Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment
Edible: By grafting natural peptide antagonists onto the cyclotide kalata B1, orally active peptides were engineered, which are potentially useful therapeutics for the treatment of inflammatory pain. For example, the entire loop 6 of kalata B1 was replaced with the peptidic bradykinin B1 receptor an...
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sg-ntu-dr.10356-983852020-03-07T12:18:20Z Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment Wong, Clarence T. T. Rowlands, Dewi K. Wong, Chi-Hang. Lo, Theodore W. C. Nguyen, Giang K. T. Li, Hoi-Yeung Tam, James P. School of Biological Sciences DRNTU::Science::Biological sciences Edible: By grafting natural peptide antagonists onto the cyclotide kalata B1, orally active peptides were engineered, which are potentially useful therapeutics for the treatment of inflammatory pain. For example, the entire loop 6 of kalata B1 was replaced with the peptidic bradykinin B1 receptor antagonist DALK (red in scheme) to obtain the cyclic bradykinin antagonist ckb-kal. 2013-07-29T08:18:14Z 2019-12-06T19:54:39Z 2013-07-29T08:18:14Z 2019-12-06T19:54:39Z 2012 2012 Journal Article Wong, C. T. T., Rowlands, D. K., Wong, C.-H., Lo, T. W. C., Nguyen, G. K. T., Li, H.-Y., et al. (2012). Orally Active Peptidic Bradykinin B1 Receptor Antagonists Engineered from a Cyclotide Scaffold for Inflammatory Pain Treatment. Angewandte Chemie International Edition, 51(23), 5620-5624. 1433-7851 https://hdl.handle.net/10356/98385 http://hdl.handle.net/10220/12497 10.1002/anie.201200984 en Angewandte chemie international edition © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. |
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DRNTU::Science::Biological sciences Wong, Clarence T. T. Rowlands, Dewi K. Wong, Chi-Hang. Lo, Theodore W. C. Nguyen, Giang K. T. Li, Hoi-Yeung Tam, James P. Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
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Edible: By grafting natural peptide antagonists onto the cyclotide kalata B1, orally active peptides were engineered, which are potentially useful therapeutics for the treatment of inflammatory pain. For example, the entire loop 6 of kalata B1 was replaced with the peptidic bradykinin B1 receptor antagonist DALK (red in scheme) to obtain the cyclic bradykinin antagonist ckb-kal. |
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School of Biological Sciences |
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School of Biological Sciences Wong, Clarence T. T. Rowlands, Dewi K. Wong, Chi-Hang. Lo, Theodore W. C. Nguyen, Giang K. T. Li, Hoi-Yeung Tam, James P. |
format |
Article |
author |
Wong, Clarence T. T. Rowlands, Dewi K. Wong, Chi-Hang. Lo, Theodore W. C. Nguyen, Giang K. T. Li, Hoi-Yeung Tam, James P. |
author_sort |
Wong, Clarence T. T. |
title |
Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
title_short |
Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
title_full |
Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
title_fullStr |
Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
title_full_unstemmed |
Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
title_sort |
orally active peptidic bradykinin b1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment |
publishDate |
2013 |
url |
https://hdl.handle.net/10356/98385 http://hdl.handle.net/10220/12497 |
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1681048897525383168 |