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Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds

[Image: see text] We have investigated the mechanism and reactivity of covalent bond formation between cysteine-84 of the regulatory domain of cardiac troponin C and compounds containing a nitrile moiety similar to the calcium sensitizer levosimendan. The results of modifications to the levosimendan...

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Autores principales: Klein, Brittney A., Robertson, Ian M., Reiz, Béla, Kampourakis, Thomas, Li, Liang, Sykes, Brian D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227049/
https://www.ncbi.nlm.nih.gov/pubmed/32426091
http://dx.doi.org/10.1021/acsmedchemlett.9b00168
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author Klein, Brittney A.
Robertson, Ian M.
Reiz, Béla
Kampourakis, Thomas
Li, Liang
Sykes, Brian D.
author_facet Klein, Brittney A.
Robertson, Ian M.
Reiz, Béla
Kampourakis, Thomas
Li, Liang
Sykes, Brian D.
author_sort Klein, Brittney A.
collection PubMed
description [Image: see text] We have investigated the mechanism and reactivity of covalent bond formation between cysteine-84 of the regulatory domain of cardiac troponin C and compounds containing a nitrile moiety similar to the calcium sensitizer levosimendan. The results of modifications to the levosimendan framework ranged from a large increase in covalent bond formation to complete inactivity. We present the biological activity of one of the most potent compounds. Limitations, including compound solubility and degradation at acidic pH, have prevented thorough investigation of the potential of these compounds. Our studies reveal the efficacious nature of the malononitrile moiety in targeting cNTnC and its potential in future cardiotonic drug design.
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spelling pubmed-72270492020-05-18 Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds Klein, Brittney A. Robertson, Ian M. Reiz, Béla Kampourakis, Thomas Li, Liang Sykes, Brian D. ACS Med Chem Lett [Image: see text] We have investigated the mechanism and reactivity of covalent bond formation between cysteine-84 of the regulatory domain of cardiac troponin C and compounds containing a nitrile moiety similar to the calcium sensitizer levosimendan. The results of modifications to the levosimendan framework ranged from a large increase in covalent bond formation to complete inactivity. We present the biological activity of one of the most potent compounds. Limitations, including compound solubility and degradation at acidic pH, have prevented thorough investigation of the potential of these compounds. Our studies reveal the efficacious nature of the malononitrile moiety in targeting cNTnC and its potential in future cardiotonic drug design. American Chemical Society 2019-05-15 /pmc/articles/PMC7227049/ /pubmed/32426091 http://dx.doi.org/10.1021/acsmedchemlett.9b00168 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Klein, Brittney A.
Robertson, Ian M.
Reiz, Béla
Kampourakis, Thomas
Li, Liang
Sykes, Brian D.
Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds
title Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds
title_full Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds
title_fullStr Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds
title_full_unstemmed Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds
title_short Thioimidate Bond Formation between Cardiac Troponin C and Nitrile-containing Compounds
title_sort thioimidate bond formation between cardiac troponin c and nitrile-containing compounds
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227049/
https://www.ncbi.nlm.nih.gov/pubmed/32426091
http://dx.doi.org/10.1021/acsmedchemlett.9b00168
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