Quinoline and Isoquinoline Based HDAC Inhibitors and Methods of Use Thereof
The present invention relates to methods of modulating activity of histone deacetylases (HDACs). The present invention also relates to methods of treating HDAC-associated diseases including, but not limited to, cancers, inflammatory disorders, and neurodegenerative disorders. The present invention also provides novel compounds and compositions thereof and methods of preparation of the same. The present invention also includes methods of inhibiting HDACs, and methods of treating HDAC-associated diseases using the compounds of the invention.
1 . A compound of Formula I-A or Formula I-B, or a salt or solvate thereof:
wherein in Formula I-A and Formula I-B:
Ring A is a 5- or 6-membered aromatic ring having 0-3 ring nitrogen atoms, and wherein Ring A may be optionally substituted with one or more R a s;
Ring B is an aromatic ring having 0-2 nitrogen atoms;
Ring C may optionally be substituted with a carbonyl group, and Ring C may optionally be substituted with one or more R c s; each R a , R b and R c is independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , OR d , OC(═O)R d , OC(═O)OR d , OC(═O)NR d R e , CR d R e R f , CR d R e OR f , C(═O)R d , C(═O)NR d R e , C(═O)OR d , NR d R e , NR d C(═O)R e , NR d C(═O)OR e , NR d C(═O)NR e R f , NR d S(═O) 2 R e , NR d S(═O) 2 NR e R f , SR d , S(═O)R d , S(═O) 2 R d , and S(═O) 2 NR d R e , C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, wherein each C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl is optionally substituted by 1, 2, 3, 4, or 5 substituents independently selected from F, Cl, Br, I, CN, NO 2 , OR d , OC(═O)R d , OC(═O)OR d , OC(═O)NR d R e , CR d R e R f , CR d R e OR f , C(═O)R d , C(═O)NR d R e , C(═O)OR d , NR d R e , NR d C(═O)R e , NR d C(═O)OR e , NR d C(═O)NR e R f , NR d S(═O) 2 R e , NR d S(═O) 2 NR e R f SR d , S(═O)R d , S(═O) 2 R d , and S(═O) 2 NR d R e , and wherein each R d , R e and R f is independently selected from the group consisting of H, and optionally substituted C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, and wherein any of R d , R e or R f may be optionally joined to form additional rings; and any R a , R b and R c may be optionally joined to form additional rings;
X is NH 2 , OH, S—R, where R is H or optionally substituted C 1-6 alkyl; and
n is an integer from 0-3.
2 . The compound of claim 1 , wherein the compound is selected from the group consisting of:
3 . A composition comprising the compound of claim 1 , or a salt or solvate thereof, and at least one pharmaceutically acceptable carrier.
4 . A method of treating a disease or disorder associated with HDACs in a subject, the method comprising administering to the subject a therapeutically effective amount of a compound of Formula I-A, or Formula I-B, or a salt or solvate thereof:
wherein in Formula I-A and Formula I-B:
Ring A is a 5- or 6-membered aromatic ring having 0-3 ring nitrogen atoms, and wherein Ring A may be optionally substituted with one or more R a s;
Ring B is an aromatic ring having 0-2 nitrogen atoms;
Ring C may optionally be substituted with a carbonyl group, and Ring C may optionally be substituted with one or more R c s;
each R a , R b and R c is independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , OR d , OC(═O)R d , OC(═O)OR d , OC(═O)NR d R e , CR d R e R f , CR d R e OR f , C(═O)R d , C(═O)NR d R e , C(═O)OR d , NR d R e , NR d C(═O)R e , NR d C(═O)OR e , NR d C(═O)NR e R f , NR d S(═O) 2 R e , NR d S(═O) 2 NR e R f , SR d , S(═O)R d , S(═O) 2 R d , and S(═O) 2 NR d R e , C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, wherein each C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl is optionally substituted by 1, 2, 3, 4, or 5 substituents independently selected from F, Cl, Br, I, CN, NO 2 , OR d , OC(═O)R d , OC(═O)OR d , OC(═O)NR d R e , CR d R e R f , CR d R e OR f , C(═O)R d , C(═O)NR d R e , C(═O)OR d , NR d R e , NR d C(═O)R e , NR d C(═O)OR e , NR d C(═O)NR e R f , NR d S(═O) 2 R e , NR d S(═O) 2 NR e R f , SR d , S(═O)R d , S(═O) 2 R d , and S(═O) 2 NR d R e , and wherein each R d , R e and R f is independently selected from the group consisting of H, and optionally substituted C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, and wherein any of R d , R e or R f may be optionally joined to form additional rings; and any R a , R b and R c may be optionally joined to form additional rings;
X is NH 2 , OH, S—R, where R is H or optionally substituted C 1-6 alkyl; and
n is an integer from 0-3.
5 . The method of claim 4 , wherein the compound is selected from the group consisting of:
6 . The method of claim 4 , wherein the compound selectively inhibits HDAC1, HDAC2, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, HDAC9, HDAC10, HDAC11, SIRT1, SIRT2, SIRT3, SIRT4, SIRT5, SIRT6, SIRT7, and combinations thereof.
7 . The method of claim 4 , wherein the compound selectively inhibits HDAC6.
8 . The method of claim 4 , wherein the compound selectively inhibits HDAC8.
9 . The method of claim 4 , wherein the subject is a human.
10 . The method of claim 4 , wherein the disease or disorder is selected from cancer, a psychiatric disease or disorder, a neurologic disease or disorder, a neurodegenerative disease or disorder, and a neuroinflammation disease or disorder.
11 . The method of claim 4 , wherein the compound is administered to the subject orally, parenterally, intravascularly, intranasally, or intrabronchially.
12 . The method of claim 4 , further comprising: administering to the subject a therapeutically effective amount of an additional therapeutic agent for the treatment of a disease or disorder.
13 . The method of claim 12 , wherein the additional therapeutic agent is selected from the group consisting of an immunomodulatory drug, an immunotherapeutic drug, a DNA-damaging chemotherapeutic, a proteasome inhibitor, an anti-androgen receptor, an antiretroviral drug, a reverse-transcriptase inhibitor, a chemotherapeutic drug, and an immunosuppressant.
14 . A method of inhibiting HDACs in a subject, the method comprising administering to the subject a therapeutically effective amount of a compound of Formula I-A, or Formula I-B, or a salt or solvate thereof:
wherein in Formula I-A and Formula I-B:
Ring A is a 5- or 6-membered aromatic ring having 0-3 ring nitrogen atoms, and wherein Ring A may be optionally substituted with one or more R a s;
Ring B is an aromatic ring having 0-2 nitrogen atoms;
Ring C may optionally be substituted with a carbonyl group, and Ring C may optionally be substituted with one or more R c s;
each R a , R b and R c is independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , OR d , OC(═O)R d , OC(═O)OR d , OC(═O)NR d R e , CR d R e R f , CR d R e OR f , C(═O)R d , C(═O)NR d R e , C(═O)OR d , NR d R e , NR d C(═O)R e , NR d C(═O)OR e , NR d C(═O)NR e R f , NR d S(═O) 2 R e , NR d S(═O) 2 NR e R f , SR d , S(═O)R d , S(═O) 2 R d , and S(═O) 2 NR d R e , C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, wherein each C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl is optionally substituted by 1, 2, 3, 4, or 5 substituents independently selected from F, Cl, Br, I, CN, NO 2 , OR d , OC(═O)R d , OC(═O)OR d , OC(═O)NR d R e , CR d R e R f , CR d R e OR f , C(═O)R d , C(═O)NR d R e , C(═O)OR d , NR d R e , NR d C(═O)R e , NR d C(═O)OR e , NR d C(═O)NR e R f , NR d S(═O) 2 R e , NR d S(═O) 2 NR e R f , SR d , S(═O)R d , S(═O) 2 R d , and S(═O) 2 NR d R e , and wherein each R d , R e and R f is independently selected from the group consisting of H, and optionally substituted C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, and wherein any of R d , R e or R f may be optionally joined to form additional rings; and any R a , R b and R c may be optionally joined to form additional rings;
X is NH 2 , OH, S—R, where R is H or optionally substituted C 1-6 alkyl; and
n is an integer from 0-3.
15 . The method of claim 14 , wherein the compound is selected from the group consisting of:
16 . The method of claim 14 , wherein the subject has a disease or disorder selected from the group consisting of cancer, a psychiatric disease or disorder, a neurologic disease or disorder, a neurodegenerative disease or disorder, and a neuroinflammation disease or disorder.
17 . A method of immunomodulation for organ transplant, the method comprising administering to a patient a therapeutically effective amount of a compound of claim 1 .
18 . A kit for inhibiting an HDAC or for treating a disease or disorder associated with an HDAC in a subject, comprising an amount of a compound of claim 1 , or a salt or solvate thereof, and an instruction manual for the use thereof.
19 . A kit for treating a disease or disorder associated with an HDAC in a subject, comprising an amount of a compound of claim 1 , or a salt or solvate thereof, and an instruction manual for the use thereof.
20 . A probe for imaging, diagnosing, or theragnosting a disease or disorder associated with an HDAC in a subject, comprising a compound of claim 1 , or a salt or solvate thereof.