Proteins as possible targets for antitumor metal complexes: biophysical studies of their interactions
There is considerable interest today for the reactions of anticancer metallodrugs with proteins as these interactions might feature processes that are crucial for the biodistribution, the toxicity and even the mechanism of action of this important group of anticancer agents. Valuable structural and...
Saved in:
| Main Author: | |
|---|---|
| Format: | Electronic Book Chapter |
| Language: | No linguistic content, Not applicable |
| Published: |
Firenze University Press
2009
|
| Series: | Premio Tesi di Dottorato
|
| Subjects: | |
| Online Access: | DOAB: download the publication DOAB: description of the publication |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
MARC
| LEADER | 00000naaaa2200000uu 4500 | ||
|---|---|---|---|
| 001 | doab_20_500_12854_57248 | ||
| 005 | 20210212 | ||
| 003 | oapen | ||
| 006 | m o d | ||
| 007 | cr|mn|---annan | ||
| 008 | 20210212s2009 xx |||||o ||| 0|||| d | ||
| 020 | |a 978-88-8453-940-3 | ||
| 020 | |a 9788884539403 | ||
| 040 | |a oapen |c oapen | ||
| 024 | 7 | |a 10.36253/978-88-8453-940-3 |c doi | |
| 041 | 0 | |a zxx | |
| 042 | |a dc | ||
| 072 | 7 | |a PS |2 bicssc | |
| 100 | 1 | |a Chiara Gabbiani |4 auth | |
| 245 | 1 | 0 | |a Proteins as possible targets for antitumor metal complexes: biophysical studies of their interactions |
| 260 | |b Firenze University Press |c 2009 | ||
| 300 | |a 1 electronic resource (74 p.) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Premio Tesi di Dottorato | |
| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 520 | |a There is considerable interest today for the reactions of anticancer metallodrugs with proteins as these interactions might feature processes that are crucial for the biodistribution, the toxicity and even the mechanism of action of this important group of anticancer agents. Valuable structural and functional information on these adducts could be derived from several biophysical studies mainly relying on the application of X-ray diffraction and ESI MS techniques. The structural and functional information achieved on the respective metallodrug-protein adducts allowed us to identify some general trends in the reactivity of anticancer metallodrugs with protein targets. | ||
| 540 | |a Creative Commons |f https://creativecommons.org/licenses/by-nd/4.0/ |2 cc |4 https://creativecommons.org/licenses/by-nd/4.0/ | ||
| 650 | 7 | |a Biology, life sciences |2 bicssc | |
| 653 | |a Chimica | ||
| 653 | |a Biologia | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://www.fupress.com/redir.ashx?RetUrl=3852.pdf |7 0 |z DOAB: download the publication |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/57248 |7 0 |z DOAB: description of the publication |