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Indole Inhibitors of MMP-13 for Arthritic Disorders

[Image: see text] Here, we described the design, by fragment merging and multiparameter optimization, of selective MMP-13 inhibitors that display an appropriate balance of potency and physicochemical properties to qualify as tool compounds suitable for in vivo testing. Optimization of potency was gu...

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Autores principales: Taylor, Steven J., Abeywardane, Asitha, Liang, Shuang, Xiong, Zhaoming, Proudfoot, John R., Farmer, Bennett Sandy, Gao, Donghong A., Heim-Riether, Alexander, Smith-Keenan, Lana Louise, Muegge, Ingo, Yu, Yang, Zhang, Qiang, Souza, Donald, Panzenbeck, Mark, Goldberg, Daniel, Hill-Drzewi, Melissa, Margarit, Mariana, Collins, Brandon, Li, John Xiang, Zuvela-Jelaska, Ljiljana, Li, Jun, Farrow, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319936/
https://www.ncbi.nlm.nih.gov/pubmed/34337203
http://dx.doi.org/10.1021/acsomega.1c01320
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author Taylor, Steven J.
Abeywardane, Asitha
Liang, Shuang
Xiong, Zhaoming
Proudfoot, John R.
Farmer, Bennett Sandy
Gao, Donghong A.
Heim-Riether, Alexander
Smith-Keenan, Lana Louise
Muegge, Ingo
Yu, Yang
Zhang, Qiang
Souza, Donald
Panzenbeck, Mark
Goldberg, Daniel
Hill-Drzewi, Melissa
Margarit, Mariana
Collins, Brandon
Li, John Xiang
Zuvela-Jelaska, Ljiljana
Li, Jun
Farrow, Neil A.
author_facet Taylor, Steven J.
Abeywardane, Asitha
Liang, Shuang
Xiong, Zhaoming
Proudfoot, John R.
Farmer, Bennett Sandy
Gao, Donghong A.
Heim-Riether, Alexander
Smith-Keenan, Lana Louise
Muegge, Ingo
Yu, Yang
Zhang, Qiang
Souza, Donald
Panzenbeck, Mark
Goldberg, Daniel
Hill-Drzewi, Melissa
Margarit, Mariana
Collins, Brandon
Li, John Xiang
Zuvela-Jelaska, Ljiljana
Li, Jun
Farrow, Neil A.
author_sort Taylor, Steven J.
collection PubMed
description [Image: see text] Here, we described the design, by fragment merging and multiparameter optimization, of selective MMP-13 inhibitors that display an appropriate balance of potency and physicochemical properties to qualify as tool compounds suitable for in vivo testing. Optimization of potency was guided by structure-based insights, specifically to replace an ester moiety and introduce polar directional hydrogen bonding interactions in the core of the molecule. By introducing polar enthalpic interactions in this series of inhibitors, the overall beneficial physicochemical properties were maintained. These physicochemical properties translated to excellent drug-like properties beyond potency. In a murine model of rheumatoid arthritis, treatment of mice with selective inhibitors of MMP-13 resulted in a statistically significant reduction in the mean arthritic score vs control when dosed over a 14 day period.
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spelling pubmed-83199362021-07-30 Indole Inhibitors of MMP-13 for Arthritic Disorders Taylor, Steven J. Abeywardane, Asitha Liang, Shuang Xiong, Zhaoming Proudfoot, John R. Farmer, Bennett Sandy Gao, Donghong A. Heim-Riether, Alexander Smith-Keenan, Lana Louise Muegge, Ingo Yu, Yang Zhang, Qiang Souza, Donald Panzenbeck, Mark Goldberg, Daniel Hill-Drzewi, Melissa Margarit, Mariana Collins, Brandon Li, John Xiang Zuvela-Jelaska, Ljiljana Li, Jun Farrow, Neil A. ACS Omega [Image: see text] Here, we described the design, by fragment merging and multiparameter optimization, of selective MMP-13 inhibitors that display an appropriate balance of potency and physicochemical properties to qualify as tool compounds suitable for in vivo testing. Optimization of potency was guided by structure-based insights, specifically to replace an ester moiety and introduce polar directional hydrogen bonding interactions in the core of the molecule. By introducing polar enthalpic interactions in this series of inhibitors, the overall beneficial physicochemical properties were maintained. These physicochemical properties translated to excellent drug-like properties beyond potency. In a murine model of rheumatoid arthritis, treatment of mice with selective inhibitors of MMP-13 resulted in a statistically significant reduction in the mean arthritic score vs control when dosed over a 14 day period. American Chemical Society 2021-07-19 /pmc/articles/PMC8319936/ /pubmed/34337203 http://dx.doi.org/10.1021/acsomega.1c01320 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Taylor, Steven J.
Abeywardane, Asitha
Liang, Shuang
Xiong, Zhaoming
Proudfoot, John R.
Farmer, Bennett Sandy
Gao, Donghong A.
Heim-Riether, Alexander
Smith-Keenan, Lana Louise
Muegge, Ingo
Yu, Yang
Zhang, Qiang
Souza, Donald
Panzenbeck, Mark
Goldberg, Daniel
Hill-Drzewi, Melissa
Margarit, Mariana
Collins, Brandon
Li, John Xiang
Zuvela-Jelaska, Ljiljana
Li, Jun
Farrow, Neil A.
Indole Inhibitors of MMP-13 for Arthritic Disorders
title Indole Inhibitors of MMP-13 for Arthritic Disorders
title_full Indole Inhibitors of MMP-13 for Arthritic Disorders
title_fullStr Indole Inhibitors of MMP-13 for Arthritic Disorders
title_full_unstemmed Indole Inhibitors of MMP-13 for Arthritic Disorders
title_short Indole Inhibitors of MMP-13 for Arthritic Disorders
title_sort indole inhibitors of mmp-13 for arthritic disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319936/
https://www.ncbi.nlm.nih.gov/pubmed/34337203
http://dx.doi.org/10.1021/acsomega.1c01320
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