ExLibris header image
SFX Logo
Title: Bioisosteres of Indomethacin as Inhibitors of Aldo-Keto Reductase 1C3
Source:

Acs Medicinal Chemistry Letters [1948-5875] Lolli, Marco yr:2019


Collapse list of basic services Basic
Full text
Full text available via American Chemical Society Journals
GO
Full text available via PubMed Central
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Pippione, Agnese C. "Hydroxytriazole derivatives as potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors discovered by bioisosteric scaffold hopping approach." European journal of medicinal chemistry 139 (2017): 936-946. Link to SFX for this item
2. DeRatt, Lindsey G. "A carboxylic acid isostere screen of the DHODH inhibitor Brequinar." Bioorganic & medicinal chemistry letters 30.22 (2020): 127589-127589. Link to SFX for this item
3. Sainas, S. "Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds." European journal of medicinal chemistry 129 (2017): 287-302. Link to SFX for this item
4. Pippione, Agnese C. "Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid." European journal of medicinal chemistry 150 (2018): 930-945. Link to SFX for this item
Select All Clear All

Expand list of advanced services Advanced