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Contribution of H-Bonding to the Preference of Platinum Anti-Tumour Drugs for Particular Bases and Particular Cross-Links
The stereochemical factors that influence the tendencies for sequence specific binding of platinum antitumour drugs to DNA are examined. The NHs of the platinum-amine moiety can form hydrogen bonds to the O6 of guanine or to a phosphate oxygen of DNA. Modelling the stereochemistry of the NH atoms ca...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1994
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364910/ https://www.ncbi.nlm.nih.gov/pubmed/18476245 http://dx.doi.org/10.1155/MBD.1994.311 |
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author | Natile, Giovanni |
author_facet | Natile, Giovanni |
author_sort | Natile, Giovanni |
collection | PubMed |
description | The stereochemical factors that influence the tendencies for sequence specific binding of platinum antitumour drugs to DNA are examined. The NHs of the platinum-amine moiety can form hydrogen bonds to the O6 of guanine or to a phosphate oxygen of DNA. Modelling the stereochemistry of the NH atoms can lead to compounds with a strong preference for forming one type of adduct with DNA. |
format | Text |
id | pubmed-2364910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23649102008-05-12 Contribution of H-Bonding to the Preference of Platinum Anti-Tumour Drugs for Particular Bases and Particular Cross-Links Natile, Giovanni Met Based Drugs Research Article The stereochemical factors that influence the tendencies for sequence specific binding of platinum antitumour drugs to DNA are examined. The NHs of the platinum-amine moiety can form hydrogen bonds to the O6 of guanine or to a phosphate oxygen of DNA. Modelling the stereochemistry of the NH atoms can lead to compounds with a strong preference for forming one type of adduct with DNA. Hindawi Publishing Corporation 1994 /pmc/articles/PMC2364910/ /pubmed/18476245 http://dx.doi.org/10.1155/MBD.1994.311 Text en Copyright © 1994 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Natile, Giovanni Contribution of H-Bonding to the Preference of Platinum Anti-Tumour Drugs for Particular Bases and Particular Cross-Links |
title | Contribution of H-Bonding to the Preference of Platinum
Anti-Tumour Drugs for Particular Bases and Particular Cross-Links |
title_full | Contribution of H-Bonding to the Preference of Platinum
Anti-Tumour Drugs for Particular Bases and Particular Cross-Links |
title_fullStr | Contribution of H-Bonding to the Preference of Platinum
Anti-Tumour Drugs for Particular Bases and Particular Cross-Links |
title_full_unstemmed | Contribution of H-Bonding to the Preference of Platinum
Anti-Tumour Drugs for Particular Bases and Particular Cross-Links |
title_short | Contribution of H-Bonding to the Preference of Platinum
Anti-Tumour Drugs for Particular Bases and Particular Cross-Links |
title_sort | contribution of h-bonding to the preference of platinum
anti-tumour drugs for particular bases and particular cross-links |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364910/ https://www.ncbi.nlm.nih.gov/pubmed/18476245 http://dx.doi.org/10.1155/MBD.1994.311 |
work_keys_str_mv | AT natilegiovanni contributionofhbondingtothepreferenceofplatinumantitumourdrugsforparticularbasesandparticularcrosslinks |