Draft:Asengeprast
Submission declined on 28 July 2024 by DoubleGrazing (talk).
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- Comment: Primary sources do not establish notability per WP:GNG. DoubleGrazing (talk) 12:56, 28 July 2024 (UTC)
This is a draft article. It is a work in progress open to editing by anyone. Please ensure core content policies are met before publishing it as a live Wikipedia article. Find sources: Google (books · news · scholar · free images · WP refs) · FENS · JSTOR · TWL Last edited by Reba16 (talk | contribs) 21 days ago. (Update)
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Names | |
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Other names
FT011
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Identifiers | |
3D model (JSmol)
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PubChem CID
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Properties | |
C17H20NO5 | |
Molar mass | 318.349 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Asengeprast (development code FT011) is an experimental scleroderma drug candidate. It is a small molecule inhibitor of the G-protein coupled receptor GPR68 with antifibrotic activity.[1] It is being developed by Certa Therapeutics. Asengeprast was invented at the University of Melbourne.[2]
The European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA) has granted orphan drug status to FT011, for systemic sclerosis (SSc).[3]
Asengeprast has been reported to attenuate fibrosis and chronic heart failure in experimental diabetic cardiomyopathy.[4] It was developed by structure-activity optimization of the antifibrotic activity of cinnamoyl anthranilates, by assessment of their ability to prevent TGF-beta-stimulated production of collagen.[5]
References
[edit]- ^ "Certa Therapeutics website".
- ^ "University of Melbourne - Research". 11 September 2023.
- ^ "Scleroderma News".
- ^ Zhang Y, Edgley AJ, Cox AJ, Powell AK, Wang B, Kompa AR, Stapleton DI, Zammit SC, Williams SJ, Krum H, Gilbert RE, Kelly DJ (May 2012). "FT011, a new anti-fibrotic drug, attenuates fibrosis and chronic heart failure in experimental diabetic cardiomyopathy". European Journal of Heart Failure. 14 (5): 549–62. doi:10.1093/eurjhf/hfs011. PMID 22417655.
- ^ Zammit SC, Cox AJ, Gow RM, Zhang Y, Gilbert RE, Krum H, Kelly DJ, Williams SJ (December 2009). "Evaluation and optimization of antifibrotic activity of cinnamoyl anthranilates". Bioorganic & Medicinal Chemistry Letters. 19 (24): 7003–7006. doi:10.1016/j.bmcl.2009.09.120. PMID 19879136.
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