IP Library › Granted Patent US 11,253,529
Granted Patent B2
US 11,253,529 · App. 16/629,057 · Granted Feb 22, 2022

Flex-nucleoside analogues, novel therapeutics against filoviruses and flaviviruses

Inventor: Katherine L. Radtke (Baltimore, MD)
Assignee: UNIVERSITY OF MARYLAND, BALTIMORE COUNTY
A61K31/683A61K31/506A61K31/675A61K45/06
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Quick Facts
Patent No.
US 11,253,529
App. No.
16/629,057
Granted
Feb 22, 2022
Kind
B2
Abstract

The present invention is directed to compounds, methods and compositions for treating or preventing viral infections using nucleosides analogs. Specifically, the present invention provides for the design and synthesis of acyclic fleximer nucleoside analogues having increased flexibility and ability to alter their conformation structures to provide increased antiviral activity potential with the result of inhibiting flaviviruses, filoviruses and/or coronaviruses.

Claims (10)

1. A method of treating and/or reducing the effects of a filovirus, flavivirus or coronavirus in a subject in need of such treatment, the method comprising administering to the subject therapeutically effective amount of an acyclic fleximer nucleoside analogue selected from the group consisting of:

and a pharmaceutically acceptable salt, isomer, hydrate, prodrug or solvate thereof.

2. The method of claim 1 , wherein the acyclic fleximer nucleoside analogue is structure 9 and the coronavirus is severe acute respiratory syndrome (SARS) or Middle East respiratory syndrome (MERS).

3. The method of claim 1 , wherein the acyclic fleximer nucleoside analogue is structure 9 and the Flavivirus is Dengue, Zika or West Nile.

4. The method of claim 1 , wherein the acyclic fleximer nucleoside analogue is structure 3 and the Filovirus is Ebola, Sudan or and Marburg.

5. The method of claim 1 , wherein the acyclic fleximer nucleoside analogue is in a composition further comprising a pharmaceutically acceptable carrier.

6. The method of claim 5 , wherein the acyclic fleximer nucleoside analogue is in a composition further comprising an additional antiviral agent.

7. The method of claim 1 , wherein the therapeutically effective amount of the acyclic fleximer nucleoside analogue is from 0.05 to 50 mg per kilogram body weight of the subject per day.

8. A method of binding to natural and/or mutated polymerases of a filovirus, flavivirus or coronavirus in a subject in need of such treatment, the method comprising administering to the subject a therapeutically effective amount of an acyclic fleximer nucleoside analogue selected from the group consisting of:

and a pharmaceutically acceptable salt, isomer, hydrate, prodrug or solvate thereof.

Continuity (2)
Provisional Application 62539034 · Jul 31, 2017
Related Publication 20200171060A1 · Jun 4, 2020