiewicz-Adamczyk, K Piska… - European Journal of …, 2020 - Elsevier
Doxorubicin (DOX) therapy is limited by both cancer cells resistance and cardiotoxicity. DOX
biotransformation to doxorubicinol (DOXol) by reductases enzymes (mainly by CBR1; …

Small-molecule inhibitors of the SOX18 transcription factor

F Fontaine, J Overman, M Moustaqil, S Mamidyala… - Cell chemical …, 2017 - cell.com
Pharmacological modulation of transcription factors (TFs) has only met little success over the
past four decades. This is mostly due to standard drug discovery approaches centered on …

Principles, implementation, and application of biology-oriented synthesis (BIOS)

W Wilk, TJ Zimmermann, M Kaiser… - Biological …, 2010 - degruyter.com
Biology-oriented synthesis (BIOS) represents an alternative approach for the generation of
compound collections for biological applications. In BIOS, biologically relevant and …

Structure–activity relationship of flavonoids as potent inhibitors of carbonyl reductase 1 (CBR1)

Y Arai, S Endo, N Miyagi, N Abe, T Miura, T Nishinaka… - Fitoterapia, 2015 - Elsevier
Abstract Human carbonyl reductase 1 (CBR1), a member of the short-chain dehydrogenase/
reductase superfamily, reduces a variety of carbonyl compounds including therapeutic …

The modulation of carbonyl reductase 1 by polyphenols

I Boušová, L Skálová, P Souček… - Drug metabolism …, 2015 - Taylor & Francis
Abstract Carbonyl reductase 1 (CBR1), an enzyme belonging to the short-chain
dehydrogenases/reductases family, has been detected in all human tissues. CBR1 …

Efficient synthesis of anacardic acid analogues and their antibacterial activities

SK Mamidyala, S Ramu, JX Huang… - Bioorganic & medicinal …, 2013 - Elsevier
Anacardic acid derivatives exhibit a broad range of biological activities. In this report, an
efficient method for the synthesis of anacardic acid derivatives was explored, and a small set …

Synthesis of 8-hydroxy-2-iminochromene derivatives as selective and potent inhibitors of human carbonyl reductase 1

D Hu, N Miyagi, Y Arai, H Oguri, T Miura… - Organic & …, 2015 - pubs.rsc.org
Human carbonyl reductase 1 (CBR1), a member of the short-chain dehydrogenase/
reductase superfamily, reduces anthracycline anticancer drugs to their less potent …