BMP inhibitors and methods of use thereof
The present invention provides small molecule inhibitors of BMP signaling. These compounds may be used to modulate cell growth, differentiation, proliferation, and apoptosis, and thus may be useful for treating diseases or conditions associated with BMP signaling, including inflammation, cardiovascular disease, hematological disease, cancer, and bone disorders, as well as for modulating cellular differentiation and/or proliferation. These compounds may also be used to reduce circulating levels of ApoB-100 or LDL and treat or prevent acquired or congenital hypercholesterolemia or hyperlipoproteinemia; diseases, disorders, or syndromes associated with defects in lipid absorption or metabolism; or diseases, disorders, or syndromes caused by hyperlipidemia.
1. A method of treating a disease or condition in a subject that would benefit from inhibition of Bone Morphogenetic Protein (BMP) signaling, comprising administering to the subject a compound having a structure of Formula I or a pharmaceutically acceptable salt, ester, or prodrug thereof,
wherein
X and Y are independently selected from CR 15 and N;
Z is selected from CR 3 and N;
Ar is selected from substituted or unsubstituted aryl and heteroaryl;
L 1 is absent or selected from substituted or unsubstituted alkyl and heteroalkyl;
G, J, K, and M are all absent or, independently for each occurrence, are selected from CR 16 and N;
A, B, and E, independently for each occurrence, are selected from CR 16 and N;
provided that:
no more than three of A, B, E, G, J, K, and M are N,
at least one of E and M is N, and
that if G, J, K, and M are absent, then the carbon atom drawn as connected to variable M is optionally substituted with R 16 ;
R 3 is selected from H, halogen, cyano, and substituted or unsubstituted alkyl, cycloalkyl, acylamino, carbamate, sulfonyl, sulfoxido, sulfamoyl, and sulfonamido;
R 4 is selected from hydroxyl, carboxyl, and substituted or unsubstituted alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, acyl, ester, alkoxyl, alkylthio, acyloxy, amino, acylamino, carbamate, amido, amidino, sulfonyl, sulfoxido, sulfamoyl, and sulfonamido;
R 15 , independently for each occurrence, is selected from H, halogen, cyano, and substituted or unsubstituted alkyl, cycloalkyl, heterocyclyl, cycloalkylalkyl, heterocyclylalkyl, acylamino, carbamate, sulfonyl, sulfoxido, sulfamoyl, and sulfonamido; and
R 16 , independently for each occurrence, is absent or is selected from H, OH, halogen, cyano, carboxyl, and substituted or unsubstituted alkyl, alkenyl, alkynyl, aralkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, heteroaralkyl, cycloalkylalkyl, heterocyclylalkyl, acyl, ester, alkoxy, alkylthio, acyloxy, amino, acylamino, carbamate, amido, amidino, sulfonyl, sulfoxido, sulfamoyl, and sulfonamide;
provided that:
i) if Ar is a phenyl ring, it is substituted with at least one non-protium ( 1 H) substituent;
ii) B is C—R 25 when E is N, or K is C—R 25 when M is N, or both, such that at least one of B and K is C—R 25 , wherein
R 25 is selected from deuterium, halogen, hydroxyl, lower alkyl, and lower alkoxy; and/or
iii) R 4 is
W is N, CH, or CCH 3 ;
R 5 is selected from H and substituted or unsubstituted alkyl, acyl, and ester; and
R 6 and R 7 are each independently H or alkyl, or
R 6 forms a one- or two-carbon bridge to the carbon atom adjacent to R 7 and NR 5 ;
wherein either W is CH or CCH 3 , or R 6 and R 7 are not both H;
wherein the disease or condition is selected from pulmonary hypertension, hereditary hemorrhagic telangiectasia syndrome, cardiac valvular malformations, cardiac structural malformations, fibrodysplasia ossificans progressiva, juvenile familial polyposis syndrome, parathyroid disease, anemia, vascular calcification, atherosclerosis, valve calcification, renal osteodystrophy, ankylosing spondylitis, vascular inflammation, anemia of inflammation, inflammatory bowel disease, seronegative spondyloarthropathies, psoriasis, atherosclerosis, tuberculosis, infections with viruses, bacteria, fungi, and parasites, breast carcinoma, prostate carcinoma, renal cell carcinoma, bone metastasis, lung metastasis, osteosarcoma, and multiple myeloma.
2. The method of claim 1 , wherein the disease or condition is selected from breast carcinoma, prostate carcinoma, renal cell carcinoma, bone metastasis, lung metastasis, osteosarcoma, and multiple myeloma.
3. The method of claim 1 , wherein the disease or condition is ankylosing spondylitis.
4. The method of claim 1 , where the disease or condition is fibrodysplasia ossificans progressiva or anemia.
5. A method of inhibiting Bone Morphogenetic Protein (BMP) signaling in a subject, comprising administering to the subject a compound having a structure of Formula I or a pharmaceutically acceptable salt, ester, or prodrug thereof,
wherein
X and Y are independently selected from CR 15 and N;
Z is selected from CR 3 and N;
Ar is selected from substituted or unsubstituted aryl and heteroaryl;
L 1 is absent or selected from substituted or unsubstituted alkyl and heteroalkyl;
G, J, K, and M are all absent or, independently for each occurrence, are selected from CR 16 and N;
A, B, and E, independently for each occurrence, are selected from CR 16 and N;
provided that:
no more than three of A, B, E, G, J, K, and M are N,
at least one of E and M is N, and
that if G, J, K, and M are absent, then the carbon atom drawn as connected to variable M is optionally substituted with R 16 ;
R 3 is selected from H, halogen, cyano, and substituted or unsubstituted alkyl, cycloalkyl, acylamino, carbamate, sulfonyl, sulfoxido, sulfamoyl, and sulfonamido;
R 4 is selected from hydroxyl, carboxyl, and substituted or unsubstituted alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, acyl, ester, alkoxyl, alkylthio, acyloxy, amino, acylamino, carbamate, amido, amidino, sulfonyl, sulfoxido, sulfamoyl, and sulfonamido;
R 15 , independently for each occurrence, is selected from H, halogen, cyano, and substituted or unsubstituted alkyl, cycloalkyl, heterocyclyl, cycloalkylalkyl, heterocyclylalkyl, acylamino, carbamate, sulfonyl, sulfoxido, sulfamoyl, and sulfonamido; and
R 16 , independently for each occurrence, is absent or is selected from H, OH, halogen, cyano, carboxyl, and substituted or unsubstituted alkyl, alkenyl, alkynyl, aralkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, heteroaralkyl, cycloalkylalkyl, heterocyclylalkyl, acyl, ester, alkoxy, alkylthio, acyloxy, amino, acylamino, carbamate, amido, amidino, sulfonyl, sulfoxido, sulfamoyl, and sulfonamide;
provided that:
i) if Ar is a phenyl ring, it is substituted with at least one non-protium ( 1 H) substituent;
ii) B is C—R 25 when E is N, or K is C—R 25 when M is N, or both, such that at least one of B and K is C—R 25 , wherein
R 25 is selected from deuterium, halogen, hydroxyl, lower alkyl, and lower alkoxy; and/or
iii) R 4 is
W is N, CH, or CCH 3 ;
R 5 is selected from H and substituted or unsubstituted alkyl, acyl, and ester; and
R 6 and R 7 are each independently H or alkyl, or
R 6 forms a one- or two-carbon bridge to the carbon atom adjacent to R 7 and NR 5 ;
wherein either W is CH or CCH 3 , or R 6 and R 7 are not both H.