US2017348295A1PendingUtilityA1

Small molecule inhibitors of viral protein interactions with human t-rna

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Assignee: SIRGA ADVANCED BIOPHARMA INCPriority: Aug 6, 2012Filed: Mar 12, 2017Published: Dec 7, 2017
Est. expiryAug 6, 2032(~6.1 yrs left)· nominal 20-yr term from priority
A61K 31/427A61K 31/47A61K 31/4745A61K 31/44A61K 31/63A61K 31/519A61K 31/18A61K 31/136A61K 31/37A61K 31/222A61K 31/4468A61K 31/517A61K 31/5377A61K 31/085A61K 31/473A61K 31/4453A61K 31/445A61K 31/55A61K 31/428A61K 31/53
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Claims

Abstract

Disclosed herein are compounds, compositions and methods of their use to treat HIV/AIDS disease in a subject in need thereof, wherein the compositions comprise small molecule inhibitors that inhibit viral preparation or viral recruitment of human tRNA 3 Lys .

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating HIV/AIDS disease in a patient in need thereof, said method comprising administering a therapeutically effective amount of one or more compounds of formula (IV), (V) or (VI). 
     
     
         2 . The method according to  claim 1  wherein said compound of formula (IV), (V) or (VI) is selected from the group consisting of 8391-1, 8391-2, 8391-3, 8391-4, 8391-5, 8391-6, 8391-7, 8391-8, 8391-9, 8391-10, 8391-11, 8391-12, 8391-13, 8391-14, 8391-15, 8391-16, 8391-17, 8391-18, 8391-19, 8391-20, 8391-21. 
     
     
         3 . The method according to  claim 1 , wherein said patient is administered a therapeutically effective amount of one or more compounds of formula V or VI. 
     
     
         4 . The method according to  claim 3 , wherein said compound of formula V or VI is selected from the group consisting of 8391-6, 8391-7, 8391-10 and 8391-12. 
     
     
         5 . The method according to  claim 1 , wherein HIV/AIDS is treated by inhibiting interaction of one or more viral and/or host proteins with human tRNA in a subject in need thereof. 
     
     
         6 . A method of inhibiting viral preparation or viral recruitment of tRNA 3 Lys comprising contacting said tRNA 3 Lys with one or more compound of formula (IV), (V) or (VI) in an amount effective to inhibit viral preparation or viral recruitment of tRNA 3 Lys. 
     
     
         7 . The method according to  claim 6  wherein said compound of formula (IV), (V) or (VI) is selected from the group consisting of 8391-1, 8391-2, 8391-3, 8391-4, 8391-5, 8391-6, 8391-7, 8391-8, 8391-9, 8391-10, 8391-11, 8391-12, 8391-13, 8391-14, 8391-15, 8391-16, 8391-17, 8391-18, 8391-19, 8391-20, 8391-21. 
     
     
         8 . The method according to  claim 6 , wherein viral preparation or viral recruitment of tRNA 3 Lys is inhibited by contacting said tRNA 3 Lys with one or more compounds of formula V or VI. 
     
     
         9 . The method according to  claim 8 , wherein said compound of formula V or VI is selected from the group consisting of 8391-6, 8391-7, 8391-10 and 8391-12.

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