US2017348295A1PendingUtilityA1
Small molecule inhibitors of viral protein interactions with human t-rna
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-modifiedWhat 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.Cited by (0)
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