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INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology

[Image: see text] A data-centric medicinal chemistry approach led to the invention of a potent and selective IDO1 inhibitor 4f, INCB24360 (epacadostat). The molecular structure of INCB24360 contains several previously unknown or underutilized functional groups in drug substances, including a hydroxy...

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Autores principales: Yue, Eddy W., Sparks, Richard, Polam, Padmaja, Modi, Dilip, Douty, Brent, Wayland, Brian, Glass, Brian, Takvorian, Amy, Glenn, Joseph, Zhu, Wenyu, Bower, Michael, Liu, Xiangdong, Leffet, Lynn, Wang, Qian, Bowman, Kevin J., Hansbury, Michael J., Wei, Min, Li, Yanlong, Wynn, Richard, Burn, Timothy C., Koblish, Holly K., Fridman, Jordan S., Emm, Tom, Scherle, Peggy A., Metcalf, Brian, Combs, Andrew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430407/
https://www.ncbi.nlm.nih.gov/pubmed/28523098
http://dx.doi.org/10.1021/acsmedchemlett.6b00391
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author Yue, Eddy W.
Sparks, Richard
Polam, Padmaja
Modi, Dilip
Douty, Brent
Wayland, Brian
Glass, Brian
Takvorian, Amy
Glenn, Joseph
Zhu, Wenyu
Bower, Michael
Liu, Xiangdong
Leffet, Lynn
Wang, Qian
Bowman, Kevin J.
Hansbury, Michael J.
Wei, Min
Li, Yanlong
Wynn, Richard
Burn, Timothy C.
Koblish, Holly K.
Fridman, Jordan S.
Emm, Tom
Scherle, Peggy A.
Metcalf, Brian
Combs, Andrew P.
author_facet Yue, Eddy W.
Sparks, Richard
Polam, Padmaja
Modi, Dilip
Douty, Brent
Wayland, Brian
Glass, Brian
Takvorian, Amy
Glenn, Joseph
Zhu, Wenyu
Bower, Michael
Liu, Xiangdong
Leffet, Lynn
Wang, Qian
Bowman, Kevin J.
Hansbury, Michael J.
Wei, Min
Li, Yanlong
Wynn, Richard
Burn, Timothy C.
Koblish, Holly K.
Fridman, Jordan S.
Emm, Tom
Scherle, Peggy A.
Metcalf, Brian
Combs, Andrew P.
author_sort Yue, Eddy W.
collection PubMed
description [Image: see text] A data-centric medicinal chemistry approach led to the invention of a potent and selective IDO1 inhibitor 4f, INCB24360 (epacadostat). The molecular structure of INCB24360 contains several previously unknown or underutilized functional groups in drug substances, including a hydroxyamidine, furazan, bromide, and sulfamide. These moieties taken together in a single structure afford a compound that falls outside of “drug-like” space. Nevertheless, the in vitro ADME data is consistent with the good cell permeability and oral bioavailability observed in all species (rat, dog, monkey) tested. The extensive intramolecular hydrogen bonding observed in the small molecule crystal structure of 4f is believed to significantly contribute to the observed permeability and PK. Epacadostat in combination with anti-PD1 mAb pembrolizumab is currently being studied in a phase 3 clinical trial in patients with unresectable or metastatic melanoma.
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spelling pubmed-54304072017-05-18 INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology Yue, Eddy W. Sparks, Richard Polam, Padmaja Modi, Dilip Douty, Brent Wayland, Brian Glass, Brian Takvorian, Amy Glenn, Joseph Zhu, Wenyu Bower, Michael Liu, Xiangdong Leffet, Lynn Wang, Qian Bowman, Kevin J. Hansbury, Michael J. Wei, Min Li, Yanlong Wynn, Richard Burn, Timothy C. Koblish, Holly K. Fridman, Jordan S. Emm, Tom Scherle, Peggy A. Metcalf, Brian Combs, Andrew P. ACS Med Chem Lett [Image: see text] A data-centric medicinal chemistry approach led to the invention of a potent and selective IDO1 inhibitor 4f, INCB24360 (epacadostat). The molecular structure of INCB24360 contains several previously unknown or underutilized functional groups in drug substances, including a hydroxyamidine, furazan, bromide, and sulfamide. These moieties taken together in a single structure afford a compound that falls outside of “drug-like” space. Nevertheless, the in vitro ADME data is consistent with the good cell permeability and oral bioavailability observed in all species (rat, dog, monkey) tested. The extensive intramolecular hydrogen bonding observed in the small molecule crystal structure of 4f is believed to significantly contribute to the observed permeability and PK. Epacadostat in combination with anti-PD1 mAb pembrolizumab is currently being studied in a phase 3 clinical trial in patients with unresectable or metastatic melanoma. American Chemical Society 2017-03-06 /pmc/articles/PMC5430407/ /pubmed/28523098 http://dx.doi.org/10.1021/acsmedchemlett.6b00391 Text en Copyright © 2017 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 Yue, Eddy W.
Sparks, Richard
Polam, Padmaja
Modi, Dilip
Douty, Brent
Wayland, Brian
Glass, Brian
Takvorian, Amy
Glenn, Joseph
Zhu, Wenyu
Bower, Michael
Liu, Xiangdong
Leffet, Lynn
Wang, Qian
Bowman, Kevin J.
Hansbury, Michael J.
Wei, Min
Li, Yanlong
Wynn, Richard
Burn, Timothy C.
Koblish, Holly K.
Fridman, Jordan S.
Emm, Tom
Scherle, Peggy A.
Metcalf, Brian
Combs, Andrew P.
INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
title INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
title_full INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
title_fullStr INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
title_full_unstemmed INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
title_short INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
title_sort incb24360 (epacadostat), a highly potent and selective indoleamine-2,3-dioxygenase 1 (ido1) inhibitor for immuno-oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430407/
https://www.ncbi.nlm.nih.gov/pubmed/28523098
http://dx.doi.org/10.1021/acsmedchemlett.6b00391
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