Immunomodulators

Abstract

The present disclosure provides novel macrocyclic peptides which inhibit the PD-1/PD-L1 and PD-L1/CD80 protein/protein interaction, and thus are useful for the amelioration of various diseases, including cancer and infectious diseases.

What is claimed is: 
     
         1 . A compound of formula (I) 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, wherein:
 A is selected from a bond, 
 
       
         
           
           
               
               
           
         
       
       wherein:
    denotes the point of attachment to the carbonyl group and   denotes the point of attachment to the nitrogen atom; 
 z is 0, 1, or 2; 
 w is 1 or 2; 
 n is 0 or 1; 
 m is 1 or 2; 
 m′ is 0 or 1; 
 p is 0, 1, or 2; 
 R x  is selected from hydrogen, amino, hydroxy, and methyl; 
 R 14  and R 15  are independently selected from hydrogen and methyl; and 
 R z  is selected from hydrogen and —C(O)NHR 16 ; wherein R 16  is selected from hydrogen, —CHR 17 C(O)NH 2 , —CHR 17 C(O)NHCHR 18 C(O)NH 2 , and —CHR 17 C(O)NHCHR 18 C(O)NHCH 2 C(O)NH 2 ; wherein R 17  is selected from hydrogen and —CH 2 OH and wherein R 18  is selected from hydrogen and methyl; 
 R v  is hydrogen or a natural amino acid side chain; 
 Q is selected from 
 
       
         
           
           
               
               
           
         
       
       wherein R b  is defined below, and a five- or six-membered ring containing one, two, or three double bonds and optionally containing one, two, or three heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein the ring is optionally substituted with one, two, three, or four substituents independently selected from C 1 -C 6 alkoxycarbonyl, C 1 -C 3 alkyl, amino, C 1 -C 3 alkylamino, carboxy, C 1 -C 3 dialkylamino, halo, and haloC 1 -C 3 alkyl;
 U is selected from 
 
       
         
           
           
               
               
           
         
       
       wherein R k  is defined below, and a five- or six-membered ring containing one, two, or three double bonds and optionally containing one, two, or three heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein the ring is optionally substituted with one, two, three, or four substituents independently selected from C 1 -C 6 alkoxycarbonyl, C 1 -C 3 alkyl, amino, C 1 -C 3 alkylamino, carboxy, C 1 -C 3 dialkylamino, halo, and haloC 1 -C 3 alkyl; provided that at least one of Q and U is a five- or six-membered ring containing one, two, or three double bonds and containing one, two, or three heteroatoms independently selected from nitrogen, oxygen, and sulfur;
 R c , R f , R h , R i , R m , and R n  are hydrogen; 
 R a , R e , R j  and R k , are each independently selected from hydrogen and methyl; 
 R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , and R 13  are independently selected from a natural amino acid side chain and an unnatural amino acid side chain or form a ring with the corresponding vicinal R group as described below; 
 R e  and R k  can each form a ring with the corresponding vicinal R group and the atoms to which they are attached selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, and hydroxy; 
 R b  is methyl or, R b  and R 2 , together with the atoms to which they are attached, form a ring selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, and hydroxy; 
 R d  is hydrogen or methyl, or, R d  and R 4 , together with the atoms to which they are attached, can form a ring selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, hydroxy, and phenyl; 
 R g  is hydrogen or methyl or R g  and R 7 , together with the atoms to which they are attached, can form a ring selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, benzyl optionally substituted with a halo group, benzyloxy, cyano, cyclohexyl, methyl, halo, hydroxy, isoquinolinyloxy optionally substituted with a methoxy group, quinolinyloxy optionally substituted with a halo group, and tetrazolyl; and wherein the pyrrolidine and the piperidine ring are optionally fused to a cyclohexyl, phenyl, or indole group; and 
 R 1  is methyl or, R 1  and R 12 , together with the atoms to which they are attached, form a ring selected from azetidine and pyrollidine, wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, and hydroxy. 
 
     
     
         2 . A compound of  claim 1 , or a pharmaceutically acceptable salt thereof, wherein:
 Q is selected from   
       
         
           
           
               
               
           
         
       
       and a five-membered ring containing one or two double-bonds and containing one, two, three, or four nitrogen atoms; and
 U is selected from 
 
       
         
           
           
               
               
           
         
       
       and a five-membered ring containing one or two double-bonds and containing one, two, three, or four nitrogen atoms. 
     
     
         3 . A compound of  claim 2 , or a pharmaceutically acceptable salt thereof, wherein A is 
       
         
           
           
               
               
           
         
       
     
     
         4 . A compound of  claim 3 , or a pharmaceutically acceptable salt thereof, wherein
 z and w are each 1;   R 14  and R 15  are hydrogen; and   R z  is —C(O)NHR 16 ; wherein R 16  is —CHR 17 C(O)NH 2 .   
     
     
         5 . A compound of  claim 4  wherein
 R 1  is phenylC 1 -C 3 alkyl wherein the phenyl is optionally substituted with hydroxy; 
 R 2  is C 1 -C 7 alkyl or, Rb and R 2 , together with the atoms to which they are attached, form a morpholine or piperidine ring; 
 R 3  is selected from —CH 2 CO 2 H and —CH 2 C(O)NH 2 ; 
 R 4  and R d , together with the atoms to which they are attached, form a pyrrolidine ring; 
 R 5  is selected from —CH 2 NH 2  and —CH 2 (imidazolyl); 
 R 6  is selected from C 1 -C 7 alkyl, —CH 2 CH 2 C(O)NH 2 , —CH 2 CH 2 CH 2 CH 2 NH 2 , and —CH 2 CH 2 CO 2 H; 
 R 7  is hydrogen or R 7  and R g , together with the atoms to which they are attached, form a pyrroldine ring optionally substituted with a hydroxy group; 
 R 8  is —(CH 2 )indolyl; 
 R 9  is selected from aminomethyl, hydroxymethyl, —CH 2 CH 2 NH 2 , and CH 2 CH 2 CH 2 CH 2 NH 2 ; 
 R 10  is selected from —(CH 2 )indolyl, —(CH 2 )naphthyl, and —(CH 2 )benzothienyl, each optionally substituted with —CH 2 CO 2 H; 
 R 11  is C 1 -C 7 alkyl; and 
 R 12  is C 1 -C 7 alkyl. 
 
     
     
         6 . A compound of formula (II) 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, wherein:
 A is selected from a bond, 
 
       
         
           
           
               
               
           
         
       
       wherein:
    denotes the point of attachment to the carbonyl group and   denotes the point of attachment to the nitrogen atom; 
 n is 0 or 1; 
 R 14  and R 15  are independently selected from hydrogen and methyl; and 
 R 16  is selected from 
 
       hydrogen, —CHR 17 C(O)NH 2 , —CHR 17 C(O)NHCHR 18 C(O)NH 2 , 
       and —CHR 17 C(O)NHCHR 18 C(O)NHCH 2 C(O)NH 2 ; 
       wherein R 17  is selected from hydrogen and —CH 2 OH and wherein R 18  is selected from hydrogen and methyl;
 Q is a five- or six-membered ring containing one, two, or three double bonds and optionally containing one, two, or three heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein the ring is optionally substituted with one, two, three, or four substituents independently selected from C 1 -C 6 alkoxycarbonyl, C 1 -C 3 alkyl, amino, C 1 -C 3 alkylamino, carboxy, C 1 -C 3 dialkylamino, halo, and haloC 1 -C 3 alkyl; 
 R a , R f , R j , R k , R l , and R m  are hydrogen; 
 R b  and R c  are methyl; 
 R g  is selected from hydrogen and methyl; 
 R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 10 , R 11 , and R 12  are independently selected from a natural amino acid side chain and an unnatural amino acid side chain or form a ring with the corresponding vicinal R group as described below; 
 R 20  is hydrogen; 
 R 8  is selected from a natural amino acid side chain, an unnatural amino acid chain, or can form a ring with the corresponding vicinal R group as described below, or, alternatively, R 8  can form a three- to six-membered carbocyclic ring with R 20 ; 
 R d  is selected from hydrogen and methyl, or, R d  and R 4 , together with the atoms to which they are attached, form a ring selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, halomethyl, and hydroxy; 
 R e  is selected from hydrogen and methyl, or, R e  and R 5 , together with the atoms to which they are attached, form a ring selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, halomethyl, and hydroxy; and 
 R h  is selected from hydrogen and methyl, or, R h  and R 8 , together with the atoms to which they are attached, form a ring selected from azetidine, pyrollidine, morpholine, piperidine, piperazine, and tetrahydrothiazole; wherein each ring is optionally substituted with one to four groups independently selected from amino, cyano, methyl, halo, halomethyl, and hydroxy. 
 
     
     
         7 . A compound of  claim 6 , or a pharmaceutically acceptable salt thereof, wherein Q is a five-membered ring containing one or two double-bonds and containing one, two, three, or four nitrogen atoms. 
     
     
         8 . A compound of  claim 7 , or a pharmaceutically acceptable salt thereof, wherein A is 
       
         
           
           
               
               
           
         
       
     
     
         9 . A compound of  claim 8 , or a pharmaceutically acceptable salt thereof, wherein:
 R 1  and R 2  are phenylC 1 -C 3 alkyl;   R 3  is C 1 -C 7 alkyl;   R 4  is hydrogen;   R 5  is carboxymethyl;   R 6  is C 1 -C 7 alkyl;   R 7  is phenylC 1 -C 3 alkyl;   R 8  is phenylC 1 -C 3 alkyl wherein the phenyl is substituted with hydroxy, or, alternatively, R 8  and R 20  form a six-membered carbocyclic ring;   R 9  is hydrogen;   R 10  is —(CH 2 )indolyl;   R 11  is phenylC 1 -C 3 alkyl substituted with hydroxy; and   R 12  is C 1 -C 7 alkyl.   
     
     
         10 . A compound selected from:
 Example 1001; Example 1002; Example 1003; Example 1004; Example 1005; Example 1006; Example 1007; Example 1010; Example 1012; Example 1013; Example 1014; Example 1050; Example 1051; Example 1052; Example 1053; Example 1054; Example 1055; Example 1056; Example 1057; Example 1058; Example 1059; Example 1060; Example 1061; Example 1100; Example 1101; Example 1102; Example 1103; Example 1104; Example 1105; Example 1106; Example 1107; Example 1108; Example 1109; Example 1110; Example 1111; Example 1113; Example 1114; Example 3001; Example 3002; Example 3003; or a pharmaceutically acceptable salt thereof.   
     
     
         11 . A compound which is Example 1115. 
     
     
         12 . A method of enhancing, stimulating, and/or increasing the immune response in a subject in need thereof, said method comprising administering to the subject a therapeutically effective amount of a compound of  claim 1  or a therapeutically acceptable salt thereof. 
     
     
         13 . The method of  claim 12  further comprising administering an additional agent prior to, after, or simultaneously with the compound of  claim 1  or a therapeutically acceptable salt thereof. 
     
     
         14 . The method of  claim 13  wherein the additional agent is an antimicrobial agent, an antiviral agent, a cytotoxic agent, and/or an immune response modifier. 
     
     
         15 . The method of  claim 13  wherein the additional agent is an HDAC inhibitor. 
     
     
         16 . The method of  claim 13  wherein the additional agent is a TLR7 and/or TLR8 agonist 
     
     
         17 . A method of inhibiting growth, proliferation, or metastasis of cancer cells in a subject in need thereof, said method comprising administering to the subject a therapeutically effective amount a compound of  claim 1  or a therapeutically acceptable salt thereof. 
     
     
         18 . The method of  claim 17  wherein the cancer is selected from melanoma, renal cell carcinoma, squamous non-small cell lung cancer (NSCLC), non-squamous NSCLC, colorectal cancer, castration-resistant prostate cancer, ovarian cancer, gastric cancer, hepatocellular carcinoma, pancreatic carcinoma, squamous cell carcinoma of the head and neck, carcinomas of the esophagus, gastrointestinal tract and breast, and hematological malignancies. 
     
     
         19 . A method of treating an infectious disease in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a compound of  claim 1  or a therapeutically acceptable salt thereof. 
     
     
         20 . The method of  claim 19  wherein the infectious disease is caused by a virus. 
     
     
         21 . The method of  claim 20  wherein the virus is selected from HIV, Hepatitis A, Hepatitis B, Hepatitis C, herpes viruses, and influenza. 
     
     
         22 . A method of treating septic shock in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a compound of  claim 1  or a therapeutically acceptable salt thereof. 
     
     
         23 . A method blocking the interaction of PD-L1 with PD-1 and/or CD80 in a subject, said method comprising administering to the subject a therapeutically effective amount of a compound of  claim 1  or a therapeutically acceptable salt thereof.