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Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives

In this study, three type II phenolic acids (caffeic acid, p-hydroxycinnamic acid, and ferulic acid) were used to synthesize a total of 18 phenolic acid derivatives. With molecular docking for molecule design and target protein (factors) screening, in combination with the confirmation of target prot...

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Autores principales: Luo, Xuan, Du, Chuanrong, Cheng, Hui, Chen, Jian-hua, Lin, Cuiwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149684/
https://www.ncbi.nlm.nih.gov/pubmed/29182552
http://dx.doi.org/10.3390/molecules22122047
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author Luo, Xuan
Du, Chuanrong
Cheng, Hui
Chen, Jian-hua
Lin, Cuiwu
author_facet Luo, Xuan
Du, Chuanrong
Cheng, Hui
Chen, Jian-hua
Lin, Cuiwu
author_sort Luo, Xuan
collection PubMed
description In this study, three type II phenolic acids (caffeic acid, p-hydroxycinnamic acid, and ferulic acid) were used to synthesize a total of 18 phenolic acid derivatives. With molecular docking for molecule design and target protein (factors) screening, in combination with the confirmation of target proteins (factors) by surface plasmon resonance, and the evaluation of haemostatic and anticoagulant activities with five blood assays (plasma recalcification time, prothrombin time, activated partial thromboplastin time, fibrinogen, and thrombin time), the data indicated that caffeic acid derivatives showed certain anticoagulant or procoagulant activities and that two other series contained compounds with the best anticoagulant activities. Using Materials Studio analysis, particular functional groups that affect anticoagulant or procoagulant activities were revealed, and these conclusions can guide the discovery of compounds with better activities.
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spelling pubmed-61496842018-11-13 Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives Luo, Xuan Du, Chuanrong Cheng, Hui Chen, Jian-hua Lin, Cuiwu Molecules Article In this study, three type II phenolic acids (caffeic acid, p-hydroxycinnamic acid, and ferulic acid) were used to synthesize a total of 18 phenolic acid derivatives. With molecular docking for molecule design and target protein (factors) screening, in combination with the confirmation of target proteins (factors) by surface plasmon resonance, and the evaluation of haemostatic and anticoagulant activities with five blood assays (plasma recalcification time, prothrombin time, activated partial thromboplastin time, fibrinogen, and thrombin time), the data indicated that caffeic acid derivatives showed certain anticoagulant or procoagulant activities and that two other series contained compounds with the best anticoagulant activities. Using Materials Studio analysis, particular functional groups that affect anticoagulant or procoagulant activities were revealed, and these conclusions can guide the discovery of compounds with better activities. MDPI 2017-11-28 /pmc/articles/PMC6149684/ /pubmed/29182552 http://dx.doi.org/10.3390/molecules22122047 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Luo, Xuan
Du, Chuanrong
Cheng, Hui
Chen, Jian-hua
Lin, Cuiwu
Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives
title Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives
title_full Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives
title_fullStr Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives
title_full_unstemmed Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives
title_short Study on the Anticoagulant or Procoagulant Activities of Type II Phenolic Acid Derivatives
title_sort study on the anticoagulant or procoagulant activities of type ii phenolic acid derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149684/
https://www.ncbi.nlm.nih.gov/pubmed/29182552
http://dx.doi.org/10.3390/molecules22122047
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