US2024025860A1PendingUtilityA1

Sars-cov-2 inhibitors for treating coronavirus infections

Assignee: INSILICO MEDICINE IP LTDPriority: Nov 2, 2021Filed: Jun 22, 2023Published: Jan 25, 2024
Est. expiryNov 2, 2041(~15.3 yrs left)· nominal 20-yr term from priority
C12N 2770/20022C07K 14/005C07D 493/08C07D 417/14C07D 417/12C07D 413/12C07D 405/14C07D 405/12C07D 401/12C07D 261/08C07D 239/30C07D 239/26C07D 213/85C07D 213/64C07D 213/61C07B 59/002A61K 31/506A61K 31/505A61K 31/4433A61K 31/4412A61K 31/44A61K 31/42C07D 233/96A61P 31/14C07D 403/12C07D 213/56C07B 2200/05
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Claims

Abstract

Provided herein are compounds, pharmaceutical compositions, and methods for treating a SARS-CoV-2 infection.

Claims

exact text as granted — not AI-modified
1 .- 62 . (canceled) 
     
     
         63 . A method of treating or preventing a coronavirus infection in a patient in need thereof, comprising administering to the patient a pharmaceutical composition comprising (i) a compound of Formula (Ia), or a pharmaceutically acceptable salt or stereoisomer thereof: 
       
         
           
           
               
               
           
         
         wherein: 
         R 1  is fluoro and R 2  is chloro; 
       
       
         
           
           
               
               
           
         
         L is —(CR 4 R 4 ) p —; 
         each R 4  is independently hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, or C 1 -C 6 heteroalkyl; 
         p is 0; 
         R 5  is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, or C 1 -C 6 heteroalkyl; 
       
       
         
           
           
               
               
           
         
         R 7  is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, or C 1 -C 6 heteroalkyl; and 
       
       
         
           
           
               
               
           
         
       
       and
 (ii) a pharmaceutically acceptable excipient. 
 
     
     
         64 . The method of  claim 63 , wherein R 5  is C 1 -C 6 alkyl. 
     
     
         65 . The method of  claim 63 , wherein R 5  is methyl. 
     
     
         66 . The method of  claim 63 , wherein R 7  is hydrogen. 
     
     
         67 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt or stereoisomer thereof. 
     
     
         68 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         69 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         70 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         71 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         72 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         73 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         74 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         75 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         76 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         77 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         78 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         79 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         80 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         81 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         82 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         83 . The method of  claim 63 , wherein the compound of Formula (Ia) is selected from the group consisting of

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