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Prolylhydroxylase/atf4 inhibitors and methods of use for treating neural cell injury or death and conditions resulting therefrom

a technology of atf4 inhibitors and inhibitors, which is applied in the field of neural cell injury or death treatment methods, can solve problems such as the methodology remains elusiv

Inactive Publication Date: 2020-11-19
CORNELL UNIVERSITY
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

Nevertheless, until now, such a methodology has remained elusive.

Method used

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  • Prolylhydroxylase/atf4 inhibitors and methods of use for treating neural cell injury or death and conditions resulting therefrom
  • Prolylhydroxylase/atf4 inhibitors and methods of use for treating neural cell injury or death and conditions resulting therefrom
  • Prolylhydroxylase/atf4 inhibitors and methods of use for treating neural cell injury or death and conditions resulting therefrom

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[0106]Secondary injury from ICH has been attributed to hemin, a breakdown product of hemoglobin (from lysed red blood cells). To investigate the mechanisms of hemin toxicity to neurons in vitro, this experiment exposed primary cortical neurons, immortalized hippocampal neuroblasts (HT22 cells), and immortalized striatal neuroblasts (Q7 cells) to hemin for 24 hours. As expected, a dose dependent loss in viability as measured by MTT reduction or LIVE / DEAD assay in all three cell types was observed. Heroin treatment of primary neurons at the LD50 (50 μM) resulted in a time-dependent increase in heme-oxygenase expression and iron content suggesting that hemin is taken up into neurons and metabolized. To examine whether iron-dependent HIF PHD enzymes can be modulated to protect neurons from hemin-induced toxicity, this experiment examined structurally diverse inhibitors of the HIF PHDs: desferoxamine, cyclopirox, and dihydroxybenzoic acid. Co-treatment of neurons with hemin with structur...

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Abstract

Methods for treating a patient suffering from neural cell injury, the method comprising administering to the patient an effective amount of a HIE prolyl-4-hydroxylase inhibiting compound having the following general formula (1) wherein R1 is a cyclic group containing at least three and up to seven carbon atoms and optionally containing one or more heteroatoms selected from O, N, and S, and optionally attached to the shown carbon atom by a linking group; R2 is independently selected from said cyclic groups of R1 and a cyclic hydrocarbon groups R5 containing up to twenty carbon atoms; R3 is selected from hydrogen atom and hydrocarbon groups containing up to six carbon atoms; R6 and R7 are independently selected from hydrogen atom, hydrocarbon groups containing up to three carbon atoms, halogen atom, and polar groups, as well as methylene-linked versions thereof; and t is 0 or 1.

Description

CROSS REFERENCE TO RELATED APPLICATION[0001]This application is a divisional of U.S. patent application Ser. No. 15 / 104,012 filed Jun. 13, 2016, which claims the benefit of priority from U.S. Provisional Application No. 61 / 915,068, filed on Dec. 12, 2013.FIELD OF THE INVENTION[0002]The invention relates generally to methods for treating neural cell injury or death (e.g., brain and spinal cord injury), and more particularly, methods that include administering to a subject with such injury an inhibitor of hypoxia inducible factor (HIF) prolyl-4-hydroxylases (PHDs) and / or inhibitor of ATF4. The invention is also directed to particular compounds and pharmaceutical compositions useful in treating neural cell injury and conditions or diseases caused thereby or resulting therefrom.BACKGROUND OF THE INVENTION[0003]Brain or spinal cord injury is associated with significant morbidity and mortality and can occur as a result of, for example, intracerebral hemorrhage (ICH), stroke, traumatic bra...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/4709A61K31/47
CPCA61K31/47A61K31/4709A61P25/00
Inventor RATAN, RAJIV R.KARUPPAGOUNDER, SARAVANAN S.
Owner CORNELL UNIVERSITY