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 …
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
Molecular chaperones have recently emerged as fundamental regulators of salient
biological routines, including metabolic adaptations to environmental changes. Yet, many of …
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 …
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; …
biotransformation to doxorubicinol (DOXol) by reductases enzymes (mainly by CBR1; …
Small-molecule inhibitors of the SOX18 transcription factor
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 …
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 …
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 …
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 …
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 …
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 …
reductase superfamily, reduces anthracycline anticancer drugs to their less potent …